Hirata Noriko, Naruto Shunsuke, Inaba Kazunori, Itoh Kimihisa, Tokunaga Masashi, Iinuma Munekazu, Matsuda Hideaki
School of Pharmacy, Kinki University, 3-4-1 Kowakae, Higashiosaka, Osaka 577-8502, Japan.
Biol Pharm Bull. 2008 Oct;31(10):1973-6. doi: 10.1248/bpb.31.1973.
Oral administration of a methanolic extract of Piper nigrum leaf (PN-ext, 50, 200 and 500 mg/kg) showed a potent dose-dependent inhibition of dinitrofluorobenzene (DNFB)-induced cutaneous reaction at 1 h [immediate phase response (IPR)] after and 24 h [late phase response (LPR)] after DNFB challenge in mice which were passively sensitized with anti-dinitrophenyl (DNP) IgE antibody. Ear swelling inhibitory effect of PN-ext (50, 200 and 500 mg/kg, per os (p.o.)) on very late phase response (vLPR) in the model mice was significant but weaker than that on IPR. Oral administration of PN-ext (50, 200 and 500 mg/kg for 7 d) inhibited picryl chloride (PC)-induced ear swelling in PC sensitized mice. PN-ext exhibited in vitro inhibitory effect on compound 48/80-induced histamine release from rat peritoneal mast cells. Two lignans of PN-ext, (-)-cubebin (1) and (-)-3,4-dimethoxy-3,4-desmethylenedioxycubebin (2), were identified as major active principles having histamine release inhibitory activity.
给被动致敏抗二硝基苯基(DNP)IgE抗体的小鼠口服黑胡椒叶甲醇提取物(PN-ext,50、200和500mg/kg),在二硝基氟苯(DNFB)激发后1小时[即时相反应(IPR)]和24小时[迟相反应(LPR)]显示出强效的剂量依赖性抑制DNFB诱导的皮肤反应。PN-ext(50、200和500mg/kg,口服(p.o.))对模型小鼠极迟相反应(vLPR)的耳肿胀抑制作用显著,但弱于对IPR的抑制作用。口服PN-ext(50、200和500mg/kg,持续7天)可抑制氯化苦基(PC)致敏小鼠中PC诱导的耳肿胀。PN-ext对化合物48/80诱导的大鼠腹膜肥大细胞组胺释放具有体外抑制作用。PN-ext中的两种木脂素,(-)-荜澄茄素(1)和(-)-3,4-二甲氧基-3,4-去亚甲基二氧基荜澄茄素(2),被确定为具有组胺释放抑制活性的主要活性成分。