首页   按字顺浏览 期刊浏览 卷期浏览 Impaired glomerular permselectivity for albumin in chemically medullectomized WKY rats
Impaired glomerular permselectivity for albumin in chemically medullectomized WKY rats

 

作者: G. BERGSTRÖM,   E. JOHNSSON,   K. LINDSTRÖM,   J. RUDENSTAM,   B. HARALDSSON,  

 

期刊: Acta Physiologica Scandinavica  (WILEY Available online 1996)
卷期: Volume 156, issue 1  

页码: 61-67

 

ISSN:0001-6772

 

年代: 1996

 

DOI:10.1046/j.1365-201X.1996.435160000.x

 

出版商: Blackwell Science Ltd

 

关键词: albumin;2‐bromo‐ethylamine hydrobromide;capillary permeability;glomerular filtration rate;hypertension;isolated kidney perfusions;rats;renal medulla

 

数据来源: WILEY

 

摘要:

Chemical renal medullectomy with 2‐bromo‐ethylamine hydrobromide (BEA) has been used to study the importance of the renal medulla in blood pressure regulation. However, conclusive evidence as to whether BEA treatment affects the glomerular barrier is lacking. In the present study, the effects of BEA upon glomerular permselectivity for albumin were studied using isolated kidneys (IPK) perfused at a low temperature (8 °C) to inhibit tubular reabsorption of proteins. Sixteen WKY rats (WB) received an i.v. injection of BEA (150 mg kg‐1) while 10 rats served as controls (WC). Volume balance, urinary osmolality and creatinine clearance (GFR) were measured in metabolic cages. Acute paired experiments (n=9) were performed 5–7 weeks after BEA. The rats were anaesthetized and the totalin vivoalbumin excretion was recorded. The kidneys were then isolated and perfused for measurements of inulin clearance (GFR) and fractional albumin clearance without tubular reabsorption of protein. The nine BEA treated rats showed polyuria and hypoosmotic urine.In vivoGFR was lower in the BEA treated groups when measured with creatinine clearance (459±22 vs. 213±41 μL min‐1100 g‐1body wt,P<0.001), while GFR was not significantly changed in the IPK (WC=135±27, WB=92±14 μL min‐1100 g‐1body wt, n.s.) when perfused at identical pressures. The fractional albumin clearance was increased three times in the BEA group (WB=9.6±3.4J,P<0.05). Moreover, albumin excretionin vivowas similar in the two groups despite low GFR in the BEA group. We conclude that BEA treatment affects glomerular perm

 

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