Shinde U A, Kulkarni K R, Phadke A S, Nair A M, Mungantiwar A A, Dikshit V J, Saraf M N
Department of Pharmacology, Bombay College of Pharmacy, Kalina, Mumbai, India.
Indian J Exp Biol. 1999 Mar;37(3):258-61.
Volatile oil of C. deodara, administered orally at the doses of 50, 100 and 200 mg/kg body weight, significantly inhibited the pedal edema induced by compound 48/80 in rats. The oil significantly inhibited compound 48/80 induced degranulation of isolated rat peritoneal mast cells at concentrations ranging from 25-200 micrograms/ml. C. deodara wood oil also significantly inhibited the enzyme lipoxygenase at a concentration of 200 micrograms/ml. Thus, the anti-inflammatory activity of C. deodara wood oil could be attributed to its mast cell stabilizing activity and the inhibition of leukotriene synthesis.
喜马拉雅雪松挥发油,以50、100和200毫克/千克体重的剂量口服给药,能显著抑制化合物48/80诱导的大鼠足跖水肿。该挥发油在25 - 200微克/毫升的浓度范围内,能显著抑制化合物48/80诱导的离体大鼠腹腔肥大细胞脱颗粒。喜马拉雅雪松木油在200微克/毫升的浓度下也能显著抑制脂氧合酶。因此,喜马拉雅雪松木油的抗炎活性可能归因于其肥大细胞稳定活性和对白三烯合成的抑制作用。