Loria Analia S, Osborn Jeffrey L
Department of Pharmacology and Nutritional Sciences, University of Kentucky, Lexington, Kentucky; and
Department of Biology, University of Kentucky, Lexington, Kentucky.
Am J Physiol Renal Physiol. 2017 Jul 1;313(1):F47-F54. doi: 10.1152/ajprenal.00591.2016. Epub 2017 Mar 22.
Adult rats exposed to maternal separation (MatSep) are normotensive but display lower glomerular filtration rate and increased renal neuroadrenergic drive. The aim of this study was to determine the renal α-adrenergic receptor density and the renal vascular responsiveness to adrenergic stimulation in male rats exposed to MatSep. In addition, baroreflex sensitivity was assessed to determine a component of neural control of the vasculature. Using tissue collected from 4-mo-old MatSep and control rats, α-adrenergic receptors (α-ARs) were measured in renal cortex and isolated renal vasculature using receptor binding assay, and the α-AR subtype gene expression was determined by RT-PCR. Renal cortical α-AR density was similar between MatSep and control tissues (B = 44 ± 1 vs. 42 ± 2 fmol/mg protein, respectively); however, MatSep reduced α-AR density in renal vasculature (B = 47 ± 4 vs. 62 ± 4 fmol/mg protein, < 0.05, respectively). In a separate group of rats, the pressor, bradycardic, and renal vascular constrictor responses to acute norepinephrine injection (NE, 0.03-0.25 μg/μl) were determined under anesthesia. Attenuated NE-induced renal vasoconstriction was observed in rats exposed to MatSep compared with control ( < 0.05). A third group of rats was infused at steady state with the α agonist phenylephrine (10 μg/min iv) and vasodilator sodium nitroprusside (5 μg/min iv). The difference between the change in heart rate/mean arterial pressure slopes was indicative of reduced baroreflex sensitivity in MatSep vs. control rats (-0.45 ± 0.04 vs. -0.95 ± 0.07 beats·min·mmHg, < 0.05). These data support the notion that reduced α-adrenergic receptor expression and function in the renal vasculature could develop secondary to MatSep-induced overactivation of the renal neuroadrenergic tone.
成年大鼠若经历母婴分离(MatSep),血压正常,但肾小球滤过率较低,且肾神经肾上腺素能驱动增加。本研究旨在确定经历MatSep的雄性大鼠的肾α-肾上腺素能受体密度以及肾血管对肾上腺素能刺激的反应性。此外,评估压力反射敏感性以确定血管系统神经控制的一个组成部分。使用从4月龄的MatSep大鼠和对照大鼠收集的组织,通过受体结合测定法在肾皮质和分离的肾血管中测量α-肾上腺素能受体(α-ARs),并通过逆转录聚合酶链反应(RT-PCR)确定α-AR亚型基因表达。MatSep组和对照组肾皮质α-AR密度相似(分别为B = 44±1与42±2 fmol/mg蛋白质);然而,MatSep降低了肾血管中的α-AR密度(分别为B = 47±4与62±4 fmol/mg蛋白质,P<0.05)。在另一组大鼠中,在麻醉状态下测定急性注射去甲肾上腺素(NE,0.03 - 0.25μg/μl)后的升压、心动过缓和肾血管收缩反应。与对照组相比,经历MatSep的大鼠中观察到NE诱导的肾血管收缩减弱(P<0.05)。第三组大鼠以稳态输注α激动剂去氧肾上腺素(10μg/min静脉注射)和血管扩张剂硝普钠(5μg/min静脉注射)。心率/平均动脉压斜率变化的差异表明,与对照大鼠相比,MatSep大鼠的压力反射敏感性降低(-0.45±0.04与-0.95±0.07次·分钟·mmHg,P<0.05)。这些数据支持这样一种观点,即肾血管中α-肾上腺素能受体表达和功能的降低可能继发于MatSep诱导的肾神经肾上腺素能张力过度激活。