Gamma-glutamyl carboxylated Gas6 mediates the beneficial effect of vitamin K on lowering hyperlipidemia via regulating the AMPK/SREBP1/PPARα signaling cascade of lipid metabolism

被引:32
|
作者
Bordoloi, Jijnasa [1 ,2 ]
Ozah, Dibyajyoti [3 ]
Bora, Thaneswar [3 ]
Kalita, Jatin [1 ,2 ]
Manna, Prasenjit [1 ,2 ]
机构
[1] CSIR, NEIST, Biotechnol Grp, Biol Sci & Technol Div, Jorhat 785006, Assam, India
[2] CSIR, NEIST, Acad Sci & Innovat Res, Jorhat, Assam, India
[3] CSIR, North East Inst Sci & Technol, Clin Ctr, Jorhat, Assam, India
来源
关键词
Impaired lipid metabolism; Hyperlipidemia; Growth arrest specific protein 6 (Gas6); Vitamin K; Gamma-glutamyl carboxylated Gas6 (Gla-Gas6); ACTIVATED PROTEIN-KINASE; VASCULAR INFLAMMATION; HEPATIC STEATOSIS; LIVER; ATHEROSCLEROSIS; HEPATOCYTES; PATHWAY; MICE;
D O I
10.1016/j.jnutbio.2019.05.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The present study for the first time aims to examine the hypothesis that circulating gamma-glutamyl carboxylated growth arrest specific protein 6 (Gla-Gas6) deficiency may be associated with hyperlipidemia and vitamin K (VK) supplementation may ameliorate the impaired lipid homeostasis via activating Gas6 protein. Subjects with hyperlipidemia (n=22) and age-matched healthy controls (n=19) were included in this study. Results showed that plasma levels of Gla-Gas6 protein and VK were significantly lower in hyperlipidemic subjects compared to control. Moreover, Gla-Gas6 levels were significantly and positively correlated with VK (P=.034, r=0.452) and negatively with triglyceride (P=.022, r=-0.485) and total cholesterol (P=.043, r=-0.435) in hyperlipidemic subjects, which suggest that VK supplementation may have a positive effect in activating Gas6 protein and thereby reducing the aberrant plasma lipid levels. Further studies with high-fat diet (HFD)-fed animal model of hyperlipidemia demonstrated that VK supplementation (5 mu g/kg body weight, 8 weeks) reduced the plasma lipid levels, stimulated both the plasma levels and the hepatic protein expression of Gla-Gas6 protein, and regulated the AMPK/SREBP1/PPAR alpha signaling pathways of hepatic lipid metabolism in HFD-fed mice. Moreover, by using palmitic acid (PA, 0.75 mM)-treated both control and GGCX knockdown hepatocytes, this study dissected the direct role of Gla-Gas6 in mediating the positive effect of VK on preventing the PA-induced impaired hepatic lipid metabolism via regulating AMPK/SREBP1/PPAR alpha. pathways. Combining all, the present study demonstrated the beneficial effect of VK supplementation in preventing the impaired lipid homeostasis via activating VK-dependent Gas6 protein. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:174 / 184
页数:11
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