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Gender specific Elovl3 expression and metabolic activity in adipose tissue depots
Stockholm University, Faculty of Science, Wenner-Gren Institute for Experimental Biology.
Manuscript (Other academic)
URN: urn:nbn:se:su:diva-25708OAI: diva2:200322
Part of urn:nbn:se:su:diva-8469Available from: 2009-02-05 Created: 2009-01-28 Last updated: 2010-01-13Bibliographically approved
In thesis
1. Regulation of Elovl and fatty acid metabolism
Open this publication in new window or tab >>Regulation of Elovl and fatty acid metabolism
2009 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Fatty acids are important regulators in the control of mammalian energy homeostasis. They are ingested in the diet but a significant amount are also endogenously produced by de novo lipogenesis. Fatty acid elongation beyond 16 carbons (palmitic acid) can occur to generate very long chain fatty acids (VLCFA), a process that is initiated by the rate-limiting condensation reaction. To date, six mammalian enzymes responsible for this reaction, ELOVL1-6 (Elongation of very long chain fatty acid), have been characterized. All of them exert substrate specificity and tissue-specific gene expression. In this thesis, factors that regulate fatty acid metabolism and, in particular, fatty acid synthesis and elongation will be presented.

The enclosed papers discuss issues as to how Elovl3 is regulated in liver and in different adipose depots and what effects ablation of this enzyme causes to lipid homeostasis. Hepatic Elovl3 gene expression followed a circadian rhythm, present exclusively in sexually mature male mice. In contrast to the expression of several other lipogenic genes, Elovl3 gene expression was not affected by fasting or refeeding. Instead, the gene expression was influenced by steroid hormones such as glucocorticoids and sex hormones.

Interestingly, despite reduced levels of leptin, Elovl3-ablated mice were shown to be resistant to diet induced weight gain, which seemed to be due to a decreased ratio between energy intake and energy expenditure. This phenotype was more pronounced in female mice.

Place, publisher, year, edition, pages
Stockholm: Wenner-Grens institut för experimentell biologi, 2009. 58 p.
fatty acid metabolism, fatty acid elongation
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Research subject
urn:nbn:se:su:diva-8469 (URN)978-91-7155-798-8 (ISBN)
Public defence
2009-02-27, Nordenskiöldsalen, Geovetenskapens hus, Svante Arrhenius väg 8 C, Stockholm, 10:00
At the time of the doctoral defense, the following papers were unpublished and had a status as follows: Paper 2: Manuscript. Paper 3: Manuscript.Available from: 2009-02-05 Created: 2009-01-28 Last updated: 2011-02-23Bibliographically approved

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