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Shexiang Tongxin dropping pill ameliorates microvascular obstruction via downregulating ALOX12 after myocardial ischemia-reperfusion.
- Source :
-
International journal of cardiology [Int J Cardiol] 2024 Dec 01; Vol. 416, pp. 132481. Date of Electronic Publication: 2024 Aug 22. - Publication Year :
- 2024
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Abstract
- Background: Microvascular dysfunction (MVD) is common in patients with myocardial infarction receiving reperfusion therapy and is associated with adverse cardiac prognosis. Accumulating evidence suggests a protective role of Shexiang Tongxin dropping pill (STDP) in MVD. However, the specific effects and the underlying mechanisms of STDP in the context of MVD after myocardial ischemia-reperfusion (IR) remains unclear.<br />Aims: We aimed to elucidate the role of STDP in MVD induced by IR and the potential mechanisms involved.<br />Methods: Mice were orally administered with STDP or normal saline for 5 days before receiving myocardial IR. Cardiac function and microvascular obstruction was measured. Proteomics and single-cell RNA sequencing was performed on mouse hearts. In vitro hyoxia/reoxygenation model was established on mouse cardiac microvascular endothelial cells (MCMECs).<br />Results: STDP improved cardiac function and decreased microvascular obstruction (MVO) in mice after myocardial IR. Proteomics identified ALOX12 as an important target of STDP. Single-cell RNA sequencing further revealed that downregulation of ALOX12 by STDP mainly occurred in endothelial cells. The involvement of ALOX12 in the effect of STDP on MVO was validated by manipulating ALOX12 via endothelial-specific adeno-associated virus transfection in vivo and in vitro. In vivo, overexpression of ALOX12 increased whereas knockdown of ALOX12 decreased MVO and thrombus formation. STDP treatment alleviated the detrimental effects of overexpression of ALOX12. In vitro, overexpression of ALOX12 increased endothelial cell inflammation and platelet adhesion to endothelial cells, which was abolished by STDP treatment.<br />Conclusion: Our findings suggest that STDP alleviates MVO after IR, with ALOX12 playing a crucial role.<br />Competing Interests: Declaration of competing interest On behalf of all authors, the corresponding author states that there is no conflict of interest and all authors agree to submit the manuscript to your journal.<br /> (Copyright © 2024 Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Mice
Male
Microvessels drug effects
Microvessels metabolism
Disease Models, Animal
Drugs, Chinese Herbal pharmacology
Myocardial Reperfusion Injury metabolism
Myocardial Reperfusion Injury drug therapy
Myocardial Reperfusion Injury genetics
Down-Regulation drug effects
Arachidonate 12-Lipoxygenase metabolism
Arachidonate 12-Lipoxygenase genetics
Mice, Inbred C57BL
Subjects
Details
- Language :
- English
- ISSN :
- 1874-1754
- Volume :
- 416
- Database :
- MEDLINE
- Journal :
- International journal of cardiology
- Publication Type :
- Academic Journal
- Accession number :
- 39179033
- Full Text :
- https://doi.org/10.1016/j.ijcard.2024.132481