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l-麻黄碱是中药方剂毛布氏赛新汤的主要成分之一,该方剂对大鼠口服后被动皮肤过敏反应有即时抑制作用。

l-Ephedrine is a major constituent of Mao-Bushi-Saishin-To, one of the formulas of Chinese medicine, which shows immediate inhibition after oral administration of passive cutaneous anaphylaxis in rats.

作者信息

Shibata H, Nabe T, Yamamura H, Kohno S

机构信息

Central Research Laboratory, Kotaro Pharmaceutical Co. Ltd., Takatsuki, Osaka, Japan.

出版信息

Inflamm Res. 2000 Aug;49(8):398-403. doi: 10.1007/s000110050607.

Abstract

OBJECTIVE AND DESIGN

Whether Mao-Bushi-Saishin-To (MBST), one of the formulas of classical Chinese medicine, is effective on 48-h passive cutaneous anaphylaxis (PCA) in rats and which substance in the formula is responsible for its inhibitory action were examined.

TREATMENT

In the studies on PCA, MBST (hot water extract of the whole herbal formula), extracts of Ephedra herb (Mao), l-ephedrine and other reference drugs were orally administered immediately or at various times before or 5 min after the antigen challenge. In the experiments on anaphylactic histamine release from rat peritoneal mast cells, l-ephedrine and d-pseudoephedrine were added at 10(-4)-10(-7) g/ml at 30, 10, 3 or 0 min before antigen provocation.

RESULTS

The time course study indicated that MBST produced a prompt and long lasting inhibition of PCA. Among the constituents of Mao, l-ephedrine exerted this prompt inhibitory activity, but d-pseudoephedrine did not. Neither pseudoephedrine nor l-ephedrine prevented the anaphylactic histamine release from isolated peritoneal mast cells.

CONCLUSIONS

It is strongly emphasised that the rapid suppression of PCA by orally administered l-ephedrine must be exerted by a mechanism distinct from that of suppression produced following gastrointestinal absorption of the drug, because the time required for the inhibition was extraordinarily short. However, direct inhibition of anaphylactic histamine release from isolated mast cells was excluded in this inhibition of PCA.

摘要

目的与设计

考察中药经典方剂之一的麻黄附子细辛汤(MBST)对大鼠48小时被动皮肤过敏反应(PCA)是否有效,以及该方剂中的何种物质具有抑制作用。

治疗

在PCA研究中,立即或在抗原攻击前的不同时间或攻击后5分钟口服给予MBST(全草药配方的热水提取物)、麻黄草提取物(麻黄)、l-麻黄碱及其他参考药物。在大鼠腹膜肥大细胞过敏性组胺释放实验中,在抗原激发前30、10、3或0分钟加入10(-4)-10(-7) g/ml的l-麻黄碱和d-伪麻黄碱。

结果

时程研究表明,MBST对PCA有迅速且持久的抑制作用。在麻黄的成分中,l-麻黄碱具有这种迅速的抑制活性,而d-伪麻黄碱则没有。伪麻黄碱和l-麻黄碱均不能阻止分离的腹膜肥大细胞释放过敏性组胺。

结论

需着重强调的是,口服l-麻黄碱对PCA的快速抑制作用必定是通过一种与药物经胃肠道吸收后产生的抑制作用不同的机制实现的,因为抑制所需时间极短。然而,在这种对PCA的抑制作用中排除了对分离肥大细胞过敏性组胺释放的直接抑制作用。

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