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胃饥饿素O-酰基转移酶抑制剂对体外培养的胃黏膜细胞中胃H-K-ATP酶活性及GOAT/胃饥饿素系统的影响

The effect of ghrelin O-acyltransferase inhibitor on gastric H-K-ATPase activity and GOAT/ghrelin system in gastric mucosal cells in vitro.

作者信息

Du Gai Mei, Luo Bi Ping, Hu Zhi Hua, Wu Jie Ge, Yan Wen Mei, Han Zheng Qiang, Zhang Yu Hong, Liu Mao Jun

机构信息

Department of Animal Science and Technology, Jinling Technology Institution, Nanjing 210038, PR China.

Institute of Veterinary Medicine, Jiangsu Academy of Agricultural Sciences, Key Laboratory of Veterinary Biological Engineering and Technology, Ministry of Agriculture, National Center for Engineering Research of Veterinary Bio-products, Nanjing 210014, PR China; Key Lab of Food Quality and Safety of Jiangsu Province-State Key Laboratory Breeding Base, Nanjing, PR China.

出版信息

Gen Comp Endocrinol. 2018 Oct 1;267:167-171. doi: 10.1016/j.ygcen.2018.06.020. Epub 2018 Jun 30.

Abstract

Ghrelin is implicated in the regulation of gastric functional development. The octanoylation of ghrelin is critical for its physiological functions which dependent upon ghrelin O-acyltransferase (GOAT) catalyzation. To investigate the effect of GOAT on gastric acid secretion and expression of ghrelin in vitro. Primary cultures of gastric mucosal cells were challenged with 1.5 × 10, 1.5 × 10 and 1.5 × 10 mol/mL GO-CoA-Tat (The GOAT inhibitor), respectively, for 24 h in order to further clarify the effect of GOAT on H-K-ATPase activity. In vitro, GO-CoA-Tat significantly increased ghrelin and GOAT mRNA expression at 1.5 × 10, 1.5 × 10 and 1.5 × 10 mol/mL, and augmented cell total ghrelin secretion at 1.5 × 10 mol/mL. But cell acylated ghrelin secretion was reduced at 1.5 × 10 mol/mL GO-CoA-Tat (P < 0.05). And cell acylated ghrelin synthesis was reduced at 1.5 × 10 and 1.5 × 10 mol/mL GO-CoA-Tat (P < 0.05). In accordance with acylated ghrelin level, H-K-ATPase activity were decreased with 1.5 × 10 and 1.5 × 10 mol/mL GO-CoA-Tat (P < 0.05). These results indicated that GOAT inhibitor decreases the acylated ghrelin level and H-K-ATPase activity in vitro.

摘要

胃饥饿素与胃功能发育的调节有关。胃饥饿素的辛酰化对其生理功能至关重要,这依赖于胃饥饿素O-酰基转移酶(GOAT)的催化作用。为了研究GOAT对胃酸分泌和胃饥饿素体外表达的影响。胃黏膜细胞原代培养物分别用1.5×10、1.5×10和1.5×10 mol/mL的GO-CoA-Tat(GOAT抑制剂)处理24小时,以进一步阐明GOAT对H-K-ATP酶活性的影响。在体外,GO-CoA-Tat在1.5×10、1.5×10和1.5×10 mol/mL时显著增加胃饥饿素和GOAT mRNA表达,并在1.5×10 mol/mL时增加细胞总胃饥饿素分泌。但在1.5×10 mol/mL的GO-CoA-Tat作用下,细胞酰化胃饥饿素分泌减少(P<0.05)。在1.5×10和1.5×10 mol/mL的GO-CoA-Tat作用下,细胞酰化胃饥饿素合成减少(P<0.05)。与酰化胃饥饿素水平一致,在1.5×10和1.5×10 mol/mL的GO-CoA-Tat作用下,H-K-ATP酶活性降低(P<0.05)。这些结果表明,GOAT抑制剂在体外可降低酰化胃饥饿素水平和H-K-ATP酶活性。

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