Age- and Urothelium-related Changes in Hydrogen Sulfide-induced Responses in Mouse Bladder.

Journal of physiological investigation Pub Date : 2025-01-01 Epub Date: 2024-12-13 DOI:10.4103/ejpi.EJPI-D-24-00078
Fatma Aydinoglu, Tugba Toyran, Nuran Ogulener
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Abstract

Abstract: The alterations in bladder function are associated with aging. Hydrogen sulfide (H 2 S) is a gaseous neurotransmitter that is synthesized in the urinary bladder and is suggested to regulate bladder smooth muscle tone. The effects of age and urothelium on the L-cysteine/H 2 S-induced relaxant responses were investigated in young (3-4 months) and aged (23-24 months) mice. The relaxant responses to endogenous H 2 S (L-cysteine) augmented in denuded urothelium bladder tissue in both age groups. However, the relaxant responses to exogenous H 2 S (sodium hydrogen sulfide: 1 μM - 3 mM) did not change by disruption of the urothelium. The contractile response to carbachol increased in intact bladder tissues of aged mice compared to young mice. On the other hand, contractile responses to carbachol decreased in the denuded bladder tissues of aged compared to young mice. In addition, cystathionine-β-synthase, cystathionine-γ-lyase (CSE), and 3 mercaptopyruvate sulfurtransferase (3-MST) enzymes which are responsible for H 2 S synthesis were intensively detected in the urothelium and vascular smooth muscle of bladder by immunohistochemistry. CSE and 3-MST were observed lesser in the smooth muscle of aged bladder tissue. These results suggest that relaxation to the L-cysteine/H 2 S pathway and contraction to carbachol of the bladder are affected by aging and urothelium. H 2 S- and urothelium-related molecular and biological changes may be responsible for bladder dysfunctions by aging. Understanding the mechanisms involved in chemical and mechanical signaling of the H 2 S pathway may provide important insights into the development of novel targets for the clinical management of age-related bladder dysfunctions in human such as overactive bladder, lower urinary tract symptoms, and other urological diseases. In this context, it is important to note that L-cysteine/H 2 S pathway may be recognized a new therapeutic target bladder disorders.

小鼠膀胱硫化氢诱导反应中与年龄和尿路神经相关的变化
摘要:膀胱功能的改变与衰老有关。硫化氢(H2S)是一种在膀胱中合成的气态神经递质,被认为能调节膀胱平滑肌张力。研究人员在幼鼠(3-4 个月)和老龄小鼠(23-24 个月)中研究了年龄和尿路神经元对 L-半胱氨酸/H2S 诱导的松弛反应的影响。在两个年龄组中,变性尿路膀胱组织对内源性 H2S(L-半胱氨酸)的松弛反应都有所增强。然而,对外源 H2S(硫化氢钠:1 μM - 3 mM)的松弛反应并没有因为尿路上皮的破坏而改变。与年轻小鼠相比,老龄小鼠完整膀胱组织对卡巴胆碱的收缩反应有所增加。另一方面,与年轻小鼠相比,老龄小鼠变性膀胱组织对卡巴胆碱的收缩反应减弱。此外,免疫组化还在膀胱的尿路神经细胞和血管平滑肌中深入检测到了负责合成 H2S 的胱硫醚-β-合成酶、胱硫醚-γ-赖氨酸酶(CSE)和 3-巯基丙酮酸硫转移酶(3-MST)。在老化膀胱组织的平滑肌中,CSE 和 3-MST 的含量较低。这些结果表明,膀胱对 L-半胱氨酸/H2S途径的松弛和对卡巴胆碱的收缩会受到衰老和尿路上皮的影响。与 H2S 和尿路神经元相关的分子和生物变化可能是导致膀胱功能障碍的原因。了解 H2S 通路的化学和机械信号转导机制可能会为开发新的靶点提供重要启示,这些靶点可用于临床治疗与年龄相关的人类膀胱功能障碍,如膀胱过度活动症、下尿路症状和其他泌尿系统疾病。在这种情况下,L-半胱氨酸/H2S 通路可能被认为是治疗膀胱疾病的新靶点,这一点很重要。
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