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      Fish oil prevents changes induced by a high‐fat diet on metabolism and adipokine secretion in mice subcutaneous and visceral adipocytes

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          Abstract

          Key points

          • Fish oil (FO), rich in omega‐3 polyunsaturated fatty acids, has beneficial effects on changes induced by obesity and partially prevents associated comorbidities.

          • The effects of FO on adipocytes from different adipose tissue depots in high‐fat (HF) diet induced obese mice have not been uninvestigated.

          • This is the first study to examine the effects of FO on changes in metabolism and adipokine production in adipocytes from s.c. (inguinal; ING) or visceral (retroperitoneal; RP) white adipose depots in a HF diet‐induced obese mice.

          • Unlike most studies performed previously, FO supplementation was initiated 4 weeks before the induction of obesity.

          • HF diet caused marked changes in ING (glucose uptake and secretion of adiponectin, tumour necrosis factor‐α and interleukin‐6 in ING) and RP (lipolysis, de novo lipogenesis and secretion of pro‐inflammatory cytokines) adipose depots.

          • Previous and concomitant FO administration prevented the changes in ING and RP adipocytes induced by the HF diet.

          Abstract

          In the present study, we investigated the effect of fish oil (FO) on metabolism and adipokine production by adipocytes from s.c. (inguinal; ING) and visceral (retroperitoneal; RP) white adipose depots in high‐fat (HF) diet‐induced obese mice. Mice were divided into CO (control diet), CO+FO, HF and HF+FO groups. The HF group presented higher body weight, glucose intolerance, insulin resistance, higher plasma total and low‐density lipoprotein cholesterol levels, and greater weights of ING and RP adipose depots accompanied by hypertrophy of the adipocytes. FO exerted anti‐obesogenic effects associated with beneficial effects on dyslipidaemia and insulin resistance in mice fed a HF diet (HF+FO group). HF raised RP adipocyte lipolysis and the production of pro‐inflammatory cytokines and reduced de novo synthesis of fatty acids, whereas, in ING adipocytes, it decreased glucose uptake and adiponectin secretion but did not change lipolysis. Therefore, the adipose depots play different roles in HF diet‐induced insulin resistance according to their location in the body. Concerning cytokine secretion, adipocytes per se in addition to white adopise tissue infiltrated leukocytes have to be considered in the aetiology of the comorbidities associated with obesity. Evidence is presented showing that previous and concomitant administration of FO can prevent changes in metabolism and the secretion of hormones and cytokines in ING and RP adipocytes induced by HF.

          Key points

          • Fish oil (FO), rich in omega‐3 polyunsaturated fatty acids, has beneficial effects on changes induced by obesity and partially prevents associated comorbidities.

          • The effects of FO on adipocytes from different adipose tissue depots in high‐fat (HF) diet induced obese mice have not been uninvestigated.

          • This is the first study to examine the effects of FO on changes in metabolism and adipokine production in adipocytes from s.c. (inguinal; ING) or visceral (retroperitoneal; RP) white adipose depots in a HF diet‐induced obese mice.

          • Unlike most studies performed previously, FO supplementation was initiated 4 weeks before the induction of obesity.

          • HF diet caused marked changes in ING (glucose uptake and secretion of adiponectin, tumour necrosis factor‐α and interleukin‐6 in ING) and RP (lipolysis, de novo lipogenesis and secretion of pro‐inflammatory cytokines) adipose depots.

          • Previous and concomitant FO administration prevented the changes in ING and RP adipocytes induced by the HF diet.

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          Author and article information

          Contributors
          alonsovale@gmail.com
          Journal
          J Physiol
          J. Physiol. (Lond.)
          10.1111/(ISSN)1469-7793
          TJP
          jphysiol
          The Journal of Physiology
          John Wiley and Sons Inc. (Hoboken )
          0022-3751
          1469-7793
          25 August 2016
          01 November 2016
          : 594
          : 21 ( doiID: 10.1113/tjp.2016.594.issue-21 )
          : 6301-6317
          Affiliations
          [ 1 ] Department of Biological Sciences Institute of Environmental Sciences Chemical and Pharmaceutical Federal University of São Paulo, Diadema Brazil
          [ 2 ] Department of Physiology and Biophysics Institute of Biomedical Sciences University of Sao Paulo Sao Paulo Brazil
          [ 3 ] Campus of Exact Science and Technology State University of Goias Anapolis Brazil
          Author notes
          [*] [* ] Corresponding author M. I. C. Alonso Vale: Department of Biological Sciences, Institute of Environmental, Chemical and Pharmaceutical Sciences, Federal University of São Paulo, 210, São Nicolau Street, Diadema 09913‐030, Brazil. Email: alonsovale@ 123456gmail.com
          Author information
          http://orcid.org/0000-0003-4949-5668
          Article
          PMC5088242 PMC5088242 5088242 TJP7437
          10.1113/JP272541
          5088242
          27558442
          7f24c4d4-c26f-42c2-b86c-2cccca66cc07
          © 2016 The Authors. The Journal of Physiology © 2016 The Physiological Society
          History
          : 11 April 2016
          : 22 June 2016
          Page count
          Figures: 8, Tables: 3, Pages: 17, Words: 9107
          Funding
          Funded by: FAPESP
          Award ID: 2011/51627‐8, 2010/07596‐8, 2010/05669‐8 and 2013/03268‐4
          Funded by: CNPq
          Funded by: CAPES
          Funded by: Guggenheim Foundation
          Categories
          Endocrinology and Metabolism
          Metabolism and Regulation
          Research Paper
          Renal and endocrine
          Editor's Choice
          Custom metadata
          2.0
          tjp7437
          1 November 2016
          Converter:WILEY_ML3GV2_TO_NLMPMC version:4.9.6 mode:remove_FC converted:01.11.2016

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