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(-)-普萘洛尔在离体兔虹膜中的分布。

The distribution of (-)-propranolol in the isolated rabbit iris.

作者信息

Fleig H A, Krieglstein G K

出版信息

Int Ophthalmol. 1986 May;9(2-3):195-201. doi: 10.1007/BF00159849.

Abstract

It has been postulated that propranolol lowers the intraocular pressure by adrenergic neurone block. However, in the isolated iris of albino rabbits, there was only a small degree of cocaine-sensitive (i.e., neuronal) accumulation of 3H-(-)-propranolol, and none at all after pretreatment of the animals with reserpine. Moreover, after preloading of the iris with 3H-(-)-propranolol, veratridine failed to release any labelled material. Hence, any adrenergic neurone blocking action of propranolol is highly unlikely. Albino and pigmented irides were first exposed to 3H-(-)-propranolol and then washed out. The results and their compartmental analysis indicated an extensive binding of 3H-(-)-propranolol in or at pigment cells; the binding is characterized by a low dissociation constant. It is very likely that the initial binding and the subsequent slow dissociation from pigment cells explains the long duration of action of beta-adrenoceptor antagonists in human therapy.

摘要

据推测,普萘洛尔通过肾上腺素能神经元阻滞来降低眼压。然而,在白化兔的离体虹膜中,3H-(-)-普萘洛尔仅有少量可卡因敏感(即神经元性)蓄积,在用利血平预处理动物后则完全没有蓄积。此外,在虹膜预先加载3H-(-)-普萘洛尔后,藜芦碱未能释放任何标记物质。因此,普萘洛尔的任何肾上腺素能神经元阻滞作用极不可能。首先将白化和有色虹膜暴露于3H-(-)-普萘洛尔,然后冲洗掉。结果及其房室分析表明,3H-(-)-普萘洛尔在色素细胞内或其表面有广泛结合;这种结合的特点是解离常数低。很可能最初的结合以及随后从色素细胞的缓慢解离解释了β-肾上腺素能受体拮抗剂在人类治疗中的长效作用。

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