4.7 Article

LongShengZhi alleviated cardiac remodeling via upregulation microRNA-150-5p with matrix metalloproteinase 14 as the target

Journal

JOURNAL OF ETHNOPHARMACOLOGY
Volume 291, Issue -, Pages -

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jep.2022.115156

Keywords

LongShengZhi capsule; mircroRNA-150-5p; Cardiac remodeling; Matrix metalloproteinase 14

Funding

  1. Affiliated Huaian No.1 People's Hospital of Nanjing Medical University [YGRS202006]
  2. Natural Science Research Program of Huai'an [HAB202025]

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The study shows that LongShengZhi capsule (LSZ) can alleviate cardiac remodeling induced by Ang II by upregulating miR-150-5p to target MMP14. Administration of LSZ, upregulation of miR-150-5p, or targeting of MMP14 may be strategies for cardiac remodeling therapy.
Ethnopharmacological relevance: LongShengZhi capsule (LSZ), a traditional Chinese medicine, is used for treatment of patients with vascular diseases. LSZ reduced doxorubicin-induced heart failure by reducing production of reactive oxygen species and inhibiting inflammation and apoptosis. Aim of the study: This study was to explore whether LSZ could alleviate cardiac remodeling via upregulation of microRNA (miR)-150-5p and the downstream target. Cardiac remodeling was induced by Ang II in vivo and in vitro. Results: LSZ attenuated Ang II-induced cardiac hypertrophy and fibrosis in rats, and in primary cardiomyocytes (CMs) and primary cardiac fibroblasts (CFs). MiR-150-5p was downregulated in Ang II-induced rat heart, CMs and CFs, and these decreases were reserved by LSZ. In vivo overexpression of miR-150-5p by transfection of miR150-5p agomiR protected Ang II-induced cardiac hypertrophy and fibrosis in rats. Meanwhile, its overexpression also reversed Ang II-induced upregulation of atrial natriuretic peptide (ANP), brain natriuretic peptide (BNP) and beta-myosin heavy chain (beta-MHC) in rat hearts and primary CMs, as well as upregulation of collagen I, collagen III and transforming growth factor-beta (TGF-beta) in rat hearts and primary CFs. Matrix metalloproteinase 14 (MMP14) was validated as the target gene of miR-150-5p, which was overexpressed in Ang II-induced rat heart, rat primary CMs and primary CFs. Notably, overexpression of MMP14 induced cardiac remodeling, and reversed the protective role of miR-150-5p in downregulating Ang II-induced upregulation of hypertrophy and fibrosis markers in vitro. Conclusion: Collectively, LSZ protects Ang II-induced cardiac dysfunction and remodeling via upregulation of miR-150-5p to target MMP14. Administration of LSZ, upregulation of miR-150-5p or targeting of MMP14 may be strategies for cardiac remodeling therapy.

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