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可乐定和替扎尼定对大鼠脊髓切片中P物质释放的抑制作用及α-肾上腺素能受体拮抗剂的拮抗作用。

Inhibitory effects of clonidine and tizanidine on release of substance P from slices of rat spinal cord and antagonism by alpha-adrenergic receptor antagonists.

作者信息

Ono H, Mishima A, Ono S, Fukuda H, Vasko M R

机构信息

Department of Toxicology and Pharmacology, Faculty of Pharmaceutical Sciences, University of Tokyo, Japan.

出版信息

Neuropharmacology. 1991 Jun;30(6):585-9. doi: 10.1016/0028-3908(91)90077-o.

Abstract

Effects of clonidine and tizanidine, which have antinociceptive and alpha 2-agonistic actions, were studied on the release of substance P from slices of spinal cord from the rat. Veratridine-evoked depolarization induced a 2-3-fold increase in the release of substance P from the slices of spinal cord. Exposure of the cord tissue to 10 microM clonidine and tizanidine significantly reduced the release of substance P. The inhibitory effects of clonidine and tizanidine were attenuated by pre-exposure of the tissue to 10 microM piperoxane, which has alpha 2-antagonistic activity and the inhibitory effect of clonidine was attenuated by 10 microM yohimbine. Moreover, the inhibitory effects of clonidine and tizanidine were also blocked by a small dose of prazosin, an antagonist for alpha 1- and alpha 2B-receptors. None of the antagonists had any effect on release of substance P, when given alone. These results suggest that alpha 2B-adrenoceptors are involved in the inhibitory effects of clonidine and tizanidine on the release of substance P.

摘要

研究了具有抗伤害感受和α2-激动作用的可乐定和替扎尼定对大鼠脊髓切片中P物质释放的影响。藜芦碱诱发的去极化使脊髓切片中P物质的释放增加了2 - 3倍。将脊髓组织暴露于10微摩尔的可乐定和替扎尼定可显著减少P物质的释放。预先将组织暴露于具有α2-拮抗活性的10微摩尔哌罗克生可减弱可乐定和替扎尼定的抑制作用,而10微摩尔育亨宾可减弱可乐定的抑制作用。此外,小剂量的哌唑嗪(一种α1-和α2B-受体拮抗剂)也可阻断可乐定和替扎尼定的抑制作用。单独给予这些拮抗剂时,对P物质的释放均无影响。这些结果表明,α2B-肾上腺素能受体参与了可乐定和替扎尼定对P物质释放的抑制作用。

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