4.6 Article

Puerarin alleviates coronary heart disease via suppressing inflammation in a rat model

Journal

GENE
Volume 771, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.gene.2020.145354

Keywords

Puerarin; Coronary heart disease; Inflammation; Apoptosis

Funding

  1. Suzhou Science and Technology Development Program Guidance Project Fund [SYSD2013093]
  2. Youth Natural Science Fund of Soochow University [SDY2013A32]
  3. Research Fund of the Second Affiliated Hospital of Soochow University [SDFEYGJ1405]
  4. Xinxin Heart (SIP) Foundation [2019-CCA-ACCESS-058]

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The research showed that puerarin could alleviate coronary heart disease in rats by suppressing inflammation, improving cardiac function, and regulating the expression of key proteins and factors, including those affecting cholesterol and lipid levels.
Background: Puerarin shows inhibitory effects on inflammation in chronic heart failure (CHF), but its efficacy in coronary heart disease (CHD) remained vague. Methods: Rat CHD model was constructed, and serum parameters were determined using a blood liquid biochemical analyzer. Also, contents of creatine kinase (CK), creatine kinase MB isoenzyme (CK-MB), lactate dehydrogenase (LDH) and cardiac troponin (cTnT) were measured using colorimetry. Histological examination was conducted with Hematoxylin-Eosin (H&E) staining, and cardiac function was assessed by Echocardiography. Cell apoptosis was detected using Terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) assay. Relative expressions were measured using quantitative real-time polymerase chain reaction (qRT-PCR) and Western blot as needed. Results: In CHD rats, the levels of TC, LDL and TG and the expressions of matrix metalloproteinase-9 (MMP-9), CD40 ligand (CD40L), tumor necrosis factor-alpha (TNF-alpha) and C-reactive protein (CRP) were increased while HDL level was decreased, accompanied with inflammatory cell infiltration and cardiac malfunction. Also, the contents of CK, CK-MB, LDH and cTnT, the percentage of apoptotic cells, the expressions of Bcl-2 associated X protein (Bax), cleaved Caspase-3, TNF-alpha, Interleukin-beta (IL-beta), IL-6 and Lipoprotein-associated Phospholipase A2 (Lp-PLA2) expressions and the levels of oxidized-(ox-)LDL and malondialdehyde (MDA) were upregulated, while the level of super oxidase dismutase (SOD) and the expressions of B cell lymphoma-2 (Bcl-2) and vascular endothelial growth factor (VEGF) were downregulated. However, Puerarin ameliorated the effects of CHD model construction, suppressed nuclear factor-(NF-)kappa B expression, and enhanced the expressions of Farnesoid X Receptor (FXR), phosphorylated-AKT (p-AKT) and phosphorylated-signal transducer and activator of transcription 3 (p-STAT3). Conclusion: Puerarin alleviated CHD in rats via inhibiting inflammation, providing possible method for CHD treatment.

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