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The mechanism of tilianin against ischemia-reperfusion injury of H9c2 cells
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Jie YANG1, Rui-fang ZHENG2, Yan-wen DU2, Hai-ning LI3, Shao-jiang LI1, Di-wei LIU2, *, Jian-guo XING2, *
Acta Pharmaceutica Sinica | 2021, 56(4) : 1070 - 1078
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Acta Pharmaceutica Sinica | 2021, 56(4): 1070-1078
Original Articles
The mechanism of tilianin against ischemia-reperfusion injury of H9c2 cells
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Jie YANG1, Rui-fang ZHENG2, Yan-wen DU2, Hai-ning LI3, Shao-jiang LI1, Di-wei LIU2, *, Jian-guo XING2, *
Affiliations
  • 1. Xinjiang Medical University, Urumqi 830011, China
  • 2. Xinjiang Institute of Materia Medica, Urumqi 830002, China
  • 3. Shihezi University, Shihezi 832000, China
Published: 2021-04-12 doi: 10.16438/j.0513-4870.2020-1636
Outline
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Z-VAD-FMK was combined with hypoxia-reoxygenation (H/R) injury to establish a necroptosis model of H9c2 cells to mimic the pathological changes of myocardial ischemia reperfusion injury (MIRI) in vitro and to study the effect and mechanism of tilianin against myocardial ischemia-reperfusion injury. A cell counting kit-8 (CCK-8) was used to detect cell viability, and commercial kits were used to detect lactate dehydrogenase (LDH) and superoxide dismutase (SOD) in the cell culture supernatant. Hoechst 33342/PI immunofluorescence staining was used to detect cell death. DCFH-DA, BBcellProbeTMM61, and JC-1 probes were used to detect reactive oxygen species (ROS), mitochondrial permeability transition pore (mPTP), and mitochondrial membrane potential (MMP), respectively. An enzyme-linked immunosorbent assay (ELISA) method was used to detect the release of tumor necrosis factor alpha (TNF-α), interleukin-1 beta (IL-1β), and interleukin-6 (IL-6). The results show that the cell viability, SOD activity, and MMP of the model group induced by H/R injury decreased, as compared with control group, but the necroptosis rate, LDH level, and ROS release increased significantly. Furthermore, mPTP of the model group cells opened, and TNF-α, IL-1β, and IL-6 levels were significantly higher. Molecular docking modeling showed that tilianin can bind to calmodulin-dependent protein kinase Ⅱ (CaMKII), and Western blot results showed that compared with control group, the expression levels of p-CaMKII and phospho-mixed lineage kinase domain-like protein increased in the model group, and tilianin could decrease the expression level of these proteins. The above results indicate that tilianin can protect H9c2 cells by inhibiting the phosphorylation of CaMKII at threonine 287, protecting mitochondrial function, and inhibiting the opening of mPTP to prevent necroptosis. This study has value for research on new methods to treat H/R injury.

tilianin  /  myocardial ischemia-reperfusion injury  /  necroptosis  /  calcium/calmodulin-dependent protein kinase Ⅱ  /  mitochondrial permeability transition pore
Jie YANG, Rui-fang ZHENG, Yan-wen DU, Hai-ning LI, Shao-jiang LI, Di-wei LIU, Jian-guo XING. The mechanism of tilianin against ischemia-reperfusion injury of H9c2 cells[J]. Acta Pharmaceutica Sinica, 2021 , 56 (4) : 1070 -1078 . DOI: 10.16438/j.0513-4870.2020-1636
Year 2021 volume 56 Issue 4
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Article Info
doi: 10.16438/j.0513-4870.2020-1636
  • Receive Date:2020-10-19
  • Online Date:2025-12-18
  • Published:2021-04-12
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History
  • Received:2020-10-19
  • Revised:2020-11-27
Funding
Affiliations
    1. Xinjiang Medical University, Urumqi 830011, China
    2. Xinjiang Institute of Materia Medica, Urumqi 830002, China
    3. Shihezi University, Shihezi 832000, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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