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β1肾上腺素能受体拮抗剂可增强游泳应激对小鼠的抗惊厥作用。

Beta-1 adrenoceptor antagonists potentiate the anticonvulsive effect of swim stress in mice.

作者信息

Pericic D, Jazvinscak M, Svob D, Mirkovic K

机构信息

Laboratory for Molecular Neuropharmacology, Division of Molecular Medicine, Ruder Boskovic Institute, PO Box 180, 10002, Zagreb, Croatia.

出版信息

Pharmacol Biochem Behav. 2000 Nov;67(3):507-10. doi: 10.1016/s0091-3057(00)00385-3.

Abstract

To explore the possible involvement of beta adrenoceptor antagonists in the previously observed anticonvulsive effect of swim stress, the mice were, prior to administration of convulsants, pre-treated with propranolol (a non-selective beta adrenoceptor antagonist), betaxolol (a selective beta-1 adrenoreceptor antagonist), or ICI 118,551 (a selective beta-2 adrenoreceptor antagonist). In control unstressed animals, only propranolol [10 mg/kg, intraperitoneally (ip)] produced a significant change. It enhanced the threshold dose of picrotoxin producing tonic hindlimb extension. However, in swim-stressed animals, propranolol enhanced doses of picrotoxin producing tonic hindlimb extension and death, while betaxolol (20 mg/kg, i.p.) enhanced doses of picrotoxin producing running/bouncing clonus, tonic hindlimb extension and death. Pre-treatment with ICI 118,551 (4 mg/kg, i.p.) failed to affect doses of picrotoxin producing convulsions and death. The results demonstrate that blockade of beta-1 adrenoceptors potentiates the anticonvulsant effect of swim stress against convulsions produced by picrotoxin, a noncompetitive GABA(A) receptor antagonist.

摘要

为了探究β肾上腺素能受体拮抗剂是否可能参与先前观察到的游泳应激的抗惊厥作用,在给予惊厥剂之前,用普萘洛尔(一种非选择性β肾上腺素能受体拮抗剂)、倍他洛尔(一种选择性β-1肾上腺素能受体拮抗剂)或ICI 118,551(一种选择性β-2肾上腺素能受体拮抗剂)对小鼠进行预处理。在对照未应激动物中,只有普萘洛尔[10毫克/千克,腹腔注射(ip)]产生了显著变化。它提高了产生强直性后肢伸展的苦味毒的阈剂量。然而,在游泳应激动物中,普萘洛尔提高了产生强直性后肢伸展和死亡的苦味毒剂量,而倍他洛尔(20毫克/千克,腹腔注射)提高了产生奔跑/弹跳阵挛、强直性后肢伸展和死亡的苦味毒剂量。用ICI 118,551(4毫克/千克,腹腔注射)预处理未能影响产生惊厥和死亡的苦味毒剂量。结果表明,β-1肾上腺素能受体的阻断增强了游泳应激对由非竞争性GABA(A)受体拮抗剂苦味毒引起的惊厥的抗惊厥作用。

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