Antioxidant and In Vivo Hypoglycemic Activities of Ethanol Extract from the Leaves of Engelhardia roxburghiana Wall, a Comparative Study of the Extract and Astilbin

The leaves of Engelhardia roxburghiana Wall (LERW) has been used as sweet tea in China throughout history. In this study, the ethanol extract of LERW (E-LERW) was prepared and the compositions were identified by HPLC-MS/MS. It indicates that astilbin was the predominant component in E-LERW. In addition, E-LERW was abundant in polyphenols. Compared to astilbin, E-LERW presented much more powerful antioxidant activity. The E-LERW also had stronger affinity with α-glucosidase and exerted more vigorous inhibitory effect on the enzyme. Alloxan-induced diabetic mice had significantly elevated glucose and lipid levels. Treatment with E-LERW at the medium dose (M) of 300 mg/kg could reduce the levels of glucose, TG, TC, and LDL by 16.64%, 12.87%, 32.70%, and 22.99%, respectively. In addition, E-LERW (M) decreased food intake, water intake, and excretion by 27.29%, 36.15%, and 30.93%, respectively. Moreover, E-LERW (M) therapy increased the mouse weight and insulin secretion by 25.30% and 494.52%. With respect to the astilbin control, E-LERW was more efficient in reducing the food and drink consumption and protecting pancreatic islet and body organs from alloxan-induced damage. The study demonstrates that E-LERW may be a promising functional ingredient for the adjuvant therapy of diabetes.


Introduction
Nowadays, diabetes is a high incidence disease seriously challenging human health. Diabetic patients occupy 10% of the world's population. The complications of diabetes include renal injury, retinopathy, diabetic cataract, diabetic foot, coronary disease, and so on, which not only make the patients suffer great pain but also bring heavy economic burden on families and society. How to protect and treat diabetes has become a major concern in food and medicinal fields. Natural plants and their active ingredients exhibit multitarget, multi-pathway, and multi-directional hypoglycemic characteristics. Compared to chemical drugs, herbal medicines have mild and sustained effects with low toxicity. The multi-target property not only benefits glucose modulation, but also contributes to the alleviation of diabetic complications. A natural product with known hypoglycemic activity is becoming a promising alternative to the current drugs for diabetic therapy. Engelhardtia roxburghiana Wall (ERW) is a subtropical tree grown in the Guangdong, Guangxi, and Fujian provinces of China. The leaves of ERW (LERW) have been used as sweet tea in Chinese folk medicine to treat obesity, fever, and pain for a long time. Due to the abundance in flavonoids and phenols, LERW has multiple physiological activities, including inhibition of aldose reductase, bladder protection, as well as anticoagulant, hypolipidemic, and antioxidant activities [1]. Flavonoids such as astilbin, taxifolin, and engeletin are the main

Total Phenols
The total phenols in E-LERW were determined using the methods reported by Yao et al. and Dirar et al. [12,13] and were expressed as mg gallic acid (GA) equivalent (mg GE)/g. The absorbance of the reference GA was linear with the concentration ranging from 10 to 500 µg/mL. The regression equation was Y = 102.2X + 0.0616 (r 2 = 0.9991).

Astilbin
The sample was analyzed by a LD-20AD HPLC system (Shimadzu, Tokyo, Japan). The separation was performed on a SinoChrom ODS-BP column (4.6 mm × 150 mm, 5 µm). The detection conditions were the same as described in Section 2.3. The detection wavelength was 291 nm with the injection volume of 20 µL. In the range of 0.02 to 1.0 mg/mL, the peak area of astilbin was linear with the concentration. The regression equation was Y = 54756X − 255.86 (r 2 = 0.9992).
2.5. Antioxidant Activity 2.5.1. Scavenging DPPH Free Radicals E-LERW and astilbin were prepared into a series of solutions, which contained astilbin from 0.2 to 1 mg/mL, respectively. The determination was carried out according to what Makgatho et al. reported [14]. Ascorbic acid was set as the positive control.

Scavenging ABTS + Radicals
The measurement was conducted following the method reported by Aruwa et al. [15].

Ferric Reducing Activity of Power
The ferric reducing activity of power (FRAP) of E-LERW and astilbin were determined conforming to the method proposed by Hao et al. [16].

Inhibition of Lipid Membrane Oxidation
The lyophilized liposomes were re-dispersed in deionized water, from which 0.5 mL was drawn out and blended with 0.5 mL of E-LERW or astilbin at different concentrations. The sample was incubated at 37 • C for 1 h. Subsequently, 1 mL of 1% thiobarbituric acid was added, boiled for 10 min, and cooled to room temperature. The solution was centrifuged at 1000 r/min for 10 min. The absorbance of the supernatant was measured at 532 nm (A). Meanwhile, the absorbance of blank control (A 0 ) was determined using 0.5 mL deionized water in place of the sample. Tannic acid was set as the positive control. The inhibitory rate was calculated according to the following equation (Equation (1)) [17]:

Inhibitory Effect on α-Glucosidase
The inhibitory effect on α-glucosidase was examined according to the method described by Broholm et al. [18]. Briefly, the sample of 50 µL was blended with 50 µL α-glucosidase of 0.5 U/mL, and incubated under 37 • C for 30 min. Afterward, 1 mM substrate pNPG of 50 µL was added and reacted at 37 • C for another 30 min. The reaction was terminated by adding 0.2 M sodium carbonate of 50 µL. The absorbance at 405 nm was determined. In addition, using PBS to replace the enzyme, the background absorbance was measured in parallel. The inhibitory curve was constructed using the inhibitory rates versus astilbin concentrations. Acarbose was set as the positive control.

Kinetic Analysis on the Inhibition of α-Glucosidase
The concentration of α-glucosidase was fixed at 0.5 U/mL. The inhibitory velocity of E-LERW and astilbin on α-glucosidase was determined under different concentrations of substrate pNPG [19]. The double reciprocal curves were plotted based on the following Lineweaver-Burk equation: and a secondary plot was constructed as Equation (3): where v is the inhibitory velocity of the sample on α-glucosidase and [I] and [S] represent the concentration of inhibitor and substrate, respectively. K i and K m are the inhibition constant and Michaelis-Menten constant, respectively. α is a constant standing for the ratio of uncompetitive inhibition to competitive inhibition.

Animal Experiment Design
The animal experiment was approved by the Ethics Committee of Chengdu University, Chengdu, China (protocol number: CDPS 2020-122), and all procedures adhered to European Community Guidelines (86/609/EEC) for the Care and Use of Laboratory Animals. Male Kunming mice, weighing 18 to 22 g, were purchased from Chengdu Dashuo Experimental Animal Company (Chengdu, China). Before the experiment, all mice were allowed to adapt to the environment for 3 days. The mice in the normal control (NC) group were fasted but had free access to water for 12 h, and fasting blood glucose (FBG) was measured via the tail vein, which was used as the basic blood glucose level of normal mice. The rest of the mice were fasted for 24 h, followed by the intraperitoneal injection of alloxan at 200 mg/kg to develop a diabetic mouse model [20]. The fasting blood glucose was measured after 3 days. The mice with the blood glucose level over 11.1 mmol/L were diagnosed as diabetic mice and were randomly divided into 6 groups with 6 mice in each group. The groups include the model control of diabetes (MC); astilbin control (AC) with the dosage of 30 mg/kg; the positive control (PC) of metformin hydrochloride at the dose of 100 mg/kg; and E-LERW groups of high (H), medium (M) and low dose (L) at 600, 300, and 150 mg/kg, which were equivalent to the dose of 56.88, 28.44, and 14.22 mg astilbin/kg, respectively. The oral gavage was performed twice a day and consecutively lasted for 28 d [21]. The scheme of the experimental design was displayed in Figure 1. respectively. The oral gavage was performed twice a day and consecutively lasted for 28 d [21]. The scheme of the experimental design was displayed in Figure 1.

Oral Glucose Tolerance Test
At the final week of treatment, all mice were orally given a glucose solution of 1.5 g/kg after being fasted for 12 h [22]. The blood glucose level was measured every half hour. Oral glucose tolerance test was expressed as AUC in 2 h.

Blood Sample Analysis
When the experiment was completed, the mice were sacrificed by breathing carbon dioxide. The mouse blood was collected in a tube pre-coated with heparin sodium and was centrifuged at 3000 r/min for 10 min. The supernatant serum was stored at −20 °C until measurement. The levels of insulin, triglyceride (TG), total cholesterol (TC), high density lipoprotein (HDL), and low-density lipoprotein (LDL) were measured by commercial ELISA kits (Nanjing Jiancheng Bioengineering Institute, Najing, China). All the determinations were carried out according to the instructions of the reagent kits.

Organ Index
After the mice were sacrificed, the livers and kidneys were detached from the body, placed on filter paper to remove blood, and weighed, respectively. The weight ratios of organ to body (organ indexes) were calculated.

Data Analysis
All data are expressed as mean ± standard error. The diagrams were plotted using Origin 8.0 (OriginLab Corporation, Northampton, MA, USA). The difference between the data was evaluated by one-way analysis of variance (ANOVA) and Duncan's test using SPSS version 10.0 software (IBM SPSS Inc., Chicago, IL, USA). The difference was considered statistically significant when p < 0.05.

Oral Glucose Tolerance Test
At the final week of treatment, all mice were orally given a glucose solution of 1.5 g/kg after being fasted for 12 h [22]. The blood glucose level was measured every half hour. Oral glucose tolerance test was expressed as AUC in 2 h.

Blood Sample Analysis
When the experiment was completed, the mice were sacrificed by breathing carbon dioxide. The mouse blood was collected in a tube pre-coated with heparin sodium and was centrifuged at 3000 r/min for 10 min. The supernatant serum was stored at −20 • C until measurement. The levels of insulin, triglyceride (TG), total cholesterol (TC), high density lipoprotein (HDL), and low-density lipoprotein (LDL) were measured by commercial ELISA kits (Nanjing Jiancheng Bioengineering Institute, Najing, China). All the determinations were carried out according to the instructions of the reagent kits.

Organ Index
After the mice were sacrificed, the livers and kidneys were detached from the body, placed on filter paper to remove blood, and weighed, respectively. The weight ratios of organ to body (organ indexes) were calculated.

Data Analysis
All data are expressed as mean ± standard error. The diagrams were plotted using Origin 8.0 (OriginLab Corporation, Northampton, MA, USA). The difference between the data was evaluated by one-way analysis of variance (ANOVA) and Duncan's test using SPSS version 10.0 software (IBM SPSS Inc., Chicago, IL, USA). The difference was considered statistically significant when p < 0.05.

HPLC-MS/MS Analysis
The chromatogram and MS identification results of E-LERW are shown in Figure 2 and Table 1, respectively. A total of 10 components were identified with reference to the database of the instrument.  [24] and 125.0231, which were assigned to pyrogallol [23]. The MS 2 of citric acid included the ions of m/z 111.0074 and 87.0074, which was in accordance with what AliAbadi et al. reported [25]. Compound 6 and 7 failed to be detected in the MS 2 due to the weak fragment signals.

HPLC-MS/MS Analysis
The chromatogram and MS identification results of E-LERW are shown in Figure 2 and Table 1, respectively. A total of 10 components were identified with reference to the database of the instrument. α-Lactose was determined by the molecular ions of m/z 360.1497 (M+NH4) + and 365.1050 (M+Na) + . The ion with m/z 145.0494 was assigned to hydroxypropyl pyran, which removed one water and formed the ion of m/z 127.0390. The ion further dissociated one propylene and yielded the ion with m/z 85.0289. Malic acid had the MS 2 [24] and 125.0231, which were assigned to pyrogallol [23]. The MS 2 of citric acid included the ions of m/z 111.0074 and 87.0074, which was in accordance with what AliAbadi et al. reported [25]. Compound 6 and 7 failed to be detected in the MS 2 due to the weak fragment signals.   Table 1.
The flavonoid-like compounds from 4 to 9 had the maximum absorbance wavelength of around 290-295 nm [26]. Quercetin and maritimetin included the maximum wavelength of over 300 nm due to longer conjugate structure. Citric acid λ max is the wavelength with the maximum absorbance in the UV spectrum, which was determined by DAD.

Determination of Active Components
The contents of astilbin, total flavonoids, and total phenols in E-LERW were 94.79 ± 2.49 mg/g, 153.42 ± 2.74 mg RE/g, and 255.74 ± 4.16 mg GE/g, respectively. It indicates that E-LERW is enriched in polyphenols.

Antioxidant Activity
The results of E-LERW in scavenging DPPH free radicals, ABTS+ free radicals, FRAP, and inhibition against lipid membrane oxidation are shown in Figure 3. The activity of both E-LERW and astilbin presented a concentration-dependent mode. The activity increased with the elevation of concentration. At different concentrations, the capacity of E-LERW in scavenging free radicals was significantly higher than that of astilbin (p < 0.05, Figure 2A,B). Meanwhile, E-LERW also exhibited much stronger FRAP over astilbin (p < 0.05, Figure 2C). E-LERW presented a more potent capacity in inhibiting the oxidation of lipid membrane as well ( Figure 2D). When the concentration amounted to 2 mg/mL, E-LERW prevented 75% lipid membrane from oxidation while the inhibitory rate of astilbin was only less than 20% at the same concentration. The inhibitory effect of astilbin kept low even as the concentration reached 10 mg/mL. The control of ascorbic acid presented much stronger antioxidant activity over both astilbin and E-LERW in the examined concentration range (p < 0.01). When the concentration was below 1.5 mg/mL, tannic acid exhibited significantly higher inhibitory capacity against lipid membrane oxidation (p < 0.01). LERW prevented 75% lipid membrane from oxidation while the inhibitory rate of astilbin was only less than 20% at the same concentration. The inhibitory effect of astilbin kept low even as the concentration reached 10 mg/mL. The control of ascorbic acid presented much stronger antioxidant activity over both astilbin and E-LERW in the examined concentration range (p < 0.01). When the concentration was below 1.5 mg/mL, tannic acid exhibited significantly higher inhibitory capacity against lipid membrane oxidation (p < 0.01).

Inhibition on α-Glucosidase
The inhibitory effect of E-LERW and astilbin on α-glucosidase is shown in Figure 4A. The inhibitory rates of both the samples and the control acarbose presented a concentration-dependent manner. The effect increased with the elevation of concentration. The inhibitory strength of E-LERW was remarkedly higher than that of astilbin in the examined concentration range (p < 0.05). Meanwhile, the control acarbose displayed much stronger inhibitory activity than E-LERW and astilbin (p < 0.05). The concentration with 50% inhibitory rate (IC50) of E-LERW, astilbin, and acarbose was 0.46 ± 0.09, 1.12 ± 0.17, and 0.19 ± 0.03 mg/mL, respectively.

Inhibition on α-Glucosidase
The inhibitory effect of E-LERW and astilbin on α-glucosidase is shown in Figure 4A. The inhibitory rates of both the samples and the control acarbose presented a concentrationdependent manner. The effect increased with the elevation of concentration. The inhibitory strength of E-LERW was remarkedly higher than that of astilbin in the examined concentration range (p < 0.05). Meanwhile, the control acarbose displayed much stronger inhibitory activity than E-LERW and astilbin (p < 0.05). The concentration with 50% inhibitory rate (IC 50 ) of E-LERW, astilbin, and acarbose was 0.46 ± 0.09, 1.12 ± 0.17, and 0.19 ± 0.03 mg/mL, respectively.

Inhibitory Kinetic Analysis
The Lineweaver-Burk curves of E-LERW and astilbin are shown in Figure 4B,C, respectively. The increase of the concentration accompanied with the elevation of the vertical axis intercept (1/V max ), as well as the decrease of the net value of horizonal axis intercept, indicate that the interaction between the samples and α-glucosidase belonged to a mixed mode [19]. The secondary plot using slope-versus-inhibitor concentration was linear ( Figure 4D,E), showing that both E-LERW and astilbin had a single inhibitory site on αglucosidase. The calculated Ki of E-LERW and astilbin was 0.145 and 0.474 mg/mL, respectively. spectively. The increase of the concentration accompanied with the elevation of the vertical axis intercept (1/Vmax), as well as the decrease of the net value of horizonal axis intercept, indicate that the interaction between the samples and α-glucosidase belonged to a mixed mode [19]. The secondary plot using slope-versus-inhibitor concentration was linear ( Figure 4D,E), showing that both E-LERW and astilbin had a single inhibitory site on α-glucosidase. The calculated Ki of E-LERW and astilbin was 0.145 and 0.474 mg/mL, respectively.  3.5. Hypoglycemic Activity In Vivo 3.5.1. Body Weight, Food Intake, Water Intake and Excretion Table 2 shows the body weight, the amounts of excretion, and food and water consumption of mice in different groups. On the first day of alloxan injection, the diabetic mice had similar food intake to normal mice, but with more than threefold the water consumption and, as a result, over three times the excretion compared to the normal mice. This demonstrated a successful establishment of a diabetic mouse model. Though the body weights of mice in all groups increased after 28 d, the weights of the mice injected with alloxan were significantly lower than those in normal control (NC) group, who received no injection (p < 0.05). Nevertheless, compared to the model control (MC) group without any therapy, the groups with the treatment of metformin (PC), astilbin (AC), and E-LERW of high (H) and medium dosage (M) had the weight increment of 49%, 18%, 38%, and 25%, respectively, affirming the remedy effectiveness of metformin, astilbin, and E-LERW on diabetes. Though the weights of diabetic mice decreased, their food intake, water intake, and excretion increased dramatically (p < 0.01). The food and drink consumed by the mice in MC group were 1.8 and 6.3 times the amount consumed by normal mice. After the treatment of metformin, astilbin, and E-LERW at high (H), medium (M), and low dosage (L), the food intake diminished to 1.13, 1.38, 1.18, 1.31, and 1.74 times the normal intake, respectively. The drinking dropped to 2.79, 4.38, 3.33, 4.02, and 6.16 times normal drinking, respectively. The excretion of MC mice was seven times that of normal mice. Through treatment with different samples, the excretion reduced to 3.21, 6.30, 3.93, 5.04, and 7.09 times the normal amount, respectively. The results show that metformin (PC) has the most powerful therapeutic effect, followed by E-LERW (H) and (M). Astilbin (AC) and E-LERW (L) have weak activity in alleviating the symptoms triggered by a high glucose level.   Figure 5A shows the fasting blood glucose (FBG) levels of mice receiving different treatments during 28 d. As time progressed, the MC and the group fed with E-LERW (L) maintained high and invariable glucose levels. Other diabetic mice treated with different samples had a gradually declining FBG. On day 28 of the therapy, the FBG of the mice receiving metformin, astilbin, and E-LERW (H) and (M) was reduced to 35%, 87%, 65%, and 83% level of MC group, respectively. Metformin again presented the strongest hypoglycemic activity. Astilbin and E-LERW exhibited moderate strength. E-LERW (M) included approximately 10% astilbin, which was equivalent to the AC group. Figure 5B indicates that the injection of alloxan severely damaged the function of islet. The insulin level of MC mice was only 4.7% that of normal mice. Under the treatment of metformin, astilbin, and E-LERW (H, M and L), insulin secretion was restored to 72.0%, 15.0%, 59.5%, 28.0%, and 5.4% normal level, implying that astilbin and E-LERW helped to restore the damaged islets.

Fasting Blood Glucose and Insulin
hypoglycemic activity. Astilbin and E-LERW exhibited moderate strength. E-LERW (M) included approximately 10% astilbin, which was equivalent to the AC group. Figure 5B indicates that the injection of alloxan severely damaged the function of islet. The insulin level of MC mice was only 4.7% that of normal mice. Under the treatment of metformin, astilbin, and E-LERW (H, M and L), insulin secretion was restored to 72.0%, 15.0%, 59.5%, 28.0%, and 5.4% normal level, implying that astilbin and E-LERW helped to restore the damaged islets. Figure 5. Effects of astilbin and E-LERW on the fasting blood glucose level (A), insulin secretion (B), oral glucose tolerance test (C), and AUC (D). All values were expressed as the mean ± SD (n = 6). Data analysis was performed by one-way ANOVA and Duncan's test. Different letters indicate significant differences among groups (p < 0.05).

Oral Glucose Tolerance Test
Oral glucose tolerance and the corresponding area under the curve (AUC) of each group are displayed in Figure 4C,D, respectively. The results show that the glucose peak values of all groups were reached in 30 min after the oral administration of glucose, followed by a gradual decrease. The glucose peak concentration of MC was increased to 3.74 times that of normal mice. After the treatment of metformin, astilbin, and E-LERW (H, M, and L) for 28 d, the peak level was reduced to 1.81, 3.38, 2.70, 3.41, and 3.71 times the normal level, showing the therapeutic effect of metformin, astilbin, and E-LERW in improving the oral glucose tolerance of diabetic mice.
AUC is another indicator to assess the oral glucose tolerate. The AUC of MC was 3.94 times that of normal mice, verifying the alloxan-induced impairment of glucose tolerate. The value was reduced to 1.67 and 3.43 times the normal level after the remedy of . All values were expressed as the mean ± SD (n = 6). Data analysis was performed by one-way ANOVA and Duncan's test. Different letters indicate significant differences among groups (p < 0.05).

Oral Glucose Tolerance Test
Oral glucose tolerance and the corresponding area under the curve (AUC) of each group are displayed in Figure 4C,D, respectively. The results show that the glucose peak values of all groups were reached in 30 min after the oral administration of glucose, followed by a gradual decrease. The glucose peak concentration of MC was increased to 3.74 times that of normal mice. After the treatment of metformin, astilbin, and E-LERW (H, M, and L) for 28 d, the peak level was reduced to 1.81, 3.38, 2.70, 3.41, and 3.71 times the normal level, showing the therapeutic effect of metformin, astilbin, and E-LERW in improving the oral glucose tolerance of diabetic mice.
AUC is another indicator to assess the oral glucose tolerate. The AUC of MC was 3.94 times that of normal mice, verifying the alloxan-induced impairment of glucose tolerate. The value was reduced to 1.67 and 3.43 times the normal level after the remedy of metformin and astilbin, respectively. E-LERW (H, M, and L) decreased the AUC to 2.64, 3.33, and 3.93 times the normal value. The trend was similar to the effects of various samples in diminishing glucose peak concentration. Meanwhile, the hypoglycemic activity of E-LERW (M) was consistent with that of astilbin control.

Blood Lipid Analysis
Patients with diabetes and prediabetes are always at increased risk of dyslipidemia and cardiovascular disease [27]. As shown in Table 3, the injection of alloxan also significantly increased the levels of TG, TC, and LDL, and remarkedly reduced the concentration of HDL in MC mice (p < 0.01). The administration of various samples decreased the lipid levels and boosted HDL concentration to different degrees. The lipid lowering strength was metformin > E-LERW (H) > astilbin and E-LERW (M) > E-LERW (L) (p < 0.05). E-LERW (M) presented stronger activity in reducing TC and LDL with respect to astilbin, but the difference was not significant (p > 0.05).

Effects of E-LERW on Organ Indexes of Liver and Kidney
The status of high glucose level impairs livers and kidneys as well. The organ indexes of mice in each group are shown in Table 4. Compared to the normal mice, the liver index of the MC group increased 33%. Other groups such as metformin, astilbin, and E-LERW (H, M, and L) elevated 8%, 27%, 12%, 21%, and 34%, respectively. The kidney index of the MC group increased 67%, while that of the treatment groups rose 8%, 51%, 27%, 44%, and 65%, respectively. It indicates that diabetes exerts a more detrimental impact on kidneys. E-LERW has the function of preventing liver and kidney swelling. The medium dose exhibited stronger capacity than the purified compound astilbin in protecting the organs.

Discussion
Compared to astilbin, the LERW presented much stronger antioxidant as well as α-glucosidase-inhibitory activity in vitro. Perez-Najera et al. obtained astilbin enriched extract from Smilax aristolochiifolia Root with astilbin at 48.76 mg/g [28]. The inhibitory rate of the extract against α-glucosidase was lower than 10%. The vigorous strength of E-LERW may originate from the integrative effect from both astilbin and other flavonoids present in LERW, such as quercetin and engeletin. Moreover, in the inhibitory kinetic test, the Ki of astilbin was 3.27 times that of LERW, implying that the affinity between the enzyme and LERW was much stronger than astilbin.
In the animal experiment, E-LERW significantly lowered blood glucose levels of mice triggered by alloxan. The group of E-LERW (M) had a similar content of astilbin to the group of astilbin control (AC). Though E-LERW exhibited much stronger antioxidant and glucosidase-inhibitory effects over astilbin, compared to AC, E-LERW (M) did not display more powerful effect in lowering fasting glucose level or enhancing oral glucose tolerance. The possible reason is that the hypoglycemic process involves various complex mechanisms-for example, decreasing glucose absorption from small intestine, hindering glucose production in vivo, prompting glucose uptake by tissues, enhancing glucose clearance from body, and so on [29]. Recent studies found that DNA methylation, histone modification, and non-coding RNA expressing also contribute to the pathogenesis of diabetes [30]. Inhibition on α-glucosidase only means the yield of glucose is reduced and glucose absorption is slowed down. It indicates that compound astilbin is the major component responsible for the hypoglycemic function of E-LERW.
Though the glucose level of the mice treated with E-LERW (M) was similar to those with astilbin, E-LERW (M) group had significantly higher insulin concentration than AC group, implying the protective capacity of flavonoids and polyphenols present in the extract on the islet β-cells. Flavonoids were able to increase the numbers of islets and β-cells, restore the pancreatic tissues impaired by alloxan, decrease β-cell apoptosis, and activate insulin receptors, which resulted in the increase of insulin secretion [31]. The underlying mechanisms for flavonoids and polyphenols to preserve β-cells include the blocking of NF-kappa B signaling, activation of the PI3K/Akt pathway, as well as the release decrease of nitric oxide (NO) and reactive oxygen species (ROS) [32].
Alloxan injections led to hyperglycemia accompanied with significant weight loss, while food intake, water intake, and excretion amount increased dramatically ( Table 2). The phenomena were in accordance with what Leme et al. reported [33]. Administration of astilbin and E-LERW (H) and (M) significantly alleviated diabetes-induced weight loss, food intake, water intake, and excretion amount (p < 0.05). Compared to astilbin, E-LERW (M) reduced water intake and excretion more efficiently (p < 0.05). Hyperglycemia also damaged the liver and kidney and made the two organs swell. E-LERW protected the liver and kidney by remarkedly diminishing the organ indexes. The group with E-LERW (M) had lower organ indexes of liver and kidney compared to the astilbin group, exhibiting more potent protective power on organs. This function is associated with the strong antioxidant activity of E-LERW [34]. Hyperglycemia mellitus is related to high yield of ROS, which may cause DNA oxidation. High levels of genomic damage led to liver and renal failure [35,36]. Antioxidant phytochemicals such as phenolic compounds and flavonoids help to scavenge ROS and protect the organs from radical related impairment [34]. The antioxidant components could also enhance the activity of antioxidant enzymes such as glutathione peroxidase and catalase [37] and lower the elevated levels of malondialdehyde (MDA) and NO in streptozotocin (STZ)-induced diabetic rats [38]. In addition, polyphenols and flavonoids were able to hinder the activity change of hepatic enzymes, for example, alanine aminotransferase (ALT), aspartate aminotransferase (AST) and lactate dehydrogenase (LDH), and attenuated the hepatic toxicity caused by STZ [39].

Conclusions
Astilbin was the principal component of E-LERW. Compared to astilbin, E-LERW presented significantly higher activity in scavenging radicals, FRAP, and inhibiting the oxidation of lipid membrane. E-LERW also displayed stronger affinity with α-glucosidase with more powerful inhibitory strength on the enzyme, which was evidenced by Lineweaver-Burk curves. After the alloxan injection, the plasma levels of FBG, oral glucose tolerance, TG, TC, and LDL of the mice increased to 4.18, 3.93, 2.04, 2.84, and 4.63 times the normal levels, respectively. Meanwhile, insulin secretion and HDL levels were reduced to 4.72% and 38.97% of normal mice. Alloxan also impaired the organs, causing the indexes of the liver and kidney to elevate 33% and 67%, respectively. Treatment with E-LERW (M) and (H) can efficiently lower the increased glucose and lipid levels induced by alloxan and boost the levels of insulin and HDL. In addition, E-LERW alleviated hyperglycemia-induced organ damage and decreased the liver and kidney indexes. Compared to astilbin control, E-LERW did not show more potent capacity in lowering glucose level and oral glucose tolerance, but presented a more efficient ability in preventing weight loss, reducing food intake, water intake, and excretion. Moreover, E-LERW was superior to astilbin in enhancing insulin secretion and protecting organs. The study indicates that E-LERW may be a promising functional ingredient in alleviating symptoms of diabetic patients. Informed Consent Statement: Not applicable.

Data Availability Statement:
The data used to support the findings of this study can be made available by the corresponding author upon request.