Abstract
Increased levels of neuropeptide Y have been reported in transthyretin-null mice.
This effect might be related to transthyretin ligands (retinol and thyroxine) since,
through binding to nuclear receptors, they modulate the expression of genes that control
cellular metabolism. The retinoic X receptors form obligatory heterodimers with peroxisome
proliferator-activated receptors and liver X receptors - potent regulators of fat,
glucose and cholesterol homeostasis. We used transthyretin-null mice to investigate
whether the absence of transthyretin influences metabolism. Transthyretin-null mice
do not differ from controls in body weight and white adipose tissue morphology, nor
in basal or fast-induced circulating levels of glucose, lipids, and leptin. Glucose
tolerance tests show that transthyretin-null mice have normal capacity to remove and
metabolize energy substrates. Expression of genes encoding lipid transporters and
nuclear receptors are also similar in transthyretin-null and control mice. Therefore,
the absence of transthyretin does not seem to influence the regulation of lipid and
glucose metabolism.
Key words
Transthyretin - retinoids - RXR - PPAR - LXR - thyroxine
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R9-R10
Correspondence
J. A. Palha
Life and Health Sciences Research Institute (ICVS)
School of Health Sciences
University of Minho
Campus de Gualtar
4710-057 Braga
Portugal
Phone: +351/253/60 48 17
Fax: +351/253/60 48 09
Email: japalha@ecsaude.uminho.pt