Bradykinin elevates cytosolic Ca2+ concentration in smooth muscle cells isolated from rat duodenum

被引:0
作者
Wassdal, I [1 ]
Larsen, K [1 ]
Iversen, JG [1 ]
机构
[1] Univ Oslo, Inst Basic Med Sci, Dept Physiol, N-0317 Oslo, Norway
来源
ACTA PHYSIOLOGICA SCANDINAVICA | 1999年 / 165卷 / 03期
关键词
bradykinin; isolated smooth muscle cells; kinin; lantan phospholipase C; second messenger;
D O I
暂无
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The effect of bradykinin on the cytosolic Ca2+ concentration were measured in single, Fura-2 loaded, smooth muscle cells isolated from rat duodenum. Ail cells responded with a Ca2+ signal when exposed to bradykinin. The bradykinin response consisted of an initial Ca2+ spike followed by a plateau. Pre-treatment of single muscle cells with either the phospholipase C blocker U-73122 or thapsigargin, which is a potent inhibitor of the endoplasmic reticulum Ca2+-ATPase, inhibited the response to bradykinin. Pre-treatment of the cells with EGTA or La3+ to inhibit the Ca2+ influx, abolished the response induced by bradykinin. We conclude that bradykinin applied to single smooth muscle cells from rat duodenum, increases cytosolic Ca2+ by emptying intracellular Ca2+ stores, and by contribution from extracellular Ca2+. In contrast to bradykinin-induced response in isolated rat duodenum (a relaxation followed by a contraction), we did not observe a biphasic effect of bradykinin on cytosolic Ca2+ in single muscle cells. Bradykinin may thus cause relaxation of duodenal smooth muscle indirectly through an effect on neighbouring cells as dilatation is brought about by this agent in blood vessels.
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页码:259 / 264
页数:6
相关论文
共 18 条
[1]   RELAXING EFFECT OF BRADYKININ ON INTESTINAL SMOOTH MUSCLE [J].
ANTONIO, A .
BRITISH JOURNAL OF PHARMACOLOGY, 1968, 32 (01) :78-+
[2]   5-hydroxytryptamine, angiotensin and bradykinin transiently increase intracellular calcium concentrations and PKC-alpha activity, but do not induce mitogenesis in human vascular smooth muscle cells [J].
Assender, JW ;
Irenius, E ;
Fredholm, BB .
ACTA PHYSIOLOGICA SCANDINAVICA, 1997, 160 (03) :207-217
[3]   BRADYKININ-INDUCED MESENTERIC VASODILATION IS MEDIATED BY B2-SUBTYPE RECEPTORS AND NITRIC-OXIDE [J].
BERGUER, R ;
HOTTENSTEIN, OD ;
PALEN, TE ;
STEWART, JM ;
JACOBSON, ED .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (03) :G492-G496
[4]  
BLEASDALE JE, 1990, J PHARMACOL EXP THER, V255, P756
[5]   Mechanism of contraction induced by bradykinin in the rabbit saphenous vein [J].
Eguchi, D ;
Nishimura, J ;
Kobayashi, S ;
Komori, K ;
Sugimachi, K ;
Kanaide, H .
BRITISH JOURNAL OF PHARMACOLOGY, 1997, 120 (03) :371-378
[6]  
FABER DB, 1973, ARCH INT PHARMACOD T, V205, P226
[7]  
FARMER SG, 1992, ANNU REV PHARMACOL, V32, P511
[8]  
GRYNKIEWICZ G, 1985, J BIOL CHEM, V260, P3440
[9]   HUMAN URINARY KININ EXCRETION [J].
HORTON, EW .
BRITISH JOURNAL OF PHARMACOLOGY AND CHEMOTHERAPY, 1959, 14 (01) :125-132
[10]   EFFECTS OF MECH, THAPSIGARGIN, AND LA-3+ ON PLASMALEMMAL AND INTRACELLULAR CA-2+ TRANSPORT IN LACRIMAL ACINAR-CELLS [J].
KWAN, CY ;
TAKEMURA, H ;
OBIE, JF ;
THASTRUP, O ;
PUTNEY, JW .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 258 (06) :C1006-C1015