KALLIKREIN EXCRETION IN DAHL SALT-SENSITIVE AND SALT-RESISTANT RATS WITH NATIVE AND TRANSPLANTED KIDNEYS

被引:14
作者
CHURCHILL, PC
CHURCHILL, MC
BIDANI, AK
RABITO, SF
机构
[1] LOYOLA UNIV, DEPT INTERNAL MED, MAYWOOD, IL 60141 USA
[2] HINES VET AFFAIRS HOSP, MAYWOOD, IL 60141 USA
[3] COOK CTY HOSP, DEPT ANESTHESIOL, CHICAGO, IL 60612 USA
[4] UNIV ILLINOIS, CHICAGO, IL 60612 USA
关键词
GENETIC HYPERTENSION; RENAL FUNCTION; KALLIKREIN-KININ SYSTEM;
D O I
10.1152/ajprenal.1995.269.5.F710
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Urinary kallikrein excretion is decreased in Dahl salt-sensitive (S) vs. salt-resistant (R) rats, and several lines of reasoning suggest not only that decreased kallikrein excretion is a marker for salt-sensitive hypertension but also that kallikrein might play a pathogenic role. Because previous cross-transplantation studies have demonstrated that the kidney's genotype plays a role in determining the blood pressure of the recipient in Dahl S and R rats, the present experiments were designed to determine whether both blood pressure and urinary kallikrein excretion ''traveled with the kidney'' in transplantation. The Rapp strains of S and R were maintained on a low- NaCl (0.13%) diet until kidney transplantation (bilaterally nephrectomized recipients), at which time the diet was switched to high NaCl (7.8%). Sixteen days later, blood pressures (tail-cuff plethysmography) of the cross-transplant groups (R/S and S/R, indicating kidney genotype/recipient genotype) were nearly identical to each other and intermediate between the blood pressures of the control groups with transplanted kidneys (R/R and S/S). Renal function studies, performed on anesthetized rats 17 days after surgery, demonstrated that R kidneys had higher glomerular filtration rates, renal plasma flows, and urinary kallikrein excretion rates than S kidneys. These differences tended to be preserved in the cross-transplant groups, and therefore they must be genetically determined intrinsic differences between R and S kidneys. This was especially striking with respect to urinary kallikrein excretion. The rank order of urinary kallikrein excretion was R/R = R/S > S/R = S/S, which implies that it is completely determined by the genotype of the kidney. Finally, although these intrinsic differences between the kidneys might play a role in determining blood pressure, they cannot be the entire explanation, because blood pressures in the cross-transplant groups were nearly identical. Thus, in conclusion, extrarenal genetic factors in the recipient also have a decisive role in control of blood pressure.
引用
收藏
页码:F710 / F717
页数:8
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