The role of L-cysteine/H2S pathway in CaSRs-mediated relaxations in mouse bladder tissue.

IF 1.9 4区 医学 Q3 PHYSIOLOGY
Physiological research Pub Date : 2025-07-23
F Aydinoglu, K Gonbe, N Ogulener
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引用次数: 0

Abstract

The activation of Calcium-Sensing Receptors (CaSRs) reduces detrusor activity in bladder tissues. Also, hydrogen sulfide (H2S) produces in bladder tissue and regulates the bladder smooth muscles tone. However, there is no evidence of the interaction between CaSRs and H2S in bladder tissue. The aim of this study is to investigate the possible contribution of L-cysteine/H2S pathway in CaSRs-mediated relaxation responses in isolated mouse bladder tissue. CaCl2 (1, 2, 3, 5, 10 mM) was applied to isolated mouse bladder tissues pre-contracted with carbachol (1 microM). CaCl2-induced relaxations were performed in the presence of PAG (10 mM), AOAA (1 mM), and Calhex-231 (5 microM), cystathionine-gamma-lyase (CSE), cystathionine-beta-synthase (CBS) and CaSR inhibitor, respectively. L-cysteine (1 microM-10 mM), an H2S substrate, was used to induced a concentration-dependent relaxant response in isolated bladder tissues pre-contracted with carbachol. L-cysteine induced relaxations were performed in the presence of PAG (CSE inhibitor, 10 mM), AOAA (CBS inhibitor, 1 mM) and Calhex-231 (CaSR inhibitor, 5 microM). CaCl2-induced relaxations were decreased by PAG and AOAA. Also, Calhex-231 decreased the CaCl2-induced relaxant responses. L-cysteine-induced relaxant responses were reduced in the presence of PAG (10 mM) and AOAA (1 mM). Calhex-231 (5 microM) caused a significant decrease in L-cysteine-induced relaxations. Also, Calhex-231 reduced the increase in H2S production in the presence of L-cysteine. In addition, CaCl2 increased basal H2S generation, and PAG (10 mM), AOAA (1 mM) and Calhex-231 (5 microM) reduced the increase in H2S production stimulated with CaCl2. In conclusion, CSE and CBS-derived endogenous H2S formation may, at least in part, contribute to CaSR-mediated relaxation responses, and CaSRs involve in endogenous H2S relaxation responses in isolated mouse bladder tissue. Key words Bladder o CaSRs " Calhex-231 " Hydrogen sulfide " L-cysteine " Mouse.

l -半胱氨酸/H2S通路在casrs介导的小鼠膀胱组织松弛中的作用。
钙敏感受体(CaSRs)的激活可降低膀胱组织的逼尿肌活性。此外,硫化氢(H2S)在膀胱组织中产生并调节膀胱平滑肌张力。然而,没有证据表明CaSRs和H2S在膀胱组织中相互作用。本研究的目的是探讨l -半胱氨酸/H2S通路在离体小鼠膀胱组织中casrs介导的松弛反应中的可能作用。CaCl2(1、2、3、5、10 mM)分别作用于经甲乙醇(1微米)预收缩的离体小鼠膀胱组织。分别在PAG (10 mM)、AOAA (1 mM)、calhexx -231(5微米)、胱硫氨酸- γ -裂解酶(CSE)、胱硫氨酸- β -合成酶(CBS)和CaSR抑制剂存在下进行cacl2诱导的松弛。l -半胱氨酸(1微米-10毫米),H2S底物,用于诱导浓度依赖性松弛反应的离体膀胱组织预收缩与乙醇。在PAG (CSE抑制剂,10 mM)、AOAA (CBS抑制剂,1 mM)和calhexx -231 (CaSR抑制剂,5微米)存在的情况下进行l -半胱氨酸诱导的松弛。PAG和AOAA可降低cacl2诱导的弛豫。Calhex-231还能降低cacl2诱导的松弛反应。l -半胱氨酸诱导的松弛反应在PAG (10 mM)和AOAA (1 mM)存在时减弱。Calhex-231(5微米)引起l -半胱氨酸诱导的松弛明显减少。此外,在l -半胱氨酸存在的情况下,Calhex-231减少了H2S产量的增加。此外,CaCl2增加了H2S的基础生成,PAG (10 mM)、AOAA (1 mM)和Calhex-231(5微米)降低了CaCl2刺激下H2S生成的增加。综上所述,CSE和cbs衍生的内源性H2S形成可能至少部分地促进了casr介导的松弛反应,而casr参与了离体小鼠膀胱组织的内源性H2S松弛反应。关键词膀胱CaSRs calhexx -231硫化氢l -半胱氨酸小鼠
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来源期刊
Physiological research
Physiological research 医学-生理学
CiteScore
4.00
自引率
4.80%
发文量
108
审稿时长
3 months
期刊介绍: Physiological Research is a peer reviewed Open Access journal that publishes articles on normal and pathological physiology, biochemistry, biophysics, and pharmacology. Authors can submit original, previously unpublished research articles, review articles, rapid or short communications. Instructions for Authors - Respect the instructions carefully when submitting your manuscript. Submitted manuscripts or revised manuscripts that do not follow these Instructions will not be included into the peer-review process. The articles are available in full versions as pdf files beginning with volume 40, 1991. The journal publishes the online Ahead of Print /Pre-Press version of the articles that are searchable in Medline and can be cited.
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