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Phytochemical and Pharmacological Investigations on Moringa peregrina (Forssk) Fiori
Seham A. Elbatran,Omar M. Abdel-Salam,Khaled A. Abdelshfeek,Naglaa M. Nazif,Shams I. Ismail,Faiza M. Hammouda 한국생약학회 2005 Natural Product Sciences Vol.11 No.4
Investigation of M. peregrina aerial parts revealed the isolation and identification of 4-flavonoidalcompounds, quercetin, quercetin-3-0-rutinoside (rutin), chrysoeriol-7-0-rhamnoside and 6,8,3/,5/-tetramethoxyapigenin. The compounds were identified by TLC, PC, MS, and H1-NMR. The fatty acids and unsaponifiablematter were studied. The LD50 for M. peregrina was 113.4 mg/100 g b.wt. Repeated intraperitoneal injection of 1/20 and 1/10 LD50 (5.67 mg and 11.34 mg/100 g b.wt.) of defatted alcoholic extract of M. peregrina for 30 daysinduced significant decrease in serum glucose, liver enzymes and lipid components. M. peregrina administeredi.p., 30 min prior to carrageenan at the above doses significantly inhibited the rat paw oedema response. In acuteM. peregrina exhibited markedanalgesic properties. In addition, M. peregrina administered at time of indomethacin injection inhibited thedevelopment of gastric lesions in rats.