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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Neuroprotection of Sanhua Decoction against Focal Cerebral Ischemia/Reperfusion Injury in Rats through a Mechanism Targeting Aquaporin 4
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Neuroprotection of Sanhua Decoction against Focal Cerebral Ischemia/Reperfusion Injury in Rats through a Mechanism Targeting Aquaporin 4

机译:三花汤通过水通道蛋白4靶向机制对大鼠局灶性脑缺血/再灌注损伤的神经保护作用

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Sanhua decoction (SHD) is a famous classic Chinese herbal prescription for ischemic stroke, and aquaporin 4 (AQP4) is reported to play a key role in ischemic brain edema. This study aimed to investigate neuroprotection of SHD against focal cerebral ischemia/reperfusion (I/R) injury in rats and explore the hypothesis that AQP4 probably is the target of SHD neuroprotection against I/R rats. Lentiviral-mediated AQP4-siRNA was inducted into adult male Sprague-Dawley rats via intracerebroventricular injection. The focal cerebral ischemia/reperfusion model was established by occluding middle cerebral artery. Neurological examinations were performed according to Longa Scale. Brain water content, was determined by wet and dry weight measurement. Western blot was adopted to test the AQP4 expression in ipsilateral hippocampus. After the treatment, SHD alleviated neurological deficits, reduced brain water content and downregulated the expression of AQP4 at different time points following I/R injury. Furthermore, neurobehavioral function and brain edema after I/R were significantly attenuated via downregulation of AQP4 expression when combined with AQP4-siRNA technology. In conclusion, SHD exerted neuroprotection against focal cerebral I/R injury in rats mainly through a mechanism targeting AQP4.
机译:三花汤(SHD)是缺血性中风的著名经典中药处方,据报道水通道蛋白4(AQP4)在缺血性脑水肿中起关键作用。本研究旨在研究SHD对大鼠局灶性脑缺血/再灌注(I / R)损伤的神经保护作用,并探讨AQP4可能是SHD对I / R大鼠的神经保护作用的假设。通过脑室内注射将慢病毒介导的AQP4-siRNA导入成年雄性Sprague-Dawley大鼠。通过闭塞大脑中动脉建立局灶性脑缺血/再灌注模型。根据Longa量表进行神经系统检查。通过湿重和干重的测量来确定脑中的水分含量。采用蛋白质印迹法检测同侧海马中AQP4的表达。治疗后,SHD可减轻I / R损伤后不同时间点的神经功能缺损,减少脑水含量并下调AQP4的表达。此外,当与AQP4-siRNA技术结合使用时,通过下调AQP4表达,I / R后的神经行为功能和脑水肿显着减弱。总之,SHD主要通过针对AQP4的机制对大鼠局灶性脑I / R损伤发挥神经保护作用。

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