首页> 外文期刊>European Journal of Pharmacology: An International Journal >Presynaptic BK type Ca(2+)-activated K(+) channels are involved in prostanoid TP receptor-mediated inhibition of noradrenaline release from the rat gastric sympathetic nerves.
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Presynaptic BK type Ca(2+)-activated K(+) channels are involved in prostanoid TP receptor-mediated inhibition of noradrenaline release from the rat gastric sympathetic nerves.

机译:突触前BK型Ca(2+)激活K(+)通道参与类前列腺素TP受体介导的去甲肾上腺素从大鼠胃交感神经释放的抑制作用。

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摘要

Previously, we reported that prostanoid TP receptor mediates the inhibition of electrically evoked noradrenaline release from gastric sympathetic nerves in rats. Prostanoid TP receptor has been shown to activate phospholipase C (PLC), which catalyzes the hydrolysis of phosphatidylinositol 4,5-bisphosphate to inositol 1,4,5-triphosphate (IP(3)) and diacylglycerol; IP(3) triggers the release of Ca(2+) from intracellular stores and diacylglycerol activates protein kinase C. In the present study, therefore, we examined whether these PLC-mediated mechanisms are involved in the TP receptor-mediated inhibition of gastric noradrenaline release using an isolated, vascularly perfused rat stomach. U-46619 (9,11-dideoxy-9alpha,11alpha-methanoepoxy PGF(2alpha)) (a prostanoid TP receptor agonist)-induced inhibition of noradrenaline release from the stomach was reduced by U-73122 [1-[6-[[(17beta)-3-methoxyestra-1,3,5(10)-trien-17-yl]-amino]hexyl]-1H-pyrrole-2, 5-dine] (a PLC inhibitor) and ET-18-OCH(3) (1-O-octadecyl-2-O-methyl-sn-glycero-3-phosphorylcholine) (a phosphatidylinositol-specific PLC inhibitor), respectively. 2-APB (2-aminoethyldiphenyl borate) (a putative IP(3) receptor antagonist) also abolished the U-46619-induced inhibition of noradrenaline release, but Ro 31-8220 [2-{1-[3-(amidinothio)propyl]-1H-indol-3-yl}-3-(1-methylindol-3-yl)-maleimide] (a protein kinase C inhibitor) had no effect. Furthermore, a small dose of tetraethylammonium and charybdotoxin [blockers of BK type Ca(2+)-activated K(+) channel] abolished the U-46619-induced inhibition, but apamin (a blocker of SK-type Ca(2+)-activated K(+) channel) had no effect. These results suggest that BK type Ca(2+)-activated K(+) channels are involved in prostanoid TP receptor-mediated inhibition of electrically evoked noradrenaline release from the gastric sympathetic nerve terminals in rats.
机译:以前,我们报道前列腺素TP受体介导抑制大鼠胃交感神经中电诱发的去甲肾上腺素释放。前列腺素TP受体可激活磷脂酶C(PLC),该酶催化磷脂酰肌醇4,5-双磷酸酯水解为肌醇1,4,5-三磷酸酯(IP(3))和二酰基甘油; IP(3)触发细胞内存储释放Ca(2+)和二酰基甘油激活蛋白激酶C。因此,在本研究中,我们检查了这些PLC介导的机制是否参与TP受体介导的胃去甲肾上腺素的抑制作用使用隔离的血管灌注大鼠胃释放。由U-73122降低了U-46619(9,11-双脱氧9alpha,11alpha-甲基环氧PGF(2alpha)(前列腺素TP受体激动剂)-诱导的去甲肾上腺素从胃释放的抑制作用[1- [6-[[ (17beta)-3-methoxyestra-1,3,5(10)-trien-17-yl]-氨基]己基] -1H-吡咯-2,5-dine](PLC抑制剂)和ET-18-OCH (3)分别是(1-O-十八烷基-2-O-甲基-sn-甘油-3-磷酸胆碱)(磷脂酰肌醇特异性PLC抑制剂)。 2-APB(2-氨基乙基二苯基硼酸酯)(一种推定的IP(3)受体拮抗剂)也废除了U-46619诱导的去甲肾上腺素释放抑制,但Ro 31-8220 [2- {1- [3-([硫代)丙基] Ro ] -1H-吲哚-3-基} -3-(1-甲基吲哚-3-基)-马来酰亚胺](蛋白激酶C抑制剂)没有作用。此外,小剂量的四乙铵和Charybdoxin [BK型Ca(2+)激活的K(+)通道的阻滞剂]取消了U-46619诱导的抑制作用,但取消了apamin(SK型Ca(2+)的阻滞剂)的抑制作用。激活的K(+)通道)无效。这些结果表明,BK型Ca(2+)激活的K(+)通道参与了前列腺素TP受体介导的大鼠胃交感神经末梢电诱发的去甲肾上腺素释放的抑制作用。

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