EVIDENCE THAT ANGIOTENSIN-II ENHANCES NORADRENALINE RELEASE FROM SYMPATHETIC-NERVES IN MOUSE ATRIA BY ACTIVATING PROTEIN-KINASE-C

被引:29
作者
MUSGRAVE, IF [1 ]
FOUCART, S [1 ]
MAJEWSKI, H [1 ]
机构
[1] UNIV MELBOURNE,DEPT PHARMACOL,PARKVILLE,VIC 3052,AUSTRALIA
来源
JOURNAL OF AUTONOMIC PHARMACOLOGY | 1991年 / 11卷 / 04期
关键词
D O I
10.1111/j.1474-8673.1991.tb00319.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
1 Mouse atria were incubated with [H-3]-noradrenaline and the outflow of radioactivity induced by electrical field stimulation (5 Hz, 60 s) was used as an index of noradrenaline release. Angiotensin II (1 x 10(-8) M) significantly enhanced the stimulation-induced (S-I) outflow of radioactivity. 2 Phorbol 12-myristate 13-acetate (0.001-1.0 x 10(-6) M) and phorbol 12, 13-dibutyrate (0.001-1.0 X 10(-6) M), protein kinase C activating phorbol esters, significantly enhanced the S-I outflow of radioactivity. Phorbol dibutyrate produced a greater maximal enhancement of S-I outflow of radioactivity than phorbol myristate acetate. The enhancement of S-I outflow of radioactivity produced by the combination of phorbol dibutyrate (1.0 x 10(-7) M) and phorbol myristate acetate (1.0 x 10(-7) M) was no greater than that produced by phorbol dibutyrate (1.0 x 10(-7) M) alone. The enhancement of S-I outflow of radioactivity produced by phorbol myristate acetate (1.0 x 10(-7) M) was constant whether the tissue was exposed for 15, 45 or 75 min. 3 When angiotensin II (1.0 x 10(-8) M) was present with the maximally effective concentration of phorbol dibutyrate (1.0 x 10(-7) M) it did not increase S-I outflow of radioactivity. 8-bromo-cyclic AMP (9.0 x 10(-5) M) by itself increased the S-I outflow of radioactivity and in the presence of the maximally effective concentration of phorbol dibutyrate the enhancement of S-I outflow of radioactivity produced by 8-bromo-cyclic AMP was maintained. 4 A protein kinase inhibitor, K-252a (1.0 x 10(-6) M), did not affect S-I outflow of radioactivity. K-252a significantly reduced the enhancement of S-I outflow of radioactivity produced by both phorbol myristate acetate (0.03 or 0. 1 x 10(-6) M) and phorbol dibutyrate (0.01 or 1.0 x 10(-6) M). 5 K-252a (1.0 x 10(-6) M) blocked the enhancement of S-I outflow of radioactivity produced by angiotensin II (1.0 x 10(-8) M) and tetraethylammonium (1.0 X 10(-4) M). 6 These results suggest that angiotensin II receptors may enhance noradrenaline release through the pool of protein kinase C that is activated by phorbol dibutyrate.
引用
收藏
页码:211 / 220
页数:10
相关论文
共 39 条
[1]  
ARMSTRONG CM, 1965, J GEN PHYSIOL, V48, P858
[2]  
ATCHISON WD, 1988, J PHARMACOL EXP THER, V245, P394
[3]   EFFECT OF PHORBOL ESTERS ON NORADRENALINE RELEASE FROM CEREBRAL-ARTERIES [J].
BALFAGON, G ;
DESAGARRA, MR ;
BARRUS, MT ;
ARRIVAS, S ;
CAPILLA, MI ;
MARIN, J .
BRAIN RESEARCH, 1989, 477 (1-2) :196-201
[4]   TEMPORAL PATTERNS OF PROTEIN-PHOSPHORYLATION AFTER ANGIOTENSIN-II, A23187 AND OR 12-O-TETRADECANOYLPHORBOL 13-ACETATE IN ADRENAL GLOMERULOSA CELLS [J].
BARRETT, PQ ;
KOJIMA, I ;
KOJIMA, K ;
ZAWALICH, K ;
ISALES, CM ;
RASMUSSEN, H .
BIOCHEMICAL JOURNAL, 1986, 238 (03) :893-903
[5]  
BERRIDGE MJ, 1987, ANNU REV BIOCHEM, V56, P159, DOI 10.1146/annurev.bi.56.070187.001111
[6]   INVITRO STUDIES ON THE MODE OF ACTION OF THE PHORBOL ESTERS, POTENT TUMOR PROMOTERS .1. [J].
BLUMBERG, PM .
CRC CRITICAL REVIEWS IN TOXICOLOGY, 1980, 8 (02) :153-197
[7]   2ND MESSENGERS ASSOCIATED WITH THE ACTION OF AII AND DOPAMINE-D2 RECEPTORS IN ANTERIOR-PITUITARY - RELATIONSHIP WITH PROLACTIN SECRETION [J].
BOCKAERT, J ;
JOURNOT, L ;
ENJALBERT, A .
JOURNAL OF RECEPTOR RESEARCH, 1988, 8 (1-4) :225-243
[8]  
CASTAGNA M, 1982, J BIOL CHEM, V257, P7847
[9]   PHORBOL ESTER INCREASES CALCIUM CURRENT AND SIMULATES THE EFFECTS OF ANGIOTENSIN-II ON CULTURED NEONATAL RAT-HEART MYOCYTES [J].
DOSEMECI, A ;
DHALLAN, RS ;
COHEN, NM ;
LEDERER, WJ ;
ROGERS, TB .
CIRCULATION RESEARCH, 1988, 62 (02) :347-357
[10]   RECEPTOR ACTIVATION AND INOSITOL LIPID HYDROLYSIS IN NEURAL TISSUES [J].
FISHER, SK ;
AGRANOFF, BW .
JOURNAL OF NEUROCHEMISTRY, 1987, 48 (04) :999-1017