TSH increases synthesis of hepatic ATP-binding cassette subfamily A member 1 in hypercholesterolemia

被引:4
作者
Zhang, Tiantian [1 ]
Zhou, Lingyan [1 ]
Cong, Cong [2 ]
Shi, Hong [3 ]
Zhou, Xinli [1 ]
机构
[1] Shandong Univ, Shandong Clin Med Ctr Endocrinol & Metab, Inst Endocrinol & Metab, Shandong Acad Clin Med,Shandong Prov Hosp,Dept En, Jinan 250021, Shandong, Peoples R China
[2] Shandong Univ, Jinan Cent Hosp, Jinan 250021, Shandong, Peoples R China
[3] Shandong Univ Tradit Chinese Med, Affiliated Hosp 2, Dept Pediat, Jinan, Peoples R China
基金
中国国家自然科学基金;
关键词
SCH mice; ABCA1; Hypercholesteremia; ABCA1; MESSENGER-RNA; THYROTROPIN RECEPTOR; FATTY-ACIDS; CHOLESTEROL; TRANSPORTER; DISEASE; ACCUMULATION; LIPOPROTEIN; DEFICIENCY; METABOLISM;
D O I
10.1016/j.bbrc.2016.05.054
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
Epidemiological evidence suggests that thyrotropin (TSH) levels are closely correlated with the severity of hypercholesterolemia. Reverse cholesterol transfer (RCT) plays an important role in regulating bloodcholesterol. However, the molecular mechanism of hypercholesterolemia in subclinical hypothyroidism (SCH) has not been fully clarified. The SCH mouse model, which is characterized by elevated serum TSH but not thyroid hormone levels, demonstrated a significant increase in plasma cholesterol compared with controls. Interestingly, Tshr KO mice, with normal thyroid hormone levels after thyroid hormone supplementation, showed lower plasma cholesterol levels compared with their wild-type littermates. ATP binding cassette subfamily A member 1(ABCA1) is a member of the ABC superfamily, which induces transfer of intracellular cholesterol to extracellular apolipoprotein. TSH upregulated hepatic ABCA1 to promote the efflux of intercellular cumulative cholesterol, resulting in increased plasma cholesterol. These data might partially explain the pathogenesis of hypercholesterolemia in SCH. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:75 / 81
页数:7
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