Matsumoto-Miyai Kazumasa, Yoshizumi Masaru, Kawatani Masahito
Department of Neurophysiology, Akita University Graduate School of Medicine, 1-1-1 Hondo, Akita, Akita, 010-8543, Japan.
Kansai University of Nursing and Health Sciences, 1456-4 Shizuki, Awaji, Hyogo, 656-2131, Japan.
Adv Ther. 2015 Oct;32 Suppl 1:3-15. doi: 10.1007/s12325-015-0240-2. Epub 2015 Sep 21.
A growing body of evidence suggests that 5-hydroxytryptamine (5-HT; serotonin) has both physiological and pathological functions in the lower urinary tract. A wide variety of 5-HT receptor subtypes are variably expressed in different organs, both peripheral and central. On urinary bladder smooth muscle, 5-HT1A, 5-HT2, 5-HT3, and 5-HT7 subtypes could function as postjunctional receptors. Postjunctional 5-HT2 receptors induce detrusor contraction of the bladder body. 5-HT1A is suggested to have a similar effect to 5-HT2, while 5-HT3 might suppress detrusor contraction evoked by direct muscle stimulation. Postjunctional 5-HT7 is reported to induce relaxation of the bladder neck, which might be required for efficient voiding. 5-HT1A, 5-HT2A, 5-HT2C, 5-HT3, 5-HT4, and 5-HT7 subtypes also could act as prejunctional receptors in autonomic excitatory nerve terminals. 5-HT2A, 5-HT2C, 5-HT3, 5-HT4, and 5-HT7 subtypes facilitate the neurogenic contraction of the detrusor by enhancing cholinergic or purinergic transmission, whereas 5-HT1A receptors might inhibit the release of acetylcholine in the detrusor. Furthermore, 5-HT1D could be involved in the suppression of ATP release from the urothelium, aiding visceral sensation of the urinary bladder. In the central pathways controlling the micturition reflex, 5-HT1A, 5-HT2A, and 5-HT7 are involved in regulation of bladder and urethral sphincter activities. Their functions, especially that of 5-HT1A, vary in a species- and site (spinal or supraspinal)- dependent manner. In addition to urinary bladder, 5-HT could be involved in prostate contraction and cell proliferation. Evidence indicates that 5-HT receptor subtypes may be novel therapeutic targets for lower urinary tract symptoms.
Grants-in-Aid for Scientific Research (C) (KAKENHI 23590707, 24590722, and 26460694) from the Japan Society for the Promotion of Science.
越来越多的证据表明,5-羟色胺(5-HT;血清素)在下尿路中具有生理和病理功能。多种5-HT受体亚型在不同的外周和中枢器官中呈不同程度表达。在膀胱平滑肌上,5-HT1A、5-HT2、5-HT3和5-HT7亚型可作为节后受体发挥作用。节后5-HT2受体可诱导膀胱体逼尿肌收缩。5-HT1A被认为与5-HT2有类似作用,而5-HT3可能抑制直接肌肉刺激诱发的逼尿肌收缩。据报道,节后5-HT7可诱导膀胱颈松弛,这可能是有效排尿所必需的。5-HT1A、5-HT2A、5-HT2C、5-HT3、5-HT4和5-HT7亚型也可作为自主神经兴奋性神经末梢的节前受体。5-HT2A、5-HT2C、5-HT3、5-HT4和5-HT7亚型通过增强胆碱能或嘌呤能传递促进逼尿肌的神经源性收缩,而5-HT1A受体可能抑制逼尿肌中乙酰胆碱的释放。此外,5-HT1D可能参与抑制尿路上皮ATP的释放,有助于膀胱的内脏感觉。在控制排尿反射的中枢通路中,5-HT1A、5-HT2A和5-HT7参与膀胱和尿道括约肌活动的调节。它们的功能,尤其是5-HT1A的功能,因物种和部位(脊髓或脊髓上)的不同而有所差异。除膀胱外,5-HT可能参与前列腺收缩和细胞增殖。有证据表明,5-HT受体亚型可能是下尿路症状的新型治疗靶点。
来自日本学术振兴会的科学研究资助(C)(科研资助编号23590707、24590722和26460694)。