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首页> 外文期刊>Toxicology and Applied Pharmacology >Inhibition of reactive oxygen species in hypothalamic paraventricular nucleus attenuates the renin-angiotensin system and proinflammatory cytokines in hypertension
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Inhibition of reactive oxygen species in hypothalamic paraventricular nucleus attenuates the renin-angiotensin system and proinflammatory cytokines in hypertension

机译:下丘脑室旁核中活性氧的抑制减弱了高血压的肾素-血管紧张素系统和促炎细胞因子

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摘要

Aims: To explore whether reactive oxygen species (ROS) scavenger (tempol) in the hypothalamic paraventricular nucleus (PVN) attenuates renin-angiotensin system (RAS) and proinflammatory cytokines (PICs), and decreases the blood pressure and sympathetic activity in angiotensin II (ANG II)-induced hypertension. Methods and results: Male Sprague-Dawley rats were infused intravenously with ANG II (10ng/kg per min) or normal saline (NS) for 4weeks. These rats were treated with bilateral PVN infusion of oxygen free radical scavenger tempol (TEMP, 20μg/h) or vehicle (artificial cerebrospinal fluid, aCSF) for 4weeks. ANG II infusion resulted in increased mean arterial pressure (MAP) and renal sympathetic nerve activity (RSNA). These ANG II-infused rats also had higher levels of gp91phox (a subunit of NAD(P)H oxidase), angiotensin-converting enzyme (ACE), and interleukin-1beta (IL-1β) in the PVN than the control animals. Treatment with PVN infusion of TEMP attenuated the overexpression of gp91phox, ACE and IL-1β within the PVN, and decreased sympathetic activity and MAP in ANG II-infused rats. Conclusion: These findings suggest that ANG II infusion induces elevated PICs and oxidative stress in the PVN, which contribute to the sympathoexcitation in hypertension. Inhibition of reactive oxygen species in hypothalamic paraventricular nucleus attenuates the renin-angiotensin system, proinflammatory cytokines and oxidative stress in ANG II-induced hypertension.
机译:目的:探讨下丘脑室旁核(PVN)中的活性氧(ROS)清除剂(tempol)是否能减弱肾素-血管紧张素系统(RAS)和促炎性细胞因子(PICs),并降低血管紧张素II的血压和交感活性( ANG II)诱发的高血压。方法和结果:雄性Sprague-Dawley大鼠静脉注射ANG II(10ng / kg / min)或生理盐水(NS)4周。用双侧PVN输注氧自由基清除剂tempol(TEMP,20μg/ h)或溶媒(人工脑脊液,aCSF)治疗这些大鼠4周。 ANG II输注导致平均动脉压(MAP)和肾交感神经活性(RSNA)升高。这些注入ANG II的大鼠在PVN中的gp91phox(NAD(P)H氧化酶的一个亚基),血管紧张素转换酶(ACE)和白介素-1β(IL-1β)的含量也高于对照组。用TEMP的PVN输注治疗可减轻PVN内gp91phox,ACE和IL-1β的过表达,并降低ANG II注入大鼠的交感活性和MAP。结论:这些发现表明,ANG II输注可引起PVN中PIC升高和氧化应激,这有助于高血压的交感神经兴奋。下丘脑室旁核中活性氧的抑制减弱了ANG II诱发的高血压中的肾素-血管紧张素系统,促炎性细胞因子和氧化应激。

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