Martin E R, Lewicki J A, Scarborough R M, Ballermann B J
Renal Division, Brigham and Women's Hospital, Boston, Massachusetts 02115.
Am J Physiol. 1989 Oct;257(4 Pt 2):F649-57. doi: 10.1152/ajprenal.1989.257.4.F649.
The expression and regulation of atrial natriuretic peptide (ANP) receptor subtypes were examined in rat renal glomeruli and papillae. In glomeruli, approximately two-thirds of ANP binding sites represented guanylate cyclase-uncoupled ANP clearance receptors (ANPc) with a molecular mass of 64 kDa under reducing conditions. The remainder of glomerular ANP binding sites represented guanylate cyclase-coupled ANP receptors (ANPGC) with a molecular mass of 130 kDa. In rat papillae, only the 130-kDa ANPGC was expressed. In rats adapted to a low-salt diet, saline loading or acute ANP infusion resulted in a decrease in ANPC density, a difference that was not detected when glomeruli were first acidwashed to remove endogenous ANP, indicating that apparent regulation of ANPC reflected prior occupancy by endogenous ANP. Densities of glomerular ANPC and ANPGC were similar in spontaneously hypertensive rats (SHR) compared with those of the Wistar-Kyoto (WKY) controls. However, elimination of prior receptor occupancy revealed a significantly greater expression of glomerular ANPC in SHR compared with WKY rats, without significant differences in the density of the glomerular or papillary ANPGC subtype. The failure of the ANPGC subtype to be regulated may account for our previously reported findings that dietary salt intake does not affect glomerular ANP-stimulated guanosine-3',5'-cyclic monophosphate accumulation despite apparent regulation of ANP receptor density. Whether the increased expression of the ANPC subtype in SHR represents a primary defect or results from induction of ANP clearance receptor expression remains to be determined.
在大鼠肾肾小球和肾乳头中检测了心钠素(ANP)受体亚型的表达和调节。在肾小球中,约三分之二的ANP结合位点代表还原条件下分子量为64 kDa的鸟苷酸环化酶非偶联ANP清除受体(ANPc)。肾小球中其余的ANP结合位点代表分子量为130 kDa的鸟苷酸环化酶偶联ANP受体(ANPGC)。在大鼠肾乳头中,仅表达130 kDa的ANPGC。在适应低盐饮食的大鼠中,盐水负荷或急性ANP输注导致ANPc密度降低,当肾小球首先用酸洗以去除内源性ANP时未检测到这种差异,这表明ANPc的明显调节反映了内源性ANP的先前占据。与Wistar-Kyoto(WKY)对照相比,自发性高血压大鼠(SHR)肾小球中ANPc和ANPGC的密度相似。然而,消除先前的受体占据显示,与WKY大鼠相比,SHR肾小球中ANPc的表达明显更高,肾小球或肾乳头ANPGC亚型的密度没有显著差异。ANPGC亚型未能被调节可能解释了我们先前报道的发现,即尽管ANP受体密度明显受到调节,但饮食盐摄入并不影响肾小球ANP刺激的鸟苷-3',5'-环磷酸积累。SHR中ANPc亚型表达增加是代表原发性缺陷还是由ANP清除受体表达的诱导导致仍有待确定。