Journal
ENDOCRINOLOGY
Volume 153, Issue 11, Pages 5143-5149Publisher
ENDOCRINE SOC
DOI: 10.1210/en.2012-1572
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Funding
- National Institutes of Healt [HL45095, HL112233, AA020561]
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Although studies in vitro and in hypothyroid animals show that thyroid hormone can, under some circumstances, modulate the actions of low-density lipoprotein (LDL) receptors, the mechanisms responsible for thyroid hormone's lipid-lowering effects are not completely understood. We tested whether LDL receptor ( LDLR) expression was required for cholesterol reduction by treating control and LDLR-knockout mice with two forms of thyroid hormone T-3 and 3,5-diiodo-L-thyronine. High doses of both 3,5-diiodo-L-thyronine and T-3 dramatically reduced circulating total and very low-density lipoprotein/LDL cholesterol (similar to 70%) and were associated with reduced plasma T-4 level. The cholesterol reduction was especially evident in the LDLR-knockout mice. Circulating levels of both apolipoprotein B (apo)B48 and apoB100 were decreased. Surprisingly, this reduction was not associated with increased protein or mRNA expression of the hepatic lipoprotein receptors LDLR-related protein 1 or scavenger receptor-B1. Liver production of apoB was markedly reduced, whereas triglyceride production was increased. Thus, thyroid hormones reduce apoB lipoproteins via a non-LDLR pathway that leads to decreased liver apoB production. This suggests that drugs that operate in a similar manner could be a new therapy for patients with genetic defects in the LDLR. (Endocrinology 153: 5143-5149, 2012)
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