Laboratory of Veterinary Physiology, Department of Veterinary Science, Faculty of Agriculture, University of Miyazaki, 1-1 Gakuenkibanadainishi, Miyazaki, Miyazaki 889-2192, Japan.
Laboratory of Veterinary Physiology, Department of Veterinary Science, Faculty of Agriculture, University of Miyazaki, 1-1 Gakuenkibanadainishi, Miyazaki, Miyazaki 889-2192, Japan.
Biochem Biophys Res Commun. 2021 Jan 1;534:653-658. doi: 10.1016/j.bbrc.2020.11.025. Epub 2020 Nov 20.
Two novel peptides, neuromedin U precursor-related peptide (NURP) and neuromedin S precursor-related peptide (NSRP), are produced from neuromedin U (NMU) and neuromedin S (NMS) precursors, respectively, as these precursors have multiple consensus sequences for proteolytic processing. Our group has shown previously that one of these two novel peptides, NURP, stimulates body temperature and locomotor activity, but not food intake. However, the physiological function of the other peptide, NSRP, has remained unclear. Therefore, the aim of this study was to characterize differences in the regions of the rat brain targeted by the NMU/NMS peptide family, including NURP and NSRP, and their physiological functions. First, we explored the regions of c-Fos expression after intracerebroventricular (i.c.v.) injection of NURP and NSRP and found that these were fewer than after i.c.v. injection of NMU and NMS in the hypothalamus, possibly because NURP and NSRP cannot activate NMU/NMS receptors. In the ventral subiculum, which is one region of the hippocampus, c-Fos expression was evident only after i.c.v. injection of NURP. We also examined the effects of NSRP on food intake, body temperature and locomotor activity. Like NURP, NSRP increased both body temperature and locomotor activity, but not food intake, indicating that NSRP is also a functional peptide. However, these effects of NSRP were distinctly weaker than those of NURP. These findings suggest differences in the affinity of NURP and/or NSRP for specific receptors, or in their respective biological activities.
两种新型肽,即神经调节素 U 前体相关肽(NURP)和神经调节素 S 前体相关肽(NSRP),分别由神经调节素 U(NMU)和神经调节素 S(NMS)前体产生,因为这些前体具有多个用于蛋白水解加工的共识序列。我们的研究小组之前已经表明,这两种新型肽之一的 NURP 会刺激体温和运动活性,但不会刺激摄食。然而,另一种肽 NSRP 的生理功能仍不清楚。因此,本研究的目的是表征 NMU/NMS 肽家族,包括 NURP 和 NSRP,及其生理功能所针对的大鼠脑区的差异。首先,我们探索了脑室注射 NURP 和 NSRP 后 c-Fos 表达的脑区,发现与脑室注射 NMU 和 NMS 相比,下丘脑的 c-Fos 表达较少,这可能是因为 NURP 和 NSRP 不能激活 NMU/NMS 受体。在海马的一个区域腹侧下托,只有脑室注射 NURP 后才会出现 c-Fos 表达。我们还检查了 NSRP 对摄食、体温和运动活性的影响。与 NURP 一样,NSRP 也增加了体温和运动活性,但不增加摄食,表明 NSRP 也是一种功能性肽。然而,NSRP 的这些作用明显弱于 NURP。这些发现表明 NURP 和/或 NSRP 对特定受体的亲和力不同,或者它们各自的生物学活性不同。