首页> 美国卫生研究院文献>Experimental and Therapeutic Medicine >Lactuside B decreases aquaporin-4 and caspase-3 mRNA expression in the hippocampus and striatum following cerebral ischaemia-reperfusion injury in rats
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Lactuside B decreases aquaporin-4 and caspase-3 mRNA expression in the hippocampus and striatum following cerebral ischaemia-reperfusion injury in rats

机译:乳酸B降低大鼠脑缺血再灌注后海马和纹状体aquaporin-4和caspase-3 mRNA的表达

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摘要

This study aimed to investigate the effects of lactuside B (LB) on aquaporin-4 (AQP4) and caspase-3 mRNA expression in the hippocampus and the striatum following cerebral ischaemia-reperfusion (I/R) injury in rats. Cerebral I/R injury was established in Sprague-Dawley rats by occluding the middle cerebral artery for 2 h and then inducing reperfusion. Rats in the I/R + LB groups were treated with various doses of LB following reperfusion. Neurological deficit scores and brain water content were obtained to determine the pharmacodynamics of LB. Reverse transcription polymerase chain reaction was performed to determine the expression levels of AQP4 and caspase-3 mRNA in the hippocampus and the striatum. The results of the present study indicate that LB decreased the neurological deficit scores and the brain water content. In the hippocampus, AQP4 and caspase-3 mRNA expression levels were significantly downregulated in the I/R + LB groups at 24 and 72 h following drug administration, compared with those in the I/R group (P<0.05). In the striatum, LB was also shown to significantly reduce AQP4 and caspase-3 mRNA expression levels at 24 and 72 h following drug administration, compared with those in the I/R group (P<0.05). The effects became stronger as the LB dose was increased. The most significant reductions in AQP4 and caspase-3 mRNA expression were noted in the I/R + LB 25 mg/kg and I/R + LB 50 mg/kg groups at 72 h following drug administration. The results of the present study show that LB is capable of significantly downregulating AQP4 and caspase-3 mRNA expression in the hippocampus and striatum following cerebral I/R injury in rats. The mechanism by which LB improved ischaemic brain injury may be associated with changes in AQP4 and caspase-3 mRNA expression in the hippocampus and the striatum.
机译:这项研究旨在研究内酰胺B(LB)对大鼠脑缺血再灌注(I / R)损伤后海马和纹状体aquaporin-4(AQP4)和caspase-3 mRNA表达的影响。通过阻塞大脑中动脉2 h,然后诱导再灌注,在Sprague-Dawley大鼠中建立脑I / R损伤。再灌注后,I / R + LB组的大鼠接受不同剂量的LB治疗。获得神经功能缺损评分和脑含水量,以确定LB的药效学。进行逆转录聚合酶链反应以确定海马和纹状体中AQP4和caspase-3 mRNA的表达水平。本研究的结果表明LB降低了神经功能缺损评分和脑含水量。与I / R组相比,在I / R + LB组在给药后24小时和72小时,海马中的AQP4和caspase-3 mRNA表达水平显着下调(P <0.05)。在纹状体中,与I / R组相比,LB在给药后24和72 h也显着降低AQP4和caspase-3 mRNA表达水平(P <0.05)。随着LB剂量的增加,作用变得更强。在给药后72小时,在I / R + LB 25 mg / kg和I / R + LB 50 mg / kg组中,AQP4和caspase-3 mRNA表达最明显的降低。本研究的结果表明,LB能够明显下调大鼠脑I / R损伤后海马和纹状体中AQP4和caspase-3 mRNA的表达。 LB改善缺血性脑损伤的机制可能与海马和纹状体中AQP4和caspase-3 mRNA表达的变化有关。

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