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有证据表明,血清素介导了尿道-膀胱的相互作用。

Evidence for an urethro-vesical crosstalk mediated by serotonin.

机构信息

Instituto de Investigação e Inovação em Saúde, Translational Neuro-urology Group, Universidade do Porto, Porto, Portugal.

Instituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.

出版信息

Neurourol Urodyn. 2018 Nov;37(8):2389-2397. doi: 10.1002/nau.23590. Epub 2018 Apr 17.

Abstract

AIM

To study the contribution of urethral serotonin for the urethro-vesical crosstalk METHODS: Urethane-anesthetized female rats and TPH1 mice underwent isovolumetric or urethral-opened cystometries during intravesical or intraurethral infusion of saline or serotonin solutions. Human and rat bladders and urethrae were immunoreacted against serotonin and neuronal markers. Serotonin concentration and TPH1 mRNA were determined in rat tissue by HPLC and qPCR.

RESULTS

In rats, under isovolumetric conditions, intraurethral serotonin infusion, but not saline, evoked bladder contractions. This was abolished by urethral anesthesia and by treatment with serotonin receptor antagonists. Serotonin infusion into the bladder had no effect. Under urethral-opened conditions, serotonin infusion reduced the frequency and increased the amplitude of reflex voiding contractions, compared to saline infusion. TPH1 mice, under urethral-opened conditions, exhibited increased frequency and reduced amplitude of voiding contractions compared to WT. Serotonin concentration and TPH1 mRNA expression were higher in the urethra than in the bladder. Cells 5-HT were found in the human and rat urethral epithelium, close to a sub-epithelial network of cholinergic and sensory fibers, but not in the bladder.

CONCLUSIONS

Serotonin, produced and released by urethral cells activates an urethro-vesical pathway that enhances bladder reflex contractions.

摘要

目的

研究尿道内的血清素对尿道-膀胱相互作用的贡献。

方法

在对雌性大鼠和 TPH1 小鼠进行等容或尿道开放的膀胱测压期间,通过膀胱内或尿道内输注盐水或血清素溶液来进行实验。对人类和大鼠的膀胱和尿道进行血清素和神经元标志物的免疫反应。通过 HPLC 和 qPCR 来确定大鼠组织中的血清素浓度和 TPH1 mRNA。

结果

在大鼠中,在等容条件下,尿道内输注血清素,但不是盐水,会引起膀胱收缩。这种收缩被尿道麻醉和血清素受体拮抗剂的治疗所消除。膀胱内输注血清素没有影响。在尿道开放的条件下,与盐水输注相比,血清素输注减少了反射性排空收缩的频率并增加了其幅度。与 WT 相比,在尿道开放条件下的 TPH1 小鼠表现出更高的排尿收缩频率和更低的幅度。与膀胱相比,尿道中的血清素浓度和 TPH1 mRNA 表达更高。在人类和大鼠的尿道上皮中发现了 5-HT 细胞,它们靠近胆碱能和感觉纤维的上皮下网络,但不在膀胱中。

结论

尿道内细胞产生和释放的血清素激活了增强膀胱反射性收缩的尿道-膀胱途径。

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