α-NETA down-regulates CMKLR1 mRNA expression in ileum and prevents body weight gains collaborating with ERK inhibitor PD98059 in turn to alleviate hepatic steatosis in HFD-induced obese mice but no impact on ileal mucosal integrity and steatohepatitis progression

被引:2
作者
Zheng, Canbin [1 ]
Zheng, Yongping [2 ]
Chen, Xi [3 ]
Zhong, Xianyang [1 ]
Zheng, Xiaobin [2 ]
Yang, Shuhui [1 ]
Zheng, Zihui [1 ]
机构
[1] Shantou Cent Hosp, Dept Endocrine & Metab Dis, Shantou, Guangdong, Peoples R China
[2] Shantou Cent Hosp, Dept Gastroenterol, 114 Waima Rd, Shantou 515031, Guangdong, Peoples R China
[3] Shantou Cent Hosp, Dept Clin Med, Res Ctr, Shantou, Guangdong, Peoples R China
关键词
Chemerin; Chemokine-like receptor-1 (CMKLR1); 2-(alpha-naphthoyl) ethyltrimethylammonium iodide (alpha-NETA); Extracellular-regulated kinase (ERK); Western blotting; rtPCR; Zonula occluden-1(ZO-1); HIGH-FAT DIET; SMOOTH-MUSCLE; CHEMERIN; PROLIFERATION; INFLAMMATION; DISRUPTION; MIGRATION; PROMOTES; PATHWAY; CELLS;
D O I
10.1186/s12902-023-01267-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Studies on chemerin/chemokine-like receptor-1 have mainly focused on adipose and liver with the intestinal tissues largely overlooked. In this study conducted on obese mice, we have explored: 1) CMKLR1 expression in the ileums; 2) CMKLR1 inhibitor alpha-NETA on body weight and intestinal mucosa integrity hence the impact on hepatic steatosis and pathway involved.Methods Nineteen male C57BL/6 mice were randomly divided into five groups: normal diet group (ND), high-fat diet group (HFD), HFD +alpha-NETA group (NETA), HFD+ PD98059 group (PD) and HFD +alpha-NETA +PD98059 group (NETA + PD). Mice were fed either with a chow diet or HFD for 12(th) weeks. At 12(th) week, mice of ND were put on the diet as before; mice of NETA received daily treatments of alpha-NETA (30 mg/kg) via gavage; mice of PD received daily treatment of PD98059 via tail vein injection; mice of NETA + PD received daily treatment of alpha-NETA +PD98059, all for another 4 weeks. At the time intervention ended, mice were sacrificed. The body weight, the liver pathologies were assessed. Ileal CMKLR1 mRNA was evaluated by rtPCR; ZO-1, ERK1/2 protein expression of ileal tissues by western blotting; liver TNF-alpha and serum endotoxin by Elisa.Results More weight gains in mice of HFD than ND (37.90 +/- 3.00 g) vs (24.47 +/- 0.50 g), P = 0.002; alpha-NETA reduced the body weight (33.22 +/- 1.90 g) vs (37.90 +/- 3.00 g), P = 0.033; and further reduced by NETA +PD98059: (31.20 +/- 1.74 g) vs (37.30 +/- 4.05 g), P = 0.032. CMKLR1 mRNA expression was up-regulated in ileum in group HFD compared with ND and down-regulated by alpha-NETA. Steatosis was only alleviated in group PD +NETA with less weight gain. No impact of alpha-NETA on ileal ZO-1 or pERK with western blotting, and no endotoxin level changes were detected. TNF-alpha was higher in group HFD than in group ND, while no significant difference between other groups.Conclusions CMKLR1 mRNA was up-regulated in the ileum of obese mice and down-regulated by alpha-NETA along with a body weight control collaborating with ERK inhibitor PD98059. Steatosis was alleviated in a weight dependent way. alpha-NETA has no influence on intestinal mucosal integrity and no impact on steatohepatitis progression.
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页数:10
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