CYCLOSPORINE-A HEPATOTOXICITY - EFFECT OF PROLONGED TREATMENT WITH CYCLOSPORINE ON BILIARY LIPID SECRETION IN THE RAT

被引:41
作者
GALAN, AI [1 ]
FERNANDEZ, E [1 ]
MORAN, D [1 ]
MUNOZ, ME [1 ]
JIMENEZ, R [1 ]
机构
[1] UNIV SALAMANCA,DEPT PHYSIOL & PHARMACOL,E-37007 SALAMANCA,SPAIN
关键词
BILIARY LIPID; CHOLESTASIS; CYCLOSPORINE A; HEPATOTOXICITY;
D O I
10.1111/j.1440-1681.1995.tb01991.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. The effects of cyclosporine A (CyA) treatment on liver morphology, bile flow and biliary secretion of bile acid, cholesterol and phospholipid and some plasma biochemical indicators of liver function were examined. 2. Wister rats were treated i.p. with 10 or 20 mg of CyA/kg per day for 1, 2, 3 or 4 weeks. 3. Treatment increased bile acid and bilirubin plasma concentration. Bile flow and biliary secretion of bile acid, cholesterol and phospholipid were reduced in CyA-treated animals. 4. All these effecs of the drug appeared at 1 week after the start of treatment and were enhanced during prolonged treatment. Cyclosporine A-induced cholestasis was due to a decrease in both the bile acid-dependent and -independent fractions of bile flow. 5. The reduction in cholesterol and phospholipid biliary output may be secondary to the inhibition of the hepatobiliary flux of bile acid; however, perturbations in the removal of lipids from the canalicular membrane as well as intracanalicular interaction between CyA and lipid vesicles/micelles could also be involved.
引用
收藏
页码:260 / 265
页数:6
相关论文
共 32 条
[1]   CYCLOSPORINE, THE BIOLOGY OF THE BILE CANALICULUS, AND CHOLESTASIS [J].
ARIAS, IM .
GASTROENTEROLOGY, 1993, 104 (05) :1558-1560
[2]   GLUTATHIONE AS A PRIMARY OSMOTIC DRIVING FORCE IN HEPATIC BILE FORMATION [J].
BALLATORI, N ;
TRUONG, AT .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (05) :G617-G624
[3]   RELATION BETWEEN BILIARY GLUTATHIONE EXCRETION AND BILE ACID-INDEPENDENT BILE-FLOW [J].
BALLATORI, N ;
TRUONG, AT .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 256 (01) :G22-G30
[4]   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
[5]  
CADRANEL JF, 1989, GASTROEN CLIN BIOL, V13, P779
[6]   EFFECTS OF CYCLOSPORINE AND CORTICOSTEROIDS ON BILE SECRETION IN THE RAT [J].
CHANUSSOT, F ;
BOTTAFRIDLUND, D ;
DELAPORTE, PL ;
SBARRA, V ;
PORTUGAL, H ;
PAULI, AM ;
HAUTON, J ;
GAUTHIER, A ;
LAFONT, H .
TRANSPLANTATION, 1992, 54 (02) :226-231
[7]   LIPID FLOW IN BILE FORMATION [J].
COLEMAN, R ;
RAHMAN, K .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1125 (02) :113-133
[8]   CYCLOSPORINE A-INDUCED CHOLESTASIS IN THE RAT - BENEFICIAL-EFFECTS OF S-ADENOSYL-L-METHIONINE [J].
FERNANDEZ, E ;
MUNOZ, ME ;
ROMAN, ID ;
GALAN, AI ;
GONZALEZBUITRAGO, JM ;
JIMENEZ, R .
DRUG INVESTIGATION, 1992, 4 :54-63
[9]  
Galan A. I., 1993, Journal of Hepatology, V18, pS42
[10]  
GALAN AI, 1991, ARCH INT PHYSIOL BIO, V99, P373