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Higenamine attenuates isoproterenol-induced myocardial infarction via regulating METTL3/TFEB pathway
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Bao-ping XIE1, 2, Yi-xin GUO3, Man-yi YE1, Xu-can HUANG3, Xu-ping LI1, Pei-cheng ZHONG1, Da-wei WANG4, Zhong-qiu LIU1, 4, *, Yuan-yuan CHENG1, 4, *
Acta Pharmaceutica Sinica | 2022, 57(10) : 3106 - 3114
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Acta Pharmaceutica Sinica | 2022, 57(10): 3106-3114
Special Reports Ⅱ: Traditional Chinese Medicine in the Prevention and Treatment of Cardio-cerebrovascular Related Diseases
Higenamine attenuates isoproterenol-induced myocardial infarction via regulating METTL3/TFEB pathway
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Bao-ping XIE1, 2, Yi-xin GUO3, Man-yi YE1, Xu-can HUANG3, Xu-ping LI1, Pei-cheng ZHONG1, Da-wei WANG4, Zhong-qiu LIU1, 4, *, Yuan-yuan CHENG1, 4, *
Affiliations
  • 1. School of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, Guangzhou 511400, China
  • 2. Key Laboratory of Prevention and Treatment of Cardiovascular and Cerebrovascular Diseases of Ministry of Education, Gannan Medical University, Ganzhou 341000, China
  • 3. School of Basic Medical Sciences, Guangzhou University of Chinese Medicine, Guangzhou 511400, China
  • 4. Shunde Hospital of Guangzhou University of Chinese Medicine, Guangzhou University of Chinese Medicine, Foshan 528333, China
Published: 2022-10-12 doi: 10.16438/j.0513-4870.2022-0435
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In this study, we investigated the pharmacological effect and possible molecular mechanism of higenamine (HG) in isoproterenol (ISO)-induced myocardial infarction (MI). All procedures were approved by the Institutional Animal Care and Use Committee of the Guangzhou University of Chinese Medicine. ISO was used to induce MI model in rats and H9c2 cells. The effects of HG on biomarkers and cardiac function in MI rats were evaluated by enzyme linked immunosorbent assay (ELISA), echocardiography and hematoxylin-eosin staining (HE). The expression of apoptosis and autophagy related proteins were detected by Western blot in myocardial tissue and H9c2 cells, as well as methyltransferase-like 3 (METTL3) and transcription factor EB (TFEB) protein expression. Molecular docking was used to evaluate the interaction between HG and METTL3. The results showed that HG significantly improved cardiac function and pathologic changes in ISO-induced MI, and inhibited the levels of MI-related biomarkers such as creatine kinase Mb (CK-MB), creatine kinase (CK) and lactate dehydrogenase (LDH). Mechanism studies showed that HG inhibited the expression of apoptosis-related proteins (Bax/Bcl2, caspase3, cleaved-caspase3). Interestingly, HG up-regulated the expression of autophagy related protein Beclin1, promoted autophagy flux, and decreased the ratio of light chain 3B-I/light chain 3B-II (LC-3B-I/LC-3B-II). Further studies found that HG increased the autophagy regulator TFEB and inhibited METTL3 expression. Molecular docking results showed that HG had a good interaction with METTL3. Taken together, HG has a potential anti-MI effect via regulating METTL3/TFEB signaling pathway-mediated autophagy.

higenamine  /  myocardial infarction  /  apoptosis  /  autophagy  /  methyltransferase-like 3
Bao-ping XIE, Yi-xin GUO, Man-yi YE, Xu-can HUANG, Xu-ping LI, Pei-cheng ZHONG, Da-wei WANG, Zhong-qiu LIU, Yuan-yuan CHENG. Higenamine attenuates isoproterenol-induced myocardial infarction via regulating METTL3/TFEB pathway[J]. Acta Pharmaceutica Sinica, 2022 , 57 (10) : 3106 -3114 . DOI: 10.16438/j.0513-4870.2022-0435
Year 2022 volume 57 Issue 10
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Article Info
doi: 10.16438/j.0513-4870.2022-0435
  • Receive Date:2022-04-18
  • Online Date:2025-12-24
  • Published:2022-10-12
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History
  • Received:2022-04-18
  • Revised:2022-07-15
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Affiliations
    1. School of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, Guangzhou 511400, China
    2. Key Laboratory of Prevention and Treatment of Cardiovascular and Cerebrovascular Diseases of Ministry of Education, Gannan Medical University, Ganzhou 341000, China
    3. School of Basic Medical Sciences, Guangzhou University of Chinese Medicine, Guangzhou 511400, China
    4. Shunde Hospital of Guangzhou University of Chinese Medicine, Guangzhou University of Chinese Medicine, Foshan 528333, 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
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Genus
种数
Number of
species
占总种数比例
Percentage of total
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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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