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细胞因子会损害神经介导的膀胱收缩:诱导型一氧化氮合酶的作用。

Nerve-mediated bladder contraction is impaired by cytokines: involvement of inducible nitric oxide synthase.

作者信息

Johansson Rebecka, Andersson Karl-Erik, Persson Katarina

机构信息

Department of Clinical Pharmacology, Lund University Hospital, SE-221 85 Lund, Sweden.

出版信息

Eur J Pharmacol. 2003 Aug 29;476(3):221-7. doi: 10.1016/s0014-2999(03)02178-2.

Abstract

We investigated the possible involvement of inducible nitric oxide synthase (iNOS) in the effect of cytokines on neuromuscular function in isolated rat bladder strips. Bladder strips were incubated in cell culture medium for 24 h with or without tumour necrosis factor-alpha (TNF-alpha)+interleukin-1beta. Mechanical activity in response to electrical field stimulation and carbachol was recorded in organ baths. Both the electrical field stimulation- and carbachol-induced contractions were reduced by the incubation. The electrical field stimulation-induced contraction was significantly further impaired after prolonged exposure to TNF-alpha+interleukin-1beta. This impairment was restored by dexamethasone, the iNOS inhibitor aminoguanidine and partially by brain-derived neurotrophic factor (BDNF). In contrast, carbachol-induced contractions were not affected by cytokines. iNOS protein expression was detected in cytokine-incubated bladder strips by immunohistochemistry and Western blot analysis. The results demonstrated that TNF-alpha+interleukin-1beta impaired nerve-mediated bladder contractions. Aminoguanidine, and to some extent BDNF, exerted neuroprotective effects.

摘要

我们研究了诱导型一氧化氮合酶(iNOS)在细胞因子对离体大鼠膀胱条神经肌肉功能影响中的可能作用。将膀胱条在细胞培养基中培养24小时,添加或不添加肿瘤坏死因子-α(TNF-α)+白细胞介素-1β。在器官浴槽中记录对电场刺激和卡巴胆碱的机械活动。培养后,电场刺激和卡巴胆碱诱导的收缩均减弱。长时间暴露于TNF-α+白细胞介素-1β后,电场刺激诱导的收缩进一步显著受损。地塞米松、iNOS抑制剂氨基胍以及部分脑源性神经营养因子(BDNF)可恢复这种损伤。相比之下,卡巴胆碱诱导的收缩不受细胞因子影响。通过免疫组织化学和蛋白质印迹分析在细胞因子培养的膀胱条中检测到iNOS蛋白表达。结果表明,TNF-α+白细胞介素-1β损害神经介导的膀胱收缩。氨基胍以及在一定程度上BDNF发挥了神经保护作用。

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