Rehni Ashish K, Shri Richa, Singh Manjeet
Department of Pharmaceutical Sciences and Drug Research, Punjabi University, Patiala 147 002, India.
Indian J Exp Biol. 2007 Mar;45(3):247-52.
Bilateral carotid artery occlusion of 10 min followed by reperfusion for 24 hr was employed in present study to produce ischaemia and reperfusion induced cerebral injury in mice. Cerebral infarct size was measured using triphenyltetrazolium chloride staining. Short-term memory was evaluated using elevated plus maze. Inclined beam walking test was employed to assess motor incoordination. Bilateral carotid artery occlusion followed by reperfusion produced cerebral infarction and impaired short-term memory, motor co-ordination and lateral push response. A preceding episode of mesenteric artery occlusion for 15 min and reperfusion of 15 min (remote mesenteric ischaemic preconditioning) prevented markedly ischaemia-reperfusion-induced cerebral injury measured in terms of infarct size, loss of short-term memory, motor coordination and lateral push response. Glibenclamide (5 mg/kg, iv) a KATP channel blocker and caffeine (7 mg/kg, iv) an adenosine receptor blocker attenuated the neuroprotective effect of remote mesenteric ischaemic preconditioning. It may be concluded that neuroprotective effect of remote mesenteric ischaemic preconditioning may be due to activation of adenosine receptors and consequent activation of KATP channels in mice.
在本研究中,采用双侧颈动脉闭塞10分钟后再灌注24小时的方法,在小鼠中产生缺血再灌注诱导的脑损伤。使用氯化三苯基四氮唑染色测量脑梗死体积。使用高架十字迷宫评估短期记忆。采用倾斜梁行走试验评估运动不协调。双侧颈动脉闭塞后再灌注会导致脑梗死,并损害短期记忆、运动协调和侧推反应。肠系膜动脉闭塞15分钟并再灌注15分钟(远隔肠系膜缺血预处理)的先前发作,可显著预防以梗死体积、短期记忆丧失、运动协调和侧推反应衡量的缺血再灌注诱导的脑损伤。格列本脲(5毫克/千克,静脉注射)一种KATP通道阻滞剂和咖啡因(7毫克/千克,静脉注射)一种腺苷受体阻滞剂减弱了远隔肠系膜缺血预处理的神经保护作用。可以得出结论,远隔肠系膜缺血预处理的神经保护作用可能是由于小鼠体内腺苷受体的激活以及随后KATP通道的激活。