中国临床药理学与治疗学 ›› 2026, Vol. 31 ›› Issue (3): 300-312.doi: 10.12092/j.issn.1009-2501.2026.03.002
王夏颖1(
), 蒋虎刚1,2, 刘佳坤1, 马静1, 刘凯1,2, 李应东1,2, 赵信科1,2,*(
)
收稿日期:2025-05-06
修回日期:2025-06-26
出版日期:2026-03-26
发布日期:2026-04-03
通讯作者:
赵信科
E-mail:1686610858@qq.com;zxkd412@163.com
作者简介:王夏颖,女,在读硕士研究生,研究方向:中西医结合防治心血管疾病方向。E-mail:基金资助:
Xiaying WANG1(
), Hugang JIANG1,2, Jiakun LIU1, Jing MA1, Kai LIU1,2, Yingdong LI1,2, Xinke ZHAO1,2,*(
)
Received:2025-05-06
Revised:2025-06-26
Online:2026-03-26
Published:2026-04-03
Contact:
Xinke ZHAO
E-mail:1686610858@qq.com;zxkd412@163.com
摘要:
目的: 探究电离辐射对H9C2心肌细胞的影响及当归黄芪超滤物(RAS-RH)的干预效应。方法: 应用X射线建立H9C2损伤模型,并选用RAS-RH对其进行干预。通过CCK-8法检测各组H9C2的活力情况,鬼笔环肽染色观察细胞的肌丝骨架变化,JC-1染色及流式细胞术检测细胞线粒体膜电位(ΔΨm)变化,Hoechst33324染色及流式细胞术检测细胞的凋亡情况,蛋白免疫印迹法(Western blot)实验检测Drp1和HSP70相关蛋白的表达水平。结果: (1)X射线可抑制H9C2的增殖(P<0.05),破坏细胞肌丝骨架、降低细胞活力、改变ΔΨm以及促进细胞凋亡(P<0.01,P<0.05);(2)RAS-RH干预后H9C2活力升高(P<0.01)、细胞肌丝骨架恢复,且细胞的增殖能力、ΔΨm以及细胞凋亡(P<0.01、P<0.05)均得以改善;(3)RAS-RH可通过调节Drp1及HSP70蛋白的相对表达量(P<0.05)来改善H9C2生物学功能。结论: 电离辐射通过破坏细胞肌丝骨架、降低细胞活力、下调ΔΨm以及促进细胞凋亡进程来破坏H9C2的生物学功能,而RAS-RH可通过调节Drp1及HSP70蛋白的相对表达水平以修复电离辐射所带来的H9C2损伤。
中图分类号:
王夏颖, 蒋虎刚, 刘佳坤, 马静, 刘凯, 李应东, 赵信科. 当归黄芪超滤物对电离辐射诱导下心肌细胞的影响及其机制研究[J]. 中国临床药理学与治疗学, 2026, 31(3): 300-312.
Xiaying WANG, Hugang JIANG, Jiakun LIU, Jing MA, Kai LIU, Yingdong LI, Xinke ZHAO. Effect of Angelica astragalus ultrafiltration on cardiomyocytes induced by ionizing radiation and its mechanism[J]. Chinese Journal of Clinical Pharmacology and Therapeutics, 2026, 31(3): 300-312.
图 1
Fig.1 Effect of ionizing radiation on viability of H9C2 cells by using CCK-8 method ($ \overline{x} $±s, n=3) bP<0.05, cP<0.01, compared with 0 Gy group.
图 2
Fig.2 The effects of ionizing radiation on myofibrillar skeleton of H9C2 cells were observed by guaninyl penicillamine staining (inverted microscope, 400×)
图 4
Fig.4 Effect of ionizing radiation on total apoptosis rate of H9C2 cells with the flow cytometry assay ($ \overline{x} $±s, n=3) bP<0.05, cP<0.01, compared with blank group.
图 6 cP<0.01, compared with blank group; eP<0.05, fP<0.01, compared with 2 Gy group.
Fig.6 Effect of ionizing radiation on mitochondrial transmembrane potential of H9C2 cells with the flow cytometry assay ($ \overline{x} $±s, n=3) cP<0.01, compared with blank group; eP<0.05, fP<0.01, compared with 2 Gy group.
图 7
Fig.7 Effect of RAS-RH on viability of ionizing radiation-induced H9C2 cells by using CCK-8 method ($ \overline{x} $±s, n=3) cP<0.01, compared with blank group; fP<0.01, compared with model group.
图 8
Fig.8 Effect of RAS-RH on muscle silk skeleton of ionizing radiation-induced H9C2 cells by using the ghost closed-loop peptide staining (inverted microscope, 400×)
图 10
Fig.10 Effect of RAS-RH on ionizing radiation-induced apoptosis in H9C2 cells was determined by flow cytometry ($ \overline{x} $±s, n=3) cP<0.01, compared with blank group; fP<0.01, compared with model group.
图 11
Fig.11 Effect of RAS-RH on mitochondrial transmembrane potential of ionizing radiation-induced H9C2 cells by using JC-1 staining (inverted microscope, 400×)
图 12 bP<0.05, compared with blank group; eP<0.05, fP<0.01, compared with model group.
Fig.12 The effect of RAS-RH on the ionizing radiation-induced mitochondrial transmembrane potential in H9C2 cells was examined by JC-1 flow cytometry ($ \overline{x} $±s, n=3) bP<0.05, compared with blank group; eP<0.05, fP<0.01, compared with model group.
图 13 bP<0.05, cP<0.01, compared with 0 Gy group.
Fig.13 Effect of Drp1 and HSP70 proteins expression in ionizing radiation-induced H9C2 cells by using Western blot technology ($ \overline{x} $±s, n=3) bP<0.05, cP<0.01, compared with 0 Gy group.
图 14 cP<0.01, compared with blank group; eP<0.05, fP<0.01, compared with model group.
Fig.14 Effect of RAS-RH on the Drp 1 and HSP70 proteins expression in ionizing radiation-induced H9C2 cells by using Western blot technology ($ \overline{x} $±s, n=3) cP<0.01, compared with blank group; eP<0.05, fP<0.01, compared with model group.
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