下丘脑室旁核炎性细胞因子在依普利酮改善心力衰竭中的作用
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Proinflammatory Cytokines in Paraventricular Nucleus Involved in Improvement of Heart Failure by Eplerenone
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    摘要:

    目的 探讨下丘脑室旁核(PVN)炎性细胞因子在依普利酮(EPL)改善心力衰竭中的作用。方法 Wistar大鼠分为假手术组(n6)、模型组(n10)、吡咯烷二硫基甲酸盐(PDTC)组(n10)、依普利酮组(n10)。结扎左冠状动脉前降支诱导急性心肌梗死后心力衰竭,根据分组情况分别给予PDTC[(150 mg/(kg·d)]、依普利酮[30 mg/(kg·d)]和清洁蒸馏水灌胃,假手术组只在相同位置穿线而不结扎。6周后进行血流动力学测定,留取下丘脑、血浆标本,检测PVN内肿瘤坏死因子α(TNF-α)、核因子κB/p65(NF-κB/p65)、促肾上腺皮质激素释放激素(CRH)及血管紧张素Ⅱ(AngⅡ)的表达,并检测血浆TNF-α、去甲肾上腺素(NE)、醛固酮(ALD)水平。结果 依普利酮和PDTC干预后大鼠心功能较模型组明显改善。模型组血浆ALD、NE、TNF-α水平显著升高,而依普利酮和PDTC干预后ALD、NE、TNF-α水平降低(P<0.05)。模型组PVN内CRH、AngⅡ表达显著增多,依普利酮和PDTC干预后PVN内CRH、AngⅡ表达显著减少(P<0.05),NF-κB/p65在依普利酮组和PDTC组的表达较模型组显著降低(P<0.05)。依普利酮、PDTC可降低PVN内CRH阳性神经元表达。结论 心力衰竭时大鼠PVN内炎性细胞因子表达增多,依普利酮可以改善心力衰竭大鼠心功能,与抑制PVN内炎性细胞因子过表达有关。

    Abstract:

    Aim To study the effects of eplerenone (EPL) on heart failure and inflammatory cytokines in central nervous system. Methods Wistar rats were divided into sham group (n6),PDTC treatment group (n10),EPL treatment group (n10) and model group (n10). Then these rats were administrated with PDTC (150 mg/(kg·d)),EPL (30 mg/(kg·d)) and clean distilled water. After six weeks,hemodynamic data was measured,then hypothalamus and serum samples were collected. Cytokines,nuclear factor kappa B (NF-κB),corticotropin releasing hormone (CRH),aldosterone (ALD) and norepinephrine (NE) was measured. Results Eplerenone and PDTC could improve heart function. In the model group,expression of ALD,NE,TNF-α,CRH,AngⅡ and NF-κB/p65 increased. Eplerenone and PDTC decreased the expression of these indexes effectively. Expression of CRH positive neurons in the hypothalamus of rats was significantly increased in the model group,which was decreased in eplerenone and PDTC treated group. Conclusions Eplerenone could improve heart function in rats with heart failure,which may be related to the inhibition of expression of inflammatory cytokines in hypothalamic paraventricular nucleus.

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王 涛,刘 强,虞华鹏,李岱旭,贾如意.下丘脑室旁核炎性细胞因子在依普利酮改善心力衰竭中的作用[J].中国动脉硬化杂志,2015,23(09):887~890.

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  • 收稿日期:2014-12-23
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  • 在线发布日期: 2015-07-21