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To Optimize the Therapeutic Dose and Time Window of Picroside II in Cerebral Ischemic Injury in Rats by Orthogonal Test

机译:正交试验优化吡ro糖苷II在大鼠脑缺血损伤中的治疗剂量和时间窗

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The paper aims to optimize the therapeutic dose and time window of picroside II by orthogonal test in cerebral ischemic injury in rats. The forebrain ischemia models were established by bilateral common carotid artery occlusion (BCCAO) methods. The successful models were randomly divided into sixteen groups according to orthogonal experimental design and treated by injecting picroside II intraperitonenally at different ischemic time with different dose. The concentrations of neuron-specific enolase (NSE), neuroglial marker protein S100B and myelin basic protein (MBP) in serum were determined by enzyme linked immunosorbent assay to evaluate the therapeutic effect of picroside II in cerebral ischemic injury. The results indicated that best therapeutic time window and dose of picroside II in cerebral ischemic injury were ischemia 1.5 h with 20 mg/kg body weight according to the concentrations of NSE, S100B and MBP in serum. It is concluded that according to the principle of lowest therapeutic dose with longest time window, the optimized therapeutic dose and time window are injecting picroside II intraperitonenally with 20 mg/kg body weight at ischemia 1.5 h in cerebral ischemic injury in rats.
机译:本文旨在通过正交试验优化苦瓜苷Ⅱ在大鼠脑缺血损伤中的治疗剂量和时间窗。采用双侧颈总动脉闭塞(BCCAO)方法建立前脑缺血模型。根据正交实验设计,将成功的模型随机分为16组,并在不同的缺血时间,不同的剂量,不同的腹膜内注射苦味甙II进行治疗。用酶联免疫吸附法测定血清中神经元特异性烯醇化酶(NSE),神经胶质标记蛋白S100B和髓鞘碱性蛋白(MBP)的浓度,以评估苦瓜苷II在脑缺血性损伤中的治疗作用。结果表明,根据血清中NSE,S100B和MBP的浓度,在大鼠缺血性脑缺血中,苦味苦苷II的最佳治疗时间窗和剂量为缺血1.5 h,体重20 mg / kg。结论:根据最低治疗剂量和最长时间窗的原则,在大鼠脑缺血1.5 h时,腹膜内注射20 mg / kg体重的苦味苷II是优化的治疗剂量和时间窗。

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