INCREASE IN TONE AND INTRACELLULAR CA2+ IN RABBIT ISOLATED EAR ARTERY BY PLATELET-DERIVED GROWTH-FACTOR

被引:30
作者
HUGHES, AD
机构
[1] Department of Clinical Pharmacology, St. Mary's Hospital Medical School, Imperial College of Science Technology and Medicine, London, W2 1NY, South Wharf Road
关键词
PLATELET-DERIVED GROWTH FACTOR; VASCULAR SMOOTH MUSCLE; CALCIUM; TYROSINE KINASE;
D O I
10.1111/j.1476-5381.1995.tb14917.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 The effect of platelet-derived growth factor (PDGF-AB) on tone and intracellular Ca2+ ([Ca2+]) was examined in rabbit isolated ear arteries. Arteries were mounted in a myograph and loaded with the Ca2+-sensitive fluorescent indicator, fura-2, for concurrent measurements of isometric force and [Ca2+](i). 2 PDGF-AB contracted rabbit ear artery in a concentration-dependent manner. PDGF-AB induced tone was associated with a rise in [Ca2+](i). In the presence of noradrenaline, PDGF-AB induced a similar rise in [Ca2+]i but contraction in response to PDGF-AB in the presence of noradrenaline was increased compared with PDGF-AB alone. 3 PDGF-AB-induced rise in [Ca2+]i and tone were abolished by removal of extracellular Ca2+ (with addition of BAPTA, a Ca2+ chelator), and by preincubation with a dihydropyridine calcium channel blocker, (-)-202 791. Bistyrphostin, a selective inhibitor of tyrosine kinases, also inhibited PDGF-AB-induced tone, but had no effect on noradrenaline- or potassium-induced tone. 4 PDGF-AB contracts rabbit ear artery by increasing Ca2+ entry through voltage-operated calcium channels. This effect involves activation of a tyrosine kinase.
引用
收藏
页码:138 / 142
页数:5
相关论文
共 31 条
[1]   PLATELET-DERIVED GROWTH-FACTOR DOES NOT CONSTRICT RAT INTRACEREBRAL ARTERIOLES INVITRO [J].
BASSETT, JE ;
BOWENPOPE, DF ;
TAKAYASU, M ;
DACEY, RG .
MICROVASCULAR RESEARCH, 1988, 35 (03) :368-373
[2]   VASOACTIVE EFFECTS OF GROWTH-FACTORS [J].
BERK, BC ;
ALEXANDER, RW .
BIOCHEMICAL PHARMACOLOGY, 1989, 38 (02) :219-225
[3]   VASOCONSTRICTION - A NEW ACTIVITY FOR PLATELET-DERIVED GROWTH-FACTOR [J].
BERK, BC ;
ALEXANDER, RW ;
BROCK, TA ;
GIMBRONE, MA ;
WEBB, RC .
SCIENCE, 1986, 232 (4746) :87-90
[4]   TYRPHOSTINS INHIBIT PDGF-INDUCED DNA-SYNTHESIS AND ASSOCIATED EARLY EVENTS IN SMOOTH-MUSCLE CELLS [J].
BILDER, GE ;
KRAWIEC, JA ;
MCVETY, K ;
GAZIT, A ;
GILON, C ;
LYALL, R ;
ZILBERSTEIN, A ;
LEVITZKI, A ;
PERRONE, MH ;
SCHREIBER, AB .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 260 (04) :C721-C730
[5]  
BOBIK A, 1993, PHARMACOL REV, V45, P1
[6]   REGULATION OF CA2+ TRANSPORT BY PLATELET-DERIVED GROWTH FACTOR-BB IN RAT VASCULAR SMOOTH-MUSCLE CELLS [J].
CIRILLO, M ;
QUINN, SJ ;
ROMERO, JR ;
CANESSA, ML .
CIRCULATION RESEARCH, 1993, 72 (04) :847-856
[7]   TYROSINE KINASE INHIBITORS SUPPRESS AGONIST-INDUCED CONTRACTION IN SMOOTH-MUSCLE [J].
DISALVO, J ;
STEUSLOFF, A ;
SEMENCHUK, L ;
SATOH, S ;
KOLQUIST, K ;
PFITZER, G .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 190 (03) :968-974
[8]   TYRPHOSTINS .1. SYNTHESIS AND BIOLOGICAL-ACTIVITY OF PROTEIN TYROSINE KINASE INHIBITORS [J].
GAZIT, A ;
YAISH, P ;
GILON, C ;
LEVITZKI, A .
JOURNAL OF MEDICINAL CHEMISTRY, 1989, 32 (10) :2344-2352
[9]  
GRYNKIEWICZ G, 1985, J BIOL CHEM, V260, P3440
[10]  
HART CE, 1985, SCIENCE, V240, P1529