Selected Species of the Cucurbitaceae Family Used in Mexico for the Treatment of Diabetes Mellitus

In Mexico, Diabetes mellitus (DM) is a serious health problem, and although the current pharmacological treatments for DM such as insulin and oral hypoglycemics are available, the Mexican population continues to use medicinal plants in the treatment of DM. The antidiabetic properties of the plant species that belong to the Cucurbitaceae family has already been recognized worldwide. Since Mexico is one of the most important centers of diversity of Cucurbitaceae, the present work contributes to the review of the most used species of Cucurbitaceae in the treatment of DM in Mexico. The reviewed species (Cucurbita ficifolia, C. maxima, C. moschata, C. pepo, Ibervillea sonorae, Sechium edule, Citrullus lanatus, Cucumis melo, and C. sativus) revealed that the antidiabetic effects exerted are effective in a number of mechanisms involved in the complex pathogenesis of DM: hypoglycemic, antioxidant, anti-inflammatory, anti-obesity, protective effects on diverse organs and cells, as well as in the control of dyslipidemias; furthermore, the select species of the Cucurbitaceae family could also be essential components of diets for the control of DM in patients with the disease. Thus, the Cucurbitaceae species selected in the present work represent a source of antidiabetic agents that perhaps establish the bases for novel clinical treatments.


Introduction
Diabetes mellitus (DM) is a chronic disease that occurs when the pancreas is no longer able to produce insulin, or when the body cannot effectively use insulin, which causes an increase in blood glucose levels. Type 1 DM (T1DM) is caused by the loss of beta cells of pancreatic islets that produce insulin, resulting in the deficiency of insulin. In the case of Type 2 DM (T2DM), the disease is caused by insulin resistance and includes approximately 90% of all DM cases [1]. According to the International Diabetes Federation (IDF) [2], approximately 463 million persons (aged between 20 and 79 years) were living with DM worldwide in 2019, and by the year 2030, this number will rise to 700 million.
The guarantee of health services for covering the increasing demand by individuals affected by DM and associated complications represent a considerable economic burden with global impact [3]. In fact, a report on the year 2020 indicates that the persistent increasing global burden of DM varies by diabetic type, region, and country. Notoriously, in these rankings, Mexico is a country that appears in the top five places in the world: the highest prevalence of DM was registered in China (89.5 million), followed by India (67.8 million), dishes and also as sweets prepared with their seeds or fruits [30]. The entire plant and the fruit are utilized in traditional medicine: for example, in the state of Hidalgo, Mexico, the fruit has been employed topically to treat worms found under the skin (such as larva migrans) [31], and the fruit macerated in water is used for the treatment of diabetes [30,32].
A number of in vitro and in vivo tests have been carried out to show the hypoglycemic effect of C. ficifolia. Román-Ramos et al. evaluated glucose tolerance in an animal model using healthy rabbits that were treated as follows: water as a control (4 mL/kg); Tolbutamide (20 mg/kg) as a reference control, and plant preparation (C. ficifolia, 4 mL/kg). C. ficifolia exhibited the greatest decrease in the area under the glucose tolerance curve (30.7%) [33]. Previous studies by the same research group showed that C. ficifolia possesses a hypoglycemic effect equal to that of Tolbutamide in healthy rabbits with temporary hyperglycemia (induced by subcutaneous administration of glucose) and in animals with moderate diabetes induced by Alloxan (fasting glucose level 150-300 mg/dL), but not in animals with severe diabetes induced by Alloxan (fasting glucose level higher than 400 mg/dL) [34]. In this model studied by Román-Ramos et al., Tolbutamide produces hypoglycemia in healthy animals, and in diabetic animals (T2DM) induced by Alloxan, which produces the release of insulin in the beta cells of the pancreas. In animals with severe Alloxan-induced diabetes (T1DM), pancreatic beta cells are not present; therefore, Tolbutamide does not produce a hypoglycemic effect. Based on the latter, it was proposed that the juice of the fruit of C. ficifolia acts only in the presence of insulin [34]. C. ficifolia, in addition to having a hypoglycemic effect in healthy rabbits and those with moderate diabetes, improves glucose tolerance in fasting healthy rabbits; thus, it is suggested that the integration of edible plants with hypoglycemic activity into the diet involves the possibility of a high effect of controlling and preventing DM.
On the other hand, a study with 10 patients with T2DM demonstrated that the administration of C. ficifolia juice, at a dose of 4 mL/kg of body weight, caused a decrease in blood glucose levels during 5 h after ingestion of the extract. These results are consistent with the hypoglycemic effect observed in studies of animals with moderately high glucose levels [35].
Other reports comprising in vivo tests indicated that the juice from the pulp of C. ficifolia was administered intraperitoneally and orally to healthy and Alloxan-induced diabetic mice. The juice administered intraperitoneally produced the greatest decrease in blood glucose in healthy and diabetic mice, even greater than Tolbutamide. Oral administration for 14 days at a dose of 1000 mg/kg of body weight per day to diabetic mice normalized glucose levels at the end of this period. At high doses (750-1250 mg/kg) administered intraperitoneally, the highest death rates of mice were recorded, opening the need for more detailed toxicological investigations [36].
Xia and Wang have conducted various investigations on the antihyperglycemic effect of the hydromethanolic extract (70%) of C. ficifolia administered in rats with diabetes induced by Streptozotocin, at a dose of 300 and 600 mg/kg of body weight per day for a 30 day period. These authors observed a significant reduction in blood glucose, glycosylated hemoglobin, and an increase in plasma insulin and total hemoglobin [37]. These same authors, in a subsequent investigation, analyzed the lipid profile and glucose tolerance of the same C. ficifolia extract, finding not only a hypoglycemic effect but also a significant decrease in triglycerides, low-density lipoproteins (LDL) and a significant increase in the high-density lipoprotein (HDL) level. They also reported a significant effect on glucose tolerance [38].
Bayat et al. [39] evaluated the effect of the C. ficifolia extract (100 g) and probiotic yogurt (150 g) alone or in combination, in a clinical trial in patients with T2DM during 8 weeks.
The results showed that C. ficifolia extract and probiotic yogurt alone or in combination, has beneficial effects on lipid profile, glycemic control, and inflammation. Additionally, the administration of the combination of C. ficifolia extract and probiotic yogurt caused a notable decrease in atherogenic lipids and lipoproteins levels, and an increase in highdensity lipoprotein cholesterol (HDL-C), suggesting a synergistic effect. However, more studies are necessary in order to determine the role of the parts of this possible synergistic effect. Finally, authors, suggested that the consumption of C. ficifolia and probiotic yogurt may help in the treatment of patients with diabetes.
In another study, the effect of an aqueous extract of C. ficifolia (200 mg/kg) on the enzymes involved in oxidative stress, glutathione disulfide (GSSG) and reduced glutathione (GSH), was investigated in mice with Streptozotocin-induced diabetes by oral administration, for 30 days. The aqueous extract of C. ficifolia in mice with diabetes significantly reduced glycemia, polydipsia, and hyperphagia and plasma lipid peroxidation. The GSH/GSSG ratio and its redox potential were restored, which explains part of the antioxidant properties of the extract. The authors support the use of the C. ficifolia extract as an alternative treatment for the control of DM, in addition to preventing complications caused by oxidative stress [40].
Bayat et al. [39] evaluated the effect of the C. ficifolia extract (100 g) and probiotic yogurt (150 g) alone or in combination, in a clinical trial in patients with T2DM during 8 weeks. The results showed that C. ficifolia extract and probiotic yogurt alone or in combination, has beneficial effects on lipid profile, glycemic control, and inflammation. Additionally, the administration of the combination of C. ficifolia extract and probiotic yogurt caused a notable decrease in atherogenic lipids and lipoproteins levels, and an increase in high-density lipoprotein cholesterol (HDL-C), suggesting a synergistic effect. However, more studies are necessary in order to determine the role of the parts of this possible synergistic effect. Finally, authors, suggested that the consumption of C. ficifolia and probiotic yogurt may help in the treatment of patients with diabetes.
In another study, the effect of an aqueous extract of C. ficifolia (200 mg/kg) on the enzymes involved in oxidative stress, glutathione disulfide (GSSG) and reduced glutathione (GSH), was investigated in mice with Streptozotocin-induced diabetes by oral administration, for 30 days. The aqueous extract of C. ficifolia in mice with diabetes significantly reduced glycemia, polydipsia, and hyperphagia and plasma lipid peroxidation. The GSH/GSSG ratio and its redox potential were restored, which explains part of the antioxidant properties of the extract. The authors support the use of the C. ficifolia extract as an alternative treatment for the control of DM, in addition to preventing complications caused by oxidative stress [40].
In 2006, Xia and Wang [41], in search of the identification of bioactive molecules, analyzed the profile of inositols and soluble carbohydrates of the hydro-methanolic extract (70%) of the fruit of C. ficifolia through its derivatization by silylation and identification and quantification by gas chromatography. The identified carbohydrates were D-chiro-inositol (DCI) (2.9 ± 0.2 mg/g), myo-inositol (7.8 ± mg/g), fagopyritols (33.6 ± 3.9 mg/g) and sucrose (126.8 ± 9.1 mg/g) [42] (Figure 1). Previous research describes inositol molecules, especially DCI, as mediators of insulin action through the administration of synthetic D-chiro-inositol (at doses of 10 and 15 mg/kg) in Streptozotocin diabetic rats, where a decrease of between 30 and 40% in the blood glucose concentration was observed [43,44]. Xia and Wang employed the extract of C. ficifolia containing 10-20 mg/kg DCI and administered it orally to Streptozotocin-induced diabetic rats. The effect of the C. ficifolia extract was favorable by significantly reducing blood glucose and increasing the levels of liver glycogen, total haemoglobin, and plasma insulin. The effect of the administration of C. ficifolia is comparable to that of synthetic DCI, therefore, the C. ficifolia extract can be considered a natural source of DCI Previous research describes inositol molecules, especially DCI, as mediators of insulin action through the administration of synthetic D-chiro-inositol (at doses of 10 and 15 mg/kg) in Streptozotocin diabetic rats, where a decrease of between 30 and 40% in the blood glucose concentration was observed [43,44]. Xia and Wang employed the extract of C. ficifolia containing 10-20 mg/kg DCI and administered it orally to Streptozotocin-induced diabetic rats. The effect of the C. ficifolia extract was favorable by significantly reducing blood glucose and increasing the levels of liver glycogen, total haemoglobin, and plasma insulin. The effect of the administration of C. ficifolia is comparable to that of synthetic DCI, therefore, the C. ficifolia extract can be considered a natural source of DCI with hypoglycemic activity. These findings suggest that the fagopyritols also found in the C. ficifolia extract could have a certain hypoglycemic effect by being hydrolyzed in the in vivo model and releasing DCI units [41]. Fagopyritols have also been identified in tartary buckwheat (Fagopyrum tataricum) and are described as having antidiabetic activity [45]; thus, they also may contribute to the bioactivity of the C. ficifolia extract.
Fortis-Barrera et al. [46] investigated the antioxidant and anti-inflammatory effect of the aqueous extract of C. ficifolia and of synthetic DCI on adipocytes. Both, the extract and the synthetic DCI reduced oxidative stress by decreasing H 2 O 2 levels, increasing glutathione peroxidase enzyme activity, and changing the GSH/GSSG ratio. DCI caused the decrease in mRNA expression and the secretion of tumor necrosis factor-alpha (TNF-α), interleukin 6 (IL-6), and resistin. On the other hand, the C. ficifolia extract gave rise to a diminution in resistin levels and an increment in IL-6 levels. Therefore, only DCI possesses an insulin-mimetic action, and the anti-inflammatory and antioxidant effect of the C. ficifolia extract can be largely explained by its DCI content. Thus, DCI may have a beneficial effect in the treatment of obesity and T2DM.
In another investigation, the anti-inflammatory and antioxidant activities of a precipitate from a fraction of the aqueous extract of the fruit of C. ficifolia with a content of 3.31 mg/g of DCI [47] were also determined in healthy and Streptozotocin-diabetic mice. The results showed similar behavior to that found by Fortis-Barrera et al. [46], where the administration of the fraction produced an increase in GSH levels and a decrease in malondialdehyde (MDA) in the liver. TNF-α levels were diminished and IL-6 and interferon-gamma (IFN-γ) levels were increased in serum. This increase observed in the mediators may be due to the inflammatory effect of Streptozotocin or as a predictor of toxicity of the extract in mice. Hence, in addition to its hypoglycemic activity, the authors describe the extract of C. ficifolia as having antioxidant and anti-inflammatory properties, suitable for the control of DM.
A later study identified the following five of the main components of the aqueous extract of C. ficifolia: p-coumaric acid, p-hydroxybenzoic acid, salicin, stigmast-7,22-dien-3ol, and stigmast-7-en-3-ol [48] (Figure 2), while DCI was not detected in the extract. The extract of C. ficifolia was administered to Alloxan-induced diabetic mice and a histological analysis of the mouse liver revealed the accumulation of glycogen. Additionally, the extract of C. ficifolia exerted a protective effect on hepatocytes due to the absence of neither necrosis nor cell alterations, that were observed in the liver tissue of the mice. In addition, an increased glycogen synthase and decreased glycogen phosphorylase were recorded; therefore, the hypoglycemic effect of this extract may be partially explained by the glycogen accumulation in the liver. Compounds such as p-coumaric acid, p-hydroxybenzoic acid, and salicin have antioxidant, anti-inflammatory and gluconeogenesis inhibitory effects reported previously, contributing to the hypoglycemic effect of the C. ficifolia extract [48]. the synthetic DCI reduced oxidative stress by decreasing H2O2 levels, increasing glu thione peroxidase enzyme activity, and changing the GSH/GSSG ratio. DCI caused t decrease in mRNA expression and the secretion of tumor necrosis factor-alpha (TNF-α interleukin 6 (IL-6), and resistin. On the other hand, the C. ficifolia extract gave rise to diminution in resistin levels and an increment in IL-6 levels. Therefore, only DCI po sesses an insulin-mimetic action, and the anti-inflammatory and antioxidant effect of t C. ficifolia extract can be largely explained by its DCI content. Thus, DCI may have beneficial effect in the treatment of obesity and T2DM.
In another investigation, the anti-inflammatory and antioxidant activities of a pr cipitate from a fraction of the aqueous extract of the fruit of C. ficifolia with a content 3.31 mg/g of DCI [47] were also determined in healthy and Streptozotocin-diabetic mi The results showed similar behavior to that found by Fortis-Barrera et al. [46], where t administration of the fraction produced an increase in GSH levels and a decrease malondialdehyde (MDA) in the liver. TNF-α levels were diminished and IL-6 and inte feron-gamma (IFN-γ) levels were increased in serum. This increase observed in the m diators may be due to the inflammatory effect of Streptozotocin or as a predictor of to icity of the extract in mice. Hence, in addition to its hypoglycemic activity, the autho describe the extract of C. ficifolia as having antioxidant and anti-inflammatory properti suitable for the control of DM.
A later study identified the following five of the main components of the aqueo extract of C. ficifolia: p-coumaric acid, p-hydroxybenzoic acid, salicin, sti mast-7,22-dien-3-ol, and stigmast-7-en-3-ol [48] (Figure 2), while DCI was not detected the extract. The extract of C. ficifolia was administered to Alloxan-induced diabetic mi and a histological analysis of the mouse liver revealed the accumulation of glycoge Additionally, the extract of C. ficifolia exerted a protective effect on hepatocytes due to t absence of neither necrosis nor cell alterations, that were observed in the liver tissue the mice. In addition, an increased glycogen synthase and decreased glycogen pho phorylase were recorded; therefore, the hypoglycemic effect of this extract may be pa tially explained by the glycogen accumulation in the liver. Compounds such p-coumaric acid, p-hydroxybenzoic acid, and salicin have antioxidant, anti-inflammato and gluconeogenesis inhibitory effects reported previously, contributing to the hyp glycemic effect of the C. ficifolia extract [48].  Therefore, since the antidiabetic activity is related to the antioxidant and anti -inflammatory process, Table 1 presents the bioactive molecules identified in the extracts of C. ficifolia with multiple actions that could be useful in the treatment of DM. Table 1. Evaluation of the hypoglycemic, antioxidant and anti-inflammatory effects of the molecules isolated from different extracts of the fruit of C. ficifolia.

Cucurbita Maxima Duchesne
Cucurbita maxima is native to the Americas and was cultivated by the ancient civilizations of Central and South America more than 7000 years ago. Other varieties can be found in Australia, Africa (Zambia, Nigeria, and Zimbabwe), Asia (China, India, Iran, Afghanistan), and Europe (Spain and Turkey) [49,50]. It is known as winter squash, butternut squash, kalabazeam maboga, zapallo, parangi, giromon, cocozza [51], giant pumpkin, hubbard squash, kabocha squash or pumpkin [30]. Traditionally, the leaves, fruits and seeds are used to treat various ailments. The seeds are consumed orally for the treatment of intestinal worms, parasites [52,53], constipation [52], kidney problems [54], and prostatitis [55]. The leaves have been utilized for the treatment of anemia [56] and head and lung cancer [57]. Oral consumption of the fruit in traditional medicine for the treatment of urinary disorders [54], blood pressure control, and constipation has been recorded [58]. In Mexico, China, and Iran the juice of the fruit of C. maxima is employed for control of the blood glucose level [30,59].
Several investigations have been conducted to characterize the bioactivity of the flowers, seeds, and fruit of C. maxima. Among these studies, its antimicrobial, antioxidant [60] anti-inflammatory [61,62], cytotoxic [63] and antidiabetic [64] activity stands out.
In vitro, in vivo, and patient trials have been developed to determine the antidiabetic effect of extracts from leaves, flowers, and seeds of C. maxima. Some approaches for the treatment of T2DM focus on the decrease of the postprandial hyperglycemia effect. Inhibition of the enzymes responsible for hydrolyzing carbohydrates, such as α-glucosidase and α-amylase, contributes to the control of postprandial hyperglycemia [65]. Al-Shaheen et al. [64] evaluated the antioxidant and the inhibitory capacity in the α-amylase enzyme of the methanolic extract of C. maxima leaves. The extract was shown to have detectable and higher antioxidant activity than the positive controls (BHT, BHA and vitamin C), with an IC 50 value of 125 µg/mL. Similarly, the extract exhibited the potential to inhibit the enzyme α-amylase by 97.01% at a concentration of 100 mg/mL and an IC 50 value of 2.1 mg/mL.
In another research, in vitro tests also demonstrated the inhibitory activity of the aqueous extract of the seeds of C. maxima in the enzymes α-glucosidase and α-amylase, with IC 50 values of 8.11 ± 0.36 mg/mL and 7.00 ± 0.29 mg/mL, respectively. Additionally, phytoelements such as Mg, Ca, Na and, K, which have been shown to inhibit the enzymes α-glucosidase and α-amylase, were detected in the aqueous extract of the seeds, where they probably contributed to the hypoglycemic effect of the extract [66].
The methanolic extract of the flowers of C. maxima possess an inhibitory effect on the enzyme α-glucosidase with an IC 50 value of 610.52 ± 60.33 µg/mL. In this same study, the neu-roprotective, hepatoprotective, and antihypertensive effect of the methanolic extract of the flowers of C. maxima was evaluated by inhibiting the enzymes acetylcholinesterase (AChE, IC 50 = 460.78 ± 6.01 µg/mL), β-glucuronidase (64.69% ± 1.29 inhibition at 500 µg/mL), and the angiotensin converting enzyme (ACE, 46.63% ± 1.15 inhibition at 15 µg/mL). Thus, the methanolic extract of the flowers of C. maxima demonstrated antidiabetic, neuroprotective, and antihypertensive potential. Some of the most conspicuous phytochemicals of the extract were identified by gas chromatography, and included, nine organic acids, seven sugars and sugar alcohols, four amino acids, four fatty acids, and porphine [67] (Figure 3).
Molecules 2022, 27, x FOR PEER REVIEW 9 of 38 be involved in the stabilizing effect of the hepatocyte membrane and antioxidant activity that decrease the oxidative stress generated by diabetes. Other identified compounds include fatty acids, amino acids, alkaloids, disaccharides, terpenes, phytosterols, and saponins ( Figure 4), which probably present a synergistic effect to protect against the liver and pancreatic damage caused by diabetes [71].  In vivo tests have been carried out with extracts from different parts of C. maxima, which have shown a hypoglycemic effect. Lal et al. evaluated the hypoglycemic effect of the fruit juice and the hydroethanolic extract of the aerial parts in Streptozotocin induced diabetic rats at a dose of 100 and 200 mg/kg for 28 days. The extract showed a higher hypoglycemic effect than the juice [68]. Similarly, in another study, the methanolic extract of the aerial parts of C. maxima was shown to have a hypoglycemic effect at 200 and 400 mg/kg administered to Streptozotocin induced diabetic rats for 14 days. The extract also revealed an antioxidant effect by increasing the enzyme GHS and catalase (CAT) and generated a protective effect by decreasing the levels of the enzymes glutamic oxaloacetic transaminase (SGOT), serum glutamine pyruvic transaminase (SGPT), and alkaline phosphatase (ALP), which were elevated in the control group of rats with diabetes. The antioxidant and antidiabetic effect of the extract was explained by the presence of polyphenols or polysaccharides in the extract [69].
Hepatoprotective potential was exhibited for the methanolic extract of the seeds [70] and the fruit [71] of C. maxima. The extract of the seeds was shown to prevent liver damage caused by diabetes, where a decrease in the levels of AST (aspartate aminotransferase), ALT (alanine aminotransferase), and ALP (alkaline phosphatase) was found. The methanolic extract of the seeds was also shown to have a renal protective effect by the decrease of creatinine (CRTN) levels and the increase of hemoglobin (Hb) and total protein (TPR) levels in diabetic rats. Concerning the methanolic extract of the fruit of C. maxima, it was also shown to have a protective effect on the pancreas against damage caused by diabetes. This hepatoprotective effect was determined by histopathological examination of the pancreatic islet cells from diabetic rats, in which, the disappearance of severe degenerative and necrotic changes in pancreatic cells was observed. Analysis by gas chromatography coupled to mass spectrometry revealed the presence of flavonoids such as vitexin and other flavone C-glycosides, carotenoids, and polyphenols, which may be involved in the stabilizing effect of the hepatocyte membrane and antioxidant activity that decrease the oxidative stress generated by diabetes. Other identified compounds include fatty acids, amino acids, alkaloids, disaccharides, terpenes, phytosterols, and saponins ( Figure 4), which probably present a synergistic effect to protect against the liver and pancreatic damage caused by diabetes [71].
On the other hand, the hypoglycemic and antihyperlipidemic effect of petroleum ether, ethyl acetate and ethanolic extracts from the seeds of C. maxima in Streptozotocin induced diabetic rats was investigated [72]. All extracts, especially the ethanolic extract, exhibited a hypoglycemic and antihyperlipidemic effect. The oral administration of 200 mg/kg of extracts for 21 days potentiated an increase in insulin and HDL-cholesterol levels, while total cholesterol (TC), LDL, VLDV, and triglycerid (TG) levels decreased in the blood serum. In these in vivo tests, no death of any animal was reported at the administered concentrations, indicating the non-toxicity effect of the C. maxima extracts.
The hypoglycemic effect of the lyophilized fruit juice of C. maxima was evaluated in a clinical trial. A group of 20 patients, in which 12 were patients with T1DM, and eight patients with T2DM, were orally administrated with 5g of the lyophilized fruit juice every 12 h for 3 days. The lyophilized fruit juice of C. maxima showed a significant reduction in the blood glucose level and was rapid and effective, without presenting adverse effects [59].

Cucurbita Moschata Duchesne
Archaeological evidence indicates that the possible territories where C. moschata was domesticated are localized in Mexico (about 5000 B.C.), Peru (3000 B.C.) or Guatemala (2000 B.C.) [50]. Currently, C. moschata is widely distributed in Asia, America, and Africa [73]. Common names for C. moschata include butternut squash, pumpkin, cheese pumpkin, golden cushaw, Japanese pumpkin, melon squash, musky gourd, musky pumpkin, musky squash, musky winter squash, seminole pumpkin, tropical pumpkin, winter crookneck squash, winter marrow, winter pumpkin, winter squash, and winter straightneck squash [74]. C. moschata is used to prepare a variety of traditional dishes, but is also utilized in traditional medicine. The seeds are employed to relieve kidney affections, as an antiparasitic, and in the treatment of intestinal infections. The flowers are used topically to soothe minor wounds [74,75]. In China, the seeds of C. moschata are officially prescribed by traditional medicine for the treatment of DM [76]. Research on the bioactivity of C. moschata reveals that polysaccharides exhibit antioxidant [60], antibacterial [77], anti-obesity [78], antitumoral [79], antiparasitic [80], and hypoglycemic effects [81,82]. A number of studies have been carried out to delve into the antidiabetic properties of the fruits, flowers and stems of C. moschata. Several reports showed that hypoglycemic activity has been related to the carbohydrate content (Table 2).
Other evidence of the hypoglycemic effect of the C. moschata extract was shown by Zhang et al. [85]. These authors investigated the effect of the administration of a fraction of water-soluble carbohydrates obtained from the hydroethanolic extract (80%) of the C. moschata fruit in Alloxan-induced diabetic rabbits in a dose of 75 mg/kg for 21 days. The results indicated that this polysaccharide fraction improves the body-weight loss of rabbits and also a reduction in the levels of blood glucose (BG), total cholesterol (TC), triglycerides, and glycated hemoglobin (HbA1c) were observed. Additionally, in the analysis of the pancreatic tissue, the water-soluble carbohydrate fraction exerted the regeneration of damaged pancreatic islets by stimulating β-cell proliferation. The chemical analysis of this polysaccharide fraction revealed the presence of glucose, galactose, arabinose, rhamnose, and a small amount of hexuronic acid.
Chang et al. [86] reported some components of the stem of C. moschata and the hypoglycemic effect and the mechanism of action. Ten compounds from two fractions of the methanolic extract of the stem of C. moschata that presented hypoglycemic activity in Streptozotocin-induced diabetic mice were identified. These compounds include apocarotenoids (loliolide); phenolics [2-hydroxybenzoic acid; 4-hydroxycinnamic acid; fer-  Figure 5. Steroid compounds 24-methyl-6β-methoxy-5α-cholesta-7,22-diene-3β,5-diol, and 3β-hydroxy-(22E,24R)-ergosta-5,8,22-trien-7-one promoted glucose uptake in normal hepatocytes in a similar way to that of insulin. The mechanism of action of these compounds may be mediated by AMPK activation. On the other hand, despite the structural difference of compounds ferulic acid, syringaresinol, and 24-methyl-6β-methoxy-5α-cholesta-7,22-diene-3β,5-diol, they showed an insulin-sensitization and/or insulin-substitution function in insulin-resistant cells. Thus, the stem of C. moschata contains compounds with the potential to control T1 or T2DM [86]. The hypoglycemic effect of the fruit of C. moschata has also been demonstrated for the seeds. Marbun et al. [87] reported the antidiabetic activity of the ethanolic extract of the seeds and pulp of C. moschata, which was comparable to the effect of Metformin in Streptozotocin-induced diabetic mice. Preliminary tests revealed the presence of flavonoids, terpenes, saponins, and tannins in both extracts.

Cucurbita pepo L.
C. pepo is a Cucurbitaceae known as pumpkin that has been part of the human diet for more than 10,000 years and that possesses the oldest record of domesticated Mesoamerican species, over other members of the Cucurbitaceae family such as C. moschata, C. argyrosperma, and Lagenaria siceraria. Recent data suggested that pre-Columbian Mexican civilizations probably cultivated cucurbits prior to corn [88]. C. pepo is native to Mexico and today is cultivated in association with other plants as part of the cultivated corn field (milpa) or as a single crop [89]. The flowers and fruits are consumed in Mexico through the preparation of candies, cakes, or traditional dishes [90]. In traditional medicine, C. pepo had been used largely in a number of countries around the world as a diuretic and antihelminthic. However, one of the most common uses is in the treatment of irritable bladder for enlarged prostate-gland and micturition problems. Nonetheless, even these treatments with C. pepo seeds diminish micturition, it has not very effective in reducing the expanded size of the prostate gland [91].

Cucurbita pepo L.
C. pepo is a Cucurbitaceae known as pumpkin that has been part of the human diet for more than 10,000 years and that possesses the oldest record of domesticated Mesoamerican species, over other members of the Cucurbitaceae family such as C. moschata, C. argyrosperma, and Lagenaria siceraria. Recent data suggested that pre-Columbian Mexican civilizations probably cultivated cucurbits prior to corn [88]. C. pepo is native to Mexico and today is cultivated in association with other plants as part of the cultivated corn field (milpa) or as a single crop [89]. The flowers and fruits are consumed in Mexico through the preparation of candies, cakes, or traditional dishes [90]. In traditional medicine, C. pepo had been used largely in a number of countries around the world as a diuretic and antihelminthic. However, one of the most common uses is in the treatment of irritable bladder for enlarged prostate-gland and micturition problems. Nonetheless, even these treatments with C. pepo seeds diminish micturition, it has not very effective in reducing the expanded size of the prostate gland [91].
Regarding the phytochemicals reported in C. pepo, the fruit is characterized by a high total carotenoid content of 171.9 to 461.9 µg·g −1 , but also by a low content of fat (2.3%), and a poor polyphenol content, which was calculated as 0.02 mg GAE/100 mg sample by fresh fruit [92]. Nevertheless, 57 phenolics and other polar compounds were identified by HPLC coupled with two different detection systems: diode array (DAD) and quadrupole time-of-flight (Q-TOF) mass spectrometry. These phenolics were grouped as hydroxycinnamic acids and derivatives, hydroxybenzoic acids and derivatives, flavones and glycosides, flavonols and glycosides, organic acids and derivatives, amino-acids and derivatives, and nucleosides [93]. Studies on the chemicals present in the seeds of C. pepo are numerous and varied. Some variations in the composition of the main chemicals in the seeds have been detected. However, the seeds of pumpkin content are approximately 50% oil and are a good source of phytosterols, carotenoids, fatty acids, and vitamins. The seeds of C. pepo have been characterized by their tocopherol content, where γ-tocopherol is more abundant than α-tocopherol. The oils of seeds contain phenolics such as tyrosol, vanillic acid, vanillin, luteolin, and sinapic acid, where tyrosol was the most abundant compound detected in an amount of 1.6 mg/kg to 17.7 mg/kg [94]. Other reports found that p-hydroxybenzoic acid was the most conspicuous phenolic acid in all parts of the seeds of C. pepo, such as kernels and the hulls [51]. The main fatty acids reported in the pumpkin seeds are oleic, linoleic, linolenic, palmitic, and stearic acids, while among the most conspicuous carotenoids, we find lutein, α-carotene, β-carotene, auroxanthin, flavoxanthin, luteoxanthin, β-carotene violxanthin [92]. The terpenes found in the C. pepo seeds were studied by Kikuchi et al. [95], who reported the presence of 3-p-aminobenzoyl multifloranetype triterpenes, 7-epi zucchini factor A and debenzoyl zucchini factor B. Additionally, five malutiflorane-type triterpenoids, two new ent-kaurane diterpene glycosides; and a new steroid, (24S)-stigmasta-7,22E,25-trien-3-one, were identified ( Figure 6). From the sprouts of C. pepo, two novel multiflorane p-aminobenzoates were isolated: 7-epi zucchini factor A (1b) and debenzoyl zucchini factor B. None of these compounds were found in adult plants [96]. However, the triterpene squalene is one of the most conspicuous in pumpkin seeds and has been employed as a marker. Squalene has also been recognized to possess anticancer, antibacterial, and antifungal properties and plays an important role in the metabolism of cholesterol and steroid hormones [97]. The sterols are another group of compounds that are considered as prominent in C. pepo, particularly ∆7 and ∆5 sterols. ∆ stigmastatrienol and ∆ spinasterol have been considered as the main sterols isolated in seeds of C. pepo, followed by ∆ stigmasterol, stigmastadienol, and β-sitosterol [98]. Regarding the phytochemicals reported in C. pepo, the fruit is characterized by a high total carotenoid content of 171.9 to 461.9 µg·g −1 , but also by a low content of fat (2.3%), and a poor polyphenol content, which was calculated as 0.02 mg GAE/100 mg sample by fresh fruit [92]. Nevertheless, 57 phenolics and other polar compounds were identified by HPLC coupled with two different detection systems: diode array (DAD) and quadrupole time-of-flight (Q-TOF) mass spectrometry. These phenolics were grouped as hydroxycinnamic acids and derivatives, hydroxybenzoic acids and derivatives, flavones and glycosides, flavonols and glycosides, organic acids and derivatives, amino-acids and derivatives, and nucleosides [93]. Studies on the chemicals present in the seeds of C. pepo are numerous and varied. Some variations in the composition of the main chemicals in the seeds have been detected. However, the seeds of pumpkin content are approximately 50% oil and are a good source of phytosterols, carotenoids, fatty acids, and vitamins. The seeds of C. pepo have been characterized by their tocopherol content, where γ-tocopherol is more abundant than α-tocopherol. The oils of seeds contain phenolics such as tyrosol, vanillic acid, vanillin, luteolin, and sinapic acid, where tyrosol was the most abundant compound detected in an amount of 1.6 mg/kg to 17.7 mg/kg [94]. Other reports found that p-hydroxybenzoic acid was the most conspicuous phenolic acid in all parts of the seeds of C. pepo, such as kernels and the hulls [51]. The main fatty acids reported in the pumpkin seeds are oleic, linoleic, linolenic, palmitic ,and stearic acids, while among the most conspicuous carotenoids, we find lutein, α-carotene, β-carotene, auroxanthin, flavoxanthin, luteoxanthin, β-carotene violxanthin [92]. The terpenes found in the C. pepo seeds were studied by Kikuchi et al. [95], who reported the presence of 3-p-aminobenzoyl multiflorane-type triterpenes, 7-epi zucchini factor A and debenzoyl zucchini factor B. Additionally, five malutiflorane-type triterpenoids, two new ent-kaurane diterpene glycosides; and a new steroid, (24S)-stigmasta-7,22E,25-trien-3-one, were identified ( Figure 6). From the sprouts of C. pepo, two novel multiflorane p-aminobenzoates were isolated: 7-epi zucchini factor A (1b) and debenzoyl zucchini factor B. None of these compounds were found in adult plants [96]. However, the triterpene squalene is one of the most conspicuous in pumpkin seeds and has been employed as a marker. Squalene has also been recognized to possess anticancer, antibacterial, and antifungal properties and plays an important role in the metabolism of cholesterol and steroid hormones [97]. The sterols are another group of compounds that are considered as prominent in C. pepo, particularly Δ7 and Δ5 sterols. Δ stigmastatrienol and Δ spinasterol have been considered as the main sterols isolated in seeds of C. pepo, followed by Δ stigmasterol, stigmastadienol, and β-sitosterol [98].  On the other hand, some pharmacological properties of pumpkin have been reported, such as antimicrobial, hepatoprotective, lipid lowering, antioxidant, antihypertension, antiinflammatory, and antidiabetic properties [99]. However, these latter antidiabetic properties have been acquiring relevance in recent years, because of the traditional use of C. pepo in the treatment of DM in Mexico, in which local healers recommend the ingestion of crude aqueous extracts of pumpkin, which represents a source which is available for the entire population; therefore, it comprises an alternative treatment for the growing population that suffers from DM, especially in Mexico.
The hypoglycemic activity (blood sugar lowering) of C. pepo extracts was demonstrated in Alloxan-induced diabetic rats and rabbits, and interestingly, these active hypoglycemic properties of pumpkin were identified in the pulp and seed extracts, in contrast with those of the leaves and stems [99]. Pumpkin powder was administrated during 4 weeks to Alloxan-induced diabetic rats, where the results showed a significant reduction in the levels of glucose, cholesterol, triglycerides, low density lipoprotein (LDL) and C-reactive protein (CRP) levels. However, even the pumpkin powder increased the levels of blood insulin and high density lipoprotein (HDL), though not significantly. The histological analysis evidenced the restoration of the pancreatic tissue caused by the administration of the pumpkin powder, due to the increase in the diameter and number of the Langerhans islets observed in rats fed with pumpkin [100].
Other studies revealed that the antidiabetic properties of pumpkin have been observed through the antioxidant activities of the raw fruit of the pumpkin. Especially, the content of tocopherols was attractive due to its already known high antioxidant properties. Therefore, Bharti et al. [101] determined the content of tocopherol in the seeds of pumpkin by HPLC (107.4 ± 2.9 mg/100 g) and tested this on diabetic rats. In addition to glycemic profile, a variety of criteria to establish the possible impact of tocopherols on the physiology of DM was included in those investigations, such as insulinemic and lipidic profiles; histological studies; molecular docking investigations; endogenous enzymatic and nonenzymatic antioxidant levels, and GLP-1 content in the cecum. The results indicated that tocopherol induced a significant glucose lowering together with a reduction of insulinemia and a decrease in insulin resistance at the higher dose employed (5 g/kg body weight). However, the tocopherol did not exhibit benefits in the lipidic profiles. Concerning the histological studies, tocopherol induced a significant improvement in the number of pancreatic islets as well as in the grade of insulitis. In the docking studies, the tocopherol isomers exhibited considerable interaction in the active sites of the proteins. A notable reduction was also observed in the oxidative markers such as SOD, catalase, GST, TBARS, total thiols, and GSH. Finally, a remarkable increase of GLP-1 content in the cecum by the administration of tocopherol was recorded in diabetic rats along with cecal-tissue enlargement.
On the other hand, polysaccharides have been identified as crucial for the hypoglycemic properties of pumpkin. In the case of protein-bound polysaccharide (PBPP) isolated from the aqueous extract of pumpkin fruit, this showed a dose-dependent hypoglycemic effect, because of the marked effect exhibited by the dose of 1000 mg/kg when administrated in diabetic rats, over the 500 mg/kg dose, and also because of the comparison with the control group (Glibenclamide). The PBPP from pumpkin was able to increase the levels of insulin in serum and also stimulate pancreatic cells. With these characteristics, PBPP may be able to be considered as a future novel antidiabetic agent [102]. Fractions with a content of polysaccharides from pumpkin powder were able to significantly reduce the blood glucose levels in diabetic mice, but were not able to stimulate cells in the islets of Langerhans. However, pumpkin polysaccharides may play an important role in the recovery of liver function and glucose utilization. The most active fraction of polysaccharides was made up of four monosaccharides, including glucose, galactose, arabinose, and rhamnose in a proportion of 2.0:1.0:1.5:2.5 [84].
Another work reported the extraction of a polysaccharide denominated PP-PE with a molecular weight of 2.4 × 10 4 , and composed of α-(1→6)-glucan branched at the C3 position and α-(1→4)-galactan, obtained by the hot water extraction of C. pepo. This PP-PE was tested for in vivo antidiabetic activities in Alloxan-diabetic mice (a dose of 100 mg/kg/day), and in in vitro assays for measuring α-glucosidase inhibitory activity and α-amylase inhibitory activity. The results revealed that the blood glucose level decreased after 7 days of PP-PE treatment and a normal histological structure of β-cells at the central zone in the islet of Langerhans was also observed. In the in vitro tests, the PP-PE was able to inhibit α-glucosidase and α-amylase activities, and the IC 50 values were calculated as 110.32 ± 7.08 and 103.06 ± 1.60 mg/mL, respectively. Hence, C. pepo could be considered as promising in the treatments of diabetes [103].
The hypoglycemic properties of pumpkin have been reported mostly in experimental animals, but also some reports indicated the possible hypoglycemic effect of pumpkin in humans, in patients with T1DM and T2DM [104]. In addition to this, the consumption of pumpkin as a dietary component and as a source of fiber has been analyzed not only in the treatment of DM, but also to prevent the risk of other diseases such as obesity, atherosclerosis, heart diseases, colon cancer, and colorectal cancer. From the nutritional and industrial perspective, pumpkins are attractive due to the fact that they are a good source of carotenoids, pectin, mineral salts, and vitamins. Recent studies propose that the raw materials of pumpkin can be useful to produce pumpkin flour for enriching food with by a high content of dietary fiber. In this respect, pumpkin emerges as a cucurbit that is useful not only from the pharmacological perspective for the treatment of DM, but also as a central dietary component in diabetic population [105].

Ibervillea sonorae (S. Watson) Greene
Ibervillea sonorae, known as wareke o wereke, is a perennial plant distributed in the northern states of Mexico, including Sinaloa, Sonora, and Baja California, and the southern regions of the U.S. Some indigenous tribes of that Mexican region, such as the Mayo, Opata, Seri, and Yaqui, have traditionally used wareke for the treatment of skin diseases. Nevertheless, since pre-Hispanic times, knowledge about its empirical use for minor skin infections, arthritis, rheumatism, and heart conditions have been recorded [106].
In the 20th century, different activities have been found in the extracts of the roots, probably because these organs are the most notorious parts of I. sonorae, exhibiting a tuberculous appearance (root tuber) that is usually marketed. In 1993, Domínguez et al. [107,108] described the first formulas of the main chemical components of these tuberous roots of I. sonorae, describing the isolation and characterization of six compounds of the type of the cucurbitan series of tetracyclic system of 3-glycosides-tetramethyl-19-norpregnenedione-17-2,3,6,-trihydroxy-6-methyl cucurbitacin Kinoin A and Cucurbitacin B; Kinoin A and B glycosides; hexanorcucurbitacin Kinoin C [3a,16adihydroxy-4,4,9,14-tetramethyl-(9~,10~)-19-norp~gn-5-ene-l 1,20-dione] and Kinoin C triterpenes (Figure 7). These cucurbitacins were named in honor of Father Quino, an Austrian-Italian Jesuit missionary, explorer, cartographer, geographer, and astronomer, distinguished among the indigenous people in the present area of northwestern Mexico and in the southwestern U.S. for his methods of evangelization, the founder of 20 missions, and known for his ability to establish relationships between indigenous people and the religious institutions that he represented [107].
In recent decades, a number of reports have pointed out that the wereke were extensively utilized in the traditional medicine of the State of Sonora, Mexico, in a variety of uses such as a topical antibiotic, cathartic, antirheumatic, antidiabetic, and as anticancer. Particularly, this latter activity motivated Torres-Moreno et al. [109] to isolate the secondary metabolites cucurbitan-type triterpenes, Kinoin A and 3β−(2-O-α-L-rhamnosylβ-D-glucosyl) (Kinoin B), to establish the antiproliferative and induction of cell death by apoptotic activities. In recent decades, a number of reports have pointed out that the wereke were extensively utilized in the traditional medicine of the State of Sonora, Mexico, in a variety of uses such as a topical antibiotic, cathartic, antirheumatic, antidiabetic, and as anticancer. Particularly, this latter activity motivated Torres-Moreno et al. [109] to isolate the secondary metabolites cucurbitan-type triterpenes, Kinoin A and 3β−(2-O-α-L-rhamnosyl-β-D-glucosyl) (Kinoin B), to establish the antiproliferative and induction of cell death by apoptotic activities.
Other studies found that wereke has anticancer potential, in that it possesses a cytotoxic effect on T47D cancer cell lines [110] due the presence of cucurbitan-type triterpene glycosides. The isolation of Cucurbitacin IIb and the effect of the reduction in the growth of cancer cells, as well as the induction of apoptosis in HeLA and A549 at low doses, were reported by Robles-Zepeda et al. [111]. The structural differences of Cucurbitacin IIb with the less active Kinoin A and Kinoin B diglycoside, were the subject of study, where the presence in the molecule at position 2 of a hydroxyl group with β orientation, was found to enhance antiproliferative activity [112]. Recently, Zepeda et al. [113] were able to use the roots of I. sonorae in the therapy of some cancers. These authors prepared and tested two phytopreparations, Phyto-ison-EtOH and Phyto-ison-AcOEt, measuring their antiproliferative properties. From Phyto-ison-EtOH a new cucurbitacin (25-anhydro-Kinoin A diglycoside) was isolated and characterized, together with active CIIb and the diglycoside of Kinoin B. By means of experiments with the APCI-IT MsN of the two phytopreparations, the presence of Kinoin A, 3-glucoside Kinoin B and 3-diglycoside Kinoin A was also detected.
On the other hand, antibiotic, antifungal, anti-inflammatory, and antiviral properties are also attributed to wereke [30,114]. Martínez Vázquez et al. [115] isolated and characterized a new octanocucurbitacin-type triterpene (Kinoin D) with anti-inflammatory activity from the extract with ethyl acetate and the other compounds already isolated from I. sonorae (Figure 8). Sinagawa-Garcia et al. [116] carried out a bromatological analysis that indicated the nutritional composition of wereke roots. In Other studies found that wereke has anticancer potential, in that it possesses a cytotoxic effect on T47D cancer cell lines [110] due the presence of cucurbitan-type triterpene glycosides. The isolation of Cucurbitacin IIb and the effect of the reduction in the growth of cancer cells, as well as the induction of apoptosis in HeLA and A549 at low doses, were reported by Robles-Zepeda et al. [111]. The structural differences of Cucurbitacin IIb with the less active Kinoin A and Kinoin B diglycoside, were the subject of study, where the presence in the molecule at position 2 of a hydroxyl group with β orientation, was found to enhance antiproliferative activity [112]. Recently, Zepeda et al. [113] were able to use the roots of I. sonorae in the therapy of some cancers. These authors prepared and tested two phytopreparations, Phyto-ison-EtOH and Phyto-ison-AcOEt, measuring their antiproliferative properties. From Phyto-ison-EtOH a new cucurbitacin (25-anhydro-Kinoin A diglycoside) was isolated and characterized, together with active CIIb and the diglycoside of Kinoin B. By means of experiments with the APCI-IT MsN of the two phytopreparations, the presence of Kinoin A, 3-glucoside Kinoin B and 3-diglycoside Kinoin A was also detected.
On the other hand, antibiotic, antifungal, anti-inflammatory, and antiviral properties are also attributed to wereke [30,114]. Martínez Vázquez et al. [115] isolated and characterized a new octanocucurbitacin-type triterpene (Kinoin D) with anti-inflammatory activity from the extract with ethyl acetate and the other compounds already isolated from I. sonorae (Figure 8). Sinagawa-Garcia et al. [116] carried out a bromatological analysis that indicated the nutritional composition of wereke roots. In which the presence of an active proteinase at alkaline pH and the inhibitory activity of trypsin were reported, to our knowledge for the first time, in wereke. which the presence of an active proteinase at alkaline pH and the inhibitory activity of trypsin were reported, to our knowledge for the first time, in wereke. Nonetheless, in the 20th century, the decoction of wereke roots became one of the most used remedies in Mexico for the treatment of DM, not only in the northern region of Mexico, but also extending through the country. The series of works conducted by Alarcón- Aguilar et al. (2002Aguilar et al. ( -2007 [117][118][119] showed that the aqueous decoction of I. sonorae roots reduces the blood sugar concentration, validating the traditional use of the plant. Hence, according to the first of these works, the freeze-dried decoction (traditional preparation) of I. sonorae decreases the blood glucose levels in healthy mice and mild Alloxan-diabetic mice and rats. However, no changes in the levels of hyperglycemia were observed in severe Alloxan-diabetic rats [117]. In the second study, wareque root was administered, as in the traditional preparation, as the raw extract (juice), as the dichlormethane extract, and as a methanolic extract in a model of acute and chronic administration. At a dose of 600 mg/kg, the traditional preparation, the raw extract and the methanolic extract caused significant reductions of glycemia in healthy mice after intraperitoneal administration. However, the dichlormethane extract caused severe hypoglycemia that produced lethality in all of the animals treated with the same dose. Consequently, the dichlormethane extract was administered at a dose of 300 mg/kg to diabetic rats for 41 days. The levels of total cholesterol and uric acid did not exhibit any change, while the levels of glycemia, body weight, and triglycerides were incremented in comparison with those of the diabetic control group [118]. In the third work of the series, from the wereke roots, 11 compounds were isolated of the monoglycerides type, in addition to five fatty Nonetheless, in the 20th century, the decoction of wereke roots became one of the most used remedies in Mexico for the treatment of DM, not only in the northern region of Mexico, but also extending through the country. The series of works conducted by Alarcón- Aguilar et al. (2002Aguilar et al. ( -2007 [117][118][119] showed that the aqueous decoction of I. sonorae roots reduces the blood sugar concentration, validating the traditional use of the plant. Hence, according to the first of these works, the freeze-dried decoction (traditional preparation) of I. sonorae decreases the blood glucose levels in healthy mice and mild Alloxan-diabetic mice and rats. However, no changes in the levels of hyperglycemia were observed in severe Alloxan-diabetic rats [117]. In the second study, wareque root was administered, as in the traditional preparation, as the raw extract (juice), as the dichlormethane extract, and as a methanolic extract in a model of acute and chronic administration. At a dose of 600 mg/kg, the traditional preparation, the raw extract and the methanolic extract caused significant reductions of glycemia in healthy mice after intraperitoneal administration. However, the dichlormethane extract caused severe hypoglycemia that produced lethality in all of the animals treated with the same dose. Consequently, the dichlormethane extract was administered at a dose of 300 mg/kg to diabetic rats for 41 days. The levels of total cholesterol and uric acid did not exhibit any change, while the levels of glycemia, body weight, and triglycerides were incremented in comparison with those of the diabetic control group [118]. In the third work of the series, from the wereke roots, 11 compounds were isolated of the monoglycerides type, in addition to five fatty acids that showed hypoglycemic effects when administered in different mixtures to healthy and Alloxaninduced diabetic mice (Figure 9). acids that showed hypoglycemic effects when administered in different mixtures to healthy and Alloxan-induced diabetic mice (Figure 9). Hypoglycemic and anti-obesity effects were caused by the aqueous extract of I. sonorae incorporated into the diet of the mice. The wereke extract also promoted a decrease in food intake with a subsequent decrease in the body weight, and a decrease in obesity levels in mice treated with prepared diets [120]. In a different investigation, Zapata Bustos et al. [121] demonstrated that the aqueous extracts of the tuberous roots of I. sonorae induce the consumption of glucose in human adipocytes, which is the mechanism by which these roots have antidiabetic properties. In this work, the presence of flavonoids, phenolic compounds, and high amounts of gallic acid were detected. From another point of view, in recent years, the anti-hyperglycemic mechanisms of I. sonorae were studied by enzymatic inhibition studies that revealed that the aqueous extract of I. sonorae was able to inhibit the enzyme α-glucosidase in a concentration-dependent manner and competitive inhibition. Additionally, the wereke aqueous extract stimulates insulin secretion in vitro from RIN-m5F pancreatic β cells, which allows the proposal of the use of I. sonorae as a supplement in order to control the glucose blood levels of patients, as an alternative to combat the potential contraindications of wereke [122].
Estrada-Zúñiga et al. [123] established the culture of calluses from explants of I. sonorae leaves and determined the amounts of stearic, palmitic, lauric, myristic, pentadecanoic fatty acids, and the content of phenolic compounds. In terms of the complex chemical composition of these tubers, ketones, alkanes and amides, palmitic acid, and methyl palmitate, are noteworthy, which are associated with hypoglycemic activities [124]. In Table 3, the 33 compounds identified by GC-MS are found. Hypoglycemic and anti-obesity effects were caused by the aqueous extract of I. sonorae incorporated into the diet of the mice. The wereke extract also promoted a decrease in food intake with a subsequent decrease in the body weight, and a decrease in obesity levels in mice treated with prepared diets [120]. In a different investigation, Zapata Bustos et al. [121] demonstrated that the aqueous extracts of the tuberous roots of I. sonorae induce the consumption of glucose in human adipocytes, which is the mechanism by which these roots have antidiabetic properties. In this work, the presence of flavonoids, phenolic compounds, and high amounts of gallic acid were detected. From another point of view, in recent years, the anti-hyperglycemic mechanisms of I. sonorae were studied by enzymatic inhibition studies that revealed that the aqueous extract of I. sonorae was able to inhibit the enzyme α-glucosidase in a concentration-dependent manner and competitive inhibition. Additionally, the wereke aqueous extract stimulates insulin secretion in vitro from RIN-m5F pancreatic β cells, which allows the proposal of the use of I. sonorae as a supplement in order to control the glucose blood levels of patients, as an alternative to combat the potential contraindications of wereke [122].
Estrada-Zúñiga et al. [123] established the culture of calluses from explants of I. sonorae leaves and determined the amounts of stearic, palmitic, lauric, myristic, pentadecanoic fatty acids, and the content of phenolic compounds. In terms of the complex chemical composition of these tubers, ketones, alkanes and amides, palmitic acid, and methyl palmitate, are noteworthy, which are associated with hypoglycemic activities [124]. In Table 3, the 33 compounds identified by GC-MS are found. 3.6. Sechium edule (Jacq.) Sw.
Sechium edule, popularly known as, chayote, is a native, perennial climbing plant domesticated by the Aztec and Maya civilizations. Chayote is an important element of the Mexican diet and is employed to prepare salads, jams, sweets, or desserts [125]. At present, chayote is cultivated in tropical and subtropical areas worldwide and is known by different names depending on the region where it is found, such as cidrayote, chiote, cho-cho, choko, chow-chow, christophene, custard, hayatouri, huisquil, mango squash, mirliton, sayote, vegetable pear, and xuxu [126]. Chayote is recognized in a wide range of shapes and sizes, but today it can be identified due to the existence of data on its genome and its proteome [127].
In recent years, S. edule has been investigated due to the therapeutic and nutritional potential of its natural product content [128]. Among some current uses of chayote are: its employment in the food industry due the production of starch; in the cosmetic industry, as an ingredient in moisturizers, cleansers, sun lotions, toothpastes, mouthwash, shaving creams, deodorants, and shampoos; and in the animal nutrition area due to its promotion of growth in pigs, because the chayote meals prepared with fruits and leaves were found to replace the standard grower ration in the diet of the pigs without any secondary effects; and this may be one of its most salient uses: in traditional medicine [129]. Chayote has been widely utilized in the treatment of diabetes, followed by uses such as a diuretic, in renal calculi, arteriosclerosis, hypertension, vermifuge, leprosy, and asthma [130,131].
A variety of in vitro and in vivo tests have been conducted in order to detect the pharmacological properties of S. edule in various organs or systems, such as the cardiovascular and the central nervous system, the gastrointestinal system, and in the liver and kidney, but very few of these are bioguided in order to identify the bioactive compounds. The phytochemical content of the chayote is diverse and the chemicals that have been identified are alkaloids, saponins, phenolic acids, flavonoids, carotenoids, coumarins, cucurbitane triterpenoids, and phytosterols [129]. According to some authors, the flavonoid and triterpene content that are the most relevant for biological activities in S. edule; thus, some of the main flavonoids identified in S. edule are apigenin 6-C-β-D-glucopyranosyl-8-C-β-D-apiofuranoside, diosmetin 7-O-rutinoside, luteolin 7-O-rutinoside, luteolin 7-O-β-Dglucoside, and apigenin 7-O-rutinoside [125]. In the same manner, the triterpenoids in S. edule are characterized by the presence of cucurbitacins such as the cucurbitancins B, E, P, and L [132].
On the other hand, as reported by Siahaan et al., flavonoids comprise the most relevant chemical content for the hypoglycemic effects observed in S. edule. A significant decrease in the blood sugar levels of mice was observed after the administration of the ethanolic extract of S. edule in a 200 mg/kg dose. However, no changes were observed in the activity of the glutathione peroxidase enzyme. Additionally, a difference in the diameter of the pancreatic β-cell was recorded in chayote-treated mice [133]. In a subsequent study, this same research group studied the anti-hypoglycemia and antioxidant activities of S. edule in a rat model of T2DM. The ethanol extract and the ethyl acetate fraction of chayote possess antioxidant and anti-insulin resistant activities as they were able to reduce the levels of blood sugar and increase the antioxidant level of superoxide dismutase (SOD) [134].
Because the fruit of S. edule is widely recommended in Mexico for reducing not only the glucose blood levels, but also the risks related to diabetes, a series of works were carried out during the last decades. Dire et al. reported that the Sechium edule extract was able to modify the biodistribution of certain metabolites in the pancreas, such as AGE (Advanced Glycation End Products), which are characterized by inducing general inflammation in addition to other anomalies related to DM. Chayote modified and inactivated these molecules in an in vivo model with Windstar rats [135]. In another work, the relation between DM and other diseases and risk factors usually present, such as obesity, fatty liver, and hypertension, originated the search for natural alternatives that could reduce one or some of these risk factors. Hence, S. edule sprouts, as well as its fresh leaves, were prepared to be macerated and tested in fatty liver, finding mixtures of polyphenols, which reduce the accumulation of lipids in the liver, and in an in vitro model of fatty acid accumulation induced in HepG2cells [136]. Additionally, because it has been revealed in recent years that diet is crucial to controlling diabetes and related illnesses, a number of food supplements have been proposed. Chaguro is a food supplement, made from chayote and tuna fish that is useful in specific plan diets for patients with diabetes. In the elaboration of chaguro, different proportions of tuna fish and S. edule were tested. Results revealed that the combination of 75% of dry tuna fish mixed with 25% of S. edule is useful to induce lower blood glucose and improve the lipid profile in DM and dyslipidemia [137].
The nutritional content of S. edule revealed great amounts of vitamin C, starch, proteins, peroxidases, and an interesting mineral content that includes metals such as iron, manganese, zinc, and calcium. In contrast, the sugar and carbohydrate content were detected in a notoriously low amount. Then, based on the mineral and carbohydrate content present in chayote, as well as flavonoids, chayote could be considered for use in the prevention of chronic diseases such as DM, cardiovascular diseases, and the metabolic syndrome [138].

Citrullus lanatus (Thunb.) Matsum. & Nakai
The most widespread common name worldwide for Citrullus lanatus is watermelon, but it is also called sandía, tarbooz, acendría, and cooking melon among others. The fruit of this cucurbit possesses approximately 93% water, and a large and globous shape with a sweet and pulpy flesh, the reasons for it being denominated watermelon. Africa has been considered as the center of origin of watermelon, where has been cultivated for more than 4000 years. At present, watermelon is a very popular cultivar through the world, where the main producers are China, Turkey, Greece, Italy, Spain, Mexico, and Japan [139,140]. The fruit of C. lanatus is consumed fresh and raw, but also cooked, especially in some parts of Asia. With regard to the traditional use of the watermelon, there are numerous and diverse reports for using as cooling, strengthening, aphrodisiac, expectorant, diuretic, blood purifier, to cure itches, urinary tract infections, and kidney stones. The rind of the fruit is recommended for the treatment of diabetes [126,139,141]. The pharmacological properties of watermelon have been identified as antibacterial, antifungal, antiulcer, anti-inflammatory, anti-prostatic hyperplasia, anti-atherosclerotic, gastroprotective, analgesic, hepatoprotective, antioxidant and antidiabetic [139,141,142]. Among the main phytochemicals detected in watermelon are carotenoids, which represent from 31% (yellow pulp cultivar) to 99% (red pulp cultivar) of the percentage of total carotenoids. It has been considered that watermelon is one of the best sources of lycopene, after tomato, but also the carotenoids vary depending on the variety of color of the watermelon, for example, red (lycopene and beta carotene), yellow (neoxanthin, violaxanthin, and luteoxanthin), orange (beta carotene, prolycopene, phytonene, and carotene), and white (carotene). Other phytochemicals reported in watermelon comprise phenolic compounds, vitamins, aminoacids, flavonoids, and alkaloids [139,143]. On the other hand, watermelon has also been recognized as a source of L-citrulline, a neutral, non-essential amino-acid, precursor of L-arginine in mammals, and an important component of the cycle of the urea in the liver and kidneys. L-citrulline is involved in the production of endogenous nitroxide (NO), which is considered essential for regulating vasodilatation, immune responses, neurotransmission, and the adhesion of platelets and leukocytes. Thus, in recent years, the potential benefits of supplementing L-citrulline have been explored in cardiometabolic areas that include skeletal muscle and adipose tissue metabolism [142,144].
The lycopene present in the pulp of the fruit of Citrullus lanatus was investigated for its possible antidiabetic properties in an in vitro assay, where it exerted the inhibition of the α-amylase and lipase enzymes, in addition to its high content of L-citrulline [144]. In a study that included extracts prepared from different organs from the same plant (seed, flesh, rind, and leaves), the aqueous extract of the leaves of C. lanatus was able to inhibit α-glucosidase, and it also exhibited higher antioxidant capacities. Some of the molecules identified in the leaf extract were curcumenol, curcubitacin E, citrulline, 6-gingerol, citric acid, ascorbic acid, leucine, arginine, palmitic acid, arjunolic acid, naringenin 5,7-dimethyl ether 4 -O-xylosyl-(1->4)-arabinoside, 4 -apo-beta, psi-caroten-4 -al, caffeic acid 3-glucoside, luteolin 7-rhamnosyl (1->6) galactoside, and apigenin 7-(4",6"-diacetylalloside)-4 -alloside. These results permit proposing that watermelon could potentially be useful in the treatment of diabetes, but not only employing the fruit, but also the raw leaves [145]. Other work, exhibited that the administration of the juice of the watermelon to 40 Wistar rats and, was able to inhibit the enzymes α-amylase and α-glucosidase in a dose-dependent manner. The administration of different doses of watermelon juice reduced the fasting blood glucose level, serum lipid profile, glucose-6-phosphatase, lipid peroxidation, and anti-inflammatory activities in Alloxan-induced diabetic rats. These results revealed that the juice of the watermelon may be useful in the treatment of DM via multiple pathways, and could also be helpful in metabolic complications associated with DM [146]. Additionally, other investigations revealed that the ethanolic extract from the seeds of watermelon was not toxic when administered orally in rats in doses of 250, 500, 1000, and 2000 mg/kg for 28 days, in that no signs of toxicity, behavioral changes, or mortality were observed in the treated animals. Thus, the consumption of the entire pulp of the watermelon could be considered as safe [147]. The possible use of watermelon in the treatment of DM and in some related comorbidity diseases were explored in an in vivo study, where the extracts of the leaves of C. lanatus were administered in doses of 200 and 400 mg/kg to obese and diabetic-induced rats. The histological analysis demonstrated that the extracts of watermelon were able to attenuate the biochemical parameters and structural changes in the kidneys and liver of diabetic animals, indicating that the extract may be useful in complications associated with diabetes [148]. A different study showed that dietary supplementation with watermelon and L-citrulline reduced blood pressure in trials in humans probably plays an important role in the metabolism of lipids and in the control of satiety, consequently, watermelon could be useful in cardiac disease associated with diabetes [149].

Cucumis sativus L.
C. sativus known as cucumber is a Cucurbitaceae from India but it is currently widespread around the world. The fruit has been an essential part of the Mediterranean diet for centuries, it is mainly eaten fresh in salads or fermented. The pulp has been utilized for cleansing of the skin traditionally and today, cucumber extracts are employed in the cosmetic industry for many products [150]. Concerning its medicinal uses, cucumber has been reported as a laxative, as astringent, an anthelminthic, and an antipyretic. Other reported uses are in the treatment of hepatitis, bronchitis, asthma, diarrhea, and leprosy [151]. Notoriously, these traditional uses are mostly reports from Asia and Europe, but it is widely used in the entire Mexican territory for the treatment of DM [152].
The fruit possess antibacterial, antitumoral, antifungal, hepatoprotective, gastroprotective, ultraviolet protectant, wound-healing, and hypoglycemic activities [153]. This latter activity has been the object of recent studies, for example, the oral administration of 500 mg/kg of methanolic extract of the fruit caused a significant decrease in the fasting blood glucose concentration of Alloxan-induced diabetic rats, exhibiting a similar effect to that of Glibenclamide [154]. The ethanolic extract of the fruit of C. sativus demonstrated antihyperglycemic activity and also gave rise to the reduction in elevated lipid profiles in Alloxan-induced diabetic rats. It was notorious that these effects were more pronounced than those exhibited by other species of Cucurbitaceae, such as Lagenaria siceraria and Cucurbita maxima [155]. In an in vivo model, the anti-hyperglycemic effect of the decoction of C. sativus by the subcutaneous glucose tolerance in rabbits was determined. C. sativus was able to reduce the hyperglycemic peak significantly and was considered by the authors as recommendable for the prevention and treatment of DM [33]. Thus, the existing literature reveals the hypoglycemic effect of C. sativus extracts and their potential use in the treatment of DM. However, and to the best of our knowledge, none of the active molecule content in the extracts that have demonstrated this hypoglycemic activity has been isolated and identified by bio-guided studies of C. sativus.
Interestingly, and even when there is abundant literature on the phytochemicals of the cucumber from specimens around the world, and to the best to our knowledge, none of these phytochemical screenings considered biological activity (bio-guided) and even more so, they did not focus on hypoglycemic activity.

Cucumis melo L.
Cucumis melo is one of the fruits most consumed worldwide due to its delicious and juicy taste. It is also known as cantaloupe, Musk melon, sweet melon, round melon, and melón. In recent years, C. melo has become widely known because of its increasingly nutritive and medicinal functions [161,162]. Its chemical content, mainly fatty acids, polyphenols, and carotenoids have been recorded as possessing a broad range of beneficial characteristics that can also enhance health. Notoriously, the main source of these molecules is the mesocarp, which became the most studied part of the melón, compared with the skin and the seeds [163]. Some of the most abundant phenolic compounds detected in C. melo were reported in its seeds by Quian et al. [164], in which naringenin-7-O-glycoside, gallic acid, and vanillic acid were identified, while in the seed oils, γ-tocopherol, showed the highest concentration above that of α-tocopherol, β-tocopherol, and γ-tocotrienol. Flavonoids such as ß-carotene, lentin, xanthin, and cryptoxanthin were also reported.
The pharmacological properties of C. melo have been studied in recent decades and antiinflammatory, analgesic, anticancer, antioxidant, anthelminthic, antimicrobial, antidiabetic, diuretic, and hepatoprotective effects were found [165]. Even traditional medicine has described the use of the fruit and the roots, the fruit is the most utilized part in the treatment of flatulence, obesity, fever, leprosy, bronchitis, anemia, constipation, hypertension, and diabetes [166,167].
Regarding the antidiabetic properties of melón, it is known that the gut microbiota plays an important role in the production of the metabolic endotoxins that can potentiate or inhibit insulin resistance. The administration of C. melo in obese mice reduces the inflammation induced by endotoxins of the bacterial flora, in addition to activating the function of insulin [168]. On the other hand, the potential use of the juice of C. melo has been investigated in the management of T2DM with cardioprotective effects in arteriosclerosis [169]. Interestingly, because melón is a commercial crop, there are varieties that have exerted antidiabetic activity, and these have been employed in traditional medicine around the world (Table 4), however, and to the best to our knowledge, the identification of the compounds responsible for the antidiabetic activities remain unknown. ↑ Dopamine, melatonin, brain vascularendothelial growth factor levels. Protective effect by the extract was observed to oxidative stress, inflammation, and neural death cell processes [174] C. melo Lebanon Seed/Hexanic extract Inhibition of α-glucosidase and α-amylase enzymes Extract inhibited both enzymes (α-glucosidase IC 50 = 25.5 ± 1.9 µg/mL, and α-amylase IC 50 = 191.6 ± 2.7 µg/mL). Unsaturated fatty acids, linoleic and oleic acids are responsible of activity observed [175]

Discussion
The persistent increase in the number of people worldwide who are diagnosed with DM, was estimated at 10.5% (536.6 million individuals), which has led to increasing novel and effective investigations that seek to offer treatments in order to contribute in a better control of DM, its associated complications, the patients' quality of life, and, of course, to alleviate the global burden of DM in health sectors [176].
Consistently elevated blood glucose levels have been one of the major concerns for the control of patients with DM, numerous investigations have focused on the hypoglycemic effect. Nonetheless, in recent decades, the importance of the correlation among hyperglycemia, obesity, oxidative stress, and inflammation, especially during the development and progression of T2DM, has been established [177,178]. Obesity produces a state of chronic inflammation, and the oxidative stress is involved in the insulin resistance. The imbalance between the production of free radicals and their reduction by antioxidant mechanisms provoke insulin resistance and vascular complications [179,180]. Some sub-stances, such as GSH and MDA are altered in patients with T2DM: GSH decreased and MDA increased. Therefore, MDA, GSH, and the redox potential determined by the ratio of GSH/GSSH (oxidized glutathione) are used as indicators of oxidative stress. Low concentrations of GSH and high levels of GSSG have been found in patients with T2DM and diabetic experimental animals as a result of oxidative stress [47]. In turn, oxidative stress activates inflammation pathways, with the consequent production of proinflammatory cytokines such as TNF-α, IL-6, IFN-γ, and resistin [181,182]. In patients with T2DM, an increase in the levels of inflammatory markers is observed [183]. Accordingly, a number of investigations have been exploring not only the hypoglycemic effect, but also the antioxidant and anti-inflammatory properties of T2DM in the area of modern drug discovery, especially in the field of edible plants, where this latter approach has become relevant due the additional impact that diets-based-on-vegetables have in T2DM patients. One of the most prominent plant families with all of these characteristics, as mentioned previously, is the Cucurbitaceae family [51].
Although the relevance of the species belonging to the Cucurbitaceae family in the empirical treatment of DM mainly through the hypoglycemic effect has been recognized, the isolation and identification of the active molecules responsible for this action remain [184]. Probably the most frequently used Cucurbitaceae in current traditional Mexican medicine for the treatment of DM, I. sonorae, possesses abundant cucurbitacin's content in their roots. Because cucurbitacins comprise a very structurally diverse group of triterpenes that characterize the Cucurbitaceae family (but they could also be found in other families of plants) their pharmacological activity is varied. Hence, even though cucurbitacin-type triterpenes-Kinoin, which had been described, to our knowledge, for the first time in wereke, and characterizing this species, the hypoglycemic effects observed in in vitro and in vivo assays were attributed to the presence of monoglycerides and fatty acids localized in the roots [118]. Additionally, it was also observed that the antidiabetic properties of wereke may be related with the presence of flavonoids, and with high amounts of gallic acid [121]. In this manner, even with the presence of cucurbitacins, the antidiabetic properties observed in wereke were not clearly associated with these. Moreover, the cucurbitacins of wereke showed potent anticancer activity, and at present, a number of related investigations are in progress [111][112][113]. In a similar situation, the cucurbitacins present in S. edule are predominantly cucurbitancins B, E, P, and L, but pharmacological studies have described the flavonoids as the most relevant phytochemicals for hypoglycemic effects [134].
On the other hand, species from the genus Cucurbita have been the object-of-study in recent years, in that their chemical and nutritional contents have exhibited a wide spectrum of pharmacological activities. The chemical content in the species of this genus comprises carotenoids, tocopherols, phenols, terpenoids, saponins, sterols, fatty acids, carbohydrates, and polysaccharides [51]. However, the carbohydrate and polysaccharide content appears to be crucial for hypoglycemic effects and other related antidiabetic processes such as antioxidant and anti-inflammatory, in the species C. ficifolia, C. maxima, C. moschata, and C. pepo which are used in traditional Mexican medicine for the treatment of DM. Active fractions with antidiabetic properties identified in these species, were characterized with by a high content of polysaccharides from the aqueous extracts, while the antidiabetic activities also comprise pancreatic-cell protection [41,67,87,102,103].
It is interesting to note that in the case of C. lanatus and C. melo, the use in traditional medicine for the treatment of T2DM is notoriously more frequent in Mexico than in Asia, where both regions are found to be places of the commercial production of watermelon and melón. In the case of C. lanatus, the antidiabetic properties observed correlated with the presence of high amounts of lycopene and L-citrulline [144] in the fruits, while for the case of C. melo, the antidiabetic activity was associated with the presence of rutin, quercetin, gallic acid, linoleic acid, oleic acid, and unsaturated fatty acids [171,175]. As could be perceived in both cases, information on the antidiabetic effects and the active molecules responsible of this activity, are still scarce. Nonetheless, in the present work, from the total of selected species of Cucurbitaceae that are used in traditional Mexican medicine in the treatment of DM, C. sativus appears to be the least studied, in that very few reports demonstrated the hypoglycemic effects of C. sativus extracts [33], and, to best of our knowledge, none of these studies focused on the identification of the bioactive molecules. In contrast, a great number of studies that revealed the chemical composition of the essential oils of C. sativus are present in the literature, showing that the industrial application of the oils of C. sativus has probably been driving this approach.
In addition to the phytochemical content, because the Cucurbitaceae family has been recognized as one of the most widely used traditional antidiabetic family of plants worldwide, a crucial aspect in terms of continuing the research of potential new agents that could be useful in the treatment of DM, is the toxicity of the antidiabetic species. Although Marles and Farnsworth [185] reported that toxicity has been detected in the majority of the hypoglycemic species of Cucurbitaceae, in the present work, the selected species of Cucurbitaceae that are employed in Mexico to the treatment of DM are mostly edible and considered as safe, according to the literature. For the case of C. ficifolia, an acute toxicological study revealed that when the juice of immature fruits was administered to diabetic patients in a dose of 100 mg/kg, no toxicity effects were observed. Nonetheless, in an experimental model, deaths of animals were recorded in a dose of 625 mg/kg, but the dose employed in patients was evidently smaller than that used in animals. Despite this, these data revealed that the juice of C. ficifolia does not cause toxic effects in patients, more studies concerning the sub-acute administration of the juice are required [186]. The seeds of C. maxima were evaluated in an acute and subacute toxicological study. The lethal dose (DL 50 ) of the hydroalcoholic extract of C. maxima was determined as higher than 5000 mg/kg when it was orally administered. Thus, the hydroalcoholic extract from the seeds of C. maxima can be considered as safe [187]. The ethyl acetate and methanolic extract of C. pepo did not show any toxicity in mice when administered in 2000 mg/kg doses for 14 days [188]. Non-toxicity signs were recorded after the oral administration of the ethanolic extract of the seeds of C. lanatus in Wistar rats at doses of 250, 500, 1000, and 2000 mg/kg; moreover, protection to different body organs was observed at under the 1000 mg/kg doses [147]. Recent studies suggested that the extracts of the seeds of C. melo, C. lanatus, C sativus, and C. maxima are not only safe but that they can also be effectively used in chronic pain conditions due the analgesic and anti-inflammatory properties shown [62,189]. Perhaps the highest dose evaluated experimentally in order to determine the toxicity effect on the species of Cucurbitaceae, is the dose of 5000 mg/kg, which was administered to mice over 7 days by means of the methanolic extract of S. edule. The absence of signs of toxicity suggested that chayote can be considered as safe, without any harmful side effects [190]. Nonetheless, it is one of the species arousing the most interest considered in the present work, since it is probably the most used plant in traditional Mexican medicine to the treatment of DM, which, despite the potent hypoglycemic effect exerted by the extracts prepared with the roots and the possible role of wereke in the prevention of diseases correlated with diabetes such as obesity, dyslipidemia, and hyperglycaemia, the administration of high doses of the extract (>1000 mg/kg) to diabetic rats may induce toxicity [120].
Through the previously mentioned information and because DM is a chronic disease, where the pharmacological treatment is managed over the lifetime of the patients, chronictoxicity studies of the selected species of the Cucurbitaceae family considered in the present work must be exhaustively conducted in future investigations.
Another interesting aspect that we wish to highlight about the selected species of Cucurbitaceae that are included in the present work is the fact that the majority of these cucurbits are edible. These characteristic results are relevant because, in recent decades, a vegetables-based diet has shown to be central in diabetic patients for the control of DM due to the replacement of animal-derived lipids and proteins that directly impact the glucose homeostasis. Particularly, the majority of the Cucurbitaceae species are considered a good source of protein, and dietary fiber, which is important for the regulation of cholesterol, improvements of the insulinemic response in providing benefits for the intestinal function [13]. In recent years, in Mexico, efforts have been made to study edible plants that could contribute to the approach of a novel diet-therapeutic alternative to prevent chronic diseases such as DM. Then, an evaluation of the nutritional value, glycemic index (GI), and the total phenol and flavonoid content, as well as antioxidant and antidiabetic activity (inhibition of α-amylase and α-glucosidase) of plants used by the Maya population in Mexico was conducted. The results showed that C. moschata, among other plant species from different botanical families, possess antidiabetic properties that allow it to be incorporated as a food-diet in the treatment and prevention of DM [191]. Due the important role of Cucurbitaceae in the treatment of DM, a crucial study was carried out with patients with T2DM. In that study, diet was based on the consumption of the following six species of Cucurbitaceae for 2 months: C. sativus, C. pepo, C. moschata, Lagenaria siceraria, C. lanatus, and C. melo. Study results showed that the diet based on Cucurbitaceae was able to control the levels of blood sugar when employing the fasting blood sugar and glycated hemoglobin for measurements. Conveniently, the diet based on cucurbits was low in carbohydrates and lipids but rich in minerals and vitamins, according to the daily nutrimental requirements. However, certain other essentials need to be taken as supplements. Thus, this study confirms that the Cucurbitaceae family species could be useful in clinical research for the treatment of DM [27]. Interestingly, five of the six species comprised in that study are also included in the present work. Thus, the selected species of Cucurbitaceae employed in traditional Mexican medicine for the treatment of DM represent a potential source of agents for the treatment of DM from an integral perspective, in which the antidiabetic properties combined hypoglycemic, antioxidant, anti-inflammatory, and anti-obesity effects, and also for the control of dyslipidemia. Even more so, the Cucurbitaceae species considered in the present work possess the pharmacological potential to be developed as new antidiabetic agents, but also to be included as essential components of diets for the control of DM in patients with the disease. Finally, since the plant species treated in this manuscript that belong to the Cucurbitaceae family are used for the treatment of DM in Mexico are considered as safe, some future aspects to consider for research in this topic comprise the identification of the bioactive compounds in fractions or extracts that could provide fundamental information for the standardization of future antidiabetic phytomedicines, particularly, those bioactives that could possess multi-antidiabetic activities. On the other hand, another interesting aspect to explore in future research is the prevention or delay the complications associated with DM, and in which, the bioactives against DM present in Cucurbitaceae could also be beneficial. Thus, the interactions among the antidiabetic compounds present in Cucurbitaceae and the myokines that regulate the beneficial effects of the practice of exercise in patients with DM, may appear as the subject of prospective studies that could impact in the deterioration of organs caused by DM disease. In this manner, the Cucurbitaceae family represents a source of compounds that are perhaps useful in the DM therapy through different pathways.

Conclusions
The complexity of the DM disease and the increasing number of people who suffer from DM worldwide clamor for novel and effective treatments for its control. The use of plant-based traditional medicine for the treatment of DM is an extensive practice in Mexico and other countries where DM is a serious health problem. In the present work, the most used plants in the treatment of DM in Mexico that belong to the Cucurbitaceae family were reviewed with regard to their antidiabetic properties. From among the selected species, with the exception of I. sonorae, the remainder of the selected species are edible and are also considered as part of the diet recommended to diabetic patients in order to control DM. The antidiabetic effects shown by the selected Cucurbitaceae species comprise hypoglycemic, antioxidant and anti-inflammatory activities, anti-obesity and protective effects on diverse organs and cells, as well as in the control of dyslipidemias. Hence, the Cucurbitaceae species selected in the present work encourage future and expeditious investigations that would be able to make effective antidiabetic agents available that could contribute to the control of DM and perhaps establish the bases for novel clinical treatments.