REGULATION OF HEPATIC NA+-HCO3- COTRANSPORT AND PH BY MEMBRANE-POTENTIAL DIFFERENCE

被引:17
作者
FITZ, JG [1 ]
LIDOFSKY, SD [1 ]
SCHARSCHMIDT, BF [1 ]
机构
[1] UNIV CALIF SAN FRANCISCO, SAN FRANCISCO, CA 94143 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1993年 / 265卷 / 01期
关键词
SODIUM-HYDROGEN EXCHANGE; BICARBONATE; SODIUM-POTASSIUM-ADENOSINE-TRIPHOSPHATASE; HEPATIC TRANSPORT;
D O I
10.1152/ajpgi.1993.265.1.G1
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Hepatocytes possess several mechanisms for membrane acid-base transport, which work in concert to maintain intracellular pH (pH(i)) in a narrow physiological range, despite metabolic processes that produce and consume substantial quantities of H+ and HCO3. Na+-H+ and Cl-HCO3- exchangers contribute to recovery from intracellular acidosis and alkalosis, respectively, but are largely inoperative at physiological values of pH(i). Recent studies indicate that hepatocytes also possess a mechanism for coupled transport of Na+ and HCO3- across the basolateral membrane. This appears to be the dominant pathway for membrane acid-base transport operative under basal conditions, mediates influx of Na+ and HCO3-, and is an important contributor to recovery from intracellular acidosis. In this review, the properties of hepatic Na+-HCO3- cotransport are described with emphasis on its effects on pH(i) and Na+ homeostasis and on the possible role of membrane potential difference as a signal modulating the rate of HCO3- influx and pH(i) of hepatocytes through effects on this transporter.
引用
收藏
页码:G1 / G8
页数:8
相关论文
共 55 条
[1]  
ALPERN RJ, 1991, KIDNEY INT, V40, pS29
[2]   AMILORIDE AND TAURINE INHIBIT CHOLATE-INDUCED HCO3--RICH CHOLERESIS IN PERFUSED RAT LIVERS [J].
ANWER, MS ;
ATKINSON, JM ;
ZIMNIAK, P .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 259 (03) :G453-G461
[3]   INTRACELLULAR CALCIUM MEDIATED ACTIVATION OF HEPATIC NA+/H+ EXCHANGE BY ARGININE VASOPRESSIN AND PHENYLEPHRINE [J].
ANWER, MS ;
ATKINSON, JM .
HEPATOLOGY, 1992, 15 (01) :134-143
[4]   INTRACELLULAR PH INFLUENCES THE RESTING MEMBRANE-POTENTIAL OF ISOLATED RAT HEPATOCYTES [J].
BEAR, CE ;
DAVISON, JS ;
SHAFFER, EA .
BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 944 (02) :113-120
[5]   CL--HCO3- EXCHANGER IN ISOLATED RAT HEPATOCYTES - ROLE IN REGULATION OF INTRACELLULAR PH [J].
BENEDETTI, A ;
STRAZZABOSCO, M ;
CORASANTI, JG ;
HADDAD, P ;
GRAF, J ;
BOYER, JL .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (03) :G512-G522
[6]  
BIERMAN AJ, 1988, J BIOL CHEM, V263, P15253
[7]   HEPATIC TRANSPORT-SYSTEMS REGULATING PHI, CELL-VOLUME, AND BILE SECRETION [J].
BOYER, JL ;
GRAF, J ;
MEIER, PJ .
ANNUAL REVIEW OF PHYSIOLOGY, 1992, 54 :415-438
[8]   LOWERING OF PHI INHIBITS CA-2+-ACTIVATED K+ CHANNELS IN PANCREATIC B-CELLS [J].
COOK, DL ;
IKEUCHI, M ;
FUJIMOTO, WY .
NATURE, 1984, 311 (5983) :269-271
[9]   CA-2+-ACTIVATED K+ CHANNELS FROM CULTURED RENAL MEDULLARY THICK ASCENDING LIMB CELLS - EFFECTS OF PH [J].
CORNEJO, M ;
GUGGINO, SE ;
GUGGINO, WB .
JOURNAL OF MEMBRANE BIOLOGY, 1989, 110 (01) :49-55
[10]  
DIETMER JW, 1989, J PHGYSL LOND, V411, P179