Downregulation of natriuretic peptide C-receptor protein in the hypertrophied ventricle of the aortovenocaval fistula rat

被引:10
作者
Brown, LA
Rutherford, RAD
Nunez, DJR
Wharton, J
Lowe, DG
Wilkins, MR
机构
[1] Hammersmith Hosp, Royal Postgrad Med Sch, Dept Clin Pharmacol, London W12 0NN, England
[2] Hammersmith Hosp, Royal Postgrad Med Sch, Dept Histochem, London W12 0NN, England
[3] Genentech Inc, S San Francisco, CA 94080 USA
关键词
rat; volume overload; cardiac hypertrophy; autoradiography; immunocytochemistry;
D O I
10.1016/S0008-6363(97)00192-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: This study examined the expression of the C-type receptor for the natriuretic peptide family (NPR-C) in the ventricles of normal and aortovenocaval (AV)-fistula rats, the latter a model of cardiac volume overload producing hypertrophy of both ventricles. Methods: Western blotting with a rabbit anti-NPR-C antibody was used to quantify NPR-C levels in ventricular membranes. NPR-C expression was localised anatomically and measured in frozen sections of cardiac tissue by histochemistry and in vitro autoradiography. Results: Western blot analysis revealed a single band (similar to 120 kDa) in ventricular membranes which was reduced to similar to 60 kDa after treatment with beta-mercaptoethanol. NPR-C immunoreactivity and [I-125]rat ANP1-28 binding (displaceable by the NPR-C-specific ligand C-ANP 4-23) were localised to the endocardium. NPR-C protein levels, as measured by all three techniques, were reduced significantly in the hypertrophied ventricles of AV-fistula rats compared to sham-operated animals. Conclusions: Volume-induced cardiac hypertrophy in the AV-fistula rat is associated with downregulation of endocardial NPR-C. This may be one mechanism by which the endocardium regulates the myocardial response to changes in haemodynamic load. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:363 / 371
页数:9
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