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정훈(Hoon Jeong),이승룡(Seung Yong Lee),김수웅(Su Ung Kim),한만덕(Man Deuck Han),이은방(Eun Bang Lee),천선아(Seon Ah Cheon),김상미(Sang Mee Kim),김경란(Kyung Ran Kim),이승목(Seung Mok Lee),현익상(Ik Sang Hyun),이준우(June Woo Lee) 한국응용약물학회 1994 Biomolecules & Therapeutics(구 응용약물학회지) Vol.2 No.4
A polysaccharide, G009, isolated from Ganoderma lucidum IY 009, was subjected to investigating on general pharmacology. This material at the large oral doses of 1000 and 2000 ㎎/㎏ in mice did not exhibit any abnormal behaviors and another effects on central nervous system. It also had no influences on hexobarbital-induced sleeping time, rotarod test and spontaneous activity test at each oral dose of 1000 ㎎/㎏ in mice. No effects on the body temperature and on acetic acid induced writhing syndrome in mice were observed with its oral administration at 1000 ㎎/㎏, and the convulsions induced by strychnine and pentetrazole were not inhibited at its oral doses of 1000 ㎎/㎏ in mice. The solution of G009 as given intravenously at the doses of 30 and 60 ㎎/㎏ in rabbit had no influences on blood pressure and respiration rates and depth. In isolated organs of rat uterus and fundus muscles and guinea pig ileum and trachea, it did not show any contraction or relaxation at the concentrations of 2 X 10^(-3) g/㎖, and the contractive actions produced by oxytocin, acetylcholine, serotonin and histamine were not inhibited at the same doses. This material showed no effect on intestinal propulsion test in mice and gastric secretion in rats at the oral doses of 1000 ㎎/㎏. However, it is interesting that the material exhibited potent inhibition of acidified aspirin induced gastric damage at the doses of 500 and 1000 ㎎/㎏ in rats.