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缬沙坦对高血压期间小脑肾上腺髓质素系统失调的影响。

Effect of Valsartan on Cerebellar Adrenomedullin System Dysregulation During Hypertension.

作者信息

Figueira Leticia, Israel Anita

机构信息

School of Pharmacy, Laboratory of Neuropeptides, Universidad Central de Venezuela, Santa Rosa de Lima, Las Mesetas, Calle La Cima, Res. Mara, Apto 82, Caracas, Venezuela.

出版信息

Cerebellum. 2017 Feb;16(1):132-141. doi: 10.1007/s12311-016-0780-2.

Abstract

Adrenomedullin (AM) and its receptors components, calcitonin-receptor-like receptor (CRLR), and receptor activity-modifying protein (RAMP1, RAMP2, and RAMP3) are expressed in cerebellum. Cerebellar AM, AM binding sites and receptor components are altered during hypertension, suggesting a role for cerebellar AM in blood pressure regulation. Thus, we assessed the effect of valsartan, on AM and its receptor components expression in the cerebellar vermis of Wistar Kyoto (WKY) and spontaneously hypertensive (SHR) rats. Additionally, we evaluated AM action on superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPx) activity, and thiobarbituric acid reactive substances (TBARS) production in cerebellar vermis. Animals were treated with valsartan or vehicle for 11 days. Rats were sacrificed by decapitation; cerebellar vermis was dissected; and AM, CRLR, RAMP1, RAMP2, and RAMP3 expression was quantified by Western blot analysis. CAT, SOD, and GPx activity was determined spectrophotometrically and blood pressure by non-invasive plethysmography. We demonstrate that AM and RAMP2 expression was lower in cerebellum of SHR rats, while CRLR, RAMP1, and RAMP3 expression was higher than those of WKY rats. AM reduced cerebellar CAT, SOD, GPx activities, and TBARS production in WKY rats, but not in SHR rats. Valsartan reduced blood pressure and reversed the altered expression of AM and its receptors components, as well the loss of AM capacity to reduce antioxidant enzyme activity and TBARS production in SHR rats. These findings demonstrate that valsartan is able to reverse the dysregulation of cerebellar adrenomedullinergic system; and they suggest that altered AM system in the cerebellum could represent the primary abnormality leading to hypertension.

摘要

肾上腺髓质素(AM)及其受体成分,降钙素受体样受体(CRLR)和受体活性修饰蛋白(RAMP1、RAMP2和RAMP3)在小脑中表达。在高血压期间,小脑AM、AM结合位点和受体成分会发生改变,提示小脑AM在血压调节中发挥作用。因此,我们评估了缬沙坦对Wistar Kyoto(WKY)大鼠和自发性高血压(SHR)大鼠小脑蚓部中AM及其受体成分表达的影响。此外,我们评估了AM对小脑蚓部中超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和谷胱甘肽过氧化物酶(GPx)活性以及硫代巴比妥酸反应性物质(TBARS)生成的作用。动物用缬沙坦或赋形剂处理11天。通过断头处死大鼠;解剖小脑蚓部;通过蛋白质免疫印迹分析对AM、CRLR、RAMP1、RAMP2和RAMP3的表达进行定量。通过分光光度法测定CAT、SOD和GPx活性,并通过无创体积描记法测定血压。我们证明,SHR大鼠小脑中AM和RAMP2的表达较低,而CRLR、RAMP1和RAMP3的表达高于WKY大鼠。AM降低了WKY大鼠小脑的CAT、SOD、GPx活性以及TBARS生成,但对SHR大鼠没有影响。缬沙坦降低了血压,并逆转了SHR大鼠中AM及其受体成分表达的改变,以及AM降低抗氧化酶活性和TBARS生成能力的丧失。这些发现表明缬沙坦能够逆转小脑肾上腺髓质素能系统的失调;并且提示小脑中AM系统的改变可能是导致高血压的主要异常情况。

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