PMID- 33333215 OWN - NLM STAT- MEDLINE DCOM- 20210121 LR - 20210121 IS - 1879-0038 (Electronic) IS - 0378-1119 (Linking) VI - 771 DP - 2021 Mar 1 TI - Puerarin alleviates coronary heart disease via suppressing inflammation in a rat model. PG - 145354 LID - S0378-1119(20)31023-4 [pii] LID - 10.1016/j.gene.2020.145354 [doi] AB - 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-)kappaB 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. CI - Copyright (c) 2020 Elsevier B.V. All rights reserved. FAU - Zhao, Liangping AU - Zhao L AD - Department of Cardiology, The Second Affiliated Hospital of Soochow University, Gusu District, Suzhou, Jiangsu Province 215004, China. Electronic address: zhlianhping_zhaolp@163.com. FAU - Wang, Li AU - Wang L AD - Department of Cardiology, The Second Affiliated Hospital of Soochow University, Gusu District, Suzhou, Jiangsu Province 215004, China. FAU - Zhang, Daimin AU - Zhang D AD - Department of Cardiology, Nanjing First Hospital, Qinhuai District, Nanjing, Jiangsu Province 210001, China. FAU - Chen, Yuqi AU - Chen Y AD - Department of Cardiology, The Second Affiliated Hospital of Soochow University, Gusu District, Suzhou, Jiangsu Province 215004, China. FAU - Jin, Fulu AU - Jin F AD - Department of Cardiology, The Second Affiliated Hospital of Soochow University, Gusu District, Suzhou, Jiangsu Province 215004, China. LA - eng PT - Journal Article DEP - 20201215 PL - Netherlands TA - Gene JT - Gene JID - 7706761 RN - 0 (Anti-Inflammatory Agents) RN - 0 (Isoflavones) RN - 0 (Troponin C) RN - EC 1.1.1.27 (L-Lactate Dehydrogenase) RN - EC 2.7.3.2 (Creatine Kinase) RN - Z9W8997416 (puerarin) SB - IM MH - Animals MH - Anti-Inflammatory Agents/*administration & dosage/pharmacology MH - Coronary Disease/*drug therapy/genetics MH - Creatine Kinase/blood MH - Disease Models, Animal MH - Gene Expression Regulation/drug effects MH - Gene Regulatory Networks/*drug effects MH - Isoflavones/*administration & dosage/pharmacology MH - L-Lactate Dehydrogenase/blood MH - Male MH - Rats MH - Troponin C/blood OTO - NOTNLM OT - Apoptosis OT - Coronary heart disease OT - Inflammation OT - Puerarin EDAT- 2020/12/18 06:00 MHDA- 2021/01/22 06:00 CRDT- 2020/12/17 20:11 PHST- 2020/08/24 00:00 [received] PHST- 2020/10/30 00:00 [revised] PHST- 2020/12/01 00:00 [accepted] PHST- 2020/12/18 06:00 [pubmed] PHST- 2021/01/22 06:00 [medline] PHST- 2020/12/17 20:11 [entrez] AID - S0378-1119(20)31023-4 [pii] AID - 10.1016/j.gene.2020.145354 [doi] PST - ppublish SO - Gene. 2021 Mar 1;771:145354. doi: 10.1016/j.gene.2020.145354. Epub 2020 Dec 15.