Ting P, Xu S, Krumins S
Department of Pediatrics, College of Medicine, Howard University, Washington, DC.
Acta Neurochir Suppl (Wien). 1994;60:253-6. doi: 10.1007/978-3-7091-9334-1_67.
We studied changes in opioid receptors (mu, delta, kappa) concentrations during temporary middle cerebral artery occlusion (MCAO) in cats by sequential displacement of unselective opioid antagonist, [3H]-diprenorphine with highly selective ligands for mu, delta and kappa, subsites. Following threshold cerebral ischemia (rCBF < 10 ml/100 g/min) there was a 2 to 3 fold increase in the 3 opioid receptor subtype concentrations at 10 min following the release of MCAO. Further, 56% of the cats depicted early postischemic hyperemia BBB opening, at 1 h and 3 h following the release of occlusion, with significant subsequent progression of brain edema. We believe that the enhanced brain opioid activity may be relevant to the neuronal damage caused by the early postischemic BBB opening.
我们通过用针对μ、δ和κ亚位点的高选择性配体依次取代非选择性阿片样物质拮抗剂[3H]-二丙诺啡,研究了猫大脑中动脉暂时闭塞(MCAO)期间阿片样物质受体(μ、δ、κ)浓度的变化。在阈值脑缺血(rCBF < 10 ml/100 g/min)后,MCAO解除10分钟时,3种阿片样物质受体亚型浓度增加了2至3倍。此外,56%的猫在闭塞解除后1小时和3小时出现缺血后早期充血性血脑屏障开放,随后脑水肿显著进展。我们认为,增强的脑阿片样物质活性可能与缺血后早期血脑屏障开放引起的神经元损伤有关。