|Year : 2018 | Volume
| Issue : 4 | Page : 285-291
Antioxidant and α-glucosidase activities and phytochemical constituents of Chrysanthoglossum trifurcatum (Desf.)
Ahlem Ben Sassi1, Sana Amroussi1, Malek Besbes1, Mahjoub Aouni1, Fethia Skhiri2
1 Laboratory of Transmissible Diseases and Biologically Active Substances, Department of Microbiology, Faculty of Pharmacy, University of Monastir, Tunisia
2 Laboratory of Genetics, Biodiversity and Valorisation of Bioresources, Higher Institute of Biotechnology, University of Monastir, Tunisia
|Date of Submission||25-Nov-2017|
|Date of Decision||25-Jan-2018|
|Date of Acceptance||15-Feb-2018|
|Date of Web Publication||30-Apr-2018|
Ahlem Ben Sassi
Laboratory of Transmissible Diseases and Biologically Active Substances, Department of Microbiology, Faculty of Pharmacy, Avicenne street, Monastir
Source of Support: None, Conflict of Interest: None
Objective: To investigate the antioxidant and α-glucosidase properties and phytochemical constituents of roots, stems, leaves and flowers extracts and aerial parts oil of Chrysanthoglossum trifurcatum (Desf.) (C. trifurcatum). Methods: For extraction from roots, stems, leaves and flowers of C. trifurcatum, methanol, ethyl acetate and petroleum ether solvents were used. Phenols, flavonoids, flavonols and tannins contents were evaluated. More, C. trifurcatum aerial parts oil composition was determined using chromatography/mass spectrometry. The antioxidant effect was estimated by DPPH, ABTS and reducing power test systems. The α-glucosidase inhibition was determined by colorimetric assay using the enzyme from Aspergillus niger and the p-nitrophenyl glucopyranoside (pNPG) as substrate. Results: The highest amounts of polyphenols, flavonoids, flavonols and tannins were shown by the methanolic extract of leaves. The main components of the aerial parts oil were limonene (29.21%), γ -terpinene (12.96%), 4-terpenyl acetate (12.18%) and α -pinene (5.76%). The activity evaluated by DPPH, ABTS and reducing power tests was important for stems (IC50=0.68 mg/mL) and flowers (IC50=0.67 mg/mL) methanolic extracts and essential oil (IC50=0.72 mg/mL). Findings of α-glucosidase activity revealed that petroleum ether extracts of leaves and roots together with aerial parts oil showed a highest activity with IC50 of 0.044, 0.045 and 0.049 mg/mL, respectively. Conclusions: Observed antioxidant and α-glucosidase activities of oil and extracts are attributed to the presence of the active phytochemicals in C. trifurcatum organs. Thus, the C. trifurcatum can be used as a source of antioxidant compounds and dietary supplement to treat patients with type 2 diabetes.
Keywords: Antioxidant, α-glucosidase, Phenolic content, Oil, Chrysanthoglossum trifurcatum
|How to cite this article:|
Sassi AB, Amroussi S, Besbes M, Aouni M, Skhiri F. Antioxidant and α-glucosidase activities and phytochemical constituents of Chrysanthoglossum trifurcatum (Desf.). Asian Pac J Trop Med 2018;11:285-91
|How to cite this URL:|
Sassi AB, Amroussi S, Besbes M, Aouni M, Skhiri F. Antioxidant and α-glucosidase activities and phytochemical constituents of Chrysanthoglossum trifurcatum (Desf.). Asian Pac J Trop Med [serial online] 2018 [cited 2022 Jun 29];11:285-91. Available from: https://www.apjtm.org/text.asp?2018/11/4/285/231469
| 1. Introduction|| |
Many medicinal and aromatic plants contain antioxidants such as phenols. These components can have a significant role in the neutralization and absorption of radicals and peroxide decomposition or extinction. Many phenolic constituents for example flavonoids and phenolic acids have antioxidant potential thus they contribute significantly to the fight against many human diseases and contribute to the mortality reduction.,
The type 2 diabetes mellitus is one of the common metabolic diseases. Treatment of type 2 diabetes improves patient blood sugar levels and insulin secretion stimulated by drugs such as α-glucosidase inhibitors and metformin. α-glucosidase serves to inhibit postprandial hyperglycemia and reduce the glucose absorption, and it is located in small intestine epithelium. Several α-glucosidase inhibitors for example acarbose, voglibose and miglitol are clinically used. Thus, the molecules of plant origin represent a source of such inhibitors.
The Chrysanthemum genus belongs to the family of Asteraceae which is common in countries of Mediterranean basin,. We counted 13 Chrysanthemum species distributed in many regions in Tunisia. Chrysanthoglossum trifurcatum (Desf.) (synonym of Chrysanthemum trifurcatum Desf. var. macrocephalum (Viv.) Beg.) (C. trifurcatum) is largely disseminated in Tunisian regions. It used to treat problems of intestinal transit, constipation and postdelivery pains. It has been reported that extract with methanol solvent of Tunisian C. trifurcatum stimulates the contractions of duodenal smooth muscles through muscarinic receptors. The same authors reported that the hot water, methanol, ethyl acetate and petroleum extracts and essential oils of C. trifurcatum exhibited activity against many bacteria and yeasts,. On other hand, the same extracts and oils have a lower effect against Herpes simplex virus type-1. Recent findings have reported that flavonoids are the most important phytocomponents of methanol extracts of leaves, stems and flowers of C. trifurcatum. Other researchers have identified five flavonoids and one phenolic acid (caffeic acid) in the butanolic fraction of Algerian C. trifurcatum, which had an antioxidant activity.
However, no studies have been conducted to determine the antioxidant and α-glucosidase activities of C. trifurcatum growing in Tunisia. Thus, the research objectives are to evaluate reducing power, scavenging ability of ABTS and DPPH radicals, α-glucosidase inhibitor activity, total phenols, flavonoids, flavonols and tannins content of the methanolic, ethyl acetate and petroleum ether extracts of roots, leaves, stems and flowers and the composition of aerial parts oil of C. trifurcatum.
| 2. Materials and methods|| |
2.1. C. trifurcatum material
Plant material was collected in March 2015 (in flowering stage) from Monastir area in centre of Tunisia. Plant was botanically identified by Pr. Skhiri Fethia (High Institute of Biotechnology, Monastir University, Tunisia) according to the description of morphology existing in Flora of Tunisian. The fresh material (roots, stems, leaves, flowers and aerial parts) was air-dried in shadow for 10 d and powdered.
2.2. Organic extracts preparation
The material of C. trifurcatum organs (100 g) was extracted using three increasing polarity solvents: petroleum ether, ethyl acetate, and methanol. Twelve obtained extracts were evaporated and yields were determined.
2.3. Phenolic content determination
2.3.1. Total polyphenolic content
Total phenolic content was measured by Folin–Ciocalteu method,. Indeed, sample (1 mg/mL, 50 μL) and water/ Folin–Ciocalteu solution [28:2 (v/v), 750 μL] were mixed. Sodium carbonate (20%, 200 μL) was added after 3 min. After incubation in a boiling water bath for 1 min, the mixture was kept for 30 min in the dark. Methanol was used as the control sample. Absorbance was determined at 765 nm. Total phenols were evaluated by relating the absorbance in the calibration curve prepared with solutions of gallic acid ranging from 0 to 250 μg/mL (r=0.99). Results are reported as mg of gallic acid equivalent/100 g of dry weight (mg GAE/100 g DW).
2.3.2. Flavonoid content
Flavonoid content of the different plant organs was evaluated by the aluminum chloride method. Diluted sample (0.5 mL) was added to aluminum chloride solution (2%, 0.5 mL). Mixture was incubated for 15 min at ambient temperature, and then absorbance was measured at 430 nm. Catechin calibration curve ranging from 0 to 250 μg/mL (r=0.99) was used. Content of flavonoids is presented as mg catechin equivalent/100 g of dry weight (mg CE/100 g DW).
2.3.3. Flavonol content
The flavonol contents were estimated using aluminum chloride method. Extract (1 mg/mL, 1 mL) was added to aluminum chloride (2%, 1 mL) and sodium acetate (5%, 3 mL) solutions. After incubating the mixture at ambient temperature for 2.5 h, absorbance was determined at 440 nm. Catechin with calibration curve ranging from 0 to 250 μg/mL (r=0.99) was used. The content of flavonols is presented as mg catechin equivalent/100 g of dry weight (mg CE/100 g DW).
2.3.4. Tannins content
Tannins were evaluated by the method of Sun et al. with minor modifications. Thus, vanillin (4%, 3 mL) and concentrated H2SO4 (1.5 mL) solutions were mixed with diluted extract (50 μL). Absorbance was determined at 500 nm after 15 min. Tannin content is expressed as mg catechin equivalent/100 g of dry weight (mg CE/100 g DW). Catechin calibration curve ranged from 0 to 400 μg/mL (r=0.99).
2.4. Essential oil isolation
The fresh aerial parts material was submitted for 5 h for hydrodistillation. Essential oil yield was determined based on sample fresh weight.
2.5. Chromatographic analysis
Gas chromatography-mass spectrometer (GC–MS) analyses of aerial parts oil were performed as previously reported.
2.6. Antioxidant activity evaluation
Antioxidant effect of C. trifurcatum oil and extracts was measured by reducing power and DPPH and ABTS free radical- scavenging assays.
2.6.1. DPPH radical scavenging assays
Anti-radical activity was evaluated using the modified method of Ramadan et al. Thus, DPPH (950 μL, 1×104 mol/L) was mixed with diluted extract (50 μL). After 30 min, the mixture absorbance was read at 515 nm. Trolox was the positive control. The anti-radical activity was determined by the formula:
% inhibition of radical DPPH=[(Acontrol - Asample)/Acontrol)] ×100.
Where, Acontrol is control reaction absorbance, and Asample is sample test absorbance. Thereafter, IC50 value (concentration responsible to inhibit DPPH radicals to 50%) was determined.
2.6.2. ABTS radical scavenging assays
Re et al. method with minor modification was used to evaluate anti-radical activity. Thus, ABTS (7 mmol/L) were mixed with potassium peroxodisulfate (2.45 mmol/L). To a diluted ABTS+ solution (990 μL), 10 μL of the sample (1 mg/mL) were added. After 20 min, the absorbance was determined at 734 nm. Trolox is the positive control and anti-radical activity was determined by the following formula:
% inhibition of radical DPPH=[(Acontrol - Asample)/Acontrol]×100.
Where, Acontrol is control reaction absorbance, and Asample is sample test absorbance. IC50 value (concentration responsible to inhibit ABTS radicals to 50%) was determined.
2.6.3. Reducing power
The modified Sanja et al. method was adopted to evaluate the ferric-reducing power of oil and extracts. Sample solutions (0.5-3.0 mg/mL) were mixed with potassium ferric cyanide [1% (w/v), 2.5 mL]. Then, trichloroacetic acid [10% (w/v), 2.5 mL) was added after 20 min at 50 °C A centrifugation at 3 000 r/min for 10 min was made. The supernatant (2.5 mL), distilled water (2.5 mL) and ferric chloride (0.1%, 1 mL) were mixed. After 10 min at ambient temperature, absorbance was measured at 700 nm. Trolox is used as a reference product. The reducing power was determined by the formula:
% reducing power=[(A sample/A control -1)] 100.
Where, Asample is sample absorbance and Acontrol is control absorbance.
2.7. α-glucosidase inhibitory activity
The α-glucosidase inhibition effect was evaluated using the Tao et al. method. Thus, p-nitrophenyl- α -D-glucopyranoside (2.5 mmol/L) was mixed with α-glucosidase (0.3 U/mL) and extract or oil in DMSO (250 μL). The reaction mixture was incubated at 37 °C for 15 min. Acarbose was a standard. Absorbance was measured at 405 nm. Inhibition ratio (%) by samples and acarbose were determined by the equation:
% inhibition ratio=[1-(Asample/Acontrol]x100.
Where, Asample is sample absorbance and Acontrol is control absorbance. The concentration of the sample that inhibits the enzyme by 50% was evaluated.
2.8. Statistical analysis
Results are expressed as mean ± SD from three separate observations. Linear regression analysis was adopted to determine the IC50 (DPPH, ABTS and reducing power methods) values. Data were analyzed by SPSS software (SPSS v.20) and Duncan test was used to determine statistical significance (P<0.05 deemed as significant).
| 3. Results|| |
3.1. Yields and phenol contents
Yields of extractions from flowers, stems, leaves and roots of C. trifurcatum by varying polarity solvents (methanol, ethyl acetate and petroleum) are represented in [Table 1]. The highest yield was obtained by methanolic extraction. In different plant parts, the yields of methanolic extracts were 0.91% for roots, 1.10% for stems, 5.10% for flowers and 6.20% for leaves. The contents of phenol, flavonoid, flavonol and tannin varied significantly with type of extract [Table 1]. The methanolic extract of leaves had the highest contents of total phenol, flavonoid, flavonol and tannin. However, petroleum ether stem extract presented lower level of polyphenols and flavonoids. Ethyl acetate flower extract presented lower level of flavonols and tannins.
|Table 1: Total polyphenol, flavonoid, flavonol and tannin contents in C. trifurcatum according to organs and solvent extraction systems.|
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3.2. Essential oil composition
C. trifurcatum oil with the yield of 0.061% (w/w) was analyzed by GC–MS. As can be seen in [Table 2], 44 constituents, representing 98.95% of oil, were detected. Limonene (29.21%), γ-terpinene (12.96%), 4-terpenyl acetate (12.18%) and α-pinene (5.76%) were the main compounds in oil.
|Table 2: Constituents of the essential oil from the aerial parts of C. trifurcatum (Desf.).|
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3.3. Antioxidant activity
The various extracts of C. trifurcatum exhibited remarkable antioxidant activities [Table 3]. The radical scavenging and reducing power activities, expressed as inhibition percentage and IC50, varied with type of solvent and plant part [Table 3].
|Table 3: Antioxidant capacity determined by DPPH, ABTS and reducing power test systems of C. trifurcatum extracts and oil.|
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By DPPH radical scavenging test, the best activity was observed with methanolic extracts for stems and flowers, and the lowest activity was observed in petroleum ether extract for stems. By ABTS radical scavenging test, the best activity was observed in methanol extract for stems and the lowest activity was observed in ethyl acetate extract for leaves. The results by reducing power test presented in [Table 3] show that most extracts had some antioxidant activity and that the greatest activity was obtained with methanol extracts from flowers and leaves. Also, these activities were lower than a Trolox with IC50 of 0.136, 0.161 and 0.082 mg/mL by DPPH, ABTS and reducing power tests, respectively.
The results of antioxidant activity of aerial parts oil are presented in [Table 3]. Oil had an antioxidant activity with IC50 of (0.72±0.01), (0.87±0.03) and (0.92±0.09) mg/mL by DPPH and ABTS radicals scavenging and reducing power assays, respectively. This activity was lesser than that of Trolox [Table 3].
3.4. α-glucosidase inhibition activity
The α-glucosidase inhibitor effectiveness of different C. trifurcatum extracts and oil are presented in [Table 4]. The low IC50 values designated the high inhibition activity. Thus, the greatest α-glucosidase inhibition activity was obtained in petroleum ether extracts of leaves and roots and aerial parts oil, with IC50 of 0.044, 0.045 and 0.049 mg/mL, respectively. Ethyl acetate extracts of stems (IC50=0.054 mg/mL) and flowers (IC50=0.057 mg/mL) also exhibited α-glucosidase inhibition, as well as methanolic stem extract (IC50=0.064 mg/mL). This biological activity was better than that of acarbose (IC50=0.07 mg/mL).
| 4. Discussion|| |
For phenolic composition, results demonstrated that methanol was better solvent in extracting polyphenols. Therefore, the polarity of solvent will play an important role in increasing solubility of phenols,. Then, variation of phenol accumulation between plant parts should be related to their specific cells and tissues. The high presence of phenols in leaves is attributed to the phenological organ growth, transport involved in polyphenols distribution at plant level, handy interaction between plant parts and processes of degradation and/or biosynthesis.
Researchers have reported that Chrysanthemum species were found to contain several flavonoids. In the previous studies, the most important phytochemicals of methanol extracts of flowers, leaves and stems of C. trifurcatum were flavonoids. Isorhamnetin was identified in flowers, leaves and stems of C. trifurcatum. In contrast, flavones, flavonols and phenolic acid (caffeic acid) were present in flowers and leaves. Mokaddem-Daroui et al. have reported that the butanolic fraction of Algerian C. trifurcatum contained flavonoids phenolic acid (caffeic acid).
Aerial parts oil composition is somewhat similar to the compositions described in previous reports on C. trifurcatum leaves and stem oils. Thus, the oil of leaves contained 41 constituents, representing 97.84% of oil and main components were limonene, γ-terpinene, α-pinene, α-terpenyl acetate and α-thujene. In the stem oil, 29 compounds were found and representing 99.02% of oil. The main components were limonene, 4-terpenyl acetate, γ -terpinene and 2-hexenal.
We deduced that the higher antioxidant activity was obtained with polar extracts. The antioxidant effects of C. trifurcatum may be related to its richness on phenols and flavonoids. Researchers have reported that the butanolic extract of C. trifurcatum aerial parts collected in Algeria exhibited antioxidant activity by DPPH test with IC50=0.199 mg/mL. Others findings reported a potent antioxidant activity of Chrysanthemum genus such Chrysanthemum morifolium, Chrysanthemum coronarium, Chrysanthemum indicum, Chrysanthemum balsamita and Chrysanthemum fuscatum. However, Tahri et al. reported that methanol extracts of C. trifurcatum were rich in flavonoidslike luteolin and phenolic acid like caffeic acid. It is shown that the caffeic acid is a potent radical scavenger and it is more effective than Trolox. Luteolin is an important component in Chrysanthemum species. Chrysanthemum morifolium contained luteolin-7-O- β -D-glucoside which had antioxidant and inflammatory activities ,,. Chrysanthemum indicum is considered as an important source of quercitrin and myricetin. Others researchers have reported that quercetin had antioxidant activity,. Bahramikia et al. indicated that flavonoids interrupt free radical autoxidation chain propagation. According to Zhang et al., phenolic and flavonoid plant compounds generally contribute to antioxidant activity. So, the antioxidant potential of C. trifurcatum can be attributed to the existing of these constituents in different plant parts. In addition, aerial parts oil of this specie was rich in limonene and a-pinene, which are known as potent anti-oxidants,. Nevertheless, major and minor constituents can participate in this antioxidant effect and not just one or a few minority active molecules.
α-glucosidase is a major enzyme in oligosaccharide hydrolysis. The α-glucosidase inhibition is an important approach to manage level of blood glucose. However, the major disadvantage of using inhibitors of α-glucosidase is their side effects such as diarrhea, distention of abdominal and flatulence. Thus, it is important to evaluate antidiabetic activities of medicinal plants to develop alternative substances without side effects for diabetes mellitus and with low toxicity. The α-glucosidase inhibition activity of C. trifurcatum was evaluated for the first time. In this case, we can refer to some concepts such as synergism, antagonism and additivity between the chemical compounds to explain this inhibitory response for Chrysanthemum trifurcatum. A limited number of studies have evaluated α-glucosidase inhibition effect of the genus Chrysanthemum. Thus, n-butanol extract of C. fuscatum may prevent hyperglycemia and hyperlipidemia in induced diabetic rats, which can be due to various mechanisms. This extract contained active substances which they produced a reduction of diabetic blood glucose levels. Thi Luyen et al. demonstrated that the flavones are the main compounds in C. morifolium flowers and showed a strong inhibition against α-glucosidase. Therefore, these compounds may be important contributors to the hyperglycemia lowering property of this specie. The antidiabetic potential of essential oil can be due to the main constituents. Moreover, terpene constituents such as α-pinene inhibited the important enzymes related to diabetes type 2 essentially α-glucosidase. However, the oil is a complex mixture of various molecules and a synergy between all molecules or the main molecules is responsible for its biological activities.
According to our knowledge, this is the first work on α-glucosidase and antioxidant activities and global chemical composition of organic extracts of different organs and aerial parts oil of C. trifurcatum from Tunisia. The obtained results showed that the aerial parts oil was rich in limonene and the content of phenolic compounds in the extracts was highly dependent on the organ of the plant. The highest level in polyphenol and flavonoid contents is detected in the leaves which favors their use in industry for the extraction of phenolic compounds. The inhibition of α-glucosidase and antioxidant activities of Tunisian C. trifurcatum may be due to the richness of this plant in phenolic compounds. So, this study should be followed by isolation, purification and identification of the specific molecules with high activity, from this plant, to develop natural α-glucosidase inhibitors and antioxidants.
Conflict of interest statement
The authors declare that they have no conflict of interest.
| References|| |
Djeridane A, Yousfi M, Nadjemi B, Boutassouna D, Stocher P, Vidal N. Antioxidant activity of some Algerian medicinal plants extracts containing phenolic compounds. Food Chem
Fang XK, Gao J, Zhu DN. Kaempferol and quercetin isolated from Euonymus alatus
improve lucose uptake of 3T3-L1 cells without adipogenesis activity. Life Sci
Scott LJ, Spencer CM. Miglitol: A review of its therapeutic potential in type 2 diabetes mellitus. Drugs
Quezel P, Santa S. Nouvelle flore de l’Algérie et des régions désertiques méridionales. Tome II: Centre national de la recherche scientifique; 1981.
Lee KD, Yang MS, Ha TJ, Park KM, Park KH. Isolation and identification of dihydrochrysanolide and its 1-epimer from Chrysanthemum coronarium
L. Biosci Biotechnol Biochem
Pottier Alapetite G. La flore de la Tunisie: Angiospermes Dicotylédones Gamopétales. Tunisie: Publications scientifiques tunisiennes; 1981, p. 1000-1007.
Le Floc’h E, Boulos L, Véla E, Ghrabi Gammar Z, Daoud Bouattour A, Ben Saad Limam S, et al.
Flore de Tunisie, Catalogue synonymique commenté. Tunisie: Ministère de l’environnement et du développement durable et banque nationale de gènes; 2010, p. 101.
Ben Sassi A, Harzallah-Skhiri F, Chraief I, Bourgougnon N, Hammami M, Aouni M. Chemical composition and antimicrobial activities of the essential oil of (Tunisian) Chrysanthemum trifurcatum
(Desf.) Batt. and Trab. flower heads. C R Chim
Ben Sassi A, Harzallah-Skhiri F, Borgi W, Chouchène N, Aouni M. Effets de l’extrait méthanolique de Chrysanthemum trifurcatum
(Desf.) Batt. et Trab. sur la motricité duodénale de rat. C R Biol
Tahri W, Chatti A, Romero-Gonzalez R, López Gutiérrez N, Garrido Frenich A, Landoulsi A. A Phenolic profiling of the aerial part of Chrysanthemum trifurcatum
using ultra high performance liquid chromatography coupled to Orbitrap high resolution mass spectrometry. Anal Methods
Mokaddem-Daroui H, Touafek O, Kabouche A, Kabouche Z, Calliste CA, Duroux JL. Components and antioxidant activity of the polar extracts of Chrysanthemum trifurcatum. Chem Nat Compounds
Singleton VL, Rossi JA. Colorimetry of total phenolics with phosphomolybdic phosphotungstic acid reagents. Am J Enol Viticult
Official methods of analysis of the association of official analytical chemists. 14th ed. Arlington: Ass Offic Analyt Chem; 1984
Miliauskas G, Venskutonis PR, Van Beek TA. Screening of radical scavenging activity of some medicinal and aromatic plant extracts. Food Chem
Sun B, Richardo-da-Silvia JM, Spranger I. Critical factors of vanillin assay for catechins and proanthocyanidins. Agric Food Chem
Ben Sassi A, Harzallah-Skhiri F, Chraief I, Bourgougnon N, Hammami M, Aouni M. Essential oils and crude extracts from Chrysanthemum trifurcatum
leaves, stems and roots: Chemical composition and antibacterial activity. J Oleosci
Ramadan MF, Kroh LW, Morsel JT. Radical scavenging activity of black cumin (Nigella sativa
L.) coriander (Coriandrum sativum
L.) and niger (Guizotia abyssinica
Cass.) crude seed oils and oil fractions. J Agr Food Chem
Re R, Pellegrini N, Proteggente A, Pannala A, Yang M, Rice-Evans C. Antioxidant activity applyi ng an improved ABTS radical cation decolorization assay. Free Radical Biol Med
Sanja SD, Sheth NR, Patel NK, Patel D, Patel B. Characterization and evaluation of antioxidant activity of Portulaca oleracea. Int J Pharm Pharm Sci
Tao T, Zhang Y, Cheng Y, Wang Y. Rapid screening and identification of α-glucosidase inhibitors from mulberry leaves using enzyme- immobilized magnetic beads coupled with HPLC/MS and NMR. Biomed Chromatogr
Davies NW. Gas chromatographic retention indices of monoterpenes and sesquiterpenes on methyl silicon and Carbowax 20M phases. J Chromatogr A
Adams R. Identification of essential oil components by gas chromatography/quadrupole mass spectroscopy. USA: Allured, Carol Stream IL; 2001, p. 19.
Pedro LG, Santos PA, Silva JA, Figueiredo AC, Barrso JG, Deans SG. Essential oils from Azorean Laurus azorica. Phytochemistry
Sibanda S, Chigwada G, Pool M, Gwebu ET, No-letto JA, Schmidt JM, et al.
Composition and bioactivity of the leaf essential oil of Heteropyxis dehniae
from Zimbabwe. J Ethnopharmacol
Hamm S, Bleton J, Connan J, Tchapla A. A chemi-cal investigation by headspace SPME and GC-MS of volatile and semi-volatile terpenes in various olibanum samples. Phytochemistry
Roby MHH, Sarhana MA, Selima KAH, Khalel KI. Evaluation of antioxidant activity, total phenols and phenolic compounds in thyme (Thymus vulgaris
L.), sage (Salvia officinalis
L.), and marjoram (Origanum majorana
L.) extracts. Ind Crops Prod
Naczk M, Shahidi F. Phenolics in cereals, fruits and vegetables: Occurrence, extraction and analysis. J Pharm Biomed Anal
Hudaib M, Speroni E, Di Pietra AM, Cavrini V. GC/MS evaluation of thyme (Thymus vulgaris
L.) oil composition and variations during the vegetative cycle. J Pharm Biomed Anal
Ranxin S, Choon NO, Han-Ming S. Pharmacological and chemopreventive studies of Chrysanthemum
. In: Lester Packe, Choon NO, Barry H. Herbal and traditional medicine, biomolecular and clinical aspects
. Boca Raton: CRC Press; 2004, p. 372.
Guo-Hua L, Lin L, Hua-Wei L, Xin M, Jing-Ye W, Li-Ping W, et al.
Antioxidant action of a Chrysanthemum morifolium
extract protects rat brain against ischemia and reperfusion injury. J Med Food
Jiyoung K, Jung NC, Kang MK, Daejung K, Jong SK, Jung HYP, et al.
A correlation between antioxidant activity and metabolite release during the blanching of Chrysanthemum coronarium
L. Bio Sci Biotechnol Biochem
Trishna D, Hai LJ, Abul Hasnat M, Yunsuk K, Nadira BS, Pyo-Jam P, et al.
Antioxidant potential and oxidative DNA damage preventive activity of Chrysanthemum indicum
extracts. J Food Biochem
Aneta TP, Dasha SM, Iordanka NA. The effect of freezing on the antioxidant activity of Bulgarian Chrysanthemum balsamita. J BioSci Biotech
Amrani A, Zama D, Boubekri N, Ben aissa O, Meraihi Z, Benayache F, et al.
The protective effect of Chrysanthemum fantanesii
extract, vitamin E and C on sodium valproate-induced embryotoxicity in pregnant mice. J Med Plants Res
Lu Y, Foo LY. Antioxidant activities of polyphenols from sage (Salvia officinalis). Food Chem
Xie YY, Yuan D, Tian HF. Chemical constituents in the flowers of Chrysanthemum morifolium
Ramat. Chin J Med Chem
Liu JQ, Shen QQ, Liu JS, Wu DL, Wang JT. Studies on the chemical constituents from Chrysanthemum morifolium
Ramat. China J Chin Mater Med
Ha CL, Weng CY, Wang L, Lian TW, Wu MJ. Immunomodulatory effect of Glossogyne tenuifolia
in murine peritoneal macrophages and splenocytes. J Ethnopharmacol
Falleh H, Ksouri R, Oueslati S, Guyot S, Magné C, Abdelly C. Interspecific variability of antioxidant activities and phenolic composition in Mesembryanthemum
genus. Food Chem Toxicol
Ding M, Zhao JS, Bowman L, Lu YJ, Shi XL. Inhibition of AP-1 and MAPK signaling and activation of Nrf2/ARE pathway by quercitrin. Intl J Oncol
Bahramikia S, Ardestani A, Yazdanparast R. Protective effects of four Iranian medicinal plants against free radical-mediated protein oxidation. Food Chem
Zhang L, Ravipati AS, Koyyalamudi SR, Jeong SC, Reddy N, Smith PT, et al.
Antioxidant and anti-inflammatory activities of selected medicinal plants containing phenolic and flavonoid compounds. J Agric Food Chem
Wang W, Wu N, Zu YG, Fu YJ. Antioxidative activity of Rosmarinus officinalis
L. essential oil compared to its main components. Food Chem
Marostica MR, Taare S, Franch GC, Nowill A, Pastore GM, Hyslop S. Antioxidant potential of aroma compounds obtained by limonene biotransformation of orange essential oil. Food Chem
Dong HQ, Li M, Zhu F, Liu FL, Huang JB. Inhibitory potential of trilobatin from Lithocarpus polystachyus
Rehd against α-glucosidase and α-amylase linked to type 2 diabetes. Food Chem
Boubekri N, Amrani A, Zama D, Dendougui H, Benayache F, Benayache S. In vitro
antioxidant and in vivo
antidiabetic potential of n-butanol extract of Chrysanthemum fuscatum
in streptozotocin induced diabetic rats. Int J Pharm Sci Rev Res
Thi Luyen N, Hoang Tram L, Hong Hanh TT, Thanh Binh T, Hai Dang N, Van Minh C, et al.
Inhibitors of α-glucosidase, α-amylase and lipase from Chrysanthemum morifolium. Phytochem Lett
Hamden K, Keskes H, Belhaj S, Mnafgui K, Feki A, Allouche N. Inhibitory potential of omega-3 fatty and fenugreek essential oil key enzymes of carbohydrate-digestion and hypertension in diabetes rats. Lipids Health Dis
[Table 1], [Table 2], [Table 3], [Table 4]
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| ||Biocatalysis and Agricultural Biotechnology. 2019; 20: 101209 |
|[Pubmed] | [DOI]|