Tianjin Key Laboratory of Ionic-Molecular Function of Cardiovascular Disease, Department of Cardiology, Tianjin Institute of Cardiology, The Second Hospital of Tianjin Medical University, Tianjin, China.
Department of Cardiology, Tianjin Beichen Hospital, Tianjin, China.
Pharm Biol. 2022 Dec;60(1):562-569. doi: 10.1080/13880209.2022.2040543.
Paeonol (PAE) is the main phytochemical from . Its main pharmacological effects are anti-inflammatory and antioxidant, but its cardioprotective effect is unclear.
The study investigates the effects and underlying mechanisms of PAE on transverse aortic constriction (TAC)-induced heart failure (HF) in mice.
C57BL/6 mice were randomly divided into five groups: sham, TAC, PAE10 (TAC + PAE 10 mg/kg), PAE20 (TAC + PAE 20 mg/kg) and PAE 50 (TAC + PAE 50 mg/kg). Paeonol was intragastrically administered to mice for 4 weeks. Mice were anaesthetized with pentobarbital sodium and underwent cardiac echocardiography using echocardiography system. Serum levels of atrial natriuretic peptide (ANP), tumour necrosis factor-α (TNF-α) and interleukin-6 (IL-6) were measured by enzyme-linked immunosorbent assay (ELISA). Myocardial apoptosis was detected with terminal deoxynucleotidyl transferase-mediated dUTP nick end-labelling (TUNEL) staining. Haematoxylin-eosin (H&E) and Masson's staining were used for histopathological evaluation. Western and quantitative real-time PCR (qRT-PCR) were performed to detect levels of apoptosis and fibrosis-related proteins.
Echocardiography showed PAE improved cardiac function (LVEF: TAC, 52.3±6.8%; PAE20, 65.8±3.6%; PAE50, 71.4±2.5%) and H&E staining showed PAE alleviated myocardial injury (TAC: 1170.3 ± 134.6 μm; PAE50: 576.0 ± 53.5 μm). Western and qRT-PCR results showed that PAE down-regulated the levels of ANP, BNP and α-MHC. In addition, TUNEL and western results showed PAE significantly inhibited apoptosis. Masson and western results showed PAE inhibited cardiac hypertrophy. Western results showed the ERK1/2/JNK pathway could be inhibited by PAE.
Paeonol regulates ERK1/2/JNK to improve cardiac function, which provides theoretical support for the extensive clinical treatment of HF.
丹皮酚(PAE)是从 中提取的主要植物化学物质。其主要药理作用为抗炎和抗氧化,但对其心脏保护作用尚不清楚。
本研究探讨丹皮酚对小鼠主动脉缩窄(TAC)诱导的心力衰竭(HF)的作用及作用机制。
将 C57BL/6 小鼠随机分为五组:假手术组、TAC 组、PAE10 组(TAC+PAE10mg/kg)、PAE20 组(TAC+PAE20mg/kg)和 PAE50 组(TAC+PAE50mg/kg)。丹皮酚通过灌胃给药,连续给药 4 周。用戊巴比妥钠麻醉小鼠,用超声心动图系统进行心脏超声检查。采用酶联免疫吸附试验(ELISA)法检测血清心房钠尿肽(ANP)、肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6)水平。用末端脱氧核苷酸转移酶介导的 dUTP 缺口末端标记法(TUNEL)染色检测心肌细胞凋亡。苏木精-伊红(H&E)和 Masson 染色用于组织病理学评估。采用 Western blot 和实时定量 PCR(qRT-PCR)检测凋亡和纤维化相关蛋白的水平。
超声心动图显示 PAE 可改善心功能(LVEF:TAC 组为 52.3±6.8%;PAE20 组为 65.8±3.6%;PAE50 组为 71.4±2.5%),H&E 染色显示 PAE 可减轻心肌损伤(TAC 组为 1170.3±134.6μm;PAE50 组为 576.0±53.5μm)。Western blot 和 qRT-PCR 结果显示,PAE 下调 ANP、BNP 和 α-MHC 的水平。此外,TUNEL 和 Western blot 结果显示,PAE 可显著抑制细胞凋亡。Masson 和 Western blot 结果显示,PAE 可抑制心肌肥大。Western blot 结果显示,PAE 可抑制 ERK1/2/JNK 通路。
丹皮酚通过调节 ERK1/2/JNK 改善心功能,为 HF 的广泛临床治疗提供了理论支持。