Po-Chun Hsieh, Shang-Jen Chang, Hsi-Hsien Chang, Stephen Shei-Dei Yang
{"title":"The differences in the adrenergic receptors of proximal urethra between sexes.","authors":"Po-Chun Hsieh, Shang-Jen Chang, Hsi-Hsien Chang, Stephen Shei-Dei Yang","doi":"10.4103/tcmj.tcmj_221_22","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>The bladder and urethra work as a physiologically functional unit to facilitate continence in the storage and voiding phase. Sex differences have been found in the urethral contraction in response to α-adrenergic receptor activation. This study aimed to investigate the role of adrenergic receptors in the proximal urethra of male and female mice.</p><p><strong>Materials and methods: </strong>Urinary bladder and proximal urethral smooth muscle (USM) samples from male and female C57BL/6 mice were isolated and mounted in an organ bath.</p><p><strong>Results: </strong>Acetylcholine-induced contraction of the urinary bladder was compared in male and female mice. Phenylephrine and norepinephrine (NE) induced little contraction at a lower concentration, but a relaxing phase of female proximal USM was observed at a higher concentration. This contraction profile was inhibited by N<sup>G</sup>-nitro-L-arginine, lidocaine, and capsaicin. In addition, the NE-induced contraction was greater in the incubation of propranolol than that of L-NNA or lidocaine. These results suggested that the β-adrenoceptor may be the dominant receptor of female proximal USM, and the activity of calcitonin gene-related peptide sensory nerves and nitrergic nerves may pose an anti-contraction effect on the proximal urethra in female mice.</p><p><strong>Conclusion: </strong>β-adrenoceptor may be the dominant receptor of female proximal USM. The use of β-adrenergic receptor blocker agents might have the potential for the treatment of female voiding dysfunction.</p>","PeriodicalId":45873,"journal":{"name":"Tzu Chi Medical Journal","volume":null,"pages":null},"PeriodicalIF":1.4000,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/54/41/TCMJ-35-253.PMC10399842.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tzu Chi Medical Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/tcmj.tcmj_221_22","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives: The bladder and urethra work as a physiologically functional unit to facilitate continence in the storage and voiding phase. Sex differences have been found in the urethral contraction in response to α-adrenergic receptor activation. This study aimed to investigate the role of adrenergic receptors in the proximal urethra of male and female mice.
Materials and methods: Urinary bladder and proximal urethral smooth muscle (USM) samples from male and female C57BL/6 mice were isolated and mounted in an organ bath.
Results: Acetylcholine-induced contraction of the urinary bladder was compared in male and female mice. Phenylephrine and norepinephrine (NE) induced little contraction at a lower concentration, but a relaxing phase of female proximal USM was observed at a higher concentration. This contraction profile was inhibited by NG-nitro-L-arginine, lidocaine, and capsaicin. In addition, the NE-induced contraction was greater in the incubation of propranolol than that of L-NNA or lidocaine. These results suggested that the β-adrenoceptor may be the dominant receptor of female proximal USM, and the activity of calcitonin gene-related peptide sensory nerves and nitrergic nerves may pose an anti-contraction effect on the proximal urethra in female mice.
Conclusion: β-adrenoceptor may be the dominant receptor of female proximal USM. The use of β-adrenergic receptor blocker agents might have the potential for the treatment of female voiding dysfunction.
目的:膀胱和尿道作为一个生理功能单元,促进在储存和排尿阶段的尿失禁。尿道收缩对α-肾上腺素能受体激活的反应存在性别差异。本研究旨在探讨肾上腺素能受体在雄性和雌性小鼠尿道近端中的作用。材料与方法:分别取雄性和雌性C57BL/6小鼠膀胱和尿道近端平滑肌(USM)标本,置于器官浴中。结果:比较了乙酰胆碱对雌雄小鼠膀胱收缩的影响。在低浓度下,苯肾上腺素和去甲肾上腺素(NE)对雌性近端USM的收缩作用不大,而在高浓度下,雌性近端USM出现松弛期。ng -硝基- l -精氨酸、利多卡因和辣椒素抑制了这种收缩。此外,心得安的ne诱导的收缩比L-NNA和利多卡因的更大。这些结果提示,β-肾上腺素能受体可能是雌性近端USM的优势受体,降钙素基因相关肽感觉神经和氮能神经的活性可能对雌性小鼠近端尿道具有抗收缩作用。结论:β-肾上腺素受体可能是女性近端USM的显性受体。β-肾上腺素受体阻滞剂的使用可能对女性排尿功能障碍有潜在的治疗作用。
期刊介绍:
The Tzu Chi Medical Journal is the peer-reviewed publication of the Buddhist Compassion Relief Tzu Chi Foundation, and includes original research papers on clinical medicine and basic science, case reports, clinical pathological pages, and review articles.