Spondias mombin supplementation attenuated cardiac remodelling process induced by tobacco smoke

补充 Spondias mombin 可减弱烟草烟雾引起的心脏重塑过程

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作者:Maria Angélica Martins Lourenço, Mariana Gobbo Braz, Aline Garcia Aun, Bruna Letícia Buzati Pereira, Amanda Menezes Figueiredo, Renata Aparecida Cândido da Silva, Elisa Moya Kazmarek, Patrícia Helena Correa Alegre, Tatiana Fernanda Bachiega, Silmeia Garcia Zanati, Paula Schmidt Azevedo, Bertha Furla

Abstract

The objective of this study was to investigate the influence of Spondias mombin (SM) supplementation on the cardiac remodelling process induced by exposure to tobacco smoke (ETS) in rats. Male Wistar rats were divided into 4 groups: group C (control, n = 20) comprised animals not exposed to cigarette smoke and received standard chow; group ETS (n = 20) comprised animals exposed to cigarette smoke and received standard chow; group ETS100 (n = 20) received standard chow supplemented with 100 mg/kg body weight/d of SM; and group ETS250 (n = 20) received standard chow supplemented with 250 mg/kg body weight/d of SM. The observation period was 2 months. The ETS animals had higher values of left cardiac chamber diameters and of left ventricular mass index. SM supplementation attenuated these changes. In addition, the myocyte cross-sectional area (CSA) was lower in group C compared with the ETS groups; however, the ETS250 group had lower values of CSA compared with the ETS group. The ETS group also showed higher cardiac levels of lipid hydroperoxide (LH) compared with group C; and, groups ETS100 and ETS250 had lower concentrations of LH compared with the ETS group. Regarding energy metabolism, SM supplementation decreased glycolysis and increased the β-oxidation and the oxidative phosphorylation. There were no differences in the expression of Nrf-2, SIRT-1, NF-κB, interferon-gamma and interleukin 10. In conclusion, our results suggest that ETS induced the cardiac remodelling process. In addition, SM supplementation attenuated this process, along with oxidative stress reduction and energy metabolism modulation.

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