Melissa officinalis L. (Lamiaceae) had been reported in traditional Moroccan medicine to exhibit calming, antispasmodic, and strengthening heart effects. Therefore, this study is aimed at determining the anti-inflammatory activities of M. officinalis L. leaves. The effect of the essential oil of the leaves of this plant was investigated for anti-inflammatory properties by using carrageenan and experimental trauma-induced hind paw edema in rats. The essential oil extracted from leaves by hydrodistillation was characterized by means of gas chromatography-mass spectrometry (GC-MS). M. officinalis contained Nerol (30.44%), Citral (27.03%), Isopulegol (22.02%), Caryophyllene (2.29%), Caryophyllene oxide (1.24%), and Citronella (1.06%). Anti-inflammatory properties of oral administration of essential oil at the doses of 200, 400 mg/kg p.o., respectively, showed significant reduction and inhibition of edema with 61.76% and 70.58%, respectively, (P < 0.001) induced by carrageenan at 6 h when compared with control and standard drug (Indomethacin). On experimental trauma, M. officinalis L. essential oil showed pronounced reduction and inhibition of edema induced by carrageenan at 6 h at 200 and 400 mg/kg with 91.66% and 94.44%, respectively (P < 0.001). We can conclude that the essential oil of M. officinalis L. possesses potential anti-inflammatory activities, supporting the traditional application of this plant in treating various diseases associated with inflammation and pain.
La synthèse et l'étude de la réactivité de la 4-phényl-1,5-benzodiazépin-2-one nous a permis d'obtenir deux dérivés : la 4-phényl-1,3,4,5-tétrahydro-1,5-benzodiazépin-2-one et la 4-phényl-1,5-benzodiazépin-2thiole. Ces produits ont fait l'objet d'une étude toxicologique et nous avons aussi exploré leur activité sur le système nerveux central, notamment l'action analgésique, grâce à un test spécifique. Après analyse de nos résultats, nous avons constaté que les composés testés s'avèrent atoxiques à des doses thérapeutiques, avec une DL 50 supérieure à 1000 mg/kg par voie intrapéritonéale, et exercent une action analgésique modérée, surtout pour les composés 1 et 3 vis-à-vis de l'acide acétylsalicylique. Le produit 2 a une action analgésique moins importante.
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