Literature DB >> 10615946

Regulation of uncoupling protein-2 and uncoupling protein-3 mRNA expression during lipid infusion in human skeletal muscle and subcutaneous adipose tissue.

Y Khalfallah1, S Fages, M Laville, D Langin, H Vidal.   

Abstract

To study the effect of nonesterified fatty acids (NEFAs) on uncoupling protein-2 (UCP-2) and uncoupling protein-3 (UCP-3) gene expression, a triglyceride emulsion was infused for 5 h in 14 healthy volunteers. A euglycemic-hyperinsulinemic clamp was administered concomitantly in 7 of the 14 subjects. The mRNA levels of UCP-2 and of the short (UCP-3S) and long (UCP-3L) isoforms of UCP-3 were quantified by reverse transcription-competitive polymerase chain reaction in tissue biopsies taken before and at the end of the infusion periods. Plasma NEFA concentrations increased from 362+/-52 to 989+/-157 micromol/l (P = 0.018) during triglyceride infusion. UCP-3L (8+/-1 vs. 19+/-2 amol/microg total RNA, P = 0.018) and UCP-3S (11+/-2 vs. 17+/-3 amol/microg total RNA, P = 0.027) mRNA levels increased in skeletal muscle during triglyceride infusion. UCP-3L mRNA levels were positively correlated with plasma NEFA concentrations (r = 0.53, P = 0.005) and with lipid oxidation rates (r = 0.56, P = 0.004) determined by indirect calorimetry. In contrast, the expression of UCP-2 was not affected by lipid infusion in skeletal muscle or in subcutaneous adipose tissue. During the hyperinsulinemic clamp (plasma insulin concentrations 202+/-12 pmol/l), NEFA levels (405+/-49 vs. 648+/-77 micromol/l, P = 0.063) and lipid oxidation rates (0.67+/-0.09 vs. 0.84+/-0.10 mg x kg(-1) x min(-1), P = 0.091) were not significantly increased during triglyceride infusion. Under such conditions, the induction of UCP-3L and UCP-3S mRNA expression was totally prevented (8+/-2 vs. 8+/-1 and 8 +/-2 vs. 9+/-2 amol/microg total RNA, respectively). We conclude that increased plasma NEFA levels by lipid infusion for 5 h induces the expression of UCP-3 but not UCP-2 in humans. During triglyceride infusion, physiological hyperinsulinemia appears to prevent the induction of UCP-3 mRNA levels.

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Year:  2000        PMID: 10615946     DOI: 10.2337/diabetes.49.1.25

Source DB:  PubMed          Journal:  Diabetes        ISSN: 0012-1797            Impact factor:   9.461


  7 in total

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Authors:  Catherine B Chan; Mary-Ellen Harper
Journal:  Curr Diabetes Rev       Date:  2006-08

2.  Tissue-specific activity of lipoprotein lipase in skeletal muscle regulates the expression of uncoupling protein 3 in transgenic mouse models.

Authors:  D Kratky; J G Strauss; R Zechner
Journal:  Biochem J       Date:  2001-05-01       Impact factor: 3.857

3.  A rapid up-regulation in UCP3 transcriptional activity in response to moderate intensity exercise in rat skeletal muscle.

Authors:  Keiko Kusuhara; Takashi Tobe; Takaharu Negoro; Takashi Abe
Journal:  J Sports Sci Med       Date:  2005-06-01       Impact factor: 2.988

4.  Lifestyle changes and lipid metabolism gene expression and protein content in skeletal muscle of subjects with impaired glucose tolerance.

Authors:  M Mensink; E E Blaak; H Vidal; T W A De Bruin; J F C Glatz; W H M Saris
Journal:  Diabetologia       Date:  2003-07-11       Impact factor: 10.122

5.  Effect of short-term free Fatty acids elevation on mitochondrial function in skeletal muscle of healthy individuals.

Authors:  Alberto O Chavez; Subhash Kamath; Rucha Jani; Lokendra K Sharma; Adriana Monroy; Muhammad A Abdul-Ghani; Victoria E Centonze; Padma Sathyanarayana; Dawn K Coletta; Cristopher P Jenkinson; Yidong Bai; Franco Folli; Ralph A Defronzo; Devjit Tripathy
Journal:  J Clin Endocrinol Metab       Date:  2009-10-28       Impact factor: 5.958

6.  Transcription of the human uncoupling protein 3 gene is governed by a complex interplay between the promoter and intronic sequences.

Authors:  A Girousse; G Tavernier; C Tiraby; L Lichtenstein; J S Iacovoni; A Mairal; F Villarroya; D Langin
Journal:  Diabetologia       Date:  2009-05-26       Impact factor: 10.122

7.  Expression of uncoupling proteins-1, -2 and -3 mRNA is induced by an adenocarcinoma-derived lipid-mobilizing factor.

Authors:  C Bing; S T Russell; E E Beckett; P Collins; S Taylor; R Barraclough; M J Tisdale; G Williams
Journal:  Br J Cancer       Date:  2002-02-12       Impact factor: 7.640

  7 in total

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