EFFECT OF SODIUM ORTHOVANADATE ON THE HEPATOBILIARY CLEARANCE OF ROSE-BENGAL IN STREPTOZOTOCIN-INDUCED DIABETIC RATS

被引:5
作者
WATKINS, JB
BAUMAN, ME
BEATY, TM
机构
[1] Medical Sciences Program, Indiana University School of Medicine, Bloomington
关键词
BILE ACIDS; BILE PRODUCTION; BILIARY EXCRETION; CLEARANCE; HEPATOBILIARY; DIABETES; INSULIN-DEPENDENT; ORTHOVANADATE; SODIUM; PHARMACOKINETICS; ROSE BENGAL; STREPTOZOTOCIN;
D O I
10.1016/0006-2952(93)90617-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Sodium orthovanadate is known to promote glucose uptake in muscle and adipose tissues and has been suggested as a possible oral hypoglycemic agent. In addition, insulin-dependent diabetes has been shown to alter the hepatobiliary clearance of several drugs in rats. This study has determined whether orthovanadate, like insulin, can reverse diabetes-induced changes in the biliary excretion of endogenous bile acids and in the hepatobiliary clearance of rose bengal. Six groups of male Sprague-Dawley rats were used: normal, insulin-treated normal, vanadate-treated normal, diabetic, insulin-treated diabetic, and vanadate-treated diabetic. Diabetes was induced by injection of streptozotocin (45 mg/kg, i.v.). One week later, insulin (2-4 U/day, s.c.) and sodium orthovanadate (877 +/- 82 mu mol/kg/day, p.o.) treatments were initiated. After 4 weeks, the clearance and biliary excretion of rose bengal (60 mu mol/kg, i.v.) were determined for 3 hr. Bile flow rate, rose bengal excretion, and excretion of endogenous bile acids were unchanged in the two treated normal groups and in the insulin-treated diabetic rats. These parameters were increased in untreated diabetic and vanadate-treated diabetic rats as compared with normal. Pharmacokinetic analyses indicated that total and biliary clearances of rose bengal were increased in diabetic rats and that orthovanadate did not reverse these changes. However, liver weight and serum glucose concentrations were reduced by orthovanadate treatment. These data indicate that the oral insulinomimetic chemical sodium orthovanadate effectively reversed some, but not all, of the diabetes-induced alterations of hepatic function.
引用
收藏
页码:2269 / 2276
页数:8
相关论文
共 49 条
[1]   THE EFFECTS OF VANADATE ON RABBIT VENTRICULAR MUSCLE ADENYLATE-CYCLASE AND SODIUM-PUMP ACTIVITIES [J].
AITON, JF ;
CRAMB, G .
BIOCHEMICAL PHARMACOLOGY, 1985, 34 (09) :1543-1548
[2]   LONG-TERM IMPROVEMENT OF GLUCOSE-HOMEOSTASIS BY VANADATE TREATMENT IN DIABETIC RATS [J].
BRICHARD, SM ;
OKITOLONDA, W ;
HENQUIN, JC .
ENDOCRINOLOGY, 1988, 123 (04) :2048-2053
[3]   MARKED IMPROVEMENT OF GLUCOSE-HOMEOSTASIS IN DIABETIC OB OB MICE GIVEN ORAL VANADATE [J].
BRICHARD, SM ;
BAILEY, CJ ;
HENQUIN, JC .
DIABETES, 1990, 39 (11) :1326-1332
[4]   EFFECTS OF VANADATE ON INTRACELLULAR REDUCTION EQUIVALENTS IN MOUSE-LIVER AND THE FATE OF VANADIUM IN PLASMA, ERYTHROCYTES AND LIVER [J].
BRUECH, M ;
QUINTANILLA, ME ;
LEGRUM, W ;
KOCH, J ;
NETTER, KJ ;
FUHRMANN, GF .
TOXICOLOGY, 1984, 31 (3-4) :283-295
[5]   TOXIC EFFECT OF STREPTOZOTOCIN ON THE BILIARY-SECRETION OF NICOTINAMIDE-TREATED RATS [J].
CARNOVALE, CE ;
MARINELLI, RA ;
GARAY, EAR .
TOXICOLOGY LETTERS, 1987, 36 (03) :259-265
[6]   REVERSIBLE IMPAIRMENT OF HEPATOBILIARY FUNCTION INDUCED BY STREPTOZOTOCIN IN THE RAT [J].
CARNOVALE, CE ;
GARAY, EAR .
EXPERIENTIA, 1984, 40 (03) :248-250
[7]   BILE-FLOW DECREASE AND ALTERED BILE COMPOSITION IN STREPTOZOTOCIN-TREATED RATS [J].
CARNOVALE, CE ;
MARINELLI, RA ;
GARAY, EAR .
BIOCHEMICAL PHARMACOLOGY, 1986, 35 (15) :2625-2628
[8]   EFFECTS OF CHRONIC ADMINISTRATION OF VANADATE TO THE RAT ON THE SENSITIVITY OF GLYCOLYSIS AND GLYCOGEN-SYNTHESIS IN SKELETAL-MUSCLE TO INSULIN [J].
CHALLISS, RAJ ;
LEIGHTON, B ;
LOZEMAN, FJ ;
BUDOHOSKI, L ;
NEWSHOLME, EA .
BIOCHEMICAL PHARMACOLOGY, 1987, 36 (03) :357-361
[9]   ORAL VANADIUM ADMINISTRATION TO STREPTOZOTOCIN-DIABETIC RATS HAS MARKED NEGATIVE SIDE-EFFECTS WHICH ARE INDEPENDENT OF THE FORM OF VANADIUM USED [J].
DOMINGO, JL ;
GOMEZ, M ;
LLOBET, JM ;
CORBELLA, J ;
KEEN, CL .
TOXICOLOGY, 1991, 66 (03) :279-287
[10]  
DUBYAK GR, 1980, J BIOL CHEM, V255, P5306