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暴露于不可预测的慢性轻度应激的大鼠阴茎组成型一氧化氮合酶表达:炎症的作用。

Penile constitutive nitric oxide synthase expression in rats exposed to unpredictable chronic mild stress: role of inflammation.

作者信息

Şahin T D, Yazır Y, Utkan T, Göçmez S S, Bayramgürler D

机构信息

Medical Faculty, Department of Pharmacology, Kocaeli University, Kocaeli, Turkey.

Medical Faculty, Department of Histology and Embryology, Kocaeli University, Kocaeli, Turkey.

出版信息

Int J Impot Res. 2017 Mar;29(2):76-81. doi: 10.1038/ijir.2016.50. Epub 2016 Dec 1.

Abstract

Chronic psychological stress cause erectile dysfunction (ED). Considering recent evidence that tumor necrosis factor-α (TNF-α) levels are increased in serum of patients with ED, the present study investigated the effects of infliximab (a TNF-α blocker) on endothelial nitric oxide synthase (eNOS) and neuronal NOS (nNOS) immunoreactivity of rat penile corpus cavernosum in unpredictable chronic mild stress (UCMS). Male adult rats were randomly divided into three groups (n=8 per group): Control, UCMS and UCMS+infliximab. Control and UCMS groups received physiological saline, UCMS+infliximab group received infliximab (5 mg kg per week, intraperitoneally) during 8 weeks of UCMS. UCMS and UCMS+infliximab groups were subjected to different types of stressors, which were randomly applied four to five times during this time period. After 8 weeks, penile eNOS and nNOS expressions were determined immunohistochemically. In UCMS group, nNOS and eNOS immunoreactivity was found to be decreased in penile corpus cavernosum compared with the control group. Whereas in infliximab treatment group eNOS and nNOS immunoreactivity increased compared with the UCMS group. These findings support that UCMS decreases penile constitutive NOS expression via TNF-α, which may contribute to the development of ED. Blockage of TNF-α actions may represent an alternative therapeutic approach for ED in chronic psychological stress.

摘要

慢性心理应激会导致勃起功能障碍(ED)。鉴于最近有证据表明ED患者血清中肿瘤坏死因子-α(TNF-α)水平升高,本研究调查了英夫利昔单抗(一种TNF-α阻滞剂)对不可预测的慢性轻度应激(UCMS)大鼠阴茎海绵体内皮型一氧化氮合酶(eNOS)和神经元型一氧化氮合酶(nNOS)免疫反应性的影响。成年雄性大鼠随机分为三组(每组n = 8):对照组、UCMS组和UCMS + 英夫利昔单抗组。对照组和UCMS组给予生理盐水,UCMS + 英夫利昔单抗组在UCMS的8周期间接受英夫利昔单抗(每周5 mg/kg,腹腔注射)。UCMS组和UCMS + 英夫利昔单抗组接受不同类型的应激源,在这段时间内随机施加4至5次。8周后,通过免疫组织化学法测定阴茎eNOS和nNOS的表达。在UCMS组中,与对照组相比,阴茎海绵体内nNOS和eNOS免疫反应性降低。而在英夫利昔单抗治疗组中,与UCMS组相比,eNOS和nNOS免疫反应性增加。这些发现支持UCMS通过TNF-α降低阴茎组成型NOS表达,这可能有助于ED的发生。阻断TNF-α的作用可能代表慢性心理应激性ED的一种替代治疗方法。

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