Positive inotropic effect of purified green tea catechin derivative in guinea pig hearts:: The measurements of cellular Ca2+ and nitric oxide release

被引:30
作者
Hotta, Yoshihiro
Huang, Lei
Muto, Tatsuya
Yajima, Michio
Miyazeki, Kunihiro
Ishikawa, Naohisa
Fukuzawa, Yoshitaka
Wakida, Yasushi
Tushima, Hiromi
Ando, Hiroaki
Nonogaki, Tunemasa
机构
[1] Aichi Med Univ, Sch Med, Dept Pharmacol, Nagakute, Aichi 4801195, Japan
[2] Kinjo Gakuin Univ, Coll Pharm, Nagoya, Aichi 4638521, Japan
[3] Nagoya Univ, Sch Med, Dept Anesthesiol, Nagoya, Aichi 4668550, Japan
[4] Aichi Med Univ, Sch Med, Dept Internal Med, Div Gastroenterol, Aichi 4801195, Japan
关键词
guinea pig right atria; Langendorff hearts; positive inotropic effect; green tea catechin; NO release; intracellular Ca2+; pimobendan;
D O I
10.1016/j.ejphar.2006.09.017
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Each individual and pure catechin isolated from green tea was investigated as to its myocardial or blood pressure effects. The nitric oxide (NO) electrode and fluorometry were used to monitor changes in the NO and Ca2+ contents of the heart, together with simultaneous recordings of the left ventricular developed pressure. The low dose of (-)-epigallocatechin-3-gallate (EGCg: 10(-6), 10(-5) M) increased the left ventricular developed pressure with elevation of the transient fura-2 Ca2+ signal (T-Ca), but the high dose of EGCg (10(-4) M) produced a maximum left ventricular developed pressure with decreases in the basal level of T-Ca in a manner similar to the administration of the Ca-sensitizer pimobendan. However, the level of the transient NO signal (T-NO) increased dose-dependently without any increases in the width of T-NO. In the isolated right atria, the contractile force of (-)-gallocatechin-3-gallate (GCg) at 10(-8)-10(-4) M produced the highest pD(2) value, 6.7, in catechins (EGCg: 5.2, pimobendan: 5.1), but did not affect the heart rate. GCg, an artifact due to the epimerization of EGCg during the heating procedure, showed the most prolonged hypotensive effect in rabbits among the catechins. Each catechin (GCg or EGCg), like the NO donor, may have a therapeutic use as an NO-mediated vasorelaxant and may have an additional protective action in myocardial ischemia-reperfusion induced injury. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:123 / 130
页数:8
相关论文
共 31 条
[1]   Protective effects of FK409, a novel nitric oxide donor, against postischemic myocardial dysfunction in guinea-pig hearts [J].
Cao, YT ;
Hotta, Y ;
Shioi, K ;
Nagata, Y ;
Kawai, N ;
Ishikawa, N .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2001, 38 (04) :593-605
[2]   Endothelium-dependent vascular effects of Pycnogenol [J].
Fitzpatrick, DF ;
Bing, B ;
Rohdewald, P .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1998, 32 (04) :509-515
[3]   SENSITIZATION OF DOG AND GUINEA-PIG HEART MYOFILAMENTS TO CA2+ ACTIVATION AND THE INOTROPIC EFFECT OF PIMOBENDAN - COMPARISON WITH MILRINONE [J].
FUJINO, K ;
SPERELAKIS, N ;
SOLARO, RJ .
CIRCULATION RESEARCH, 1988, 63 (05) :911-922
[4]  
Goto K, 1999, J NUTR SCI VITAMINOL, V45, P135, DOI 10.3177/jnsv.45.135
[5]  
HARA S, 1990, TOXICOL LETT, V54, P271, DOI 10.1016/0378-4274(90)90194-Q
[6]   DIETARY ANTIOXIDANT FLAVONOIDS AND RISK OF CORONARY HEART-DISEASE - THE ZUTPHEN ELDERLY STUDY [J].
HERTOG, MGL ;
FESKENS, EJM ;
HOLLMAN, PCH ;
KATAN, MB ;
KROMHOUT, D .
LANCET, 1993, 342 (8878) :1007-1011
[7]  
HIRAI M, 2006, J PHARM SCI S1, V100
[8]   Protective effects of antioxidative serotonin derivatives isolated from safflower against postischemic myocardial dysfunction [J].
Hotta, Y ;
Nagatsu, A ;
Liu, W ;
Muto, T ;
Narumiya, C ;
Lu, XL ;
Yajima, M ;
Ishikawa, N ;
Miyazeki, K ;
Kawai, N ;
Mizukami, H ;
Sakakibara, J .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2002, 238 (1-2) :151-162
[9]   DIFFERENT EFFECTS OF ISOPROTERENOL AND DIHYDROOUABAIN ON CARDIAC CA2+ TRANSIENTS [J].
HOTTA, Y ;
ANDO, H ;
FUJITA, M ;
NAKAGAWA, J ;
TAKEYA, K ;
SAKAKIBARA, J .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1995, 282 (1-3) :121-130
[10]   Protective role of nitric oxide synthase against ischemia-reperfusion injury in guinea pig myocardial mitochondria [J].
Hotta, Y ;
Otsuka-Murakami, H ;
Fujita, M ;
Nakagawa, J ;
Yajima, M ;
Liu, W ;
Ishikawa, N ;
Kawai, N ;
Masumizu, T ;
Kohno, M .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1999, 380 (01) :37-48