Effect of lycopene on H9c2 cell apoptosis induced by angiotensin II

细胞凋亡 免疫印迹 标记法 刺激 活力测定 化学 分子生物学 污渍 半胱氨酸蛋白酶3 细胞 男科 内分泌学 程序性细胞死亡 生物 生物化学 医学 基因
作者
Zhefu Hu,Qi‐Zhu Tang,Yuan Liu,Li Jin
出处
期刊:Chinese Journal of Geriatrics 卷期号:34 (5): 553-556
标识
DOI:10.3760/cma.j.issn.0254-9026.2015.05.026
摘要

Objective To investigate the effect of lycopene (Lyc) on H9c2 cell apoptosis induced by angiotensin Ⅱ (Ang Ⅱ). Methods Using Ang Ⅱ (10 μmol/L) to stimulate H9c2 cells, we observed the protective effect of Lyc on H9c2 cells apoptosis. The H9c2 cells viability induced by different consideration of Lyc or Ang Ⅱ or both was detected by CCK8 assay. The expression levels of Bax and Bcl-2 in H9c2 cells were determined by real-time quantitative reverse transcription polymerase chain reaction (RT-PCR). Western blot was conducted to detect the protein expressions of Bax, Caspase 3, Caspase 9 and Bcl-2 in H9c2 cells. The apoptotic ratio of H9c2 cells was observed by TUNEL assay. Results Compared with control group, Ang Ⅱ could decrease the viability of H9c2 cells to (92.87±4.37)%. The result of RT-PCR showed that Ang Ⅱ decreased the expression level of Bcl-2, and Bax level was increased under the stimulation of Ang Ⅱ (P<0.05), while the expression level of Bcl-2 was increased and Bax level was decreased under the co-stimulation of Ang Ⅱ and Lyc in a concentration dependent manner, which indicated that Lyc ameliorated the apoptosis of H9c2 cells. The result of western blot showed that the protein expressions of Bax, Caspase 3 and Caspase 9 were increased, but Bcl-2 was decreased after the stimulation of Ang Ⅱ (P<0.05). While these phenomenon reversed apparently under the co-stimulation of Ang Ⅱ and Lyc. A large number of apoptotic cells were observed under the stimulation of Ang Ⅱ through TUNEL assay. But the number of apoptotic cells reduced significantly under the co-stimulation of Lyc and Ang Ⅱ (P<0.05). Conclusions Lyc ameliorates the H9c2 cell apoptosis induced by Ang Ⅱ, which indicates that Lyc may have an important role in the treatment of various cardiovascular diseases. Key words: Lycopersicon esculentum; Angiotensin Ⅱ; Myocytes, cardiac; Apoptosis
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