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大鼠肾脏中的利钠肽B受体和C型利钠肽

Natriuretic peptide B receptor and C-type natriuretic peptide in the rat kidney.

作者信息

Lohe A, Yeh I, Hyver T, Pratt R, Jamison R

机构信息

Division of Nephrology, Palo Alto Department of Veteran's Affairs Medical Center, CA, USA.

出版信息

J Am Soc Nephrol. 1995 Dec;6(6):1552-8. doi: 10.1681/ASN.V661552.

Abstract

Natriuretic peptide receptor B (ANP-RGC(B)) has been previously identified in the kidney. It binds C-type natriuretic peptide (CNP) with high affinity and the two other natriuretic peptides (atrial natriuretic peptide and brain natriuretic peptide) with low affinity, and mediates the biological effects of CNP. The purpose of this investigation was to identify sites of ANP-RGC(B) mRNA in the rat renal tubule and to confirm that CNP itself is synthesized in the rat kidney. Kidneys from male Sprague-Dawley rats were removed and divided into cortex, outer medulla, and inner medulla. Using reverse transcriptase and polymerase chain reaction techniques, ANP-RGC(B) mRNA was identified in the three principal regions of the kidney. Individual glomeruli and segments of the renal tubule were microdissected and subjected to reverse transcriptase-polymerase chain reaction. ANP-RGC(B) mRNA was regularly found (>60% of animals) in glomeruli, distal convoluted tubule, and cortical, outer medullary, and inner medullary tubules but not in the proximal convoluted tubule, proximal straight tubule, thin or medullary thick ascending limb. ANP-RGC(B) mRNA was also identified in outer medullary descending vasa recta. Glyceraldehyde-3-phosphate-dehydrogenase and natriuretic peptide A receptor mRNA were present in all segments. In a separate study, CNP mRNA was identified in whole kidney, cortex, and medulla. These findings confirm that CNP and its receptor are present in the rat kidney. The proximity of the ligand and receptor suggests that CNP may have paracrine or autocrine regulatory functions in the rat kidney.

摘要

利钠肽受体B(ANP-RGC(B))此前已在肾脏中被鉴定出来。它与C型利钠肽(CNP)具有高亲和力,与其他两种利钠肽(心房利钠肽和脑利钠肽)具有低亲和力,并介导CNP的生物学效应。本研究的目的是确定大鼠肾小管中ANP-RGC(B) mRNA的位点,并证实CNP本身是在大鼠肾脏中合成的。将雄性Sprague-Dawley大鼠的肾脏取出并分为皮质、外髓质和内髓质。使用逆转录酶和聚合酶链反应技术,在肾脏的三个主要区域鉴定出了ANP-RGC(B) mRNA。对单个肾小球和肾小管节段进行显微切割,并进行逆转录聚合酶链反应。在肾小球、远曲小管、皮质、外髓质和内髓质小管中经常发现ANP-RGC(B) mRNA(>60%的动物),但在近曲小管、近端直小管、细段或髓质厚升支中未发现。在外髓质下行直小血管中也鉴定出了ANP-RGC(B) mRNA。甘油醛-3-磷酸脱氢酶和利钠肽A受体mRNA存在于所有节段中。在另一项研究中,在整个肾脏、皮质和髓质中鉴定出了CNP mRNA。这些发现证实了CNP及其受体存在于大鼠肾脏中。配体和受体的接近表明CNP可能在大鼠肾脏中具有旁分泌或自分泌调节功能。

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