期刊
JOURNAL OF DIABETES RESEARCH
卷 2021, 期 -, 页码 -出版社
HINDAWI LTD
DOI: 10.1155/2021/6668506
关键词
-
资金
- National Health and Medical Research Council of Australia Postdoctoral Fellowship [GNT1037074]
- Heart Foundation of Australia Career Development Award [CR 12S 6833]
The study found that reconstituted HDL (rHDL) improved diabetes-associated cardiovascular disease and reduced the occurrence of atherosclerosis in Trail(-/-)Apoe(-/-) mice. Furthermore, rHDL also enhanced insulin and glucose metabolism in diabetic mice.
Background and Aims. Apolipoprotein A-I (ApoA-I), the main component of high-density lipoprotein (HDL), not only promotes reverse cholesterol transport (RCT) in atherosclerosis but also increases insulin secretion in pancreatic beta-cells, suggesting that interventions which raise HDL levels may be beneficial in diabetes-associated cardiovascular disease (CVD). Previously, we showed that TNF-related apoptosis-inducing ligand (TRAIL) deletion in Apolipoprotein Eknockout (Apoe(-/-)) mice results in diabetes-accelerated atherosclerosis in response to a Western diet. Here, we sought to identify whether reconstituted HDL (rHDL) could improve features of diabetes-associated CVD in Trail(-/-)Apoe(-/-) mice. Methods and Results. Trail(-/-)Apoe(-/-) and Apoe(-/-) mice on a Western diet for 12 weeks received 3 weekly infusions of either PBS (vehicle) or rHDL (containing ApoA-I (20 mg/kg) and 1-palmitoyl-2-linoleoyl phosphatidylcholine). Administration of rHDL reduced total plasma cholesterol, triglyceride, and glucose levels in Trail(-/-)Apoe(-/-) but not in Apoe(-/-) mice, with no change in weight gain observed. rHDL treatment also improved glucose clearance in response to insulin and glucose tolerance tests. Immunohistological analysis of pancreata revealed increased insulin expression/production and a reduction in macrophage infiltration in mice with TRAIL deletion. Furthermore, atherosclerotic plaque size in Trail(-/-)Apoe(-/-) mice was significantly reduced associating with increased expression of the M2 macrophage marker CD206, suggesting HDL's involvement in the polarization of macrophages. rHDL also increased vascular mRNA expression of RCT transporters, ABCA1 and ABCG1, in Trail(-/-)Apoe(-/-) but not in Apoe(-/-) mice. Conclusions. rHDL improves features of diabetes-associated atherosclerosis in mice. These findings support the therapeutic potential of rHDL in the treatment of atherosclerosis and associated diabetic complications. More studies are warranted to understand rHDL's mechanism of action.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据