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钙激动剂Bay K 8644对小鼠的行为影响:钙拮抗剂硝苯地平的拮抗作用。

The behavioral effects of the calcium agonist Bay K 8644 in the mouse: antagonism by the calcium antagonist nifedipine.

作者信息

Bolger G T, Weissman B A, Skolnick P

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1985 Feb;328(4):373-7. doi: 10.1007/BF00692903.

Abstract

Mice injected with the calcium agonist BAY K 8644 (2-4 mg/kg, i.p.) displayed profound behavioral changes including ataxia, decreased motor activity, Straub tail, arched back, limb clonus and tonus, and an increased sensitivity to auditory stimulation. BAY K 8644 significantly impaired rotorod performance in mice with an ED50 of 0.8 mg/kg. The behavioral effects of BAY K 8644 were antagonized by nifedipine, but not by the non-dihydropyridine calcium channel antagonist verapamil or the alpha-adrenoceptor antagonist prazosin. Further, the actions of BAY K 8644 were not mimicked by the alpha-adrenoceptor agonist methoxamine at doses up to 4.5 mg/kg. These observations, coupled with the findings that BAY K 8644 is a potent, competitive inhibitor of [3H]nitrendipine binding to the dihydropyridine binding site in mouse brain (Ki = 7.0 X 10(-9) M), suggests that BAY K 8644 may produce its behavioral actions via an interaction with the DHP binding site, which has been linked to the control of calcium flux across membranes in peripheral tissues.

摘要

注射钙激动剂BAY K 8644(2 - 4毫克/千克,腹腔注射)的小鼠表现出深刻的行为变化,包括共济失调、运动活动减少、斯特劳布尾、弓背、肢体阵挛和紧张度增加,以及对听觉刺激的敏感性增加。BAY K 8644显著损害小鼠的转棒试验性能,半数有效剂量(ED50)为0.8毫克/千克。硝苯地平可拮抗BAY K 8644的行为效应,但非二氢吡啶类钙通道拮抗剂维拉帕米或α - 肾上腺素能受体拮抗剂哌唑嗪则不能。此外,高达4.5毫克/千克剂量的α - 肾上腺素能受体激动剂甲氧明不能模拟BAY K 8644的作用。这些观察结果,再加上BAY K 8644是[3H]尼群地平与小鼠脑二氢吡啶结合位点结合的强效竞争性抑制剂(抑制常数Ki = 7.0×10⁻⁹ M)这一发现,表明BAY K 8644可能通过与二氢吡啶结合位点相互作用产生其行为效应,该位点与外周组织中跨膜钙通量的控制有关。

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