Sheng Letian, Shen Mengjiao, Shao Danyan
Department of Pharmacy, The Fourth Affiliated Hospital of Soochow University, Jiangsu, Suzhou, 215000, China.
Cell Biochem Biophys. 2025 Jun;83(2):2059-2066. doi: 10.1007/s12013-024-01616-y. Epub 2025 Jan 16.
Total glucosides of paeony (TGP) have been investigated for their effects on cardiomyocyte hypertrophy induced by angiotensin II (Ang II). In this study, rat cardiomyocyte H9c2 cells were treated with various doses of TGP (0, 12.5, 25, 50, 100, 200, and 400 μmol/L), and cell viability was assessed using the MTT method to determine an optimal dose. To establish the cardiomyocyte hypertrophy model, Ang II (1 μmol/L) was used. The experimental groups included the control (Ctrl) group, the hypertrophy group (Ang II), the TGP treatment group (TGP+Ang II), and a combined treatment group (TGP+Ang II+LY), where LY294002, a PI3K/Akt inhibitor, was used. The surface area of H9c2 cells was analyzed using image analysis software, and apoptosis was assessed via flow cytometry. Western blotting was employed to evaluate markers related to cell proliferation, cardiac hypertrophy, apoptosis, and autophagy, as well as the phosphorylation of the PI3K/Akt pathway. The results revealed that Ang II inhibited cell viability and increased cell surface area, apoptosis, and autophagy, all of which were significantly reversed by TGP treatment. Moreover, the addition of LY294002 partially attenuated the effects of TGP, reducing cell viability and promoting hypertrophy, apoptosis, and autophagy. Additionally, Ang II reduced PI3K/Akt signaling activity, while TGP restored it. LY treatment reversed the effects of TGP and suppressed the PI3K/Akt pathway. In conclusion, TGP improves cardiomyocyte hypertrophy induced by Ang II by activating the PI3K/Akt signaling pathway.
已对芍药总苷(TGP)对血管紧张素II(Ang II)诱导的心肌细胞肥大的影响进行了研究。在本研究中,用不同剂量的TGP(0、12.5、25、50、100、200和400 μmol/L)处理大鼠心肌细胞H9c2细胞,并使用MTT法评估细胞活力以确定最佳剂量。为建立心肌细胞肥大模型,使用了Ang II(1 μmol/L)。实验组包括对照组(Ctrl)、肥大组(Ang II)、TGP治疗组(TGP+Ang II)和联合治疗组(TGP+Ang II+LY),其中使用了PI3K/Akt抑制剂LY294002。使用图像分析软件分析H9c2细胞的表面积,并通过流式细胞术评估细胞凋亡。采用蛋白质免疫印迹法评估与细胞增殖、心肌肥大、细胞凋亡和自噬相关的标志物,以及PI3K/Akt途径的磷酸化。结果显示,Ang II抑制细胞活力并增加细胞表面积、细胞凋亡和自噬,而TGP处理可显著逆转所有这些变化。此外,添加LY294002部分减弱了TGP的作用,降低了细胞活力并促进了肥大、细胞凋亡和自噬。此外,Ang II降低了PI3K/Akt信号活性,而TGP使其恢复。LY处理逆转了TGP的作用并抑制了PI3K/Akt途径。总之,TGP通过激活PI3K/Akt信号通路改善Ang II诱导的心肌细胞肥大。