首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Bradykinin-stimulated phosphoinositide metabolism in cultured canine tracheal smooth muscle cells.
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Bradykinin-stimulated phosphoinositide metabolism in cultured canine tracheal smooth muscle cells.

机译:缓激肽刺激的犬气管平滑肌细胞中的磷酸肌醇代谢。

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摘要

1. Stimulation of bradykinin (BK) receptors coupled to phosphoinositide (PI) hydrolysis was investigated in canine cultured tracheal smooth muscle cells (TSMCs). BK, kallidin, and des-Arg9-BK, stimulated [3H]-inositol phosphates (IPs) accumulation in a dose-dependent manner with half-maximal responses (EC50) at 20 +/- 5, 13 +/- 4, and 2.3 +/- 0.7 nM, (n = 5), respectively. 2. D-Arg[Hyp3, D-Phe7]-BK and D-Arg[Hyp3, Thi5,8, D-Phe7]-BK, B2 receptor antagonists, were equipotent in blocking the BK-induced IPs accumulation with pKB = 7.1 and 7.3, respectively. 3. Short-term exposure of TSMCs to phorbol 12-myristate 13-acetate (PMA, 1 microM) attenuated BK-stimulated IPs accumulation. The concentrations of PMA that gave half-maximal and maximal inhibition of BK-induced IPs accumulation were 15 +/- 4 nM and 1 microM, n = 3, respectively. The inhibitory effect of PMA on BK-induced response was reversed by staurosporine, a protein kinase C (PKC) inhibitor, suggesting that the inhibitory effect of PMA was mediated through the activation of PKC. 4. Prolonged incubation of TSMCs with PMA for 24 h, resulted in a recovery of receptor responsiveness which may be due to down-regulation of PKC. The inactive phorbol ester, 4 alpha-phorbol 12, 13-didecanoate at 1 microM, did not inhibit this response. 5. The site of this inhibition was further investigated by examining the effect of PMA on AlF(4-)-induced IPs accumulation in canine TSMCs. AlF(4-)-stimulated IPs accumulation was inhibited by PMA treatment, suggesting that the G protein(s) can be directly activated by AlF4-, which is uncoupled from phospholipase C by PMA treatment. 6. Incubation of TSMCs in the absence of external Ca2+ or upon removal of Ca2+ by addition of EGTA, caused a decrease in IPs accumulation without changing the basal levels. Addition of Ca2+ (3-620 nM) to digitonin-permeabilized TSMCs stimulated IPs accumulation was obtained by inclusion of either guanosine 5'-O-(3-thiotriphosphate) (GTP gamma S) or BK.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.在犬培养的气管平滑肌细胞(TSMC)中研究了缓激肽(BK)受体与磷酸肌醇(PI)水解反应的刺激作用。 BK,kallidin和des-Arg9-BK以剂量依赖的方式刺激了[3H]-肌醇磷酸(IPs)积累,在20 +/- 5、13 +/- 4和20时有半数最大响应(EC50)。分别为2.3 +/- 0.7 nM(n = 5)。 2. D-Arg [Hyp3,D-Phe7] -BK和D-Arg [Hyp3,Thi5,8,D-Phe7] -BK,B2受体拮抗剂在阻断BK诱导的IP积累方面具有等价性,pKB = 7.1和7.3。 3.台积电短期暴露于佛波醇12-肉豆蔻酸酯13-醋酸酯(PMA,1 microM)会减弱BK刺激的IP积累。对BK诱导的IP积累产生半数最大和最大抑制作用的PMA浓度分别为15 +/- 4 nM和1 microM,n = 3。 staurosporine是一种蛋白激酶C(PKC)抑制剂,可以逆转PMA对BK诱导的应答的抑制作用,这表明PMA的抑制作用是通过PKC的激活介导的。 4. TSMC与PMA长时间孵育24小时,导致受体反应性恢复,这可能是由于PKC的下调所致。灭活的佛波酯,4 alpha-phorbol 12、13-十二烷酸酯在1 microM时不抑制此响应。 5.通过检查PMA对AlF(4-)诱导的犬TSMC中IP积累的影响,进一步研究了这种抑制作用的位点。 AlF(4-)刺激的IP积累受到PMA处理的抑制,表明G蛋白可以直接被AlF4-激活,而AlF4-可以通过PMA处理与磷脂酶C脱钩。 6.在不存在外部Ca2 +的情况下或通过添加EGTA去除Ca2 +后,TSMC的孵化会导致IP积累减少,而不会改变基础水平。通过加入鸟苷5'-O-(3-硫代三磷酸)(GTPγS)或BK来将钙离子(3-620 nM)添加到经洋地黄素渗透的TSMC刺激的IP积累中(在250字时截短)

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