GLOMERULAR HEMODYNAMICS IN CELL-FREE AND ERYTHROCYTE-PERFUSED ISOLATED RAT-KIDNEY

被引:3
作者
GABBAI, FB [1 ]
PETERSON, OW [1 ]
KHANG, S [1 ]
WILSON, CB [1 ]
BLANTZ, RC [1 ]
机构
[1] Scripps Res Inst, DEPT IMMUNOL, LA JOLLA, CA 92023 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1994年 / 267卷 / 03期
关键词
FILTRATION FRACTION; GLOMERULAR FILTRATION RATE; HYDROSTATIC PRESSURE; RENAL RESISTANCES;
D O I
10.1152/ajprenal.1994.267.3.F423
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The cell-free isolated perfused kidney (IPK) is characterized by normal glomerular filtration rate (GFR) and very low filtration fraction (FF). Addition of erythrocytes to the perfusate (IEPK) increases FF while maintaining ''normal'' GFR levels. Micropuncture studies were performed in IPK and IEPK to establish the determinants of the glomerular ultrafiltration process responsible for low FF in IPK and to evaluate the impact of the addition of erythrocytes on these determinants. Nephron filtration rate was similar in IPK and IEPK (40 +/- 4 vs. 39 +/- 4 nl/min), whereas nephron perfusate flow was significantly higher in IPK (1,247 +/- 100 vs. 112 +/- 13 nl/min), leading to a superficial nephron FF of 3.4 +/- 0.2% in IPK and 36 +/- 2% in IEPK. Glomerular hydrostatic pressure (PG) and transcapillary hydrostatic pressure gradient (Delta P) were 53 +/- 2 and 33 +/- 1 mmHg, respectively, in IPK and 51 +/- 3 and 34 +/- 2 mmHg in IEPK, all normal values. Glomerular arteriolar resistances were significantly lower in IPK than in IEPK, and the glomerular ultrafiltration coefficient (L(p)A) was significantly lower in IPK (0.053 +/- 0.010 vs. 0.100 +/- 0.020 nl.s(-1).mmHg(-1)), but both values are within the normal in vivo range. These results demonstrate that low FF in IPK is not due to decreased Delta P or L(p)A values but to the high renal perfusion rate required to maintain normal Po and Delta P values. Addition of erythrocytes increases glomerular arteriolar resistances and restores glomerular hemodynamics to a pattern nearly identical to in vivo conditions. These data also suggest that IEPK constitutes an excellent tool to study glomerular function in vitro.
引用
收藏
页码:F423 / F427
页数:5
相关论文
共 27 条
[1]   NITRIC-OXIDE SYNTHESIZED FROM L-ARGININE REGULATES VASCULAR TONE IN THE CORONARY CIRCULATION OF THE RABBIT [J].
AMEZCUA, JL ;
PALMER, RMJ ;
DESOUZA, BM ;
MONCADA, S .
BRITISH JOURNAL OF PHARMACOLOGY, 1989, 97 (04) :1119-1124
[2]  
BAINES AD, 1990, AM J PHYSIOL, V259, pF80
[3]  
BAYLIS C, 1978, REV PHYSIOL BIOCH P, V80, P1
[4]   RENAL FUNCTION AND RENIN-ANGIOTENSIN SYSTEM IN ISOLATED PERFUSED KIDNEY [J].
BERKOWITZ, HD ;
MILLER, LD ;
ITSKOVITZ, HD .
AMERICAN JOURNAL OF PHYSIOLOGY, 1967, 213 (04) :928-+
[5]  
BLANTZ RC, 1978, METHOD PHARMACOL, V4, P141
[6]   ROLE OF NITRIC-OXIDE IN RENAL MEDULLARY OXYGENATION - STUDIES IN ISOLATED AND INTACT RAT KIDNEYS [J].
BREZIS, M ;
HEYMAN, SN ;
DINOUR, D ;
EPSTEIN, FH ;
ROSEN, S .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (02) :390-395
[7]   AMINO-ACIDS INDUCE RENAL VASODILATATION IN ISOLATED PERFUSED KIDNEY - COUPLING TO OXIDATIVE-METABOLISM [J].
BREZIS, M ;
SILVA, P ;
EPSTEIN, FH .
AMERICAN JOURNAL OF PHYSIOLOGY, 1984, 247 (06) :H999-1004
[8]   FLOW ACTIVATES AN ENDOTHELIAL POTASSIUM CHANNEL TO RELEASE AN ENDOGENOUS NITROVASODILATOR [J].
COOKE, JP ;
ROSSITCH, E ;
ANDON, NA ;
LOSCALZO, J ;
DZAU, VJ .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (05) :1663-1671
[9]   FLOW STIMULATES ENDOTHELIAL-CELLS TO RELEASE A NITROVASODILATOR THAT IS POTENTIATED BY REDUCED THIOL [J].
COOKE, JP ;
STAMLER, J ;
ANDON, N ;
DAVIES, PF ;
MCKINLEY, G ;
LOSCALZO, J .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 259 (03) :H804-H812
[10]   EFFECT OF EXOGENOUS AND ENDOGENOUS ANGIOTENSIN-II IN THE ISOLATED PERFUSED RAT-KIDNEY [J].
DAVALOS, M ;
FREGA, NS ;
SAKER, B ;
LEAF, A .
AMERICAN JOURNAL OF PHYSIOLOGY, 1978, 235 (06) :F605-F610