Sakamoto Takumi, Mori Kenji, Nakahara Keiko, Miyazato Mikiya, Kangawa Kenji, Sameshima Hiroshi, Murakami Noboru
Department of Veterinary Physiology, Faculty of Agriculture, University of Miyazaki, Miyazaki 889-2192, Japan.
Biochem Biophys Res Commun. 2007 Sep 21;361(2):457-61. doi: 10.1016/j.bbrc.2007.07.036. Epub 2007 Jul 18.
We recently identified neuromedin S (NMS) as an endogenous ligand for the FM-4/TGR-1 receptor. Here, we examined the possible involvement of central NMS in regulation of urinary output and vasopressin (AVP) release in rats. Intracerebroventricular (icv) injection of NMS induced a dose-dependent increase in the plasma level of AVP, followed by a decrease of nocturnal urinary output. Expression of cFos after icv injection of NMS was observed in the supachiasmatic nucleus (SCN), arcuate nucleus, paraventricular nucleus (PVN), and supraoptic nucleus (SON). The cFos expressing cells in PVN and SON, but not SCN, were then double-stained using antibodies against the vasopressin. On the other hand, icv injection of neuromedin U, which also binds to the FM-4/TGR-1 receptor, required a concentration ten times higher than that of NMS in order to exert the same antidiuretic potency. These results suggest that central NMS may exert a physiological antidiuretic action via vasopressin release.
我们最近鉴定出神经介素S(NMS)是FM-4/TGR-1受体的内源性配体。在此,我们研究了中枢NMS在调节大鼠尿量和抗利尿激素(AVP)释放方面的可能作用。脑室内(icv)注射NMS可导致AVP血浆水平呈剂量依赖性升高,随后夜间尿量减少。icv注射NMS后,在视交叉上核(SCN)、弓状核、室旁核(PVN)和视上核(SON)中观察到cFos的表达。然后使用抗抗利尿激素抗体对PVN和SON中表达cFos的细胞进行双重染色,但SCN中未进行。另一方面,icv注射同样与FM-4/TGR-1受体结合的神经介素U,为发挥相同的抗利尿效力,所需浓度比NMS高十倍。这些结果表明,中枢NMS可能通过抗利尿激素释放发挥生理性抗利尿作用。