Department of Physiology, Medical College of Nanchang University, Nanchang 330006, China.
Biomed Res Int. 2020 Dec 9;2020:8818160. doi: 10.1155/2020/8818160. eCollection 2020.
Perfluorooctane sulfonate (PFOS), an environmentally persistent pollutant, has been revealed to elicit hepatic toxicity. In the current study, we investigated the protective role of grape seed proanthocyanidin extract (GSPE) against PFOS-caused steatohepatitis in mice. Animals were exposed intragastrically to PFOS (10 mg/kg/day), GSPE (150 mg/kg/day), or their combination. After 21 days of treatment, mice exposed to PFOS exhibited steatosis, oxidative stress, and inflammation in the liver. Nevertheless, simultaneous administration of GSPE resumed the declined serum hepatic enzyme activities and histological abnormalities in PFOS-exposed mice. Furthermore, GSPE supplementation reduced the contents of triglyceride (TG) and total cholesterol (TC) and expression of lipid metabolism-associated genes and fatty acid-binding protein 4 () in the liver of mice treated with PFOS. Moreover, GSPE suppressed the generation of lipid peroxidative product malondialdehyde and restored the activity of superoxide dismutase in the liver of PFOS-exposed mice. In addition, GSPE repressed the PFOS-induced hepatic overproduction of proinflammatory cytokines interleukin-6 (IL-6) and tumor necrosis factor- (TNF-). Our results demonstrate that GSPE attenuates PFOS-caused steatohepatitis in mice by regulating lipid metabolism, oxidative stress, and inflammatory response.
全氟辛烷磺酸 (PFOS) 是一种环境持久性污染物,已被证实会引起肝毒性。在本研究中,我们研究了葡萄籽原花青素提取物 (GSPE) 对 PFOS 引起的小鼠脂肪性肝炎的保护作用。动物通过胃内给予 PFOS(10mg/kg/天)、GSPE(150mg/kg/天)或两者的混合物进行暴露。治疗 21 天后,PFOS 暴露的小鼠表现出肝脂肪变性、氧化应激和炎症。然而,同时给予 GSPE 恢复了 PFOS 暴露小鼠血清肝酶活性和组织学异常。此外,GSPE 补充降低了 TG 和 TC 的含量以及与脂质代谢相关的基因的表达 和脂肪酸结合蛋白 4 () 在 PFOS 处理的小鼠的肝脏中。此外,GSPE 抑制了脂质过氧化产物丙二醛的产生,并恢复了 PFOS 暴露小鼠肝脏中超氧化物歧化酶的活性。此外,GSPE 抑制了 PFOS 诱导的促炎细胞因子白细胞介素-6 (IL-6) 和肿瘤坏死因子- (TNF-) 在肝脏中的过度产生。我们的结果表明,GSPE 通过调节脂质代谢、氧化应激和炎症反应来减轻 PFOS 引起的小鼠脂肪性肝炎。