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DOI 10.1016/j.jphs.2017.05.012

Медицинская библиотека · Journal of pharmacological sciences · 2017

Arctiin protects against cardiac hypertrophy through inhibiting MAPKs and AKT signaling pathways.

Li Jing, Yuan Yu-Pei, Xu Si-Chi, Zhang Ning, Xu Chun-Ru, Wan Chun-Xia, Ren Jie, Zeng Xiao-Feng, Tang Qi-Zhu

СтатьяПеревод пока не подготовлен

Аннотация

PURPOSE: The mitogen-activated protein kinases (MAPKs) and protein kinase B (AKT) pathways have emerged as essential intracellular signaling pathways in eukaryotic cells, particularly as regulators of cardiac hypertrophy. Previous studies indicated that arctiin, an active ingredient of biennial dried ripe burdock, could exhibit potent anti-inflammatory and anti-allergic activities via down-regulating the activation of MAPKs and AKT pathways. However, little is known about its effects on cardiac hypertrophy. Therefore, the present study aimed to explore whether arctiin could attenuate cardiac hypertrophy.

GENERAL

METHODS

Arctiin (80 mg/kg) was administered by oral gavage once daily for 3 weeks from 1 week after surgery. Then, the mice were subjected to either chronic pressure overload generated by aortic banding (AB) or sham surgery (control group). Cardiac function was assessed by echocardiography.

FINDINGS: The results indicated that arctiin attenuated cardiac hypertrophy induced by AB, and suppressed cardiac fibrosis and accumulation of collagen in vivo. Arctiin also inhibit the activation of MAPKs and AKT occurs in response to hypertrophic stimuli. Arctiin attenuated phenylephrine-induced hypertrophy of myocytes in vitro.

CONCLUSIONS

In conclusion, arctiin can improve cardiac function and prevent the development of cardiac hypertrophy by blocking the MAPKs and AKT signaling pathways.

Для цитирования: Li Jing, Yuan Yu-Pei, Xu Si-Chi, Zhang Ning, Xu Chun-Ru, Wan Chun-Xia, Ren Jie, Zeng Xiao-Feng, Tang Qi-Zhu. Arctiin protects against cardiac hypertrophy through inhibiting MAPKs and AKT signaling pathways.. Journal of pharmacological sciences. 2017. DOI: 10.1016/j.jphs.2017.05.012.

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