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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >CGRP inhibits norepinephrine induced apoptosis with restoration of Bcl-2/Bax in cultured cardiomyocytes of rat
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CGRP inhibits norepinephrine induced apoptosis with restoration of Bcl-2/Bax in cultured cardiomyocytes of rat

机译:CGRP抑制去甲肾上腺素诱导的细胞凋亡,并在大鼠培养的心肌细胞中恢复Bcl-2 / Bax

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Calcitonin gene related peptide (CGRP) and norepinephrine (NE) may interact in acute myocardial ischemia, protecting cardiomyocytes but the underlying mechanism is unclear. Here we investigated the correlation of the anti-apoptotic effect of CGRP with the change of Bcl-2/Bax. Cultured cardiomyocytes were divided into four groups: (1) control group (no treatment with any test agent), (2) NE group (treated with 10-5mol/L of NE), (3) CGRP+NE group (treated with 10-8mol/L of CGRP and NE at 10-5mol/L) and (4) CGRP8-37+CGRP+NE group (treated with 10-7mol/L of CGRP8-37, a specific antagonist of CGRP receptor, CGRP at 10-8mol/L and NE at 10-5mol/L). Apoptosis ratio was analyzed by flow cytometry. Bcl-2 and Bax and the coding mRNA were examined. It was found that the apoptosis ratio in NE group (29.4±1.8%) was significantly greater (P0.05) than that of the control group (10.1±1.7%). The effect of NE was attenuated by CGRP (18.7±2.1%), which was reversed by CGRP8-37 (24.9±2.9%). NE treatment resulted in reductions in the ratio of Bcl-2/Bax (by 33%) and their mRNA (by 53%). CGRP restored the level of Bcl-2/Bax, which was abolished by CGRP8-37. Current study suggests that norepinephrine inhibits synthesis of Bcl-2 and increases Bax and apoptosis of cardiomyocytes. CGRP restores the ratio of Bcl-2/Bax and attenuates the apoptosis induced by NE, via specific CGRP receptor.
机译:降钙素基因相关肽(CGRP)和去甲肾上腺素(NE)可能在急性心肌缺血中相互作用,保护心肌细胞,但其潜在机制尚不清楚。在这里,我们研究了CGRP的抗凋亡作用与Bcl-2 / Bax变化的相关性。培养的心肌细胞分为四组:(1)对照组(不使用任何测试剂治疗),(2)NE组(用10-5mol / L NE治疗),(3)CGRP + NE组(用10mg / L治疗) -8mol / L CGRP和NE在10-5mol / L时)和(4)CGRP8-37 + CGRP + NE组(用10-7mol / L CGRP受体特异性拮抗剂CGRP在10-10mol / L处理-8mol / L,NE为10-5mol / L)。通过流式细胞术分析细胞凋亡率。检查了Bcl-2和Bax以及编码的mRNA。发现NE组的细胞凋亡率(29.4±1.8%)显着大于对照组(10.1±1.7%)(P <0.05)。 CGRP(18.7±2.1%)减弱了NE的作用,而CGRP8-37(24.9±2.9%)则逆转了NE的作用。 NE治疗导致Bcl-2 / Bax的比例(降低了33%)及其mRNA的比例(降低了53%)。 CGRP恢复了Bcl-2 / Bax的水平,而CGRP8-37取消了该水平。当前的研究表明去甲肾上腺素抑制Bcl-2的合成并增加Bax和心肌细胞的凋亡。 CGRP通过特定的CGRP受体恢复Bcl-2 / Bax的比例,并减弱NE诱导的凋亡。

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