Hyperkalemia: An adaptive response in chronic renal insufficiency

被引:74
作者
Gennari, FJ [1 ]
Segal, AS [1 ]
机构
[1] Univ Vermont, Coll Med, Burlington, VT USA
关键词
hyperkalemia; potassium; potassium adaptation; kidney; renal failure; ROMK;
D O I
10.1046/j.1523-1755.2002.00350.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background. Hyperkalemia is a common feature of chronic renal insufficiency, usually ascribed to impaired K+ homeostasis. However, various experimental observations suggest that the increase in extracellular [K+] actually functions in a homeostatic fashion. directly stimulating renal K+ excretion through an effect that is independent of. and additive to, aldosterone. Methods. We have reviewed relevant studies in experimental animals and in human subjects that have examined the regulation of K+ excretion and its relation to plasma [K+]. Results. Studies indicate that (1) extracellular [K+] in patients with renal insufficiency correlates directly with intracellular K+ content, and (2) hyperkalemia directly promotes K+ secretion in the principal cells of the collecting duct by increasing apical and basolateral membrane conductances. The effect of hyperkalemia differs from that of aldosterone in that K+ conductances are increased as the primary event. The changes in principal cell function and structure induced by hyperkalemia are indistinguishable from the effects seen in adaptation to a high K+ diet. Conclusions. We propose that hyperkalemia plays a pivotal role in K- homeostasis in renal insufficiency by stimulating K+ excretion. In patients with chronic renal insufficiency, a new steady state develops in which extracellular [K+] rises to the level needed to stimulate K- excretion so that it again matches intake. When this new steady state is achieved, plasma [K+] remains stable unless dietary intake increases, glomerular filtration rate falls. or drugs are given that disrupt the new balance.
引用
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页码:1 / 9
页数:9
相关论文
共 88 条
[71]   K-ACTIVITY OF CCD PRINCIPAL CELLS FROM NORMAL AND DOCA-TREATED RABBITS [J].
SANSOM, SC ;
AGULIAN, S ;
MUTO, S ;
ILLIG, V ;
GIEBISCH, G .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 256 (01) :F136-F142
[72]   PREVALENCE, PATHOGENESIS, AND FUNCTIONAL-SIGNIFICANCE OF ALDOSTERONE DEFICIENCY IN HYPERKALEMIC PATIENTS WITH CHRONIC RENAL-INSUFFICIENCY [J].
SCHAMBELAN, M ;
SEBASTIAN, A ;
BIGLIERI, EG .
KIDNEY INTERNATIONAL, 1980, 17 (01) :89-101
[73]   NA-K-ATPASE IN ISOLATED RABBIT TUBULES AFTER UNILATERAL NEPHRECTOMY AND NA+ LOADING [J].
SCHERZER, P ;
WALD, H ;
CZACZKES, JW .
AMERICAN JOURNAL OF PHYSIOLOGY, 1985, 248 (04) :F565-F573
[74]   ADAPTATION TO POTASSIUM [J].
SILVA, P ;
BROWN, RS ;
EPSTEIN, FH .
KIDNEY INTERNATIONAL, 1977, 11 (06) :466-475
[75]   EXTRARENAL POTASSIUM ADAPTATION - THE ROLE OF ALDOSTERONE [J].
SPITAL, A ;
STERNS, RH .
CLINICAL SCIENCE, 1989, 76 (02) :213-219
[76]  
STANTON BA, 1987, SEMIN NEPHROL, V7, P82
[77]   POTASSIUM-TRANSPORT BY THE RENAL DISTAL TUBULE - EFFECTS OF POTASSIUM LOADING [J].
STANTON, BA ;
GIEBISCH, GH .
AMERICAN JOURNAL OF PHYSIOLOGY, 1982, 243 (05) :F487-F493
[78]   THE ROLE OF ALDOSTERONE IN POTASSIUM TOLERANCE - STUDIES IN ANEPHRIC HUMANS [J].
SUGARMAN, A ;
BROWN, RS .
KIDNEY INTERNATIONAL, 1988, 34 (03) :397-403
[79]   INCREASED SODIUM-TRANSPORT BY CORTICAL COLLECTING TUBULES FROM REMNANT KIDNEYS [J].
VEHASKARI, VM ;
HERINGSMITH, KS ;
KLAHR, S ;
HAMM, LL .
KIDNEY INTERNATIONAL, 1989, 36 (01) :89-95
[80]   ROLE OF RENIN-ANGIOTENSIN-ALDOSTERONE SYSTEM IN REGULATION OF PLASMA POTASSIUM IN CHRONIC RENAL-DISEASE [J].
WEIDMANN, P ;
MAXWELL, MH ;
ROWE, P ;
WINER, R ;
MASSRY, SG .
NEPHRON, 1975, 15 (01) :35-49