首页> 外文期刊>Food & Function >Cholesterol-lowering potentials of Lactobacillus strain overexpression of bile salt hydrolase on high cholesterol diet-induced hypercholesterolemic mice
【24h】

Cholesterol-lowering potentials of Lactobacillus strain overexpression of bile salt hydrolase on high cholesterol diet-induced hypercholesterolemic mice

机译:胆固醇降低乳杆菌菌株对高胆固醇饮食诱导的高胆固醇小鼠胆汁盐水解酶过表达的潜力

获取原文
获取原文并翻译 | 示例
           

摘要

Hypercholesterolemia is closely associated with cardiovascular disease. Supplementation with probiotics has been shown to contribute to improving lipid metabolism. The probiotic mechanisms of cholesterol reduction are complicated and remain unclear. One of the potential probiotic mechanisms for cholesterol reduction is the deconjugation of bile salts. We previously found a high bile salt hydrolase (BSH) activity of Lactobacillus casei pWQH01 (overexpression of bsh1) and Lactobacillus plantarum AR113, but found no BSH activity for Lactobacillus casei LC2W in vitro. Therefore, we decided to investigate whether the high BSH activity of L. plantarum AR113 and L. casei pWQH01 could exert a cholesterol-reducing effect in vivo. Compared to the high-cholesterol diet (HCD) group, AR113 and pWQH01 groups had a significantly lower body weight (BW), serum total cholesterol (TC), low density lipoprotein cholesterol (LDL-C) levels and atherogenic index (AI), whereas the LC2W group had a poor capability to mitigate the blood lipid levels in the hypercholesterolemic mice. In addition, the AR113 and pWQH01 groups decreased the hepatic levels of TC and LDL-C and improved hepatic steatosis compared with the HCD group. To explore their cholesterol-lowering mechanisms of action, we determined the expression levels of these genes on the cholesterol metabolic pathways. AR113 and pWQH01 groups downregulated the expression of farnesoid X receptor (FXR) and small heterodimer partner (SHP) genes, but upregulated the expression of the cholesterol 7-hydroxylase (CYP7A1) gene in the liver. Simultaneously, the expression of cholesterol liver X receptor (LXR) and low density lipoprotein receptor (LDLR) genes was upregulated in the liver. These results indicated that L. plantarum AR113 and L. casei pWQH01 could inhibit the cholesterol absorption and accelerate the cholesterol transportation. Taken together, these findings suggest that Lactobacillus strain overexpression of bile salt hydrolase has beneficial effects against hypercholesterolemia by reducing cholesterol absorption and increasing cholesterol catabolism.
机译:高胆固醇血症与心血管疾病密切相关。已经显示益生菌的补充有助于改善脂质代谢。胆固醇还原的益生菌机制是复杂的并且仍然不清楚。胆固醇还原的潜在益生菌机制之一是胆汁盐的欺骗。我们以前发现了一种高胆汁盐水解酶(BSH)活性乳杆菌PWQH01(BSH1的过度表达)和Lactobacillus Plantarum Ar113,但发现了在体外的Lactobacillus酪虫LC2W的BSH活性。因此,我们决定探讨L.Purerarum Ar113和L. casei PWQH01的高BSH活性是否可以在体内发挥胆固醇降低效果。与高胆固醇饮食(HCD)组相比,AR113和PWQHO1组具有显着降低的体重(BW),血清总胆固醇(TC),低密度脂蛋白胆固醇(LDL-C)水平和闭塞指数(AI),虽然LC2W组的能力较差,以减轻高胆固醇小鼠的血脂水平。此外,AR113和PWQH01组与HCD组相比,AR113和PWQH01组降低了Tc和LDL-C的肝水平,并改善了肝脏脂肪变性。为了探讨其胆固醇的作用机制,我们确定了这些基因对胆固醇代谢途径的表达水平。 AR113和PWQH01组下调了法呢X受体(FXR)和小异二聚体伴侣(SHP)基因的表达,但是上调胆固醇7-羟化酶(CYP7A1)基因在肝脏中的表达。同时,在肝脏中上调胆固醇肝X受体(LXR)和低密度脂蛋白受体(LDLR)基因的表达。这些结果表明,L.Purerarum Ar113和L.酪蛋白PWQH01可以抑制胆固醇的吸收并加速胆固醇运输。这些研究结果表明,通过减少胆固醇的吸收和增加胆固醇分解代谢来嗜盐水解酶的乳酸杆菌菌株过表达对高胆固醇血症具有有益的影响。

著录项

  • 来源
    《Food & Function》 |2019年第3期|共12页
  • 作者单位

    Univ Shanghai Sci &

    Technol Sch Med Instrument &

    Food Engn Shanghai Engn Res Ctr Food Microbiol Shanghai 200093 Peoples R China;

    Univ Shanghai Sci &

    Technol Sch Med Instrument &

    Food Engn Shanghai Engn Res Ctr Food Microbiol Shanghai 200093 Peoples R China;

    Univ Shanghai Sci &

    Technol Sch Med Instrument &

    Food Engn Shanghai Engn Res Ctr Food Microbiol Shanghai 200093 Peoples R China;

    Univ Shanghai Sci &

    Technol Sch Med Instrument &

    Food Engn Shanghai Engn Res Ctr Food Microbiol Shanghai 200093 Peoples R China;

    Univ Shanghai Sci &

    Technol Sch Med Instrument &

    Food Engn Shanghai Engn Res Ctr Food Microbiol Shanghai 200093 Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 食品工业;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号