Haefliger J A, Waeber B, Grouzmann E, Braissant O, Nussberger J, Nicod P, Waeber G
Department of Internal Medicine B, University Hospital, CHUV-1011 Lausanne, Switzerland.
Regul Pept. 1999 Jun 30;82(1-3):35-43. doi: 10.1016/s0167-0115(99)00031-2.
Neuropeptide Y (NPY) is a key modulator of the autonomic nervous system playing pivotal roles in cardiovascular and neuronal functions. In this study, we assessed the cellular localization and gene expression of NPY in rat kidneys. We also examined the relationship between NPY gene expression and renin in two rat models of hypertension (two-kidney, one-clip renal hypertension (2K1C), and deoxycorticosterone-salt-induced hypertension (DOCA-salt)) characterized by a similar blood pressure elevation. In situ hybridization and immunohistochemistry, using anti-NPY or anti-C-flanking peptide of NPY (CPON) antibodies, showed that NPY transcript and protein were colocalized in the tubules of rat kidneys. During experimental hypertension, NPY mRNA was decreased in both kidneys of the 2K1C animals, but not in the kidney of DOCA-salt rats. In 2K1C rats, renal NPY content was also decreased. The difference in NPY gene expression between 2K1C rats (a high renin model of hypertension) and DOCA-salt rats (a low renin model of hypertension) suggests that circulating angiotensin II plays a role in local renal NPY gene expression and that the elevated blood pressure per se is not the primary factor responsible for the control of NPY gene expression in the kidney.
神经肽Y(NPY)是自主神经系统的关键调节因子,在心血管和神经元功能中发挥着关键作用。在本研究中,我们评估了NPY在大鼠肾脏中的细胞定位和基因表达。我们还在两种高血压大鼠模型(两肾一夹肾性高血压(2K1C)和脱氧皮质酮盐诱导的高血压(DOCA-盐))中研究了NPY基因表达与肾素之间的关系,这两种模型具有相似的血压升高特征。使用抗NPY或抗NPY C端侧翼肽(CPON)抗体进行原位杂交和免疫组织化学分析,结果显示NPY转录本和蛋白共定位于大鼠肾脏的肾小管中。在实验性高血压期间,2K1C动物双侧肾脏中的NPY mRNA均降低,但DOCA-盐大鼠的肾脏中未降低。在2K1C大鼠中,肾脏NPY含量也降低。2K1C大鼠(高血压高肾素模型)和DOCA-盐大鼠(高血压低肾素模型)之间NPY基因表达的差异表明,循环中的血管紧张素II在局部肾脏NPY基因表达中起作用,且血压升高本身并非控制肾脏中NPY基因表达的主要因素。