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Chondroitin Sulfate-Rich Extract of Skate Cartilage Attenuates Lipopolysaccharide-Induced Liver Damage in Mice

机译:硫酸软骨素丰富的冰鞋软骨提取物衰减脂多糖诱导的小鼠肝脏损伤

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摘要

The protective effects of a chondroitin sulfate-rich extract (CSE) from skate cartilage against lipopolysaccharide (LPS)-induced hepatic damage were investigated, and its mechanism of action was compared with that of chondroitin sulfate (CS) from shark cartilage. ICR mice were orally administrated 200 mg/kg body weight (BW) of CS or 400 mg/kg BW of CSE for 3 consecutive days, followed by a one-time intraperitoneal injection of LPS (20 mg/kg BW). The experimental groups were vehicle treatment without LPS injection (NC group), vehicle treatment with LPS injection (LPS group), CS pretreatment with LPS injection (CS group), and CSE pretreatment with LPS injection (CSE group). Hepatic antioxidant enzyme expression levels in the CS and CSE groups were increased relative to those in the LPS group. In LPS-insulted hepatic tissue, inflammatory factors were augmented relative to those in the NC group, but were significantly suppressed by pretreatment with CS or CSE. Moreover, CS and CSE alleviated the LPS-induced apoptotic factors and mitogen-activated protein kinase (MAPK). In addition, CS and CSE effectively decreased the serum lipid concentrations and downregulated hepatic sterol regulatory element-binding proteins expression. In conclusion, the skate CSE could protect against LPS-induced hepatic dyslipidemia, oxidative stress, inflammation, and apoptosis, probably through the regulation of MAPK signaling.
机译:研究了软骨素硫酸盐硫酸盐(CSE)的保护作用,从脂多糖(LPS)引起的肝脏损伤,并将其作用机制与鲨鱼软骨的软骨素(CS)进行比较。 ICR小鼠连续3天的ORALLY给予200mg / kg体重(BW)的CS或400mg / kg BW,然后进行一次腹膜内注射LPS(20mg / kg bw)。实验组是载体处理,没有LPS注射(NC组),用LPS注射(LPS组)的载体处理,CS预处理LPS注射(CS组),以及LPS注射(CSE组)的CSE预处理。相对于LPS组中的那些,Cs和CSE基团中的肝抗氧化剂酶表达水平增加。在LPS-侮辱性肝组织中,炎症因子相对于NC组中的那些增强,但通过对Cs或CSE进行预处理被显着抑制。此外,CS和CSE缓解了LPS诱导的凋亡因子和丝裂原激活的蛋白激酶(MAPK)。此外,Cs和CSE有效地降低了血清脂质浓度和下调的肝甾醇调节元素结合蛋白表达。总之,冰鞋CSE可以防止LPS诱导的肝脏血脂血症,氧化应激,炎症和凋亡,可能是通过MAPK信号传导的调节。

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