Gratzke Christian, Streng Tomi, Waldkirch Eginhard, Sigl Katja, Stief Christian, Andersson Karl-Erik, Hedlund Petter
Department of Clinical Chemistry and Pharmacology, Lund University Hospital, Lund, Sweden.
Eur Urol. 2009 Mar;55(3):696-704. doi: 10.1016/j.eururo.2008.04.042. Epub 2008 Apr 30.
A role for the transient receptor potential (TRP) A1 ion channel in rat lower urinary tract (LUT) sensation and disease has been proposed, but in the human LUT no information on TRPA1 activity is available.
To investigate the distribution of TRPA1 in the human urethra and to study the effect of TRPA1 agonists on isolated urethral strip preparations.
DESIGN, SETTINGS, AND PARTICIPANTS: Urethral specimens were obtained preoperatively from 10 patients and were freshly prepared for Western blot, immunohistochemistry, and functional in vitro investigations.
The expression patterns of TRPA1 were studied with Western blot and immunohistochemistry. The effects of allyl isothiocyanate (AI), cinnamaldehyde (CA), and NaHS (donor of H(2)S) on tension of urethral strips were investigated in tissue baths.
TRPA1 immunoreactivity (-IR) was found in nerve fibres in the suburothelial space and was also located to nerve fibres of the muscle layer. Single TRPA1-IR nerves extended into the urothelium. A majority, but not all TRPA1-IR nerves also expressed immunoreactivity for CGRP or TRPV1. In the urothelium, TRPV1 was located to the outer layers whereas TRPA1 was observed in basal urothelial cells. Interspersed between strands of smooth muscle cells of the urethral wall, TRPA1- and vimentin-IR cells containing central nuclei and slender cytoplasmatic extensions were observed. In functional experiments, TRPA1-agonists had no contractile effect in urethral preparations. After precontraction with phenylephrine, AI, CA, and NaHS caused concentration-dependent relaxations of urethral strip preparations.
The localization of TRPA1 to nerves that also express TRPV1 and CGRP, and in urothelial cells and interstitial cells, as well as the findings that TRPA1 agonists can modify tone of urethral preparations, propose a role for TRPA1 in afferent and efferent sensory signaling of the human outflow region.
已有研究提出瞬时受体电位(TRP)A1离子通道在大鼠下尿路(LUT)感觉和疾病中发挥作用,但关于人LUT中TRPA1活性的信息尚不可得。
研究TRPA1在人尿道中的分布,并探讨TRPA1激动剂对离体尿道条制备物的影响。
设计、场所和参与者:术前从10例患者获取尿道标本,并新鲜制备用于蛋白质免疫印迹、免疫组织化学和体外功能研究。
采用蛋白质免疫印迹和免疫组织化学研究TRPA1的表达模式。在组织浴中研究异硫氰酸烯丙酯(AI)、肉桂醛(CA)和NaHS(H₂S供体)对尿道条张力的影响。
在尿道上皮下间隙的神经纤维中发现TRPA1免疫反应性(-IR),也定位于肌层的神经纤维。单个TRPA1-IR神经延伸至尿道上皮。大多数但并非所有TRPA1-IR神经也表达降钙素基因相关肽(CGRP)或瞬时受体电位香草酸亚型1(TRPV1)的免疫反应性。在尿道上皮中,TRPV1定位于外层,而TRPA1见于基底尿道上皮细胞。在尿道壁平滑肌细胞束之间,观察到含有中央核和细长细胞质突起的TRPA1和波形蛋白-IR细胞。在功能实验中,TRPA1激动剂对尿道制备物无收缩作用。用去氧肾上腺素预收缩后,AI、CA和NaHS引起尿道条制备物浓度依赖性舒张。
TRPA1定位于同时表达TRPV1和CGRP的神经、尿道上皮细胞和间质细胞,以及TRPA1激动剂可改变尿道制备物张力的发现,提示TRPA1在人排尿流出区域的传入和传出感觉信号中发挥作用。