首页> 外文期刊>The journal of sexual medicine >Endothelin A (ETA) Receptors Are Involved in Augmented Adrenergic Vasoconstriction and Blunted Nitric Oxide-Mediated Relaxation of Penile Arteries from Insulin-Resistant Obese Zucker Rats
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Endothelin A (ETA) Receptors Are Involved in Augmented Adrenergic Vasoconstriction and Blunted Nitric Oxide-Mediated Relaxation of Penile Arteries from Insulin-Resistant Obese Zucker Rats

机译:内皮素A(ETA)受体参与增强的肾上腺素血管收缩和钝性一氧化氮介导的胰岛素抵抗的肥胖祖克大鼠的阴茎动脉松弛。

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Introduction Endothelin 1 (ET-1) levels and receptors are up-regulated in the erectile tissue of diabetic patients and animal models of erectile dysfunction (ED). Aim The present study assessed the role of ET-1 receptors in the impaired adrenergic vasoconstriction and nitrergic relaxation of penile arteries from a rat model of insulin resistance. Methods The effect of ET receptor antagonists was evaluated on the contractile responses to electrical field stimulation (EFS) of penile arteries from obese Zucker rats (OZRs) compared with lean Zucker rats (LZRs). ET receptor expression was determined by immunohistochemistry. Main Outcome Measures Changes in neural nitrergic relaxation and adrenergic vasoconstriction and the expression of ET receptors in perivascular nerves were assessed. Results ET-1 (10-10M) enhanced EFS-induced vasoconstriction, and treatment with the adrenergic neurotoxin guanethidine reduced the contractions induced by ET-1 in penile arteries from both LZRs and OZRs, thus supporting the hypothesis that ET-1 releases noradrenaline from adrenergic nerves. ET-1 antagonized neural nitric oxide (NO)-mediated relaxant responses in LZR arteries, antagonizing relaxations induced by the NO donor S-nitroso-N-acetylpenicillamine to a larger extent in arteries from OZRs. ETA and ETB receptors were expressed in perivascular fibers colocalized with the neuronal marker protein gene product 9.5 in penile arteries from OZRs. The ETA receptor antagonist BQ-123 reversed the enhancing effect of ET-1 on the vasoconstriction elicited by EFS and the ET-1-induced inhibition of nitrergic relaxations in LZRs, restoring them to control levels in penile arteries of OZRs. Conclusions ET-1 enhances adrenergic vasoconstriction through presynaptic ETA receptors and antagonizes neural NO-mediated relaxation through postsynaptic smooth muscle ETA receptors in penile arteries from OZRs, which likely contributes to the augmented vasoconstriction and blunted nitrergic relaxation of erectile tissue under conditions of insulin resistance. Sanchez A, Contreras C, Martinez P, Munoz M, Martinez AC, Garcia-Sacristan A, Hernandez M, and Prieto D. Endothelin (ETA) receptors are involved in augmented adrenergic vasoconstriction and blunted nitric oxide-mediated relaxation of penile arteries from insulin-resistant obese Zucker rats. J Sex Med 2014;11:1463-1474.
机译:简介糖尿病患者的勃起组织和勃起功能障碍(ED)动物模型中内皮素1(ET-1)的水平和受体被上调。目的本研究从胰岛素抵抗大鼠模型评估了ET-1受体在肾上腺素能动性血管收缩和阴茎动脉硝化舒张受损中的作用。方法评价了ET受体拮抗剂对肥胖Zucker大鼠(OZRs)与瘦Zucker大鼠(LZRs)对阴茎动脉电场刺激(EFS)的收缩反应的影响。 ET受体表达通过免疫组织化学确定。主要观察指标:评估神经硝化舒张和肾上腺素能血管收缩的变化以及血管周围神经中ET受体的表达。结果ET-1(10-10M)增强了EFS诱导的血管收缩,肾上腺能神经毒素胍乙啶治疗减少了LZR和OZR阴茎动脉中ET-1引起的收缩,从而支持了ET-1释放去甲肾上腺素的假设。肾上腺素能神经。 ET-1拮抗LZR动脉中一氧化氮(NO)介导的舒张反应,在更大程度上拮抗NO供体S-亚硝基-N-乙酰青霉胺引起的OZRs舒张反应。 ETA和ETB受体在与OZRs的阴茎动脉中与神经元标记蛋白基因产物9.5共定位的血管周纤维中表达。 ETA受体拮抗剂BQ-123逆转了ET-1对EFS引起的血管收缩的增强作用以及ET-1诱导的LZRs的硝化舒张抑制,使它们恢复到OZRs阴茎动脉的控制水平。结论ET-1通过突触前ETA受体增强肾上腺素能血管收缩,并通过OZRs的阴茎动脉中的突触后平滑肌ETA受体拮抗神经NO介导的舒张作用,这可能有助于在胰岛素抵抗条件下勃起组织的血管收缩增加和硝化松弛性减弱。 Sanchez A,Contreras C,Martinez P,Munoz M,Martinez AC,Garcia-Sacristan A,Hernandez M和Prieto D.内皮素(ETA)受体参与增强的肾上腺素能血管收缩和钝化一氧化氮介导的胰岛素引起的阴茎动脉松弛抗肥胖肥胖的祖克大鼠。 J Sex Med 2014; 11:1463-1474。

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