Dietary flavonoid aglycones and their glycosides: Which show better biological significance?

The dietary flavonoids, especially their glycosides, are the most vital phytochemicals in diets and are of great general interest due to their diverse bioactivity. The natural flavonoids almost all exist as their O-glycoside or C-glycoside forms in plants. In this review, we summarized the existing knowledge on the different biological benefits and pharmacokinetic behaviors between flavonoid aglycones and their glycosides. Due to various conclusions from different flavonoid types and health/disease conditions, it is very difficult to draw general or universally applicable comments regarding the impact of glycosylation on the biological benefits of flavonoids. It seems as though O-glycosylation generally reduces the bioactivity of these compounds - this has been observed for diverse properties including antioxidant activity, antidiabetes activity, anti-inflammation activity, antibacterial, antifungal activity, antitumor activity, anticoagulant activity, antiplatelet activity, antidegranulating activity, antitrypanosomal activity, influenza virus neuraminidase inhibition, aldehyde oxidase inhibition, immunomodulatory, and antitubercular activity. However, O-glycosylation can enhance certain types of biological benefits including anti-HIV activity, tyrosinase inhibition, antirotavirus activity, antistress activity, antiobesity activity, anticholinesterase potential, antiadipogenic activity, and antiallergic activity. However, there is a lack of data for most flavonoids, and their structures vary widely. There is also a profound lack of data on the impact of C-glycosylation on flavonoid biological benefits, although it has been demonstrated that in at least some cases C-glycosylation has positive effects on properties that may be useful in human healthcare such as antioxidant and antidiabetes activity. Furthermore, there is a lack of in vivo data that would make it possible to make broad generalizations concerning the influence of glycosylation on the benefits of flavonoids for human health. It is possible that the effects of glycosylation on flavonoid bioactivity in vitro may differ from that seen in vivo. With in vivo (oral) treatment, flavonoid glycosides showed similar or even higher antidiabetes, anti-inflammatory, antidegranulating, antistress, and antiallergic activity than their flavonoid aglycones. Flavonoid glycosides keep higher plasma levels and have a longer mean residence time than those of aglycones. We should pay more attention to in vivo benefits of flavonoid glycosides, especially C-glycosides.     

The C‐glycosyl flavonoid,aspalathin, is absorbed,methylated and glucuronidated intact in humans

Human bioavailability of the flavonoid dihydrochalcones is little understood, and no evidence exists for C‐glycosyl flavonoid absorption in humans. The present study uses catechol‐O‐methyltransferase to generate methylated metabolites of aspalathin (a C‐glycosyl dihydrochalcone from rooibos tea). One of the methylated forms, both with and without glucuronidation, was detected using LC‐MS/MS in the urine of human subjects (n = 6), demonstrating that deglycosylation is not a prerequisite for C‐glycosyl flavonoid absorption. Methylation is catalysed by both intestine and liver cytosolic extracts. The results show that flavonoid C‐glycosides are methylated and glucuronidated in vivo in an intact form in humans.     

Metabolomics reveals consistency of the shoot system in Medicago truncatula by HPLC‐UV‐ESI‐MS/MS

Flavonoids not only play crucial roles in plant development and resistance, but also provide one of the major natural sources in human nutrition. To investigate the distribution of flavonoids in the shoot system of Medicago truncatula, a high‐performance liquid chromatography coupled with electrospray ionisation tandem mass spectrometer (HPLC‐ESI‐MS/MS) method was established and then applied to determine the quantitation of flavonoids in different parts of the plant. There were twenty‐two, fifteen and eleven different kinds of flavonoids identified from the flower, leaf and stem of M. truncatula, respectively. The identified constituents were either aglycone or glycosides of the typical flavonoid backbones, such as myricetin, quercetin, luteolin, kaempferol, tricin, apigenin and laricitrin. It was found that the shoot system of M. truncatula can be differentiated by flavonoids in terms of structures and contents. Our results provide instruction to utilise the shoot system of legume crops as fodder and herb medicine in the future.     

Chemical Acylation of Water‐Soluble Antioxidant of Bamboo Leaves (AOB‐w) and Functional Evaluation of Oil‐Soluble AOB (cAOB‐o)

Antioxidant of bamboo leaves (AOB) is a novel natural food antioxidant approved in China since 2004. Natural phenolics contained in the current AOB are usually polyhydroxy derivatives exhibiting hydrophilic character, which has been marked as water‐soluble AOB (AOB‐w). In order to broaden the application fields, oil‐soluble AOB (cAOB‐o) was obtained by chemical acylation of AOB‐w with different chain‐length fatty acids varying from C8 to C18. Results indicated that the yield and solubility of cAOB‐o in 1‐octanol solvent depended on the carbon chain length of acyl donor, and cAOB‐o derived from C12 fatty acid exhibited the more powerful antioxidant activity evaluated by β‐carotene/linoleic acid bleaching assay. Total phenolic content decreased by Folin–Ciocalteu assay. Fourier transform infrared spectra showed the increase of a carbonyl (C = O) peak at 1701 cm^?1 and a decrease in the intensity of the absorption at 3400 cm^?1 (O‐H stretching) in cAOB‐o. Acylation was inferred to mainly occur on the hydroxyl groups of flavones C‐glycosides according to the change of high‐performance liquid chromatography spectra and the contents of total flavonoids and phenolic acids. cAOB‐o with the addition of 0.02% significantly increased oxidative stability of palm oil 1.59 times, lard 3.74 times, and fried potato chips 2.08 times, which was better than the effect of oil‐soluble tea polyphenol (P < 0.01). Moreover, cAOB‐o was identified to be actually nontoxicity by an acute oral toxicity test. All the above results indicated that cAOB‐o could be used as a novel and effective oil‐soluble antioxidant in the food industry.     

Identification of Bioactive Candidate Compounds Responsible for Oxidative Challenge from Hydro‐Ethanolic Extract of Moringa oleifera Leaves

Free radicals trigger chain reaction and inflict damage to the cells and its components, which in turn ultimately interrupts their biological activities. To prevent free radical damage, together with an endogenous antioxidant system, an exogenous supply of antioxidant components to the body in the form of functional food or nutritional diet helps undeniably. Research conducted by the Natl. Inst. of Health claimed that Moringa oleifera Lam possess the highest antioxidant content among various natural food sources based on an oxygen radical absorbent capacity assay. In this study, a 90% (ethanol:distilled water—90:10) gradient solvent was identified as one of the best gradient solvents for the effectual extraction of bioactive components from M. oleifera leaves. This finding was confirmed by various antioxidant assays, including radical scavenging activity (that is, 1, 1‐diphenyl‐2‐picrylhydrazyl, H₂O₂, and NO radical scavenging assay) and total antioxidant capacity (that is, ferric reducing antioxidant power and molybdenum assay). High‐performance liquid chromatography (HPLC) fingerprints of the 90% gradient extract visually showed few specific peaks, which on further analysis, using HPLC–DAD–ESI–MS, were identified as flavonoids and their derivatives. Despite commonly reported flavonoids, that is, kaempferol and quercetin, we report here for the 1st time the presence of multiflorin‐B and apigenin in M. oleifera leaves. These findings might help researchers to further scrutinize this high activity exhibiting gradient extract and its bio‐active candidates for fruitful clinical/translational investigations.     

Two Kaempferol Glycosides Separated from Camellia Oleifera Meal by High‐Speed Countercurrent Chromatography and Their Possible Application for Antioxidation

Recently, kaempferol and its glycosides have attracted considerable attention owing to their potentially health‐benefitting properties including protection against chronic diseases. Here, a microwave‐assisted extraction (MAE) method was developed for the extraction of total flavonoid glycosides (FG) from Camellia oleifera meal, a major agrifood waste largely generated as a byproduct from the Camellia oil processing industry. Compared with traditional extraction methods, MAE enables more efficient extraction of FG. High‐speed countercurrent chromatography was then applied to separate FG from MAE extract, and two major compounds were successfully separated with purities above 90.0% as determined by HPLC. These two compounds were further identified by UV, FT‐IR, ESI‐MS, ¹H‐NMR, and ¹³C‐NMR as kaempferol 3‐O‐[α‐L‐rhamnopyranosyl‐(1→6)‐β‐D‐glucopyranosyl]‐7‐O‐β‐D‐glucopyranoside and kaempferol 3‐O‐[β‐D‐glucopyranosyl‐(1→4)‐α‐L‐rhamnopyranosyl]‐7‐O‐α‐L‐rhamnopyranoside, which were for the first time separated from C. oleifera meal. The results of antioxidant activity assay demonstrated that both compounds had excellent scavenging activity for DPPH radical, and exhibited protective effects against H₂O₂‐induced oxidative damage of vascular endothelial cells. The findings of this work suggest the possibility of employing C. oleifera meal as an attractive source of health‐promoting compounds, and at the same time facilitate its high‐value reuse and reduction of environmental burden.     

Chemical Profiling Using Uplc Q‐Tof/Ms and Antioxidant Activities of Fortunella Fruits

The fruits of Fortunella Swingle are widely consumed as fresh fruits and traditional medicine in China. China is the origin center and has the largest cultivated area of the genus Fortunella. In this study, the chemical compositions of ethanol extracts of the major Fortunella cultivated types including Fortunella japonica Swingle, Fortunella margarita Swingle, Fortunella crassifolia Swingle 1 (Lanshang) and Fortunella crassifolia Swingle 2 (Liuyang) were determined using ultra performance liquid chromatography coupled with quadrupole time‐of‐flight mass spectrometry (UPLC Q‐TOF/MS) method, and their antioxidant activities were evaluated. 12 compounds were identified and 5 compounds were tentatively characterized. The results showed that the chemical compositions of the ethanol extracts of 4 Fortunella cultivated types were largely the same. 3′, 5′‐di‐C‐glucopyranosylphloretin was the predominant flavonoid in Fortunella fruits, and Fortunella margarita Swingle had higher contents of flavonoids than other species. In addition, the data demonstrated high antioxidant activities of Fortunella fruits. The developed method could be available to rapidly analyze the chemical compounds in Fortunella fruits and its products. This study will provide information for further quality assessment and utilization of Fortunella resources.     

The Occurrence,Fate and Biological Activities of C-glycosyl Flavonoids in the Human Diet

The human diet contains a wide variety of plant-derived flavonoids, many of which are glycosylated via an O- or less commonly a C-glycosidic linkage. The distribution, quantity, and biological effects of C-glycosyl flavonoids in the human diet have received little attention in the literature in comparison to their O-linked counterparts, however, despite being present in many common foodstuffs. The structural nature, nomenclature, and distribution of C-glycosyl flavonoids in the human diet are, therefore, reviewed. Forty-three dietary flavonoids are revealed to be C-glycosylated, arising from the dihydrochalcone, flavone, and flavan-3-ol backbones, and distributed among edible fruits, cereals, leaves, and stems. C-linked sugar groups are shown to include arabinose, galactose, glucose, rutinose, and xylose, often being present more than once on a single flavonoid backbone and occasionally in tandem with O-linked glucose or rutinose groups. The pharmacokinetic fate of these compounds is discussed with particular reference to their apparent lack of interaction with hydrolytic mechanisms known to influence the fate of O-glycosylated dietary flavonoids, explaining the unusual but potentially important appearance of intact C-glycosylated flavonoid metabolites in human urine following oral administration. Finally, the potential biological significance of these compounds is reviewed, describing mechanisms of antidiabetic, antiinflammatory, anxiolytic, antispasmodic, and hepatoprotective effects.     

Antioxidant and tyrosinase inhibitory activity of Rosa roxburghii fruit and identification of main bioactive phytochemicals by UPLC‐Triple‐TOF/MS

The content of bioactive phytochemicals, antioxidant activity and tyrosinase inhibitory activity of the hydroalcoholic extracts of Rosa roxburghii were determined. Yellow fruits of cultivated R. roxburghii showed the highest phenolic content (154.81 mg gallic acid g^?1), and the green fruits of wild R. roxburghii showed higher content of flavonoid and triterpenoid. Rosa roxburghii fruits from different cultivars and maturity stages all demonstrated as good antioxidant agents and tyrosinase inhibitors, with IC50 value about twice of the positive standard in the DPPH assay and triple of the standard in the tyrosinase inhibitory activity assay. Nineteen compounds, mainly ellagic acids and its derivatives, flavonoids and their glycosides were identified by UPLC‐Triple‐TOF/MS analysis. As the first study of bioactive phytochemicals of R. roxburghii by UPLC‐MS, the present research may provide valuable information for fulfilling the potential of R. roxburghii in the functional food area.     

苦荞麸皮黄酮提取物及有效成分的抑菌活性

研究苦荞麸皮总黄酮粗品及精品对病原菌的抑制作用,并初步分析其黄酮类成分,评价不同黄酮单体的抑菌活性。通过平板打孔法及二倍稀释法检测苦荞麸皮总黄酮粗品及精品及其4种黄酮单体的抗菌活性,使用高效液相色谱法定性定量检测苦荞麸皮总黄酮粗品及精品的黄酮成分。结果表明,苦荞麸皮黄酮精品对金黄色葡萄球菌、藤黄微球菌、肠球菌、大肠杆菌、志贺氏杆菌、沙门氏菌的抑制效果优于粗品。苦荞麸皮黄酮主要黄酮成分为芦丁、山奈酚-3-O-芸香糖苷、槲皮素和山奈酚,精品的总黄酮含量是粗品总黄酮含量的2.84倍。4种黄酮单体的抑菌能力具有一定的构效关系,其中槲皮素对所有供试菌均表现出较好的抑菌活性。     

3种食品天然植物包材的抗氧化活性成分对比研究

The antioxidant components and antioxidant functions of three commonly used natural food packaging materials, including Indocalamus leaves, reed leaves and lotus leaves were investigated. The active components were extracted by ultrasonic extraction. The contents of total phenols and total flavonoids, the hydroxyl radical scavenging activity, superoxide radicals scavenging activity, DPPH free radical scavenging activity, ABTS+ free radical scavenging activity, total antioxidant activity and reducing power of plant extracts were determined. The relation between antioxidant functions and antioxidant active ingredients was tested. The results indicated that the contents of total phenols and total flavonoids in lotus leave were higher than these of Indocalamus leaves and reed leaves, and the difference was significant (P<0.05). The total phenol content of three plants was extremely significantly correlated with the hydroxyl radical scavenging activity, superoxide radicals scavenging activity, DPPH radical scavenging activity, ABTS+ scavenging activity, total antioxidant and reducing power (P<0.01). The total flavonoid content was extremely significantly correlated with the total antioxidant and reducing power (P<0.01), and significantly correlated with the ABTS+ free radical scavenging ability (P<0.05). The content of isoquercitrin was high in Indocalamus leaves, and reed leaves and the content of luteolin-6-c-glucoside was high in reed leaves and lotus leaves. These ingredients contained the 4-carbonyl group, 2, 3-double bond and o-dihydroxy group of B ring. In summary, Indocalamus leaf, reed leaf and lotus leaf contained many kinds of polyphenols, which have strong free radicals scavenging activity and other antioxidant function.     

Assessment of antiradical potential of Calluna vulgaris (L.) Hull and its major flavonoid

BACKGROUND: Antioxidant capacity of the chloroform, ethyl acetate, n‐butanol and water fractions of the aerial parts of Calluna vulgaris (L.) Hull (Ericaceae) has been assessed in this study. Antioxidant capacity of the plant was screened by assays of 2,2‐diphenyl‐β‐picrylhydrazyl, superoxide anion and hydrogen peroxide scavenging, metal‐chelating activity and reducing power. Butylated hydroxyanisole was used as reference in all assays; ethylene diamine tetraacetic acid was also used as reference in the assay of metal‐chelating activity. Total phenolic contents of the fractions were determined by the Folin–Ciocalteu method. RESULTS: Liquid chromatography/diode array detection/mass spectrometry was used for phytochemical identification of the fractions. Kaempferol‐3‐O‐β‐D ‐galactoside was found to be the major constituent in the ethyl acetate fraction (37.1 ± 0.9%), followed by the n‐butanol fraction (4.6 ± 0.1%). High occurrence of antioxidant capacity, with the exception of metal‐chelating activity, was observed in the ethyl acetate and chloroform fractions as well as in kaempferol‐3‐O‐β‐D ‐galactoside. CONCLUSION: Calluna vulgaris and its major flavonoid, kaempferol‐3‐O‐β‐D ‐galactoside, show high antioxidant capacity in various assays. As far as is known, this is the first report on antioxidant capacity of C. vulgaris and its major flavonoid. Copyright © 2009 Society of Chemical Industry     

Change in Flavonoid Composition and Antioxidative Activity during Fermentation of Onion (Allium cepa L.) by Leuconostoc mesenteroides with Different Salt Concentrations

The aim of this study is to investigate the change in flavonoid composition and antioxidative activity during fermentation of onion (Allium cepa L.) by Leuconostoc mesenteroides with different NaCl concentrations. In order to qualify and quantify the flavonoids during fermentation of onion, 7 flavonoids, [quercetin 3,7‐O‐β‐d ‐diglucopyranoside (Q3,7G), quercetin 3,4′‐O‐β‐d ‐diglucopyranoside (Q3,4′G), quercetin 3‐O‐β‐d ‐glucopyranoside (Q3G), quercetin 4′‐O‐β‐d ‐glucopyranoside (Q4′G), isorhamnetin 3‐O‐β‐d ‐glucopyranoside (IR3G), quercetin (Q), and isorhamnetin (IR)], were isolated and identified from onion. During fermentation, the contents of flavonoid glucosides (Q3,7G, Q3,4′G, Q3G, Q4′G, and IR3G) gradually decreased, whereas the contents of flavonoid aglycones (Q, IR) gradually increased. Decline rates of the flavonoid glucosides increased with the addition of L. mesenteroides. Furthermore, the activity of β‐glucosidase, which is produced by L. mesenteroides, is dose‐dependently inhibited with different NaCl concentrations during fermentation. The presence of L. mesenteroides enhanced the antioxidative activity of onion as demonstrated using the 1,1‐diphenyl‐2‐picrylhydrazyl, 2,2′‐azino‐bis(3‐ethylbenzothiazoline‐6‐sulfonic acid), and reducing power assays. The enhancement of antioxidative activity was considered because the content of flavonoid aglycones increased during fermentation. However, the addition of NaCl may decrease the antioxidative activity; we surmise that this phenomenon occurs because of the inhibition of β‐glucosidase by NaCl. Therefore, we conclude that the addition of NaCl may be useful for the regulation of antioxidative activity via the control of β‐glucosidase action, during the fermentation of flavonoid glucoside‐rich foods.     

Identification and in vitro biological activities of flavonols in garlic leaf and shoot: inhibition of soybean lipoxygenase and hyaluronidase activities and scavenging of free radicals

We isolated four flavonols from garlic (Allium sativum L) leaf and shoot and measured the in vitro antioxidant activity of the isolated flavonols and their aglycones. The chemical structures of the compounds were shown to be quercetin 3‐O‐β‐D ‐glucopyranoside (isoquercitrin), quercetin 3‐O‐β‐D ‐xylopyranoside (reynoutrin), kaempferol 3‐O‐β‐D ‐glucopyranoside (astragalin) and isorhamnetin 3‐O‐β‐D ‐glucopyranoside based on FAB‐MS and NMR analyses. Assays of DPPH (1,1‐diphenyl‐β‐picryl hydrazyl) and hydroxyl radical scavenging, inhibition of linoleic acid peroxidation, and soybean lipoxygenase (LO) and hyaluronidase (HYA) inhibition were used to evaluate the antioxidant activity. Quercetin and its glycosides showed the highest antioxidant activity among the compounds. In the LO assay, the IC₅₀ values of quercetin, isoquercitrin and reynoutrin were 16.9, 40.1 and 32.9 µM respectively. Quercetin was the most effective among the flavonols. In the HYA assay the IC₅₀ values of quercetin, isoquercitrin and reynoutrin were 23.0, 20.9 and 22.1 mM respectively. Isoquercitrin had the most potent inhibitory activity on HYA. The inhibition patterns of the flavonols on LO and HYA were elucidated as mixed types of competitive and non‐competitive inhibition according to Lineweaver–Burk plot results. Although most garlic shoots and leaves are discarded and not used at present, our results suggest that ancillary garlic parts could be utilised as functional foods or ingredients. Copyright © 2004 Society of Chemical Industry     

Antioxidant Effect of Korean Traditional Lotus Liquor (Yunyupju)

This study presented the antioxidant activities of the Korean traditional lotus liquor (Yunyupju) made from lotus blossom and leaves. The antioxidant activities are dose‐dependent and reached a plateau (about 80% inhibition) when the concentration of lotus liquor exceeded 25 μg in a modified linoleic acid peroxidation induced by haemoglobin. The concentrations to attain one absorbance unit at 700 nm were 23.6 ± 1.2 μg for Butylated hydroxytolene (BHT), and 45.7 ± 5.4 μg for lotus liquor. The scavenging activities of DPPH exerted by lotus liquor as well as α‐tocopherol were tested. Linear response curves were also obtained and the IC₅₀ were estimated as 5.6 μg for α‐tocopherol, 17.9 μg for lotus liquor. The maximum scavenging activity on hydroxyl radicals (40%) could be achieved when lotus liquor was more than 500 μg. Lotus liquor also has a potent superoxide radical scavenging activity, with value of 0.93 unit mg^?1 as superoxide dismutase equivalents. The IC₅₀ was estimated as 1.07 ± 0.04 mg for lotus liquor. The high performance liquid chromatography analysis of polyphenols was successfully achieved as these compounds appeared at 16.30 (catechin), 21.87 (rutin), 25.88 (unidentified peak), 31.51 (quercitrin), 35.19 (myricetin), and 36.72 (quercetin) min after injection of the sample, respectively.     

Antioxidant flavonoid glycosides from the leaves of Ficus pumila L.

The Okinawan folks in Japan use Ficus pumila L. as a beverage or herbal medicine to treat diabetes and high blood pressure. Four flavonoid glycosides were isolated and identified as rutin (1 and 3), apigenin 6-neohesperidose (2), kaempferol 3-robinobioside (4) and kaempferol 3-rutinoside (5). Among these compounds, rutin exhibited the strongest antioxidant activity in DPPH radical scavenging assay and superoxide radical inhibition assay. The preparation of Ooitabi leaves in water provide sufficient amount of flavonoid glycosides to the Okinawan although 50% of aqueous ethanol extracted these flavonoid glycosides more effectively. These results show the potential of Ooitabi leaves as a natural source of antioxidant for health management.     

Identification of the Major Components of Buddleja officinalis Extract and Their Metabolites in Rat Urine by UHPLC‐LTQ‐Orbitrap

Buddleja officinalis Maxim, one of the most popular herbal medicines in China, is widely prescribed for curing eye diseases for centuries. In this study, the major components of B. officinalis extract (BOE) and their metabolites in rat urine were detected and identified by ultra‐high‐pressure liquid chromatography coupled with linear ion trap‐orbitrap tandem mass spectrometry (UHPLC‐LTQ‐Orbitrap). A total of 19 compounds, including 8 flavonoids and 11 phenylethanoid glycosides, were confirmed or tentatively identified from BOE. In vivo, 33 components, including 3 prototypes and 30 metabolies, were confirmed or tentatively identified in rat urine samples. The metabolic pathways of different types of compounds were also proposed. This study would effectively narrow the range of potentially bioactive constituents of BOE and shed light to its action mechanism.     

Phenolic composition,antioxidant and cytoprotective effects of aqueous-methanol extract from Anneslea fragrans leaves as affected by drying methods

The present study is aimed to evaluate the effect of three different drying methods, including shade drying (SD), freeze drying (FD) and hot air dying (HAD), on the chemical components, antioxidant and cytoprotective activities of aqueous-methanol extracts from A. fragrans leaves. The total phenolic and flavonoid content were determined by spectroscopic methods, whereas the chemical profile of different extracts was determined by ultra-high-performance liquid chromatography coupled with a tandem mass spectrometry (UHPLC-MS/MS). A total of thirteen compounds were characterised and 9 phenolic compounds have been quantified. Two dihydrochalcone glycosides named confusoside and vacciniifolin were found to be the most abundant phenolic compounds in the SD extract of A. fragrans leaves, which also showed the strongest antioxidant and cytoprotective activities. The results showed that shade drying is an efficient method for preserving the chemical constituents and maintaining the antioxidant and cytoprotective activities of A. fragrans leaves.     

Lotus Flavonoids and Phenolic Acids: Health Promotion and Safe Consumption Dosages

Nelumbo nucifera Gaertn., also known as the sacred lotus, is extensively cultivated in Southeast Asia, primarily for food and as an herbal medicine. This article reviews studies published between 1995 and 2017, on flavonoid and phenolic acid profiles and contents of 154 different cultivars of lotus. So far, some 12 phenolic acids and 89 to 90 flavonoids (47 flavonols, 25 to 26 flavons, 8 flavan‐3‐ols, 4 flavanons, and 5 anthocyanins) have been isolated from different parts of the lotus plant, including its leaves (whole leaf, leaf pulp, leaf vein, and leaf stalk), seeds (seedpod, epicarp, coat, kernel, and embryo), and flowers (stamen, petal, pistil, and stalk), although not all of them have been quantified. Factors affecting flavonoids and phenolic acid profiles, including types of tissues and extracting factors, are discussed in this review, in order to maximize the application of the lotus and its polyphenols in the food industry. Health promotion activities, attributed to the presence of flavonoids and phenolic acids, are described along with toxicology studies, illustrating appropriate usage and safe consumption dosages of lotus extracts. This review also presents the controversies and discusses the research gaps that limit our ability to obtain a thorough understanding of the bioactivities of lotus extracts.     

Antioxidant activity screening of extracts from Sideritis species (Labiatae) grown in Bulgaria

Plant samples from several species and populations of the genus Sideritis (Labiatae) grown in Bulgaria (S scardica, S syriaca and S montana) were extracted with different solvents. Their antioxidant activities were determined by the β‐carotene bleaching test (BCBT), 2,2′‐diphenyl‐1‐picrylhydrazyl (DPPH^?) radical scavenging method and static headspace gas chromatography (HS‐GC) and compared with the antioxidant activity of two reference compounds of different polarity, viz butylated hydroxytoluene (BHT) and rosmarinic acid. The pure reference compounds were applied in a ten‐times lower concentration than the plant extracts. The highest antioxidant activity in the BCBT, close to that of BHT, was observed for the more apolar extracts. The inhibitory effect on β‐carotene bleaching of the polar extracts and rosmarinic acid was much lower than that of BHT. The inhibition of hexanal formation in bulk safflower oil by most of S syriaca and S scardica extracts was as effective as BHT but less so than rosmarinic acid. S montana extracts showed weak antioxidant or even pro‐oxidant properties. Extracts from butanol and from ethyl acetate and the total methanol extracts from all Sideritis plants studied showed a strong radical scavenging activity against DPPH^?, close to that of rosmarinic acid. S montana extracts were, as a whole, slightly weaker radical inhibitors than the extracts from the other two species. The antioxidant activity of Sideritis extracts was attributed to the presence of flavonoid and phenylpropanoid glycosides. Copyright © 2003 Society of Chemical Industry