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腺苷A(1)受体拮抗剂和线粒体ATP敏感性钾通道阻滞剂可减轻大鼠局灶性脑缺血的耐受性。

Adenosine A(1) receptor antagonist and mitochondrial ATP-sensitive potassium channel blocker attenuate the tolerance to focal cerebral ischemia in rats.

作者信息

Yoshida Mitsuyoshi, Nakakimura Kazuhiko, Cui Ying Jun, Matsumoto Mishiya, Sakabe Takefumi

机构信息

Department of Anesthesiology-Resuscitology, Yamaguchi University School of Medicine, Yamaguchi Rosai Hospital, Yamaguchi, Japan.

出版信息

J Cereb Blood Flow Metab. 2004 Jul;24(7):771-9. doi: 10.1097/01.WCB.0000122742.72175.1B.

Abstract

Involvement of adenosine and adenosine triphosphate-sensitive potassium (KATP) channels in the development of ischemic tolerance has been suggested in global ischemia, but has not been studied extensively in focal cerebral ischemia. This study evaluated modulating effects of adenosine A1 receptor antagonist DPCPX (8-cyclopentyl-1,3-dipropylxanthine) and mitochondrial KATP channel blocker 5HD (5-hydroxydecanoate) on the development of tolerance to focal cerebral ischemia in rats. Preconditioning with 30-minute middle cerebral artery occlusion (MCAO) reduced cortical and subcortical infarct volume following 120-minute MCAO (test ischemia) given 72 hours later. The neuroprotective effect of preconditioning was attenuated by 0.1 mg/kg DPCPX given before conditioning ischemia (30-minute MCAO), but no influence was provoked when it was administered before test ischemia. DPCPX had no effect on infarct volume after conditioning or test ischemia when given alone. The preconditioning-induced neuroprotection disappeared when 30 mg/kg 5HD was administered before test ischemia. These results suggest a possible involvement of adenosine A1 receptors during conditioning ischemia and of mitochondrial KATP channels during subsequent severe ischemia in the development of tolerance to focal cerebral ischemia.

摘要

在全脑缺血中,已有人提出腺苷和三磷酸腺苷敏感性钾(KATP)通道参与缺血耐受的形成,但在局灶性脑缺血中尚未进行广泛研究。本研究评估了腺苷A1受体拮抗剂DPCPX(8-环戊基-1,3-二丙基黄嘌呤)和线粒体KATP通道阻滞剂5HD(5-羟基癸酸)对大鼠局灶性脑缺血耐受形成的调节作用。用30分钟大脑中动脉闭塞(MCAO)进行预处理,可减少72小时后给予120分钟MCAO(试验性缺血)后的皮质和皮质下梗死体积。预处理的神经保护作用在预处理缺血(30分钟MCAO)前给予0.1mg/kg DPCPX时减弱,但在试验性缺血前给予时则无影响。单独给予DPCPX时,对预处理或试验性缺血后的梗死体积无影响。在试验性缺血前给予30mg/kg 5HD时,预处理诱导的神经保护作用消失。这些结果表明,在局灶性脑缺血耐受形成过程中,腺苷A1受体可能参与预处理缺血过程,而线粒体KATP通道可能参与随后的严重缺血过程。

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