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

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• 作者：Hao-ping Mao^a ; ¹ ; ² ; ^{haoping_mao@126.com" class="auth_mail" title="E-mail the corresponding author} ; ^{maohaoping19831026@hotmail.com" class="auth_mail" title="E-mail the corresponding author} ; Xing-ye Wang^a ; ¹ ; ³ ; ^{wangxingye420@163.com" class="auth_mail" title="E-mail the corresponding author} ; Yun&minus ; hang Gao^a ; ⁴ ; ^{1083747849@qq.com" class="auth_mail" title="E-mail the corresponding author} ; Yan-xu Chang^a ; Lu Chen^a ; ⁵ ; ^{18502295944@163.com" class="auth_mail" title="E-mail the corresponding author} ; Zi-chang Niu^b ; ⁶ ; ^{nzc601@sina.com" class="auth_mail" title="E-mail the corresponding author} ; Ju-qing Ai^a ; ⁷ ; ^{aijuqing1987@163.com" class="auth_mail" title="E-mail the corresponding author} ; Xiu-mei Gao^a ; ⁸ ; ^{gaoxiumei@tjutcm.edu.cn" class="auth_mail" title="E-mail the corresponding author}
• 关键词：Danhong injection ; Cardiac hypertrophy ; p38 ; NF-κb
• 刊名：Journal of Ethnopharmacology
• 出版年：2016
• 出版时间：20 June 2016
• 年：2016
• 卷：186
• 期：Complete
• 页码：20-29
• 全文大小：2204 K

文摘

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-κb. 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-κb pathway.