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Review

Flavonoids and Phenolic Acids from Oregano: Occurrence, Biological Activity and Health Benefits

by
Erick P. Gutiérrez-Grijalva
1,
Manuel A. Picos-Salas
1,
Nayely Leyva-López
2,
Marilyn S. Criollo-Mendoza
1,
Gabriela Vazquez-Olivo
1 and
J. Basilio Heredia
1,*
1
Laboratorio de Alimentos Funcionales y Nutracéuticos, Centro de Investigación en Alimentación y Desarrollo, AC. Carretera a Eldorado Km 5.5, Col. Campo el Diez, Culiacán CP 80110, Sinaloa, Mexico
2
Laboratorio de Nutrición y Planta de Alimentos, CONACYT-Centro de Investigación en Alimentación y Desarrollo, A.C., Av. Sábalo-Cerritos s/n, Mazatlán CP 82100, Sinaloa, Mexico
*
Author to whom correspondence should be addressed.
Plants 2018, 7(1), 2; https://doi.org/10.3390/plants7010002
Submission received: 11 October 2017 / Revised: 21 December 2017 / Accepted: 23 December 2017 / Published: 26 December 2017
(This article belongs to the Special Issue Plant Flavonoids)
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Abstract

:
Several herb species classified as oregano have been widely used in folk medicine to alleviate inflammation-related diseases, respiratory and digestive disorders, headaches, rheumatism, diabetes and others. These potential health benefits are partially attributed to the phytochemical compounds in oregano such as flavonoids (FL) and phenolic acids (PA). Flavonoids and phenolic acids are among the most abundant and most studied phytochemicals in oregano species. Epidemiological, in vitro and in vivo experiments have related long-term consumption of dietary FL and PA with a decreased risk of incidence of chronic diseases. The aim of this manuscript is to summarize the latest studies on the identification and distribution of flavonoids and phenolic compounds from oregano species and their potential antioxidant, anti-inflammatory and anti-cancer health benefits.

1. Introduction

It has been stated that oregano is the name used to refer to a numerous variety of plants that share a particular flavor and odor. At least 60 species and 17 genera belonging to diverse botanical families are known as oregano. However, the most relevant families are Verbenaceae and Lamiaceae [1]. Interestingly Franz and Novak [2] discusses this issue and reports a table listing species and family information of the oregano plants. Moreover, in this study we have considered as oregano the species in that list. Oregano has been traditionally used in folk medicine to alleviate conditions such as asthma, bronchitis, coughs, diarrhea, indigestion, stomachache, menstrual disorders, general infections, inflammation-related illnesses and diabetes [3]. The benefits of oregano on human health have been attributed to their phytochemical content [3,4]. Phytochemicals are a heterogeneous class of compounds derived from the secondary metabolism of plants, thus most of them do not appear to participate in essential metabolic roles. Research indicates that the main physiological function of phytochemicals is to serve as a plant defense mechanism against plant pathogens, pests, herbivores, UV-light and oxidative stress [5,6]. And their content in plants depends on factors such as cultivar, geographical localization, weather, daylight, temperature, soil conditions, water stress, harvesting time and others [7]. The most important phytochemicals found in oregano are grouped depending on their hydrophilic and hydrophobic properties into two categories: essential oils and phenolic compounds. Although research has often focused on the study of essential oils [8], they represent only one of the main groups of phytochemicals found in oregano. Thus, the study of hydrophilic compounds such as phenolic compounds is frequently ignored.
Flavonoids (FL) and phenolic acids (PA) are the main types of phenolic compounds present in oregano [9]. Oregano FL and PA have been studied due to their therapeutic potential, which has been partly attributed to their antioxidant properties [4,10]. Flavonoids and phenolic acids are molecules characterized by having at least one aromatic ring with one or more hydroxyl groups attached. FL and PA are compounds with a wide range of structures and can be classified based on the number and arrangement of their carbon atoms in: flavonoids (flavonols, flavones, flavan-3-ols, anthocyanidins, flavanones, isoflavones and others) and non-flavonoids (phenolic acids, hydroxycinnamic acids, hydroxybenzoic acids, stilbenes and others) and they are commonly found conjugated to sugars and organic acids [11,12,13]. All flavonoids are derived from the aromatic amino acids, phenylalanine and tyrosine and are C15 compounds arranged in three rings (C6-C3-C6) which are designated as A, B and C (Figure 1) [14]. Their structure varies due to the degree and pattern of hydroxylation, prenylation, alkalization or glycosylation reactions that modify the primary molecule [13]. These modifications can alter the water solubility of flavonoids, which can directly affect their bioavailability [15]. Flavones, which are the most abundant flavonoids present in oregano species, are characterized by the presence of a ketone group between C-2 and C-3 and the attachment of the B ring to C-2. Among the most widely distributed flavones in nature are apigenin, luteolin and their derivatives [14]. For further information regarding the physiological function and health effects of flavones we suggest the studies by Jiang et al. [16] and Singh et al. [17]. On the other hand, hydroxycinnamic acids are part of the non-flavonoid phenolics and the main subgroup of phenolic acids distributed in the different oregano species [18]. They are formed with an aromatic ring and a three-carbon chain (C6-C3) (Figure 1) [11]. There are four basic structures: coumaric acid, caffeic acid, ferulic acid and sinapic acid. In nature, they are usually associated with other compounds such as chlorogenic acid, which is the link between caffeic acid and quinic acid [19].

2. Flavonoids and Phenolic Acids Composition of Oregano Species

With the growing evidence on the biological activity from flavonoids and phenolic acids of oregano species, the identification of these compounds in oregano is important. Reports from different oregano species have shown that flavones are among the most abundant sub-group of FL followed by flavonols (Figure 2), flavanones and flavanols. Among the most common PA in oregano are: hydroxycinnamic acid and hydroxybenzoic acid derivatives and other phenolics [9]. The major individual FL and PA that have been identified in oregano species are rosmarinic acid, apigenin, luteolin, quercetin, scutellarein and their derivatives [4,9].
The content and distribution of FL and PA in oregano can vary depending on the cultivar, geographical and environmental factors aforementioned. It has been indicated that the flavonoid and phenolic acids profile of each oregano can be used to differentiate between oregano chemotypes within the same species. For instance, Timóteo et al. [21] reported that the flavonoids tricin-7-O-diglucuronide, chrysoeriol-7-O-diglucuronide and luteolin-7-O-glucuronide can be used to discriminate between three Brazilian chemotypes of Lippia alba. Similarly, Barbosa et al. [22] reported that two flavonoids, namely 5,5″-dihydroxy-6,4′,6″,3″,4′′′-pentamethoxy-[C7-O-C7″]-biflavone and 4′,4,5,5″-tetrahycroxy-6,6″,3′′′-trimethoxy-[C7-O-C7″]-biflavone, can be used to identify the limonene-carvone chemotype of Lippia alba. Likewise, the levels of rosmarinic acid have been reported to vary between the chemotypes within the species of O. vulgare ssp. hirtum, O. vulgare and O. syriacum [23]. Additionally, the FL and PA content of oregano species can vary depending on the vegetative stage of the plant. For instance, Baâtour et al. [24] suggested that during the late vegetative states of O. majorana L., there is a higher content of trans-2 hydroxinnamic, gallic and quercetin-3-galactoside, which makes it the best stage for harvesting O. majorana plants.
It can also be observed that oregano genotypes from the same species but from different places of origin can vary in their FL and PA composition, as is the case with the species Lippia graveolens, Lippia alba, O. majorana, O. vulgare and other oregano species. To illustrate, a recent study by Leyva-López et al. [4] reported 5 flavonoids in Lippia graveolens collected in Mexico, which are mainly flavones, namely quercetin-O-hexoside, scutellarein-7-O-hexoside, phloridzin, a trihydroxy-methoxyflavone derivative and 6-O-methylscutellarein. Whilst L. graveolens collected from Colombia reported by Stashenko et al. [25] had a different flavonoid profile with only 4 flavonoids, namely apigenin, luteolin, naringenin and quercetin. In contrast, O. vulgare collected from two different countries, China and Greece, showed a highly similar profile in their FL and PA content [26,27].
A summary of the major flavonoids and phenolic acids found in oregano species can be found in Table 1.

3. Physiological Functions of Flavonoids and Phenolic Acids from Oregano Species

Flavonoids and phenolic acids are accumulated in plant tissues (such as leaves, flowers, stems and roots) as a response to biotic and abiotic stress like pathogen and insect attack, UV radiation and wounding [13,47]. Phenolic compounds help plants survive and adapt to environmental disturbances through various physiological functions. Phenolic acids such as hydroxycinnamic acid derivatives serve as precursor molecules for the stilbenes, chalcones, flavonoids, lignans and anthocyanins [48]. These compounds are present in most tissues as conjugates (esters of carboxylic acids or sterols, amides of amino acids or amines, glycosides of mono or disaccharides) or insoluble-bound (attached to the structural components of the plant cell wall); and are rarely found in free form (monomers or dimers) [18,49].
On the other hand, flavonoids have been reported to play a variety of roles in plants, such as UV protection, pigmentation, growth regulation, stimulation of nitrogen-fixing nodules and disease resistance [11,50]. Flavonoids have the ability to absorb UV-wavelength; this ability depends on the molecular structure and the nature of substitution on different rings of their molecule. For instance, dihydroxy B ring substituted flavonoids have a better antioxidant capacity, while their monohydroxy B ring substituted analogue have greater capacity to absorb UV wavelengths [50]. The flavones orientin and luteolin are found in high levels in plants exposed to high levels of solar UV-B radiation [51]. Moreover, flavonoids are produced in the cytosol of cells and are present in high concentrations in the epidermis of leaves [52]. Besides, flavonoids may regulate auxin movement and catabolism. For instance, they modulate different phenotypes and morphoanatomical features of plants, because of their ability to create auxin gradients [50]. Furthermore, flavonoids play a role in the protection of plants against plant feeding insects and herbivores; since their presence can alter the palatability of plants and reduce their nutritive value, decrease digestibility or even act as toxins [53]. Additionally, quercetin 3-O-rutinoside (rutin) has been reported to enhance membrane rigidity and protect the membrane from oxidative damage caused by lipid peroxidation [50].
For a more detailed description of the chemistry and biological functions of flavonoids in plants, please refer to the review in the literature Samanta et al. [52].

4. Health Benefits of Flavonoids and Phenolic Compounds from Oregano Species

Epidemiological, in vitro and in vivo evidence has associated regular dietary intake of FL and PA with lower incidence of chronic diseases [54,55]. Interestingly, the flavonoids and phenolic acids that have been identified in oregano species have exhibited antioxidant, anti-inflammatory and anti-cancer properties [10,56,57]. Interestingly, some in vitro, in silico and in vivo studies have proposed a structure-activity relationship of flavonoids and phenolic acids with their biological properties [58,59,60]. For instance, Ambriz-Pérez et al. [58] summarized the following structure-anti-inflammatory activity relationship of flavonoids:
  • A planar ring system in the flavonoid molecule is needed for anti-inflammatory activity
  • Hydroxyl groups in B ring and at C5 and C7 of A ring are necessary for anti-inflammatory activity
  • The flavones and flavonoles having a hydroxyl group at 4′ position of B ring show higher anti-inflammatory activity
  • The methylation of the hydroxyl groups at 3, 5 or 4′ positions improves activity
  • The methylation of the 3-hydroxyl group reduces cytotoxicity
  • Flavones exhibited higher activities than isoflavones, flavonoles and flavanones
  • The 5, 6, 7-trihydroxyflavone core structure improves activity
  • Aglycones are more bioactive than glycosides
Furthermore, in accordance with the aforementioned, some sub-classes of flavonoids that are present in oregano species, have been related with higher activity towards certain diseases. For example, flavones have been linked with many pharmacological properties such as neuroprotective, anti-inflammatory, antioxidant, anti-asthmatic, anti-ulcer, decreased risk of cardiovascular diseases, anti-diabetic, anti-cancer, etc. [17,61,62,63]. Flavonols, for instance, have been associated with decreased risk of cardiovascular diseases [64]. Hydroxycinnamic acid derivatives have been linked with anti-diabetic, antioxidant and anti-cancer properties [65,66]. In the following sub-sections, we will briefly discuss studies regarding the antioxidant, anti-inflammatory and anti-cancer properties of oregano.

4.1. Antioxidant Properties of FL and PA from Oregano

Flavonoids and phenolic acids from oregano have been reported with antioxidant properties [4]. These compounds can be extracted using different polar solvents like water, methanol and ethanol to obtain antioxidant-rich extracts. The antioxidant capacity of a sample is usually measured by different methods typically classified in two groups: hydrogen atom transfer (HAT) and electron transfer (ET). For instance, the oxygen radical absorbance assay (ORAC) is among the most common HAT assay used. On the other hand, the most commonly used ET methods are: the inhibition of the 1,1′-diphenyl-2-picrylhydrazyl radical (DPPH), the Trolox equivalent antioxidant capacity (TEAC) method/ABTS radical cation decolorization assay (also known as ABTS assay), the ferric reducing-antioxidant power assay (FRAP), the cupric ion reducing antioxidant capacity method (CUPRAC) and total phenolic content assay. Interestingly, DPPH and ABTS can also act like HAT [67,68]. Table 2 summarizes studies regarding antioxidant capacity in oregano species.
It has been reported that the antioxidant capacity of extracts from different oregano species is somewhat dependent on the solvents used during their extraction, which has been correlated with the FL and PA yielding during the process. A different study showed that the methanolic extract of the stem has strong antioxidant capacity against the DPPH radical (96% at 200 ppm), superoxide anion radical scavenging (61% at 250 ppm) and TAC (634 μM AAE/g of extract); which is attributed to their phenolic content such as rosmarinic acid, caffeic acid, rutin, gallic acid, quercetin and p-coumaric acid as reported by HPLC analysis [69]. Moreover, Singh et al. [70] studied various leaf extracts from Eryngium foetidum, interestingly the aqueous extract had the highest phenolic content (256 mg gallic acid equivalents(GAE)/100 g fresh weight); furthermore, the methanolic extract was characterized by the presence of gallic, protocatechuic, syringic, p-coumaric, ferulic and sinapic acids.
The antioxidant capacity of oregano can also be affected by the cooking process. For instance, the effect of decoction and infusion on aqueous extracts of the leaves from Lippia alba has been studied by Timóteo et al. [21], they analyzed three chemotypes of Lippia alba and reported the presence of flavonoids of the class of flavones, especially mono and di-glucuronides of apigenin, luteolin and tricin. The authors noted that decoction samples with higher total phenolics content exhibited higher antioxidant activities (DPPH) than infusions, indicating that longer brewing time is better in the extraction of these compounds. Moreover, it was suggested that the presence of luteolin and luteolin-7-O-glucuronide in some chemotypes could improve the antioxidant capacity of Lippia alba. Aqueous extracts from Lippia graveolens (also known as Mexican oregano) have been studied for their antioxidant properties. For example, the oil free methanolic extract of L. graveolens showed a total phenolic content ranged from 211 to 270 mg GAE/g dried extract, where rosmarinic acid and naringenin were identified; meanwhile, in accordance with the TPC, the inhibition of the DPPH radical (IC50 = 152–207 μg/mL) was positively correlated to higher TPC [71]. However, another methanolic extract did not show the presence of rosmarinic acid but the flavonoids eriodictyol, naringenin, hispidulin and cirsimaritin were identified and, similarly to other studies, there was a positive correlation between the TPC and the antioxidant capacity by ORAC assay, around 5–9 mmol Trolox equivalents (TE)/mg of dry weight extract (DWE) [30].
Similarly, Lagouri and Alexandri [72] found a positive correlation between the TPC and antioxidant capacities by DPPH and FRAP of the leaves sequentially extracted with hexane, acetone and methanol, along with their infusion; they showed that the methanolic extract had higher DPPH value and the infusion higher TPC and FRAP value. Moreover, Kaliora et al. [34] observed a positive correlation between antiradical activity and quercetin protocatechuic acid, gallic acid, epicatechin, catechin, kaempferol and chlorogenic acid, found on the infusion of leaves and flowers.
Regarding Origanum glandulosum (syn. Origanum compactum), Béjaoui et al. [73] measured the antioxidant capacity of the methanolic extract, presenting an IC50 value of 0.6 mg/mL for DPPH, attributed principally to the presence of caffeic acid, which has been reported as a potent antioxidant [74]. Another widely studied oregano species regarding antioxidant capacity is Origanum majorana, characterized by the high content of rosmarinic acid. The antioxidant capacity of the microwave assisted methanolic extract from the aerial parts of O. majorana was analyzed by the CUPRAC, DPPH and TPC methods, showing high values attributed to the elevated content of rosmarinic acid, along with apigenin, caffeic acid and rutin [75]. Similarly, Elansary and Mahmoud [76] reported that rosmarinic acid and caffeic acid were the main compounds on the infusion and methanolic extract of the leaves from Origanum majorana, were the last one showed better antioxidant capacity by DPPH, β-carotene bleaching and TPC. Other flavonoids that have been found in methanolic extracts of O. majorana with correlation with TPC and ORAC values are eriodictyol and naringenin [30]. Similarly, rosmarinic acid was found to be the phenolic acid that provides the strongest antioxidant activity by FRAP and DPPH on hydromethanolic extract from Origanum majorana [39]. On the other hand, Vallverdú-Queralt et al. [77] did not find the presence of rosmarinic acid in the hydroethanolic extract of Origanum majorana, nevertheless protocatechuic acid, syringic acid and caffeic were the main compounds and the TPC exhibited a positive correlation with the DPPH and ABTS assays. Kogiannou et al. [26] reported relatively low TPC (38 mg GAE/200 mL) on the infusion of the leaves and flowers from Origanum microphyllum, with caffeic acid, syringic acid and naringenin as the main phenolics. Moreover, the antioxidant capacity was attributed to this content of phenolics, especially to caffeic acid, by FRAP assay.
Greek oregano (Origanum vulgare) is the most recognized herb as oregano around the world, generally reporting elevated content of rosmarinic acid. Yan et al. [78] analyzed the hydro-methanolic extract of the leaves from O. vulgare by TPC and ORAC, with results of 79–147 mg GAE/g DW and 1.59–3.39 mmol TE/g DW, respectively; but no correlation was found between the rosmarinic acid content and the antioxidant capacity measured by ORAC, which may indicate that other compounds are acting as antioxidant agents. In contrast, Gonçalves et al. [10] partially attributed the high antioxidant capacity (DPPH, ABTS and FRAP) of the same kind of extract to the large quantity of rosmarinic acid (23.53 mg/g of dry extract) and the presence of other active compounds like (−)-epicatechin. A study by Koldaş et al. [32] in O. vulgare associated the presence rosmarinic, chicoric and caffeic acid with the antioxidant capacity of samples. Furthermore, eriodictyol and naringenin were also found in the methanolic extract of O. vulgare leaves, which exhibited high TPC (430 μg of GAE/mg of DWE) and a positive correlation with the ORAC value (~11 mmol TE/mg DWE) [30]. Likewise, the flavonoids luteolin-7-O-glucoside and apigenin-7-O-glucoside were obtained using accelerated solvent extraction with methanol, presenting a significant positive correlation between the TPC and the FRAP value [79]. Moreover, Balkan et al. [80] found a correlation between the TPC and DPPH scavenging activity with the presence of eriodictyol, apigenin and caffeic acid in the aqueous extract of O. vulgare.
For Thymbra capitata, the ethyl acetate extracts of aerial parts exhibited higher TPC, probably related to the higher content of taxifolin di-O-glucoside; whereas, the ethanolic extract was more efficient on the superoxide scavenging activity assay, the effect attributed to the higher content of rosmarinic acid in the extract [81].
As it can be seen, the polarity of the solvents used to extract FL and PA of interest from oregano can affect the yield and profile of compounds obtained, thus affecting their antioxidant capacity.

4.2. Anti-Inflammatory Properties of FL and PA from Oregano

Inflammation is a response of the organism to detect and destroy harmful agents [82]. During inflammation, the synthesis of pro-inflammatory mediators is activated. Some of these mediators are nitric oxide (NO), reactive oxygen species (ROS), cytokines and prostaglandins (PGs), as well as enzymes such as inducible nitric oxide synthase (iNOS) and cyclooxygenases (COXs) [83]. When the inflammatory response is not well regulated an overproduction of these mediators is triggered causing pathological processes associated to diseases namely, arthritis, atherosclerosis and cancer, among others [84,85]. Therefore, the inhibition of the pro-inflammatory mediators mentioned is an important objective for the treatment of inflammation-related diseases.
It has been suggested that phenolic compounds from oregano, such as flavonoids and phenolic acids, might exert anti-inflammatory properties (Table 3) [86,87,88]. In this regard, Mueller et al. [89] evaluated the anti-inflammatory activity of Origanum onites and O. majorana hydrophilic extracts on lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophage cells. Pre-treatment of the cells with O. onites extracts at 500 μg/mL and 200 μg/mL reduced 19% and 49% the secretion of the pro-inflammatory cytokine IL-6, respectively, while the expression of iNOS was completely inhibited. Similarly, when macrophages were pre-treated with the extracts from O. majorana at 500 μg/mL and 200 μg/mL the levels of IL-6 were reduced 20% and 17%, respectively, while the iNOS expression was diminished 66%. Even though Mueller et al. [89] did not identify the compounds in the O. onites and O. majorana extracts, they mention that diosmetin, apigenin, luteolin and rosmarinic acid are the compounds to most likely be present in the hydrophilic extracts, so these molecules might be responsible for the activity of oregano extracts. On the other hand, aqueous infusion of O. vulgare was evaluated by Kogiannou et al. [26] in order to know their effect on IL-8 secretion, a pro-inflammatory and cancer promoting cytokine, in the cancerous cell lines HT-29 and PC3. When cells were treated with the O. vulgare infusion powder (0.2 μg powder/μL of medium) and stimulated with TNF-α, the IL-8 concentration on the medium was significantly reduced in both HT-29 and PC3 cells. The phenolic acid and flavonoid profile of the infusion from O. vulgare was also determined. The authors attributed to caffeic acid present in the infusion part of the anti-IL-8 activity of oregano.
Recently, it has been demonstrated that extracts from the oregano species Lippia graveolens, L. palmeri and Hedeoma patens, containing quercetin, luteolin and scutellarein derivatives and salvianolic and neochlorogenic acids, showed anti-inflammatory activity by lowering ROS and NO production in LPS-induced inflammation in lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophage cells [4].
For a better understanding on how phenolic compounds exert their anti-inflammatory activity we recommend to review the papers by Ambriz-Pérez et al. [58] and Leyva-López et al. [90].

4.3. Anti-Cancer Properties of FL and PA from Oregano

Cancer is described as “a group of diseases characterized by unregulated cell growth and the invasion and spread of cells from the site of origin, or primary site, to other sites in the body” [91]. Several factors are involved in the onset of cancer such as age, alcohol, cancer-causing substances, diet, hormones, obesity, radiation, tobacco, etc.; and they may play a direct or indirect role in the development and progressions of different types of cancers. Carcinogenesis includes five known steps: initiation, promotion, progression, invasion and metastasis. The National Cancer Institute [92] states that in vitro and in vivo studies have shown that the increased presence of antioxidants prevents free radical damage that has been associated with cancer development. Plant foods are the most significance source of natural antioxidants; from which, flavonoids and phenolic acids have attracted the most attention as potential therapeutic agents against cancer. Shukla and Gupta [93] summarized that the potential anticancer properties of FL and PA as demonstrated by laboratory studies are due to different mechanisms of action, including antioxidation, induction of detoxification enzymes and inhibition of bioactivation enzymes, estrogenic and anti-estrogenic activity, antiproliferation, cell cycle arrest and apoptosis, promotion of differentiation, regulation of host immune function and inhibition of angiogenesis and metastasis. Several of the wide variety of FL and PA that have been identified in species classified as oregano have been reported with anti-cancer properties (Table 4). Thus, research has focused on the use of oregano FL and PA as potential anti-cancer therapy.
In this subject, the ethanolic extracts from Origanum compactum showed cytotoxic activity against human breast cancer cells (MCF7) and this effect was partially attributed to its FL content [94]. Calderón et al. [95] used the methanolic extracts of Lippia cardiostegia had cytotoxic activity at values from GI50 of 5.5, 5.2 and 7.5 (µg/mL) over breast (MCF-7), lung (H-460) and central nervous system (SF-268) human cancer cell lines. Methanolic extract from Origanum compactum also exhibited cytotoxic activity against MCF-7 cells, with IC50 values from 382 μg/mL to 374 μg/mL [96]. Hesperetin isolated from Origanum majorana has shown better antiproliferative activity than 5-fluoroacil against Rattus norvegicus brain glioma (C6) and HeLa cells [97]. The FL and PA of hydroalcoholic extracts from Origanum vulgare L. subsp. viridulum showed antiproliferative activity, with 44% of inhibition of cell proliferation against human breast cancer cells (MFC-7), around 64% of inhibition against hepatic cancer cells (HepG2) and around 40% of inhibition of colorectal cancer (LoVo) cells. It is important to mention that Origanum vulgare extracts seemed to exhibit a selective antiproliferative activity against HepG2 [98].
Savini et al. [99] evaluated the ethanolic extracts from Origanum vulgare on cell proliferation and cell death in colon adenocarcinoma (Caco-2) cells; finding that at a concentration of 300 μg/mL oregano extract cell viability of decreased approximately 30% after 24 h; however, at a concentration of 500 μg/mL death time-dependently occurred. They also suggested that the mix of phenolic compounds found in O. vulgare extracts is more effective than individual phenolics, indicating a synergistic effect between compounds. Moreover, Nile et al. [100] suggested that the high cytotoxicity of Origanum vulgare extracts against breast cancer cells (MFC-7) is related to its high phenolic content
Likewise, García-Pérez et al. [57] evaluated different extracts from Poliomintha glabrescens for cytotoxic activity in colon cancer cells HT-29. The evaluated samples showed inhibition of the proliferation of HT-29 cell line, which was partially attributed to the luteolin and apigenin content in Poliomintha glabrescens.
According to all of these studies, the phenolic extracts and isolated flavonoids and phenolic acids of species classified as oregano are a promising source for the development of new drugs in the treatment of cancer, nevertheless more research is necessary to understand in detail the mechanisms of action of these compounds as well as their effects on in vivo models and the possible side effects that could occur their administration.

5. Enhancement of Flavonoid and Phenolic Acids Content in Oregano Species

As previously shown, oregano species are an important source of flavonoids and phenolic acids, which have been of special interest because of their potential use as antioxidants, anti-inflammatory and anti-cancer agents [4]. As a consequence, the enhancement of FL and PA in oregano species is desired. Consequently, research has shown that flavonoids and phenolic acids in plants can be enhanced by several methods; however, research regarding enhancement of FL and PA content in oregano is scarce [104,105,106,107,108]; nonetheless there are few studies on enhancement of FL and PA from Lamiaceae herbs, like Ocimum basilicum, that can provide information for further research in plants known as oregano. Among the most studied are the agronomic approaches and through the use of plant elicitors [109]. The main agricultural method focuses on the manipulation of FL and PA content by the manipulation of nutrient (such as application of nitrogen fertilizers) and altering irrigation strategies. On the other hand, plant elicitors are compounds that can induce plant defense reactions that could result in the production of defense secondary metabolites such as FL and PA [108].

5.1. Nutrient Manipulation

Few studies have focused on the effect of nutrient manipulation on the enhancement of flavonoid and phenolic acid content in oregano species. Briefly, boron toxicity was shown to increase phenolic content and anthocyanins in Ocimum basilicum, which is suggested to be a plant strategy to mitigate the negative effects of boron within the cells [110]. A couple of studies have also researched the effects of nitrogen manipulation on the phenolic content and antioxidant capacity in Ocimum basilicum and have shown that the levels of phenolics such as rosmarinic and caffeic acid can be enhanced as a result of nitrogen treatment [111,112]. Moreover, the total content of rosmarinic acid of Origanum vulgare can be increased when cultivated under manipulation of proline content [104]. However, caution is needed since these strategies can hinder plant growth.

5.2. Light Quality

FL and PA are secondary metabolites that are metabolized as a response to UV stress in order to avoid oxidative stress on plants. In this regard, some studies have addressed this issue by studying the effect of light quality on FL and PA content. However, research regarding the effect of light stress on FL and PA content in oregano is scarce. For instance, Shiga et al. [113] showed that the rosmarinic acid content and antioxidant capacity of Ocimum basilicum L. were increased as a result of white light irradiation. Another study in Ocimum basilicum L. by Ghasemzadeh et al. [114] reported that UV-B radiation (3.60 W/m2) improved the total phenolic and flavonoid content as well as the content of gallic acid, cinnamic acid, ferulic acid, quercetin, catechin, kaempferol, rutin and luteolin. UV treatment can also increase the content of rosmarinic acid in Origanum vulgare [106]. Additionally, UV-B treatment increased the activity of the enzyme chalcone synthase (EC: 2.3.1.74), which is a key enzyme in the phenylpropanoid metabolism, catalyzing the conversion of p-coumaroyl-CoA and malonyl-CoA to naringenin chalcone, which is a precursor of flavonoids [115].

5.3. Plant Elicitors

5.3.1. Chitosan

Chitosan is a biopolymer produced the deacetylation of chitin. And has been extensively studied as a plant elicitor in several crops [116]. Some reports have shown the use of chitosan as a FL and PA enhancer in oregano species. For instance, the content of rosmarinic acid in Ocimum basilicum L. increased after chitosan treatment [117]. Similarly, Yin et al. [108] applied chitosan oligosaccharides in Origanum vulgare ssp. hirtum, which resulted in increased content of lithospermic acid B and apigenin-6,8-diglucoside. Moreover, a combination of application of chitosan on Ocimum basilicum and reduced irrigation increased the total phenolic content and antioxidant activity [118]. Overall, these studies concluded that chitosan concentration had an impact on LF and PA stimulation.

5.3.2. Plant Growth Regulators

Growth and development in plants is regulated by endogenous phytohormones that play key roles on their metabolism. Additionally, these molecules can be used as potent elicitors. Among the most commonly used growth regulators are methyl jasmonate, jasmonic acid, spermine and arachidonic acid. In this regard, Koca and Karaman [119] showed that the application of a combination of methyl jasmonate and spermine enhanced the rosmarinic acid content in Ocimum basilicum L. Similarly, a study by Złotek et al. [120] in purple Ocimum basilicum showed an increased content of benzoic acid and rosmarinic acid after application of arachidonic and jasmonic acid. Malekpoor et al. [121] also showed an increased total phenolic content and antioxidant activity in Ocimum basilicum L. after treatment with jasmonic acid. Moreover, Kim et al. [122] showed that application of methyl jasmonate in Ocimum basilicum L. enhanced the rosmarinic and caffeic acid as well as the antioxidant activity of the samples. Additionally, acetyl salicylic acid in combination with fish protein hydrolyzate has been shown to stimulate the phenylpropanoid metabolism, which results in higher antioxidant activity [107].
Interestingly, even though enhancement FL and PA content is desired in oregano species due to their proposed human health effects, high concentrations of these compounds have shown a reduced plant growth and reproduction [109]. It is important to mention that even though the aim of this study was not to summarize flavonoid and phenolic acids enhancement methods, we consider of interest to recommend the studies by Malerba and Cerana [116], García-Mier et al. [109], Pichyangkura and Chadchawan [123] and Trivellini et al. [124].

6. Conclusions

In conclusion, due to the wide variety of herbs regarded as oregano, there is a complex mixture of flavonoids and phenolic acids that can be found throughout them, from which flavones are the main constituents. These compounds have been of particular interest for their potential bioactive properties and promising role as alternative treatment in several illnesses. Here we have summarized the most recent studies focusing on the characterization studies of oregano FL and PA as well as their antioxidant, anti-inflammatory and anti-cancer properties. Interestingly, most of the studies are based on in vitro approaches, limiting its extrapolation to human health. Hence, further in vivo research is needed to understand the bioavailability, pharmacokinetics and mechanism of action of oregano FL and PA as agents in human health improvement.

Acknowledgments

This work was financially supported by the Mexican Council for Science and Technology (CONACyT) (Proyecto Ciencia Básica 25416). Erick P. Gutiérrez-Grijalva would like to acknowledge the doctoral scholarship (Grant #391880) received from the CONACyT.

Author Contributions

Erick P. Gutiérrez-Grijalva initiated this review in partial fulfillment of his experimental education under the supervision of J. Basilio Heredia; both of them contributed with the edition of this manuscript. Nayely Leyva-López, Manuel A. Picos-Salas, Marilyn S. Criollo-Mendoza and Gabriela Vazquez-Olivo contributed to its writing.

Conflicts of Interest

The authors declare no conflict of interest.

Abbreviations

FLFlavonoids
PAPhenolic acids
BHTButylated hydroxytoluene
HATHydrogen atom transfer
ETElectron transfer
ORACOxygen radical absorbance assay
DPPH1,1′-diphenyl-2-picrylhydrazyl radical
ABTS2,2′-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid)
FRAPFerric reducing-antioxidant power assay
CUPRACCupric ion reducing antioxidant capacity
TACTotal antioxidant capacity
TPCTotal phenolic content
DWDried weight
DWEDried weight extract
NONitric oxide
ROSReactive oxygen species
IL-6Interleukin 6
IL-8Interleukin 8
IL-10Interleukin 10
TNF-αTumor necrosis factor alpha
COX-2Cyclooxygenase-2
LPSLipopolysaccharide
iNOSNitric oxide synthase
COXsCyclooxygenases

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Plants 07 00002 g001 550
Figure 1. General structure of hydroxycinnamic acids, hydroxybenzoic acids and flavonoids.
Figure 1. General structure of hydroxycinnamic acids, hydroxybenzoic acids and flavonoids.
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Plants 07 00002 g002 550
Figure 2. Chemical structure of common flavones commonly found in oregano species. (a) apigenin, (b) luteolin, (c) scutellarein, (d) apigenin-7-O-glucoside, (e) luteolin-7-O-glucoside, (f) luteolin-7-O-glucuronide. Structures from Phenol-Explorer Database, Version 3.6 [20].
Figure 2. Chemical structure of common flavones commonly found in oregano species. (a) apigenin, (b) luteolin, (c) scutellarein, (d) apigenin-7-O-glucoside, (e) luteolin-7-O-glucoside, (f) luteolin-7-O-glucuronide. Structures from Phenol-Explorer Database, Version 3.6 [20].
Plants 07 00002 g002
Table
Table 1. Principal components of flavonoids and phenolic compounds of different oregano species.
Table 1. Principal components of flavonoids and phenolic compounds of different oregano species.
Oregano SpeciesOriginExtraction SolventFlavonoids and Phenolic Acids ConstituentsReference
Hedeoma patensMexicoMethanol/acetone/water (50:40:10)3-O-caffeoylquinic acid, luteolin-7-O-glucuronide, scutellarein-7-O-hexoside, salvianolic acid A[4]
Lippia alba (Mill.) N. E. BrownBrazilMethanol 62.5%Apigenin-7-O-diglucuronide, chrysoeriol-7-O-diglucuronide, luteolin-7-O-glucuronide, tricin-7-O-diglucuronide, tricin-7-O-glucuronide[25]
Lippia alba (Mill.) N. E. BrownFranceMethanol/hydromethanolLuteolin-7-diglucuronide, verbascoside, chlorogenic acid[28]
Lippia alba (Mill.) N.E. BrownBrazilChloroform5,5′′-dihydroxy-6,4′,6′′,3′′′,4′′′-pentamethoxy-[C7–O–C7′′]-biflavone, 4′,4,5,5′′-tetrahydroxy-6,6′′,3′′′-trimethoxy-[C7–O–C7′′]-biflavone[22]
Lippia citriodoraGermanyWaterVerbasoside, luteolin-7-diglucuronide, apigenin-7-diglucuronide[29]
Lippia graveolensMexicoMethanol/acetone/water (50:40:10)Quercetin O-hexoside, scutellarein 7-O-hexoside, phloridzin, trihydroxy-methoxyflavone derivative, 6-O-methylscutellarein[4]
Lippia graveolensNR 1Methanol 70%6-Hydroxyluteolin 7-O-hexoside, pentaflavanone-B hexoside-1, pentaflavanone-B hexoside-2, scutellarein 7-O-hexoside, luteolin 7-O-glucoside, taxifolin, 6-hydroxyluteolin 7-O-rhamnoside, 6-hydroxyluteolin, 3-hydroxyphloretin 6′-O-hexoside, apigenin 7-O-glucoside, phloridzin, scutellarein, eriodictyol, luteolin, quercetin, naringenin, 6-methylscutellarein, 6,7-dimethylscutellarein, sakuranetin, pinocembrin, galangin, methylgalangin[9]
Lippia graveolensUSAMethanol 100%Eriodictyol, naringenin, hispidulin, cirsimaritin[30]
Lippia micromeraColombiaMethanol/hydromethanolNaringenin, apigenin[28]
Lippia origanoidesColombiaMethanol 62.5%Quercetin, naringenina, luteolin, pinocembrin[25]
Lippia palmeriMexicoMethanol/acetone/water (50:40:10)Quercetin-O-hexoside, luteolin 7-O-glucuronide-3′-O-glucoside, scutellarein 7-O-hexoside, trihydroxy-methoxyflavone derivative[4]
Majorana hortensis Moench.PolandWaterCaffeic acid, lithospermic acid, rosmarinic acid[31]
O. acutidensTurkeyWaterGallic acid, caffeic acid, 4-hydroxybenzaldehyde, p-coumaric acid, rosmarinic acid[32]
O. dictamusGreeceMethanol 62.5%/BHTVanillic acid, protocatechuic acid, syringic acid, gallic acid, cinnamic acid, o-coumaric acid, p-coumaric acid, caffeic acid, chlorogenic acid, rosmarinic acid, chrysin, epicatechin, naringenin, catechin, genistein, quercetin[33]
O. dictamusGreeceWaterChlorogenic acid, rutin, luteolin-7-O-glucoside, apigenin-7-O-glucoisde, rosmarinic acid, luteolin[34]
O. indercedensGreeceMethanolCaffeic acid, rosmarinic acid[35]
O. majoram L.GermanyMethanol 60%/Formic acid 1%Apigenin-6,8-di-C-glucoside, luteolin-7′-O-glucuronide, rosmarinic acid, apigenin-glucuronide, lithospermic acid A isomer a, salvianolic acid B, apigenin[36]
O. majoram L.TunisiaMethanolDihydroxybenzoic acid hexose, syringic acid, vanillic acid, dihydroxybenzoic acid, p-coumaric acid, chlorogenic acid, salvianolic acid I, caffeoyl-arbutin, rosmarinic acid, gallocatechin isomer 1, gallocatechin isomer 2, 3-O-methyl-catechin, luteolin-6,8-C-dihexose, apigenin-6,8-di-C-hexoside, isoorientin, orientin, isovitexin, kaempferol-O-sumbubioside, kaempferol-O-glucuronide, luteolin-O-glycoside, diosmin, apigenin-O-glucuronide, acacetin rutinoside, luteolin, apigenin, taxifolin, taxifolin methyl ether isomer 1, taxifolin methyl ether isomer 2, dihydrokaempferide, hesperidin, eriodictyol, sakuranetin, O-methy-quercetin, dimethyl myriceitn, quercetin dimethyl ether, jaceidin isomer 1, jaceidin isomer 2[37]
GreeceWaterVanillic acid, protocatechuic acid, syringic acid, gallic acid, cinnamic acid, o-coumaric acid, p-coumaric acid, ferulic acid, caffeic acid, sinapic acid, rosmarinic acid, chrysin, epicatechin, naringenin, catechin, kaempferol, quercetin[34]
PolandMethanolProtocatechuic acid, p-hydroxybenzoic acid, gentisic acid, chlorogenic acid, syringic acid[38]
TurkeyMethanol 80%Caffeic acid glucoside, epigallocatechin, arbutin, luteolin ruitinoside, luteolin glucuronide, rosmarinic acid, dihydroquercetin, dihydroluteolin, apigenin, quercetin, quercetin arabinoside, luteolin-7-O-glucoside gallocatechin derivative[39]
GermanyMethanol 50%Luteolin-6,8-di-C-glucoside, apigenin-6,8-di-C-glucoside, luteolin-glucuronide, rosmarinic acid, apigenin-glucuronide, lithospermic acid, apigenin[40]
O. majoram L.USAMethanol 80%Eriodictyol 6,8-di-C-glucoside, eriodictyol 7-O-glucoside, apigenin 6,8-di-C-glucoside, luteolin 7,7′-di-O-glucuronide, luteolin 7-O-glucuronide-3′-O-glucoside, apigenin 7-O-diglucuronide, luteolin 7-O-glucuronide, luteolin 7-O-glucuronide, luteolin 7-O-glucoside, apigenin 7-O-glucoside, apigenin 7-O-glucuronide, rosmarinic acid [41]
TurkeyWaterGallic acid, caffeic acid, p-coumaric acid, rosmarinic acid, chicoric acid, apigenin-7-glucoside, quercetin, kaempferol[32]
ItalyCascade extraction with ethyl acetate and ethanolEriodictyol 7-O-rutinoside, aromadendrin, eriodictyol, naringenin, luteolin, sorbifolin, cirsiliol, apigenin, cirsilineol, cirsimaritin, xanthomicrol, caffeic acid, rosmarinic acid[42]
GreeceCascade extraction with hexane and ethyl acetateSalvianolic acid H, salvianolic acid B, rosmarinic acid, salvianolic acid C, eriodictyol, naringenin[43]
FinlandMethanol 40%Calleryanin 3,4-dihydroxybenzoate, gastrodin 3,4-dihydroxybenzoate, calleryanin 3-hydroxy,4-methoxybenzoate[44]
PortugalMethanol 80%Gallic acid, 3,4-dihydroxybenzoic acid, (+)-catechin, caffeic acid, (−)-epicatechin, rosmarinic acid[10]
Oregano 2TurkeyMethanol 80%Gallic acid, syringic acid, vanillic acid, protocatechuic acid, chlorogenic acid, p-coumaric acid, quercetin-3-O-hexoside, luteolin-7-O-glucoside, ferulic acid, phloridzin, dicaffeoylquinic acid, apigenin-7-O-rutinoside, rutin, apigenin-7-O-glucoside, rosmarinic acid, luteolin-3-O-glucuronide, luteolin-7-O-rutinoside, quercetin, apigenin, 4′-methoxyapigenin, 6,7-dimethoxyscutellarein, luteolin[45]
Poliomintha longifloraNR 1Phosphate bufferVanillic acid, caffeic acid, luteolin, rosmarinic acid, hispidulin[46]
1 Not reported, 2 Species not mentioned.
Table
Table 2. A summary of the antioxidant capacity of flavonoids and phenolic acids of different oregano species.
Table 2. A summary of the antioxidant capacity of flavonoids and phenolic acids of different oregano species.
Oregano SpeciesExtractCompoundsPlant PartAntioxidant AssayReference
Coleus aromaticusMethanolRosmarinic, caffeic, p-coumaric and gallic acids; quercetin and rutinStemDPPH, superoxide, TAC[69]
Eryngium foetidumAqueous, methanolGallic, protocatechuic, syringic, p-coumaric, ferulic and sinapic acidsLeavesTPC, DPPH[70]
Lippia albaAqueousApigenin-7-O-diglucuronide, chrysoeriol-7-O-diglucuronide, tricin-7-O-diglucuronide, luteolin-7-O-glucuronideLeavesTPC, DPPH[21]
Lippia graveolensMethanolRosmarinic acid, naringeninAerial partsTPC, DPPH[71]
MethanolEriodictyol, naringenin, hispidulin, cirsimaritinLeaves, commercial herbsTPC, ORAC[30]
Origanum dictamnusSequentially with hexane, acetone and methanol; AqueousMethanolic: gallic, caffeic, ferulic and rosmarinic acids. Aqueous: gallic, caffeic, protocatechuic and rosmarinic acidsLeavesTPC, DPPH, FRAP[72]
AqueousRosmarinic, caffeic and vanillic acids, epicatechin, catechin, genisteinLeaves and flowersTPC, DPPH, FRAP[34]
Origanum glandulosumMethanol, previously deffated with n-hexaneCaffeic acid, luteolin glucosideNot specifiedDPPH, FRAP[73]
Origanum majoranaMethanol microwave-assistedRosmarinic and caffeic acid, apigenin, rutinAerial partsTPC, DPPH, CUPRAC[75]
Aqueous, methanolRosmarinic and caffeic acidsLeavesTPC, DPPH, β-carotene bleaching[76]
MethanolRosmarinic acid, eriodictyol, naringenin, hispidulin, cirsimaritinLeaves, commercial herbsTPC, ORAC[30]
MethanolRosmarinic acid, epigallocatechin, quercetin, apigeninNot specifiedDPPH, FRAP[39]
EthanolChlorogenic, ferulic, p-coumaric, p-hydroxybenzoic, protocatechuic, rosmarinic and syringic acids, quercetinNot specifiedTPC, DPPH, ABTS[77]
Origanum microphyllumAqueousp-Hydroxybenzoic, protocatechuic, syringic and caffeic acids, naringeninLeaves and flowersTPC, FRAP[26]
Origanum vulgareMethanolRosmarinic acidLeavesTPC, ORAC[78]
MethanolRosmarinic acid and (−)-epicatechinLeavesDPPH; ABTS, FRAP[10]
Water, methanol, ethyl acetate, hexaneRosmarinic, caffeic, chicoric and p-coumaric acidsLeavesTPC, DPPH, TAC, RP, superoxide[32]
MethanolRosmarinic acid, eriodictyol, naringeninLeavesTPC, ORAC[30]
Origanum vulgareMethanolRosmarinic and caffeic acids, luteolin-7-O-glucoside, apigenin-7-O-glucosideNot specifiedTPC, FRAP[79]
AqueousEriodictyol, apigenin, caffeic acid, kaempferolNot specifiedTPC, DPPH[80]
Thymbra capitataEthyl acetate, ethanolEthyl acetate: taxifolin di-O-glucoside, thymusin. Ethanol: taxifolin di-O-glucoside, rosmarinic acidAerial partsTPC, superoxide[81]
Table
Table 3. A summary of the anti-inflammatory properties of flavonoids and phenolic acids of different oregano species.
Table 3. A summary of the anti-inflammatory properties of flavonoids and phenolic acids of different oregano species.
Oregano SpeciesCompoundsEffectReference
Eryngium foetidumKaempferol, chlorogenic acid, caffeic acidReduction of NO and ROS production and inhibition of the protein levels and gene expression of IL-6, TNF-α, iNOS and COX-2 in LPS-stimulated RAW 264.7 murine macrophages[88]
Hedeoma patensNeochlorogenic acid, Luteolin-7-O-glucuronide, scutellarein-7-O-hexoside, salvianolic acid AReduction of the levels of NO and ROS produced in murine macrophage cells[4]
Lippia graveolensQuercetin-O-hexoside, scutellarein-7-O-hexoside, phloridzin, trihydroxy-methoxyflavone derivative, 6-O-methylscutellareinInhibition of the NO and ROS production in LPS-stimulated murine macrophage cells[4]
Lippia palmeriQuercetin-O-hexoside, luteolin-7-O-glucuronide-3′-O-glucoside, scutellarein-7-O-hexoside, trihydroxy-methoxyflavone derivative, 6-O-methylscutellareinDecrease of the levels of NO and ROS produced in murine macrophage cells[4]
Origanum vulgareCaffeic acidDiminution of IL-8 secretion in HT-29 and PC3 cells[26]
Table
Table 4. A summary of the anti-cancer properties of flavonoids and phenolic acids of different oregano species.
Table 4. A summary of the anti-cancer properties of flavonoids and phenolic acids of different oregano species.
Oregano SpeciesAnti-Cancer ActivityEffectReference
Origanum dictmnusCytotoxicActivity against human bronchial epidermoid carcinoma (NSCLC-N6) and murine leukemia (P388) cells line.[101]
Origanum compactumCytotoxicActivity against human breast cancer cells (MCF-7)[94]
AntiproliferativeInhibit human breast cancer (MCF-7) cell proliferation.[96]
Origanum syriacumAntiproliferativeReduction in the proliferation of human breast cancer cells (MFC-7).[102]
Origanum vulgareAntiproliferativeReduction in the proliferation of human breast cancer (MFC-7), colorectal cancer (LoVo), cervical epithelial carcinoma (HeLa) cells and selective antiproliferative activity on hepatic cancer cells (HepG2).[32,98,102]
CytotoxicShowed signs of cells death on cervical epithelial carcinoma (HeLa) cell line and cytotoxicity for breast cancer and colon adenocarcinoma (Caco-2) cells.[98,99,100,103]
Lippia cardiostegia BenthCytotoxic Activity against breast (MCF-7), lung (H-460) and central nervous system (SF-268) human cancer cell lines.[95]
Origanum marjoranaAntiproliferativeInhibit Rattus norvegicus brain glioma (C6) and cervical epithelial carcinoma (HeLa) cell proliferation.[97]
CytotoxicActivity against fibrosarcoma (HT-1080) cell line.[98]
Origanum acutidensAntiproliferativeInhibit cervical epithelial carcinoma (HeLa) cell proliferation. [32]
Poliomintha glabrescens GrayCytotoxicActivity against human colon cancer cells (HT-29).[57]

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Gutiérrez-Grijalva, E.P.; Picos-Salas, M.A.; Leyva-López, N.; Criollo-Mendoza, M.S.; Vazquez-Olivo, G.; Heredia, J.B. Flavonoids and Phenolic Acids from Oregano: Occurrence, Biological Activity and Health Benefits. Plants 2018, 7, 2. https://doi.org/10.3390/plants7010002

AMA Style

Gutiérrez-Grijalva EP, Picos-Salas MA, Leyva-López N, Criollo-Mendoza MS, Vazquez-Olivo G, Heredia JB. Flavonoids and Phenolic Acids from Oregano: Occurrence, Biological Activity and Health Benefits. Plants. 2018; 7(1):2. https://doi.org/10.3390/plants7010002

Chicago/Turabian Style

Gutiérrez-Grijalva, Erick P., Manuel A. Picos-Salas, Nayely Leyva-López, Marilyn S. Criollo-Mendoza, Gabriela Vazquez-Olivo, and J. Basilio Heredia. 2018. "Flavonoids and Phenolic Acids from Oregano: Occurrence, Biological Activity and Health Benefits" Plants 7, no. 1: 2. https://doi.org/10.3390/plants7010002

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