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首页> 外文期刊>The biochemical journal >The effects of elevated cyclic AMP levels on histamine-H1-receptor-stimulated inositol phospholipid hydrolysis and calcium mobilization in the smooth-muscle cell line DDT1MF-2
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The effects of elevated cyclic AMP levels on histamine-H1-receptor-stimulated inositol phospholipid hydrolysis and calcium mobilization in the smooth-muscle cell line DDT1MF-2

机译:循环AMP水平升高对平滑肌细胞系DDT1MF-2中组胺-H1-受体刺激的肌醇磷脂水解和钙动员的影响

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pThe effects of raising cyclic AMP levels, by forskolin stimulation, beta-adrenoceptor activation or cyclic AMP phosphodiesterase inhibition, on inositol phospholipid hydrolysis and increases in intracellular free [Ca2+] ([Ca2+]i) elicited by a range of agonists have been investigated in the hamster vas deferens smooth-muscle cell line DDT1MF-2. Isoprenaline (log [EC50 (M)] = -7.7 +/- 0.2), forskolin and the type IV cyclic AMP phosphodiesterase inhibitor rolipram elicited significant increases in the accumulation of cyclic [3H]AMP. Pretreatment with forskolin (10 microM) attenuated histamine (100 microM)- and N6-cyclopentyladenosine (CPA; 300 nM)-induced release of intracellular Ca2+, observed when cells are stimulated in Ca(2+)-free buffer containing 0.1 mM EGTA. Forskolin had no effect on ATP (100 microM)- or bradykinin (1 microM)-stimulated release of intracellular Ca2+. Histamine-induced intracellular Ca2+ release was also inhibited by pretreatment with rolipram (100 microM) or the membrane-permeant cyclic AMP analogue (Sp)-adenosine 3′,5′-monophosphothioate (100 microM). Isoprenaline (1 microM) pretreatment (in the presence of 10 microM rolipram, a concentration which on its own did not decrease the histamine response) attenuated histamine-induced intracellular Ca2+ release. Forskolin inhibited histamine (100 microM)- and CPA (100 nM) stimulated accumulation of [3H]-inositol phosphates, but was without effect on ATP or bradykinin responses. Addition of forskolin (in the presence of 100 microM rolipram) after the cells had been stimulated with histamine (in experiments initiated in Ca(2+)-free buffer) inhibited the rise in [Ca2+]i observed when extracellular Ca2+ (2 mM) was re-applied (owing to receptor-mediated Ca2+ influx). Finally, the refilling of intracellular Ca2+ stores (after receptor-mediated Ca2+ influx is blocked by mepyramine) can be demonstrated in the presence of raised cyclic AMP levels./p
机译:>通过福司柯林刺激,β-肾上腺素受体激活或环状AMP磷酸二酯酶抑制而提高环状AMP水平对肌醇磷脂水解和一系列激动剂引起的细胞内游离[Ca2 +]([Ca2 +] i)增加的影响如下:在仓鼠输精管平滑肌细胞系DDT1MF-2中进行了研究。异丙肾上腺素(log [EC50(M)] = -7.7 +/- 0.2),福司可林和IV型环状AMP磷酸二酯酶抑制剂咯利普兰引起环状[3H] AMP积累的显着增加。用Forskolin(10 microM)减毒的组胺(100 microM)和N6-环戊基腺苷(CPA; 300 nM)预处理诱导的细胞内Ca2 +释放,在含有0.1 mM EGTA的无Ca(2+)缓冲液中刺激细胞时观察到。 Forskolin对ATP(100 microM)或缓激肽(1 microM)刺激的细胞内Ca2 +释放没有影响。组胺诱导的细胞内Ca2 +释放也受到咯利普兰(100 microM)或膜渗透性环AMP类似物(Sp)-腺苷3',5'-单硫代磷酸酯(100 microM)的预处理的抑制。异丙肾上腺素(1 microM)预处理(在存在10 microM咯利普兰的情况下,其浓度本身不会降低组胺反应)减弱了组胺诱导的细胞内Ca2 +释放。 Forskolin抑制了组胺(100 microM)-和CPA(100 nM)刺激了[3H]-肌醇磷酸的积累,但对ATP或缓激肽的反应没有影响。在用组胺刺激细胞后(在无Ca(2+)缓冲液中启动的实验中),加入毛喉素(在100 microM咯利普兰的存在下)抑制了当细胞外Ca2 +(2 mM)时观察到的[Ca2 +] i的升高。重新应用(由于受体介导的Ca2 +涌入)。最后,在环AMP水平升高的情况下,可以证明细胞内Ca 2+储存的补充(在受体介导的Ca 2+流入被美吡拉明阻断后)。

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