HEPATIC CIRCULATION - POTENTIAL FOR THERAPEUTIC INTERVENTION

被引:52
作者
BALLET, F [1 ]
机构
[1] HOP ST ANTOINE, EQUINE PHYSIOL & PHARMACOL HEPAT, INSERM, U181, F-75571 PARIS 12, FRANCE
关键词
D O I
10.1016/0163-7258(90)90091-F
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In recent years, knowledge of the physiology and pharmacology of hepatic circulation has grown rapidly. Liver microcirculation has a unique design that allows very efficient exchange processes between plasma and liver cells, even when severe constraints are imposed upon the system, i.e. in stressful situations. Furthermore, it has been recognized recently that sinusoids and their associated cells can no longer be considered only as passive structures ensuring the dispersion of molecules in the liver, but represent a very sophisticated network that protects and regulates parenchymal cells through a variety of mediators. Finally, vascular abnormalities are a prominent feature of a number of liver pathological processes, including cirrhosis and liver cell necrosis whether induced by alcohol, ischemia, endotoxins, virus or chemicals. Although it is not clear whether vascular lesions can be the primary events that lead to hepatocyte injury, the main interest of these findings is that liver microcirculation could represent a potential target for drug action in these conditions. © 1990.
引用
收藏
页码:281 / 328
页数:48
相关论文
共 434 条
[1]   16,16-DIMETHYL PROSTAGLANDIN-E2 PREVENTS THE DEVELOPMENT OF FULMINANT-HEPATITIS AND BLOCKS THE INDUCTION OF MONOCYTE MACROPHAGE PROCOAGULANT ACTIVITY AFTER MURINE HEPATITIS-VIRUS STRAIN-3 INFECTION [J].
ABECASSIS, M ;
FALK, JA ;
MAKOWKA, L ;
DINDZANS, VJ ;
FALK, RE ;
LEVY, GA .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 80 (03) :881-889
[2]  
AHMAD AB, 1984, J PHARMACOL EXP THER, V230, P718
[3]   CHOLESTASIS AND CHANGES IN THE MICROCIRCULATION OF PERFUSED-RAT-LIVER CAUSED BY THE CALCIUM IONOPHORE A23187 AND TYPE-I ANTIARRHYTHMIC DRUGS [J].
AKERBOOM, T ;
LENZEN, R ;
SCHNEIDER, I ;
SIES, H .
BIOCHEMICAL PHARMACOLOGY, 1987, 36 (18) :3037-3042
[4]   EVIDENCE THAT CA-2+ FLUXES AND RESPIRATORY, GLYCOGENOLYTIC AND VASOCONSTRICTIVE EFFECTS INDUCED BY THE ACTION OF PLATELET-ACTIVATING-FACTOR AND L-ALPHA-LYSOPHOSPHATIDYLCHOLINE IN THE PERFUSED-RAT-LIVER ARE MEDIATED BY PRODUCTS OF THE CYCLOOXYGENASE PATHWAY [J].
ALTIN, JG ;
DIETER, P ;
BYGRAVE, FL .
BIOCHEMICAL JOURNAL, 1987, 245 (01) :145-150
[5]  
ALTIN JG, 1988, MOL CELL BIOCHEM, V83, P3
[7]   MODIFICATION OF GALACTOSAMINE-INDUCED LIVER-INJURY IN RATS BY RETICULOENDOTHELIAL SYSTEM STIMULATION OR DEPRESSION [J].
ALTUWAIJRI, A ;
AKDAMAR, K ;
DILUZIO, NR .
HEPATOLOGY, 1981, 1 (02) :107-113
[8]  
ALVAREZLOPEZ A, 1987, TRANSPLANT P, V19, P4105
[9]  
ANDERS MW, 1984, DRUG METABOLISM DRUG, P55
[10]  
ARAI M, 1988, HEPATOLOGY, V8, P1397