Von Lubitz D K, Lin R C, Melman N, Ji X D, Carter M F, Jacobson K A
NIH/NIDDK/LBC/Molecular Recognition Section, Bethesda, MD 20892.
Eur J Pharmacol. 1994 Apr 21;256(2):161-7. doi: 10.1016/0014-2999(94)90241-0.
The effect of chronic administration of selective adenosine A1 receptor agonists and antagonists on the outcome of cerebral ischemia is entirely unknown. Therefore, we have investigated the impact of such regimens on the hippocampal adenosine A1 receptor density, and on the recovery from 10 min forebrain ischemia in gerbils. While acutely administered N6-cyclopentyladenosine (CPA) given at 0.02 mg/kg resulted only in a significant reduction of mortality, at 1 mg/kg it improved both survival and neuronal preservation in the hippocampal CA1 region. Acute treatment with 1,3-dipropyl-8-cyclopentylxanthine (CPX) significantly worsened the outcome and enhanced neuronal destruction. The effects of chronic administration of these drugs (15 days followed by 1 drug-free day) were opposite. Thus, although chronic CPA at 0.02 mg/kg did not have any effect at all, at 1 mg/kg both survival and neuronal preservation were significantly poorer than in controls, while chronic CPX resulted in a significant improvement of both measures. These results were not accompanied by adenosine A1 receptor up- or downregulation. Our study indicates that highly selective adenosine analogues may have therapeutic potential in treatment of cerebral ischemia/stroke and possibly other neurodegenerative disorders as well.
长期给予选择性腺苷A1受体激动剂和拮抗剂对脑缺血结局的影响完全未知。因此,我们研究了此类给药方案对沙鼠海马腺苷A1受体密度以及从10分钟前脑缺血中恢复情况的影响。急性给予0.02mg/kg的N6-环戊基腺苷(CPA)仅显著降低死亡率,而1mg/kg时则改善了海马CA1区的存活率和神经元保存情况。急性给予1,3-二丙基-8-环戊基黄嘌呤(CPX)显著恶化了结局并加剧了神经元破坏。长期给予这些药物(15天,随后停药1天)的效果则相反。因此,虽然0.02mg/kg的慢性CPA根本没有任何作用,但1mg/kg时的存活率和神经元保存情况均显著低于对照组,而慢性CPX则使这两项指标均得到显著改善。这些结果并未伴随腺苷A1受体的上调或下调。我们的研究表明,高度选择性的腺苷类似物在治疗脑缺血/中风以及可能的其他神经退行性疾病方面可能具有治疗潜力。