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环匹阿尼酸和地塞米松对血清素诱导的血管平滑肌细胞钙反应的影响。

Effects of cyclopiazonic acid and dexamethasone on serotonin-induced calcium responses in vascular smooth muscle cells.

作者信息

Selli Cigdem, Tosun Metiner

机构信息

Department of Pharmacology, Faculty of Pharmacy, Ege University, 35040, Izmir, Turkey.

Applied Bioinformatics of Cancer, Edinburgh Cancer Research Centre, Institute of Genetics and Molecular Medicine, Edinburgh, EH4 2XU, UK.

出版信息

J Physiol Biochem. 2016 Jun;72(2):245-53. doi: 10.1007/s13105-016-0474-8. Epub 2016 Mar 4.

Abstract

We previously observed that sarcoendoplasmic reticulum Ca(2+) ATPase (SERCA) blockade by cyclopiazonic acid (CPA) significantly potentiates serotonin (5-hydroxytryptamine (5-HT))-induced vascular contractions. Furthermore, 5-HT receptor antagonist methysergide partially inhibited CPA-potentiated 5-HT contractions. In the present study, we further investigated whether SERCA inhibition potentiates 5-HT-induced Ca(2+) responses along with attenuating the receptor antagonism by store-operated Ca(2+) (SOC) entry and protein kinase C (PKC)-mediated mechanisms. The effects of dexamethasone that was previously shown to induce SOC entry and enhance 5-HT responses were also tested. For this purpose, intracellular Ca(2+) levels were monitored in A7r5 embryonic rat vascular smooth muscle cells by spectrofluorometry using the fluorescent indicator fura-2. The results showed that CPA, although not dexamethasone, significantly potentiated 5-HT-induced Ca(2+) elevations. Ketanserin partially decreased 5-HT-induced and CPA-potentiated Ca(2+) elevations whereas both PKC inhibitor D-sphingosine and SOC entry blocker 2-aminoethoxydiphenyl borate (2-APB) abolished the remaining responses. The data suggests that diminished antagonistic effect on 5-HT-induced Ca(2+) elevations in the presence of SERCA inhibition is induced by SOC entry and PKC activation.

摘要

我们之前观察到,环匹阿尼酸(CPA)对肌浆网Ca(2+) ATP酶(SERCA)的阻断作用显著增强了血清素(5-羟色胺(5-HT))诱导的血管收缩。此外,5-HT受体拮抗剂麦角新碱部分抑制了CPA增强的5-HT收缩作用。在本研究中,我们进一步探究了SERCA抑制作用是否通过储存式Ca(2+)(SOC)内流和蛋白激酶C(PKC)介导的机制增强5-HT诱导的Ca(2+)反应,同时减弱受体拮抗作用。我们还测试了先前显示可诱导SOC内流并增强5-HT反应的地塞米松的作用。为此,使用荧光指示剂fura-2通过荧光分光光度法监测A7r5胚胎大鼠血管平滑肌细胞内的Ca(2+)水平。结果显示,CPA而非地塞米松显著增强了5-HT诱导的Ca(2+)升高。酮色林部分降低了5-HT诱导的和CPA增强的Ca(2+)升高,而PKC抑制剂D-鞘氨醇和SOC内流阻断剂2-氨基乙氧基二苯硼酸盐(2-APB)消除了其余反应。数据表明,在存在SERCA抑制的情况下,对5-HT诱导的Ca(2+)升高的拮抗作用减弱是由SOC内流和PKC激活引起的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9f1/4873523/d1d5666147bb/13105_2016_474_Fig1_HTML.jpg

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