Biochemistry Research International

Biochemistry Research International / 2020 / Article

Research Article | Open Access

Volume 2020 |Article ID 8823209 |

Asmaa Oubihi, Hanae Hosni, Issmail Nounah, Abdessamad Ettouil, Hicham Harhar, Katim Alaoui, Mohammed Ouhssine, Zineb Guessous, "Phenolic Content, Antioxidant Activity, Anti-Inflammatory Potential, and Acute Toxicity Study of Thymus leptobotrys Murb. Extracts", Biochemistry Research International, vol. 2020, Article ID 8823209, 7 pages, 2020.

Phenolic Content, Antioxidant Activity, Anti-Inflammatory Potential, and Acute Toxicity Study of Thymus leptobotrys Murb. Extracts

Academic Editor: Tzi Bun Ng
Received13 Jul 2020
Revised05 Sep 2020
Accepted10 Sep 2020
Published18 Sep 2020


Thymus leptobotrys is a medicinal plant belonging to the Lamiaceae family, endemic in Morocco, and used in traditional medicine. The present work aims to study the phenolic compounds, the antioxidant activity, the anti-inflammatory effect, and the toxicity of two ethanolic and methanolic extracts of Thymus leptobotrys aerial part. The yield of the methanolic extraction (22.2%) is higher than that of the ethanolic extraction (15.8%) and is characterized by higher contents of polyphenols 243.08 mg/g GAE (mg/g of gallic acid), flavonoids 179.28 mg/g RE (mg/g of rutin), and tannins 39.31 mg/g CE (mg/g of catechin). The in vitro measurement of antioxidant activity with the 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical reduction test and Trolox equivalent antioxidant capacity (TEAC) test demonstrates the higher performance of the methanolic extract. The evaluation of the anti-inflammatory effect in vivo on adult Wistar female rats leads to a very significant decrease in the inflammation of the edema compared to the standard drug (indomethacin) and the control group. The toxicity test reveals that both extracts showed no toxicity within an LD50 above 2000 mg/kg body weight of the rats.

1. Introduction

Oxidative stress causes significant damage that accelerates cellular aging. This aging process leads to serious pathologies such as cancer, cardiovascular disease, diabetes, neurodegenerative disease, inflammation, digestive diseases, and metabolic syndrome [13]. Several situations in daily life lead to the production of free radicals responsible for oxidative stress. These include endogenous overproduction of inflammatory oxidative agents, free radical overproduction (tobacco, alcohol, drugs, pollution, and pesticides), and a decrease in the antioxidant capacity of foodborne vitamins and trace elements [2, 4, 5]. The use of currently available synthetic antioxidant molecules is being questioned because of potential health risks [2, 6]. The search for natural antioxidants, mainly carotenoids, polyphenols (flavonoids and phenols acids), and vitamins (mainly vitamins C and E) [7] derived from plant materials, is growing rapidly and is based on the characterization of endemic plants. Typically, these natural antioxidants, particularly polyphenols, show evidence of a broad variety of biological effects, such as antiplasmodial, antimicrobial, antiarthritic, anticancer, and anti-inflammatory effects [8, 9].

The medicinal plant sector in Morocco has a rich and varied flora with very marked endemism [10]. The species of Thymus L. (Lamiaceae) are perennial, aromatic herbs, and widely used in the Mediterranean Basin [11]. Thymus leptobotrys Murb. is an endemic species of southern Morocco traditionally used in the treatment of bronchitis, indigestion, whooping cough, and rheumatism [12] and has antifungal, antimicrobial, analgesic, insecticidal, antioxidant, and antiviral properties [1316].

No studies regarding the in vivo anti-inflammatory effect of Thymus leptobotrys were conducted previously to our knowledge. The present work is part of the valorization of Moroccan aromatic and medicinal plants. Its objective is to study the phenolic compounds, the antioxidant activity, the in vivo anti-inflammatory effect, and the acute toxicity of ethanolic and methanolic extracts of Thymus leptobotrys.

2. Materials and Methods

2.1. Plant Material

The aerial parts of Thymus leptobotrys are recovered in the region of Sidi Mzal, a small Berber village in the mountains of the Moroccan Anti-Atlas (N 29°86′/W 08°88′) during the harvest period (April–June 2017). The identification is made at the Laboratory of Botany and Plant Protection, Ibn Tofaïl University, Kenitra, Morocco. The sample is dried at room temperature and then ground and stored in sterile bags until analysis.

2.2. Animals

Adult female Wistar rats (180 to 230 g) are used for testing anti-inflammatory activity and acute toxicity. The animals are reared in the Animal Center of the Faculty of Medicine and Pharmacy of Mohammed V University in Rabat, under standard experimental conditions, where the temperature varies between 20 and 25°C with a 12-hour photoperiodic cycle. The study was conducted in accordance with the accepted principles set out in the report “Guide for the care and use of laboratory animals” prepared by the National Academy of Sciences and published by the National Institutes of Health [17].

2.3. Extraction of Plant Samples

50 g of the powder of the aerial part of Thymus leptobotrys is placed in a cartridge and placed in the Soxhlet extractor [18]. The flask is filled with 300 ml methanol for the methanolic extract and 300 ml ethanol for the ethanolic extract, and the flask is placed on a heater. When heated, the solvent evaporates, condenses in the cooler, falls back into the Soxhlet extractor, solubilizes the active ingredients, and returns to the recovery flask: the operation is repeated several times for 6 hours until the powder is completely depleted. The extract solution is cooled to room temperature, filtered through a filter paper, and then freed of all traces of solvent by means of a rotary vacuum evaporator at 40°C. The extracts are stored in hermetically sealed brown glass vials at 4°C. The extract yield (%) is calculated as follows:

2.4. Determination of Phenolic Content
2.4.1. Total Phenol Content

The total content of polyphenol is determined by the Folin–Ciocalteu reagent protocol as described by Nounah et al. [19]. First, 0.5 mL of the extract is mixed with 2.5 mL of Folin–Ciocalteu reagent diluted 1/10 with distilled water. Then, 4 mL of 7.5% Na2CO3 (w/v) is added, followed immediately by incubation for 30 min at 45°C. The spectrophotometric reading at 760 nm is taken against a blank. The calibration curve is performed with gallic acid at concentrations between 2.5 and 250 μg/mL. The total content of phenols is expressed in mg of gallic acid equivalent (GAE) per gram of extract (mg GAE/g E).

2.4.2. Total Flavonoid Content

The total content of flavonoids is determined using the aluminum chloride colorimetric method [19]. 0.25 mL of the extract is placed in a test tube containing 1.25 mL of distilled water, followed by the addition of 0.075 mL of sodium nitrite solution NaNO3 (5%), and the mixture is kept at rest for 5 minutes. Then 0.15 mL of 10% aluminum chloride is added. After 6 min, 0.5 mL 1M sodium hydroxide is added. The mixture is diluted with 0.275 mL of distilled water. The final mixture is then incubated for 30 minutes in the dark at room temperature, and the absorbance is measured at 510 nm. The flavonoid content is expressed in mg of rutin equivalent (RE) per gram of extract (mg RE/g E).

2.4.3. Total Tannin Content

The total content of condensed tannins is determined by the acidic vanillin method [20]. 500 μL of extract solution is mixed with 3 mL of 4% vanillin-methanol solution and 1.5 mL hydrochloric acid. The mixture is allowed to stand in the dark for 15 min. The absorbance is measured at 500 nm. The calibration curve for catechin is constructed from the concentrations from 30 to 1000 μg/mL. The content of condensed tannins is expressed in mg of catechin equivalent (CE) per gram of extract (mg CE/g E).

2.5. Antioxidant Activity
2.5.1. DPPH Free Radical Scavenging

The free radical scavenging activity of the extracts was measured by DPPH using the method described by Re et al. [21]. A 0.2 mM solution of DPPH is prepared in methanol or ethanol, and 0.5 mL of this solution is added to 2.5 mL of the sample. After vigorous shaking, the mixture is kept in the dark for 30 min. The absorbance is measured at 517 nm. Trolox is used as a reference compound. The experiment is performed in triplicate. The ability to recover the DPPH radical is measured using the following equation:where A0 is the absorbance of the negative control and A1 is the absorbance of the sample.

The scavenging activity is expressed by the IC50 which represents the sample concentration required to inhibit 50% of the free radical scavenging activity.

2.5.2. Trolox Equivalent Antioxidant Capacity (TEAC)

The ABTS radical scavenging activity is determined by the protocol described by Nounah et al. [22]. Stock solutions of 7 mM ABTS and 2.4 mM potassium persulfate (K2S2O8) in identical volumes are kept in the dark for sixteen hours at room temperature. Prior to testing, the ABTS+ solution is diluted in methanol or ethanol to give an absorbance of 0.700 ± 0.02 at 734 nm. 2 mL of the resulting solutions is allowed to react with 200 μL of the sample (2 mg/mL), and the absorbance is measured after 30 min at 734 nm. The same procedure is used with Trolox at different concentrations (from 5 to 100 μg/mL). The percentage of ABTS+ inhibition by different concentrations is calculated, and the antioxidant power of the sample is represented in Trolox equivalent (mg TE/g sample). The test is performed in triplicate.

2.6. Acute Toxicity Study

The acute toxicity study of T. leptobotrys extracts is evaluated on adult rats in accordance with the Organization for Economic Cooperation and Development 423 guidelines [23, 24]. After a fasting period of 3-4 h, the body weight of each animal is measured to determine the dose to be administered orally, expressed as mg extract per kg body weight. The animals are arbitrarily divided into three groups of six rats (n = 6). The first and second groups receive methanolic and ethanolic extracts from T. leptobotrys at doses of 300 and 2000 mg/kg, and the third group (control group) is given distilled water (control vehicle) orally. Signs of toxicity evaluated are general behavioral symptoms, changes in body weight, ingestion of water and food, respiration, convulsions, and mortality. They are assessed systematically for each group during the first few hours and then 14 days after treatment. The 50% lethal dose (LD50) is determined according to the protocol described in guidelines 423 [23].

2.7. Anti-Inflammatory Effect

The anti-inflammatory effect is studied using the carrageenan-induced paw edema method [25, 26]. Wistar rats are divided into four groups (n = 6). The animals were fasted for 18 hours prior to testing. The groups of rats were given different oral concentrations of T. leptobotrys extracts (300 and 600 mg/kg). The control group receives distilled water while the last group receives indomethacin (10 mg/kg) as the reference drug. After 30 minutes, all rats are injected subcutaneously with carrageenan solution (0.05 mL of 1% carrageenan suspended in 0.9% NaCl) into the subplantar region of the left hind paw. The paw volumes of the rats were recorded with a LE7500 plethysmometer just before the carrageenan injection (V0), then at 1 h 30 min, 3 h, and 6 h after the carrageenan injection (Vt). Anti-inflammatory effect is calculated using the following equation [27]:

2.8. Statistical Analysis

The data are expressed as mean values ± standard deviation for each measurement and analyzed by means of analysis of variance (one-way ANOVA) followed by Tukey posttests. The statistical study is performed using GraphPad Prism 8 software. A probability of indicates that the values are considered statistically significant.

3. Results and Discussion

3.1. Extraction Yield

The yield of the methanolic extract is around 22.2%, higher than that of ethanolic extract (15.8%).

3.2. Determination of Phenolic Content

Table 1 shows the total content of phenolics (TCP), flavonoids (TCF), and condensed tannins (CCT) of methanolic and ethanol extracts of T. leptobotrys. The highest TCP, TCF, and CCT are found in the methanolic extract. The ethanolic extract, on the other hand, has slightly lower levels of TCP and TCF, while the content of CCT is extremely low. This variation in results clearly shows that the difference in polarity of the solvents influences the extraction of phenolic compounds [28].

ExtractsTCP (mg GAE/g E)TCF (mg RE/g E)CCT (mg CE/g E)

Methanol extract243.08 ± 2.911179.28 ± 0.92239.31 ± 0.441
Ethanol extract214.26 ± 2.079144.41 ± 1.5373.06 ± 0.200

3.3. Antioxidant Activity

The antioxidant capacity of methanolic and ethanol extracts of T. leptobotrys was studied using two different methods: DPPH and ABTS radical absorption capacity (Table 2). A low IC50 value indicates significant antioxidant activity. According to the DPPH method, both types of extracts have significant antioxidant activity (Table 2), especially the methanolic extract (IC50 = 12.363 ± 0.324 μg/mL), compared to the ethanolic extract (IC50 = 20.693 ± 0.182 μg/mL). In both cases, the IC50s are higher than that of the Trolox standard (IC50 = 1.810 ± 0.017 μg/mL). The antioxidant activity of T. leptobotrys extracts, according to the ABTS test, shows that the methanolic extract has a powerful antioxidant activity of the order of 930.935 ± 1.513 mg TE/g extract, higher than that found in the ethanolic extract (860.309 ± 0.954 mg TE/g).

ExtractsDPPH (IC50 μg/mL)ABTS (mg TE/g extract)

Methanol extract12.363 ± 0.324930.935 ± 1.513
Ethanol extract20.693 ± 0.182860.309 ± 0.954
Trolox1.850 ± 0.017

The methanolic extract of the aerial part of T. leptobotrys has a higher DPPH antioxidant activity than both the methanolic extract of the leaves of T. leptobotrys (IC50 = 1950 μg/mL) and the methanolic extract of the stems of T. leptobotrys (IC50 = 430 μg/mL) using the DPPH test [29]. Thus, the whole aerial part of the plant is logically more active than individual leaves or stems.

Comparison of the results with the other studies is however not appropriate for the following two reasons: on the one hand, the antioxidant content is strongly influenced by the type of solvent used, and on the other hand, the results are expressed in caffeine equivalents or Trolox equivalents, which makes the results not directly comparable [30].

The important antioxidant activity of the methanolic extract of Thymus leptobotrys to the DPPH and ABTS radical could be explained by its richness in phenolic compounds. There is indeed a correlation between the antioxidant activity and content of phenolic compounds [3133]. On the other hand, many studies have reported that phenolic compounds are often known by their antioxidant activity [3436].

3.4. Acute Toxicity Study

The acute toxicity study of methanol and ethanol extracts of T. leptobotrys showed no mortality or clinical signs of toxicity in each group of animals all through the fourteen days of study. At 2000 mg/kg, rats showed no signs of changes in behavioral patterns or undesirable pathology or weight loss (Table 3). Ethanol and methanol extracts of T. leptobotrys can be classified as category 5 and are considered to be nontoxic by the oral route [23].

TreatmentsDose mg/kgMortalityToxic symptomsChanges in body weight (g)
1st day14th dayDifference

Methanol extract2000None185.03 ± 1.02197.83 ± 2.62+12.8
Ethanol extract2000None185.63 ± 2.42197.86 ± 1.37+12.23
Control186.03 ± 1.77199.06 ± 0.68+13.03

3.5. Anti-Inflammatory Effect

The anti-inflammatory effect of ethanolic and methanolic extracts is evaluated by the carrageenan-induced rat paw edema method. The results are presented in Table 4 and Figures 1 and 2. Six hours after administration of T. leptobotrys at 600 mg/kg extract, the volume of edema decreased notably compared to the control group () (Figures 1 and 2). Rats treated with methanol and ethanol extracts showed the greatest decrease in inflammation (90.04% and 83.88%, respectively) after 1.5 h of carrageenan injection. This reduction in edema was greater than that of indomethacin 76.77% (Table 4) and was maintained throughout the observation period. Based on these results, it can be concluded that T. leptobotrys extracts act within the first hour on the initial phase of inflammation, just like indomethacin.

Treatments (mg/kg)Inhibition of edema induced by carrageenan (%)
1 h 30 min3 h6 h

Indomethacin, 1076.7775.7861.37
Methanol extract, 30065.8764.1257.51
Methanol extract, 60090.0484.3075.10
Ethanol extract, 30068.2461.4355.36
Ethanol extract, 60083.8876.6862.66

Carrageenan-induced paw edema is due to cyclooxygenase and lipoxygenase. The cyclooxygenase enzyme is directly involved in inflammation through prostaglandin production while lipoxygenase indirectly causes an inflammatory response [7, 37]. Thus, the anti-inflammatory power of methanolic and ethanol extracts of T. leptobotrys can be explained by an inhibitory action exerted on cyclooxygenases. The inhibition of cyclooxygenases may be due to the richness of methanolic and ethanolic extracts in polyphenolic constituents. Polyphenols prevent the formation of prostaglandins that cause inflammation [38]. Tannins and flavonoids also contribute to the anti-inflammatory effect through their ability to inhibit the production of 5 proinflammatory mediators such as lipoxygenase, prostaglandins, cyclooxygenase, serotonin, histamines, and cytokines such as IL-8, TNF-α, or IL-1β [3941].

4. Conclusion

The methanolic and ethanolic extracts’ chemical analysis of the aerial part of Thymus leptobotrys reveals their phenolic compounds abundance. Overall, the methanolic extract has the highest levels of phenolic compounds as well as a more pronounced antioxidant activity using both DPPH and ABTS methods, with values of IC50 = 12.363 ± 0.324 μg/mL and 930.935 ± 1.513 μg extract TE/g, respectively. The decrease in leg edema in adult rats after 6 hours of administrating 600 mg extract/kg shows a strong anti-inflammatory effect for both extracts. The toxicity test indicates an LD50 above 2000 mg/kg for both extracts. These results show the presence of bioactive molecules in the aerial fraction of Thymus leptobotrys. Further studies for future use against diseases due to oxidative stress are recommended.

Data Availability

All data supporting the findings are adequately included within the article.

Conflicts of Interest

The authors declare that they have no conflicts of interest.


The author Asmaa Oubihi is extremely thankful to all coauthors for their valuable contribution. Moreover, many thanks go to Pr. Zidane Lahcen (Laboratory of Botany and Plant Protection, Ibn Tofail University, Kenitra, Morocco) for plant authentication. Special thanks are due to all members of the Laboratory of Pharmacology and Toxicology, Faculty of Medicine and Pharmacy, Mohammed V University, Rabat, Morocco, especially to Fatima Zahrae Bellaoui for her advice and help.


  1. E. Köksal, E. Bursal, İ. Gülçin et al., “Antioxidant activity and polyphenol content of Turkish thyme (Thymus vulgaris) monitored by liquid chromatography and tandem mass spectrometry,” International Journal of Food Properties, vol. 20, no. 3, pp. 514–525, 2017. View at: Publisher Site | Google Scholar
  2. D. Awa, Y. Konan, S. Youssouf, T. B. F. Honora, B. Adama, and K. M. Witabouna, “Pouvoir antioxydant et teneurs en composés phénoliques de deux espèces du genre Albertisia: Albertisia cordifolia (Mangenot & J. Miège) Forman et Albertisia scandens (Mangenot & J. Miège) Forman (Menispermaceae),” European Scientific Journal, vol. 14, no. 30, p. 128, 2018. View at: Publisher Site | Google Scholar
  3. E. Todirascu-Ciornea, H. A. S. El-Nashar, N. M. Mostafa et al., “Schinus terebinthifolius essential oil attenuates scopolamine-induced memory deficits via cholinergic modulation and antioxidant properties in a zebrafish model,” Evidence-Based Complementary and Alternative Medicine, vol. 2019, Article ID 5256781, 11 pages, 2019. View at: Publisher Site | Google Scholar
  4. R. S. Sohal, R. J. Mockett, and W. C. Orr, “Mechanisms of aging: an appraisal of the oxidative stress hypothesis,” Free Radical Biology and Medicine, vol. 33, no. 5, pp. 575–586, 2002. View at: Publisher Site | Google Scholar
  5. A. Favier, “Le stress oxydant,” L’Actualité Chimique, vol. 108, 2003. View at: Google Scholar
  6. Z. Liu and L. Yang, “Antisolvent precipitation for the preparation of high polymeric procyanidin nanoparticles under ultrasonication and evaluation of their antioxidant activity in vitro,” Ultrasonics Sonochemistry, vol. 43, pp. 208–218, 2018. View at: Publisher Site | Google Scholar
  7. M. E. Islam, K. M. D. Islam, M. M. Billah, R. Biswas, M. H. Sohrab, and S. M. M. Rahman, “Antioxidant and anti-inflammatory activity of Heritiera fomes (Buch.-Ham), a mangrove plant of the Sundarbans,” Advances in Traditional Medicine, vol. 20, no. 2, pp. 189–197, 2019. View at: Publisher Site | Google Scholar
  8. K. Esseh, Y.-G. Afanyibo, K. Y. S. Ahama-Esseh et al., “Screening phytochimique, étude toxicologique, évaluation des activités antiplasmodiale et antiradicalaire de la tige feuillée de Senna occidentalis Linn (Fabaceae),” European Scientific Journal, vol. 15, no. 6, 2019. View at: Publisher Site | Google Scholar
  9. A. Saleem, M. Saleem, and M. F. Akhtar, “Antioxidant, anti-inflammatory and antiarthritic potential of Moringa oleifera Lam: an ethnomedicinal plant of Moringaceae family,” South African Journal of Botany, vol. 128, pp. 246–256, 2020. View at: Publisher Site | Google Scholar
  10. C. Sauvage and C. Raynaud, “Catalogue des végétaux vasculaires de Talassemtane (rif occidental),” in Etude de Certains Milieux du Maroc et de Leur Évolution Récente, pp. 143–178, Centre National de la Recherche Scientifique, Paris, France, 1974. View at: Google Scholar
  11. H. Ismaili, L. Milella, S. Fkih-Tetouani et al., “In vivo topical anti-inflammatory and in vitro antioxidant activities of two extracts of thymus satureioides leaves,” Journal of Ethnopharmacology, vol. 91, no. 1, pp. 31–36, 2004. View at: Publisher Site | Google Scholar
  12. J. Bellakhdar, “Medicinal plants in North Africa and basic care,” Handbook of Modern Herbal Medicine, Fennec Press, Casablanca, Morocco, 2006. View at: Google Scholar
  13. F. Amarti, B. Satrani, M. Ghanmi et al., “Composition chimique et activité antimicrobienne des huiles essentielles de Thymus algeriensis Boiss. & Reut. et Thymus ciliatus (Desf.) Benth. du Maroc,” Biotechnologie, Agronomie, Société et Environnement, vol. 14, pp. 141–148, 2010. View at: Google Scholar
  14. K. Elhabazi, A. Ouacherif, A. Laroubi et al., “Analgesic activity of three thyme species, Thymus satureioides, Thymus maroccanus and Thymus leptobotrys,” African Journal of Microbiology Research, vol. 2, pp. 262–267, 2008. View at: Google Scholar
  15. F. Amarti, M. El Ajjouri, M. Ghanmi et al., “Composition chimique, activité antimicrobiennne et antioxydante de l’huile essentielle de Thymus zygis du Maroc,” Phytothérapie, vol. 9, no. 3, pp. 149–157, 2011. View at: Publisher Site | Google Scholar
  16. C. A. Jamali, A. Kasrati, K. Bekkouche et al., “Phenological changes to the chemical composition and biological activity of the essential oil from Moroccan endemic thyme (Thymus maroccanus Ball),” Industrial Crops and Products, vol. 49, pp. 366–372, 2013. View at: Publisher Site | Google Scholar
  17. K. Sayah, L. Chemlal, I. Marmouzi, M. El Jemli, Y. Cherrah, and M. E. A. Faouzi, “In vivo anti-inflammatory and analgesic activities of Cistus salviifolius (L.) and Cistus monspeliensis (L.) aqueous extracts,” South African Journal of Botany, vol. 113, pp. 160–163, 2017. View at: Publisher Site | Google Scholar
  18. O. R. Alara, N. H. Abdurahman, and C. I. Ukaegbu, “Soxhlet extraction of phenolic compounds from Vernonia cinerea leaves and its antioxidant activity,” Journal of Applied Research on Medicinal and Aromatic Plants, vol. 11, pp. 12–17, 2018. View at: Publisher Site | Google Scholar
  19. I. Nounah, A. Hajib, A. Oubihi et al., “Phytochemical screening and biological activity of leaves and stems extract of hammada scoparia,” Moroccan Journal of Chemistry, vol. 7, pp. 7–1, 2019. View at: Google Scholar
  20. S. Haida, A. Kribii, and A. Kribii, “Chemical composition, phenolic content and antioxidant capacity of Haloxylon scoparium extracts,” South African Journal of Botany, vol. 131, pp. 151–160, 2020. View at: Publisher Site | Google Scholar
  21. R. Re, N. Pellegrini, A. Proteggente, A. Pannala, M. Yang, and C. Rice-Evans, “Antioxidant activity applying an improved ABTS radical cation decolorization assay,” Free Radical Biology and Medicine, vol. 26, no. 9-10, pp. 1231–1237, 1999. View at: Publisher Site | Google Scholar
  22. I. Nounah, A. Hajib, H. Harhar et al., “Chemical composition and antioxidant activity of Lawsonia inermis seed extracts from Morocco,” Natural Product Communications, vol. 12, no. 4, 2017. View at: Publisher Site | Google Scholar
  23. Organisation for Economic Co-operation and Development (OECD), Guidelines for Testing of Chemical, Guideline 423. Acute Oral Toxicity e Acute Toxic Class Method, Organisation for Economic Co-operation and Development, Paris, France, 2002.
  24. M. El Jemli, R. Kamal, I. Marmouzi et al., “Chemical composition, acute toxicity, antioxidant and anti-inflammatory activities of Moroccan Tetraclinis articulata L.,” Journal of Traditional and Complementary Medicine, vol. 7, no. 3, pp. 281–287, 2017. View at: Publisher Site | Google Scholar
  25. C. A. Winter, E. A. Risley, and G. W. Nuss, “Carrageenin-induced edema in hind paw of the rat as an assay for antiinflammatory drugs,” Experimental Biology and Medicine, vol. 111, no. 3, pp. 544–547, 1962. View at: Publisher Site | Google Scholar
  26. A. Bounihi, G. Hajjaj, R. Alnamer, Y. Cherrah, and A. Zellou, “In vivo potential anti-inflammatory activity of Melissa officinalis L. essential oil,” Advances in Pharmacological Sciences, vol. 2013, Article ID 1, 7 pages, 2013. View at: Publisher Site | Google Scholar
  27. M. T. Saénz, M. D. García, and M. A. Fernández, “Anti-inflammatory activity and acute toxicity of Anredera leptostachys,” Phytomedicine, vol. 5, no. 3, pp. 195–198, 1998. View at: Publisher Site | Google Scholar
  28. A. O. Bolanle, A. S. Funmilola, and A. Adedayo, “Proximate analysis, mineral contents, amino acid composition, anti-nutrients and phytochemical screening of brachystegia eurycoma harms and pipper guineense schum and thonn,” American Journal of Food and Nutrition, vol. 2, pp. 11–17, 2014. View at: Publisher Site | Google Scholar
  29. A. Sayout, F. Bahi, M. Ouknin et al., “Phytochemical screening and antioxidant activity of four Moroccan Thymus species: T. leptobotrys Murb., T. pallidus Batt., T. broussonetti Boiss. and T. maroccanus Ball,” Arabian Journal of Medicinal and Aromatic Plants, vol. 1, pp. 117–128, 2015. View at: Google Scholar
  30. I. Méndez-Tovar, S. Sponza, M. C. Asensio-S-Manzanera, and J. Novak, “Contribution of the main polyphenols of Thymus mastichina subsp. mastichina to its antioxidant properties,” Industrial Crops and Products, vol. 66, pp. 291–298, 2015. View at: Publisher Site | Google Scholar
  31. A. Djeridane, M. Yousfi, B. Nadjemi, D. Boutassouna, P. Stocker, and N. Vidal, “Antioxidant activity of some Algerian medicinal plants extracts containing phenolic compounds,” Food Chemistry, vol. 97, no. 4, pp. 654–660, 2006. View at: Publisher Site | Google Scholar
  32. F. Saad, H. N. Mrabti, K. Sayah et al., “Phenolic content, acute toxicity of Ajuga iva extracts and assessment of their antioxidant and carbohydrate digestive enzyme inhibitory effects,” South African Journal of Botany, vol. 125, pp. 381–385, 2019. View at: Publisher Site | Google Scholar
  33. I. Aouam, Y. El Atki, A. Taroq, F. El Kamari, and A. Abdellaoui, “Chemical composition, antimicrobial, and antioxidant activities of two Moroccan thymus essential oils,” Asian Journal of Pharmaceutical and Clinical Research, vol. 12, no. 1, pp. 447–451, 2019. View at: Publisher Site | Google Scholar
  34. K. Sayah, I. Marmouzi, H. Naceiri Mrabti, Y. Cherrah, and M. E. A. Faouzi, “Antioxidant activity and inhibitory potential of Cistus salviifolius (L.) and Cistus monspeliensis (L.) aerial parts extracts against key enzymes linked to hyperglycemia,” BioMed Research International, vol. 2017, Article ID 2789482, 7 pages, 2017. View at: Publisher Site | Google Scholar
  35. D. Granato, F. Shahidi, R. Wrolstad et al., “Antioxidant activity, total phenolics and flavonoids contents: should we ban in vitro screening methods?” Food Chemistry, vol. 264, pp. 471–475, 2018. View at: Publisher Site | Google Scholar
  36. A. Phuyal, P. K. Ojha, B. Guragain, and N. K. Chaudhary, “Phytochemical screening, metal concentration determination, antioxidant activity, and antibacterial evaluation of Drymaria diandra plant,” Beni-Suef University Journal of Basic and Applied Sciences, vol. 8, no. 1, p. 16, 2019. View at: Publisher Site | Google Scholar
  37. G. P. Pidgeon, J. Lysaght, S. Krishnamoorthy et al., “Lipoxygenase metabolism: roles in tumor progression and survival,” Cancer and Metastasis Reviews, vol. 26, no. 3-4, p. 503, 2007. View at: Publisher Site | Google Scholar
  38. M. N. U. Chy, M. Adnan, A. K. Rauniyar et al., “Evaluation of anti-nociceptive and anti-inflammatory activities of Piper sylvaticum (Roxb.) stem by experimental and computational approaches,” Advances in Traditional Medicine, vol. 20, no. 3, p. 327, 2019. View at: Publisher Site | Google Scholar
  39. C. Pérez-Guerrero, M. D. Herrera, R. Ortiz, M. Alvarez de Sotomayor, and M. A. Fernández, “A pharmacological study of Cecropia obtusifolia Bertol aqueous extract,” Journal of Ethnopharmacology, vol. 76, no. 3, pp. 279–284, 2001. View at: Publisher Site | Google Scholar
  40. T. Vezza, A. Rodríguez-Nogales, F. Algieri, M. Utrilla, M. Rodriguez-Cabezas, and J. Galvez, “Flavonoids in inflammatory bowel disease: a review,” Nutrients, vol. 8, no. 4, p. 211, 2016. View at: Publisher Site | Google Scholar
  41. N. M. Mostafa, E. A. Abd El-Ghffar, H. G. Hegazy, and O. A. Eldahshan, “New methoxyflavone from Casimiroa sapota and the biological activities of its leaves extract against lead acetate induced hepatotoxicity in rats,” Chemistry & Biodiversity, vol. 15, Article ID e1700528, 2018. View at: Publisher Site | Google Scholar

Copyright © 2020 Asmaa Oubihi et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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