Yoshiyama Mitsuharu, Mochizuki Tsutomu, Nakagomi Hiroshi, Miyamoto Tatsuya, Kira Satoru, Mizumachi Ryoji, Sokabe Takaaki, Takayama Yasunori, Tominaga Makoto, Takeda Masayuki
Department of Urology, University of Yamanashi Graduate School of Medical Sciences, Chuo, Yamanashi, Japan;
Pharmacology Department, Nonclinical Research Center, Drug Development Service Segment, LSI Medience Corporation, Uto, Kumamoto, Japan;
Am J Physiol Renal Physiol. 2015 May 15;308(10):F1128-34. doi: 10.1152/ajprenal.00016.2015. Epub 2015 Mar 11.
The present study used a dual analysis of voiding behavior and reflex micturition to examine lower urinary tract function in transient receptor potential vanilloid (TRPV)1 knockout (KO) mice and TRPV4 KO mice. In metabolic cage experiments conducted under conscious conditions (i.e., voluntary voiding behavior), TRPV4 KO mice showed a markedly higher voiding frequency (VF; 19.3 ± 1.2 times/day) and a smaller urine volume/voiding (UVV; 114 ± 9 μl) compared with wild-type (WT) littermates (VF: 5.2 ± 0.5 times/day and UVV: 380 ± 34 μl). Meanwhile, TRPV1 KO mice showed a similar VF to WT littermates (6.8 ± 0.5 times/day) with a significantly smaller UVV (276 ± 20 μl). Water intake among these genotypes was the same, but TRPV4 KO mice had a larger urine output than the other two groups. In cystometrogram experiments conducted in decerebrate unanesthetized mice (i.e., reflex micturition response), no differences between the three groups were found in any cystometrogram variables, including voided volume, volume threshold for inducing micturition contraction, maximal voiding pressure, and bladder compliance. However, both TRPV1 KO and TRPV4 KO mice showed a significant number of nonvoiding bladder contractions (NVCs; 3.5 ± 0.9 and 2.8 ± 0.7 contractions, respectively) before each voiding, whereas WT mice showed virtually no NVCs. These results suggest that in the reflex micturition circuit, a lack of either channel is involved in NVCs during bladder filling, whereas in the forebrain, it is involved in the early timing of urine release, possibly in the conscious response to the bladder instability.
本研究采用排尿行为和反射性排尿的双重分析方法,来检测瞬时受体电位香草酸亚型1(TRPV)1基因敲除(KO)小鼠和TRPV4基因敲除小鼠的下尿路功能。在清醒状态下进行的代谢笼实验(即自主排尿行为)中,与野生型(WT)同窝小鼠相比,TRPV4基因敲除小鼠的排尿频率(VF;19.3±1.2次/天)显著更高,每次排尿量(UVV;114±9微升)更小(野生型同窝小鼠的排尿频率为5.2±0.5次/天,每次排尿量为380±34微升)。同时,TRPV1基因敲除小鼠的排尿频率与野生型同窝小鼠相似(6.8±0.5次/天),但每次排尿量显著更小(276±20微升)。这些基因型小鼠的饮水量相同,但TRPV4基因敲除小鼠的尿量比其他两组更多。在去大脑未麻醉小鼠中进行的膀胱压力容积测定实验(即反射性排尿反应)中,三组在任何膀胱压力容积测定变量上均未发现差异,包括排尿量、诱发排尿收缩的容积阈值、最大排尿压力和膀胱顺应性。然而,TRPV1基因敲除小鼠和TRPV4基因敲除小鼠在每次排尿前均出现大量无排尿膀胱收缩(分别为3.5±0.9次和2.8±0.7次收缩),而野生型小鼠几乎没有无排尿膀胱收缩。这些结果表明,在反射性排尿回路中,缺乏任一通道均与膀胱充盈期间的无排尿膀胱收缩有关,而在前脑,它与尿液释放的早期时机有关,可能与对膀胱不稳定的意识反应有关。