Kim H M, Lee E H, Jeoung S W, Kim C Y, Park S T, Kim J J
Department of Oriental Pharmacy, College of Pharmacy, Wonkwang University, Iksan-city, Chonbuk, South Korea.
J Ethnopharmacol. 1999 Jan;64(1):45-52. doi: 10.1016/s0378-8741(98)00105-6.
We investigated the effect of the herbal formulation 'Chung-Dae-San' (CDS) on anaphylactic reactions. CDS inhibited compound 48/80-induced anaphylactic shock 100% with the dose of 10(0) g/kg body weight (BW). When CDS was given as pretreatment at concentrations ranging from 10(-4) to 10(0) g/kg BW, the serum histamine levels induced by compound 48/80 were reduced in a dose-dependent manner. We also investigated the effect of CDS on mast cell-dependent passive cutaneous anaphylaxis (PCA) activated by anti-dinitrophenyl (DNP) IgE antibody. CDS potently inhibited PCA when administered orally, topically, intraperitoneally or intradermally. However, it did not show inhibitory activity when administered intravenously. CDS dose-dependently inhibited the histamine release from the rat peritoneal mast cells (RPMC) by compound 48/80 and anti-DNP IgE. Moreover, the level of cAMP in RPMC, when CDS was added, significantly increased about 4-fold at 4 min compared with that of basal cells. These results indicate that CDS may possess strong antianaphylactic activity and also suggest the differential activity following administration routes may be caused by difference in bioavailability.
我们研究了草药配方“Chung-Dae-San”(CDS)对过敏反应的影响。CDS以10⁰g/kg体重(BW)的剂量可100%抑制化合物48/80诱导的过敏性休克。当CDS以10⁻⁴至10⁰g/kg BW的浓度进行预处理时,化合物48/80诱导的血清组胺水平呈剂量依赖性降低。我们还研究了CDS对由抗二硝基苯基(DNP)IgE抗体激活的肥大细胞依赖性被动皮肤过敏反应(PCA)的影响。CDS经口服、局部、腹腔内或皮内给药时均能有效抑制PCA。然而,静脉内给药时它没有显示出抑制活性。CDS剂量依赖性地抑制化合物48/80和抗DNP IgE诱导的大鼠腹膜肥大细胞(RPMC)组胺释放。此外,添加CDS时,RPMC中的cAMP水平在4分钟时与基础细胞相比显著增加约4倍。这些结果表明CDS可能具有强大的抗过敏活性,也提示给药途径后的差异活性可能是由生物利用度的差异引起的。