Literature DB >> 24488489

Is there an optimal dose for dietary linoleic acid? Lessons from essential fatty acid deficiency supplementation and adipocyte functions in rats.

Isabelle Harant-Farrugia1, Jésus Garcia, Mari-Carmen Iglesias-Osma, Maria José Garcia-Barrado, Christian Carpéné.   

Abstract

Differential effects of n-3 and n-6 polyunsaturated fatty acids (PUFAs) have been demonstrated on adipose tissue physiology. Facing to the widely recognized beneficial effects of n-3 PUFAs, the n-6 PUFA effects remain controversial. Thus, we further analyzed the linoleic acid (LA) influence on adipocyte functions. To this aim, we treated by LA supplementation at three distinct doses (1, 2.5, or 5% of energy intake) rats with essential fatty acids deficiency (EFAD). PUFA composition was determined in blood and white adipose tissue (WAT), while lipolytic and lipogenic activities were measured in isolated adipocytes. EFAD rats exhibited reduced WAT mass and increased EFAD biomarkers. WAT mass was completely recovered after supplementation, irrespective of LA dose. However, neither body mass nor EFAD biomarkers returned to control with 1% LA, while LA abundance doubled in adipocytes from rats supplemented with 5% LA. Regarding lipolysis, 2.5% LA normalized the EFAD-induced alterations. A trend to decrease the maximal stimulation of lipolysis was observed with 1 and 5% LA. Regarding lipogenesis, the lower and higher LA doses increased basal activity and hampered insulin to further stimulate glucose incorporation into lipids whereas 2.5% LA normalized the basal or insulin-stimulated levels. Our results show that dietary linoleate at 2.5% restored anatomical, biochemical, and functional disturbances induced by EFAD. At higher dose, LA tended to reduce triacylglycerol breakdown, to increase triacylglycerol assembly, and to provoke insulin resistance. Therefore, LA influence on adipocyte functions does not appear to follow a typical dose-response relationship, adding further complexity to the definition of its dietary requirement.

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Year:  2014        PMID: 24488489     DOI: 10.1007/s13105-014-0315-6

Source DB:  PubMed          Journal:  J Physiol Biochem        ISSN: 1138-7548            Impact factor:   4.158


  48 in total

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  4 in total

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Journal:  Br J Pharmacol       Date:  2018-05-06       Impact factor: 8.739

2.  High intake of dietary tyramine does not deteriorate glucose handling and does not cause adverse cardiovascular effects in mice.

Authors:  Christian Carpéné; Stéphane Schaak; Céline Guilbeau-Frugier; Josep Mercader; Jeanne Mialet-Perez
Journal:  J Physiol Biochem       Date:  2015-12-03       Impact factor: 4.158

3.  Variations in adrenal gland medulla and dopamine effects induced by the lack of Irs2.

Authors:  Leonardo Catalano-Iniesta; María Carmen Iglesias-Osma; Virginia Sánchez-Robledo; Marta Carretero-Hernández; Enrique J Blanco; José Carretero; María José García-Barrado
Journal:  J Physiol Biochem       Date:  2018-10-26       Impact factor: 4.158

4.  High doses of tyramine stimulate glucose transport in human fat cells.

Authors:  Christian Carpéné; Francisco Les; Josep Mercader-Barceló; Nathalie Boulet; Anaïs Briot; Jean-Louis Grolleau
Journal:  J Physiol Biochem       Date:  2022-01-23       Impact factor: 4.158

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