Logan M, Sweeney M I
Department of Physiology, University of Saskatchewan, Saskatoon, Canada.
Mol Chem Neuropathol. 1997 Jun;31(2):119-33. doi: 10.1007/BF02815237.
Administration of adenosine A1 receptor agonists in vivo is neuroprotective in various stroke models. Experiments using either mixed cultures of neurons and astrocytes or brain slices, in which several cell types are present, have demonstrated that activation of A1 receptors also id protective against hypoxia and/or hypoglycemia in vitro. In this study, we have examined the effect of the A1 agonist cyclopentyladenosine (CPA) on cellular damage, measured by efflux of lactate dehydrogenase (LDH), in highly enriched primary cultures of either neurons of astrocytes exposed to different metabolic insults. CPA reduced neuronal LDH release induced by a combination of hypoxia and substrate deprivation ("simulated ischemia"; IC50 = 28 nM) of by hypoxia alone (IC50 = 170 nM). In contrast, CPA had no effect on neuronal damage induced by substrate deprivation alone, not did it affect ischemic death to astrocytes. The neuroprotective effect of CPA during simulated ischemia and hypoxia were reversed by the A1 antagonist 1,3-dipropyl-8-cyclopentylxanthine (DPCPX). These data demonstrate that activation of an adenosine A1 receptor on neurons, but not astrocytes, is protective against cellular damage of death induced specifically by hypoxia as opposed to other metabolic insults such as hypoglycemia.
在多种中风模型中,体内给予腺苷A1受体激动剂具有神经保护作用。使用神经元和星形胶质细胞混合培养物或包含多种细胞类型的脑片进行的实验表明,在体外,A1受体的激活对缺氧和/或低血糖也具有保护作用。在本研究中,我们检测了A1激动剂环戊腺苷(CPA)对暴露于不同代谢损伤的星形胶质细胞或神经元高度富集原代培养物中细胞损伤的影响,细胞损伤通过乳酸脱氢酶(LDH)外流来衡量。CPA减少了由缺氧和底物剥夺联合作用(“模拟缺血”;IC50 = 28 nM)或单独缺氧(IC50 = 170 nM)诱导的神经元LDH释放。相反,CPA对单独由底物剥夺诱导的神经元损伤没有影响,对星形胶质细胞的缺血性死亡也没有影响。在模拟缺血和缺氧期间,CPA的神经保护作用被A1拮抗剂1,3 - 二丙基 - 8 - 环戊基黄嘌呤(DPCPX)逆转。这些数据表明,神经元而非星形胶质细胞上腺苷A1受体的激活,对由缺氧而非其他代谢损伤(如低血糖)特异性诱导的细胞死亡损伤具有保护作用。