Literature DB >> 10939637

Sympathetic control of glucagon receptor mRNA levels in brown adipose tissue of cold-exposed rats.

A Morales1, J Lachuer, A Gélöen, B Georges, C Duchamp, H Barré.   

Abstract

Brown adipose tissue (BAT) is implicated in both cold-induced thermogenesis and regulation of energy expenditure and is mainly controlled by sympathetic innervation. To clarify the permissive and/or complementary roles of glucagon in cold-induced BAT activation, glucagon receptor gene expression and its modulation by sympathetic activity were investigated in rats. One pad of interscapular BAT was surgically denervated while the other pad was sham operated, then rats were either cold-exposed (CE) for 1 week at 4 degrees C or kept near thermoneutrality (25 degrees C, TN). Using a semi-quantitative reverse transcriptase-polymerase chain reaction (RT-PCR) assay, it was shown that cold exposure decreased (-44%) the relative abundance of BAT glucagon receptor mRNA, an effect which was prevented by unilateral surgical sympathectomy of BAT. The present results show a negative control by sympathetic nervous activity of glucagon receptor gene expression and/or of glucagon receptor mRNA stability in BAT of cold-exposed rats. The down-regulation of glucagon receptor expression during cold exposure does not support a major role of the peptide in the thermogenic control of BAT.

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Year:  2000        PMID: 10939637     DOI: 10.1023/a:1007058525309

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  21 in total

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Journal:  FEBS Lett       Date:  1999-02-12       Impact factor: 4.124

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Journal:  Nature       Date:  1983 Oct 20-26       Impact factor: 49.962

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Journal:  Mol Cell Endocrinol       Date:  1995-04-01       Impact factor: 4.102

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Journal:  Am J Physiol       Date:  1982-03
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  1 in total

Review 1.  The metabolic actions of glucagon revisited.

Authors:  Kirk M Habegger; Kristy M Heppner; Nori Geary; Timothy J Bartness; Richard DiMarchi; Matthias H Tschöp
Journal:  Nat Rev Endocrinol       Date:  2010-10-19       Impact factor: 43.330

  1 in total

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