4.7 Article

Danhong injection attenuates isoproterenol-induced cardiac hypertrophy by regulating p38 and NF-κb pathway

Journal

JOURNAL OF ETHNOPHARMACOLOGY
Volume 186, Issue -, Pages 20-29

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jep.2016.03.015

Keywords

Danhong injection; Cardiac hypertrophy; p38; NF-kappa b

Funding

  1. National Natural Science Funds [81303247]
  2. Research Fund for the Doctoral Program of Higher Education of China [20121210120009]

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Ethnopharmacological relevance: Danhong injection (DHI), derived from Rhizoma Salviae Miltiorrhizae (Salvia miltiorrhiza Bge., Labiatae, Danshen in Chinese) and Flos Carthami (Carthamus tinctorius L., Compositae, Salvia militiorrhiza Bunge), is an extensively-used Chinese material standardized clinical product for treatment of cardiovascular diseases. Aim of the study: Cardiac hypertrophy (CH) is an adaptive response of cardiomyocytes. Long-lasting cardiac hypertrophy results in the loss of compensation by cardiomyocytes which could ultimately develop into heart failure. In the present study, we aimed to investigate the effect and exact mechanisms of DHI on isoproterenol (ISO)-induced CH. Materials and methods: H9c2 cells and male Wistar rats were stimulated by ISO in the present study to establish CH models in vitro and in vivo. CCk-8 assay, Western blot, real time-polymerase chain reaction (RT-PCR), electrophoretic mobility shift assay (EMSA) and Echocardiography were used in the present study. Results: DHI significantly attenuated ISO-induced CH of H9c2 cells (p < 0.01). DHI decreased ISO-induced atrial natriuretic peptide (ANP) and brain natriuretic peptide (BNP) elevation both at the mRNA and protein levels (p < 0.05 and p < 0.01, respectively). Western blot showed that DHI down-regulated the phosphorylation of p38. Furthermore, we found that DHI inhibited the nuclear translocation and activation of NF-kappa b. Echocardiography from ISO-induced CH rats showed that DHI significantly decreased left ventricle (LV) mass, the thickness of the LV end-systolic posterior wall (LVPWs), and the LV end-diastolic posterior wall (LVPWd) elevated by ISO (p < 0.01 and p < 0.05, respectively). Conclusion: These data demonstrate that DHI might exert anti-cardiac hypertrophic effects by regulating p38 and NF-kappa b pathway. (C) 2016 Elsevier Ireland Ltd. All rights reserved.

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