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腺苷A1受体增强剂PD 81,723与沙鼠脑缺血/再灌注损伤

Adenosine A1 receptor enhancer, PD 81,723, and cerebral ischemia/reperfusion injury in the gerbil.

作者信息

Cao X, Phillis J W

机构信息

Department of Physiology, Wayne State University School of Medicine, Detroit, MI 48201, USA.

出版信息

Gen Pharmacol. 1995 Nov;26(7):1545-8. doi: 10.1016/0306-3623(95)00042-9.

DOI:10.1016/0306-3623(95)00042-9
PMID:8690243
Abstract
  1. The adenosine A1 receptor enhancer, PD 81,723, was tested for its neuroprotective activity in a Mongolian gerbil model of forebrain ischemia/reperfusion cerebral ischemia. 2. Gerbils were injected with PD 81,723 (1, 10 and 125 mg/kg i.p.) 20 min before a 5-min episode of forebrain ischemia. The extent of ischemic injury was assessed by monitoring the increases in locomotor activity and from the degree of damage to the CA1 hippocampal pyramidal cell layer after 5 days of recovery. 3. By both criteria, PD 81,723, at all three dose levels, failed to protect against ischemia/reperfusion evoked cerebral injury.
摘要
  1. 对腺苷A1受体增强剂PD 81,723在前脑缺血/再灌注脑缺血的蒙古沙鼠模型中进行神经保护活性测试。2. 在5分钟的前脑缺血发作前20分钟,给沙鼠腹腔注射PD 81,723(1、10和125毫克/千克)。通过监测运动活动的增加以及恢复5天后海马CA1锥体细胞层的损伤程度来评估缺血损伤的程度。3. 根据这两个标准,所有三个剂量水平的PD 81,723均未能预防缺血/再灌注诱发的脑损伤。

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