Varma D R, Yue T L
Br J Pharmacol. 1986 Mar;87(3):587-94. doi: 10.1111/j.1476-5381.1986.tb10201.x.
The cholinoceptor antagonists anisodamine and anisodine are widely used in the People's Republic of China for the management of acute circulatory shock but the mechanism of their beneficial effects is not fully known; we therefore investigated if these agents possessed adrenoceptor blocking properties. The antagonistic effect of anisodamine and anisodine against the specific binding of the alpha 1-adrenoceptor ligand [3H]-WB-4101 to cardiac and brain tissue membrane preparations and against the effects of phenylephrine on isolated aortic strips and left atria of rats were compared with classical muscarinic receptor and adrenoceptor blocking agents. Both anisodamine and anisodine possessed alpha 1-adrenoceptor blocking properties; the order of potency of various agents in displacing the binding of [3H]-WB-4101 to receptors and in antagonizing the effects of phenylephrine on aortic strips and left atria was: prazosin greater than atropine greater than anisodamine greater than scopolamine greater than anisodine. It is concluded that both anisodamine and to a lesser extent anisodine possess alpha 1-adrenoceptor blocking properties; this antagonistic activity of anisodamine may contribute to its salutary effects on the microcirculation. However, it is unlikely that anisodine produces a significant adrenoceptor blockade in the clinically used dose-range.
抗胆碱能受体药物山莨菪碱和樟柳碱在中华人民共和国被广泛用于治疗急性循环性休克,但其有益作用的机制尚不完全清楚;因此,我们研究了这些药物是否具有肾上腺素能受体阻断特性。将山莨菪碱和樟柳碱对α1-肾上腺素能受体配体[3H]-WB-4101与心脏和脑组织膜制剂特异性结合的拮抗作用,以及对去氧肾上腺素对大鼠离体主动脉条和左心房作用的拮抗作用,与经典的毒蕈碱受体和肾上腺素能受体阻断剂进行了比较。山莨菪碱和樟柳碱均具有α1-肾上腺素能受体阻断特性;各种药物在取代[3H]-WB-4101与受体结合以及拮抗去氧肾上腺素对主动脉条和左心房作用方面的效力顺序为:哌唑嗪>阿托品>山莨菪碱>东莨菪碱>樟柳碱。得出的结论是,山莨菪碱和在较小程度上樟柳碱均具有α1-肾上腺素能受体阻断特性;山莨菪碱的这种拮抗活性可能有助于其对微循环的有益作用。然而,樟柳碱在临床使用剂量范围内不太可能产生显著的肾上腺素能受体阻断作用。