Vasodilating and hypotensive effects of fangchinoline and tetrandrine on the rat aorta and the stroke-prone spontaneously hypertensive rat

被引:60
作者
Kim, HS [1 ]
Zhang, YH [1 ]
Oh, KW [1 ]
Ahn, HY [1 ]
机构
[1] CHUNGBUK NATL UNIV,COLL MED,DEPT PHARMACOL,CHONJU 360763,CHUNGBUK,SOUTH KOREA
关键词
tetrandrine; fangchinoline; vasodilation; calcium channel blockers; antihypertensive activity; stroke-prone spontaneously hypertensive rats (SHRSP);
D O I
10.1016/S0378-8741(97)00092-5
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Comparative studies of the effects of tetrandrine (TET) and fangchinoline (FAN), two major components of the Radix of Stephannia tetrandrae, on vasodilations and on calcium movement in vascular smooth muscle, and studies of hypotensive effects on stroke-prone spontaneously hypertensive rats (SHRSP) were performed in the following experiments. TET and FAN inhibited high K+ (65.4 mM) and induced sustained contraction in the rat aorta smooth muscle strips. IC50 values for TET and FAN were 0.27 +/- 0.05 mu M (n = 6) and 9.53 +/- 1.57 mu M (n = 6), respectively, and this inhibition was antagonized by increasing the Ca2+ concentration in the medium. The IC50 of TET for norepinephrine (NE)-induced contraction (0.86 +/- 0.04 g) was 3.08 +/- 0.05 mu M (n = 4), and the IC50 of FAN for NE-induced contraction (0.88 +/- 0.07 g) was 14.20 +/- 0.40 mu M (n = 4). At the molecular level, radiolabelled Ca-45(2+) uptake tests revealed that TET and FAN also inhibited high K+ (65.4 mM) and 1 mu M NE-stimulated Ca2+ influx in rat aorta strips at the maximal concentration was needed to inhibit the contraction. TET (3 mg/kg) and FAN (30 mg/kg) administered by intravenous (i.v.) bolus injection also lowered the mean arterial pressure (MAP) significantly during the period of observation in conscious SHRSP, respectively. These results showed that TET was more potent than FAN in blocking calcium channels and antihypertensive activity. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:117 / 123
页数:7
相关论文
共 22 条
[1]  
Editorial Committee, 1985, PHARMACOPOEIA P R CH, V1, P121
[2]   BIS(BENZYLISOQUINOLINE) ANALOGS OF TETRANDRINE BLOCK L-TYPE CALCIUM CHANNELS - EVIDENCE FOR INTERACTION AT THE DILTIAZEM-BINDING SITE [J].
FELIX, JP ;
KING, VF ;
SHEVELL, JL ;
GARCIA, ML ;
KACZOROWSKI, GJ ;
BICK, IRC ;
SLAUGHTER, RS .
BIOCHEMISTRY, 1992, 31 (47) :11793-11800
[3]   A LIGHT STABILIZER (TINUVIN-770) THAT ELUTES FROM POLYPROPYLENE PLASTIC TUBES IS A POTENT L-TYPE CA2+-CHANNEL BLOCKER [J].
GLOSSMANN, H ;
HERING, S ;
SAVCHENKO, A ;
BERGER, W ;
FRIEDRICH, K ;
GARCIA, ML ;
GOETZ, MA ;
LIESCH, JM ;
ZINK, DL ;
KACZOROWSKI, GJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (20) :9523-9527
[4]  
HU XM, 1994, COMPLETE WORKS SECRE, V1
[5]  
Jiangsu College of New Medicine, 1975, ENC MAT MED, V1, P981
[6]  
KANG J, 1993, CHIN J TUBERC RESP D, V16, P93
[7]  
KARAKI H, 1979, J PHARMACOL EXP THER, V211, P86
[8]   STRUCTURE AND HYPOTENSIVE ACTIVITY RELATIONSHIPS OF TETRANDRINE DERIVATIVES IN STROKE-PRONE SPONTANEOUSLY HYPERTENSIVE RATS [J].
KAWASHIMA, K ;
HAYAKAWA, T ;
MIWA, Y ;
OOHATA, H ;
SUZUKI, T ;
FUJIMOTO, K ;
OGINO, T ;
CHEN, ZX .
GENERAL PHARMACOLOGY-THE VASCULAR SYSTEM, 1990, 21 (03) :343-347
[9]  
KING VF, 1988, J BIOL CHEM, V263, P2238
[10]  
KWAN CY, 1992, ACTA PHARM SINIC, V13, P385