EFFECTS OF REPEATED ADMINISTRATION OF KW-3902, A NOVEL ADENOSINE A(1)-RECEPTOR ANTAGONIST, ON ITS PHARMACOLOGICAL ACTIONS

被引:5
作者
KUSAKA, H
KARASAWA, A
机构
[1] Department of Pharmacology, Pharmaceutical Research Laboratories, Kyowa Hakko Kogyo Co., Ltd., Shizuoka 411, 1188 Shimotogari, Nagaizumi-cho, Sunto-gun
关键词
KW-3902; ADENOSINE A(1)-RECEPTOR ANTAGONIST; DIURETIC EFFECT; RENAL PROTECTIVE EFFECT; TOLERANCE;
D O I
10.1254/jjp.63.513
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Effects of repeated administration of KW-3902, a novel adenosine Al-receptor antagonist, on its pharmacological actions were studied with regards to: 1) in vivo adenosine A(1)-antagonism, 2) diuretic effects and 3) renal protective effects against glycerol-induced acute renal failure (ARF). After repeated oral administration of KW-3902 (0.1 mg/kg/day) for 24 days, neither enhancement of the sensitivity to 5'-N-ethylcarboxamidoadenosine (NECA) nor reduction of the inhibitory effect of KW-3902 on the NECA-induced bradycardic response were observed. After repeated oral administration of KW-3902 (0.01 and 0.1 mg/kg/day) for 20 days, the diuretic effects of KW-3902 did not change. Renal protective effects against glycerol-induced ARF were not reduced by repeated oral administration of KW-3902 (0.01 and 0.1 mg/kg/ day) for 23 days. These results suggest that repeated oral administration of KW-3902 has no effect on its pharmacological actions. Additionally, changes in serum parameters, which occurred after repeated administration of furosemide or trichlormethiazide, were minimal after repeated oral administration of KW3902 (0.001-1mg/kg/day) for 27 days. From these results, KW-3902 proved to be a diuretic which has renal protective effects with less side effects.
引用
收藏
页码:513 / 519
页数:7
相关论文
共 23 条
[1]  
BROGDEN RN, 1980, DRUGS, V15, P251
[2]  
COLLIS M G, 1984, British Journal of Pharmacology, V83, p413P
[3]   DIURETIC AND SALIURETIC EFFECTS OF 1,3-DIPROPYL-8-CYCLOPENTYLXANTHINE, A SELECTIVE ADENOSINE-A1-RECEPTOR ANTAGONIST [J].
COLLIS, MG ;
SHAW, G ;
KEDDIE, JR .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1991, 43 (02) :138-139
[4]   EVIDENCE THAT A NOVEL 8-PHENYL SUBSTITUTED XANTHINE DERIVATIVE IS A CARDIOSELECTIVE ADENOSINE RECEPTOR ANTAGONIST INVIVO [J].
FREDHOLM, BB ;
JACOBSON, KA ;
JONZON, B ;
KIRK, KL ;
LI, YO ;
DALY, JW .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1987, 9 (04) :396-400
[5]  
GREEN A, 1987, J BIOL CHEM, V262, P15072
[6]   DESENSITIZATION OF ADENOSINE RECEPTOR-MEDIATED INHIBITION OF LIPOLYSIS - THE MECHANISM INVOLVES THE DEVELOPMENT OF ENHANCED CYCLIC ADENOSINE-MONOPHOSPHATE ACCUMULATION IN TOLERANT ADIPOCYTES [J].
HOFFMAN, BB ;
CHANG, H ;
DALLAGLIO, E ;
REAVEN, GM .
JOURNAL OF CLINICAL INVESTIGATION, 1986, 78 (01) :185-190
[7]  
KARASAWA A, 1988, ARZNEIMITTELFORSCH, V38-2, P1684
[8]   AMELIORATION OF GLYCEROL-INDUCED ACUTE RENAL-FAILURE IN THE RAT WITH 8-CYCLOPENTYL-1,3-DIPROPYLXANTHINE [J].
KELLETT, R ;
BOWMER, CJ ;
COLLIS, MG ;
YATES, MS .
BRITISH JOURNAL OF PHARMACOLOGY, 1989, 98 (03) :1066-1074
[9]   ADENOSINE INDUCES A CALCIUM-DEPENDENT GLOMERULAR CONTRACTION [J].
LOPEZNOVOA, JM ;
DEARRIBA, G ;
BARRIO, V ;
RODRIGUEZPUYOL, D .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1987, 134 (03) :365-367
[10]   CHRONIC THEOPHYLLINE TREATMENT INCREASES ADENOSINE-A1, BUT NOT ADENOSINE-A2, RECEPTOR-BINDING IN THE RAT-BRAIN - AN AUTORADIOGRAPHIC STUDY [J].
LUPICA, CR ;
BERMAN, RF ;
JARVIS, MF .
SYNAPSE, 1991, 9 (02) :95-102