دورية أكاديمية

Intermittent hypoxia-induced insulin resistance is associated with alterations in white fat distribution.

التفاصيل البيبلوغرافية
العنوان: Intermittent hypoxia-induced insulin resistance is associated with alterations in white fat distribution.
المؤلفون: Poulain L; Université Grenoble Alpes, Laboratoire HP2, Grenoble, F-38042, France.; Inserm U1042, Laboratoire HP2, Grenoble, F-38042, France., Mathieu H; Université Grenoble Alpes, IRMaGe, Grenoble, F-38000, France.; Inserm, US017, Grenoble, F-38043, France.; CNRS, UMS 3552, Grenoble, F-38043, France.; CHU Grenoble-Alpes, IRMaGe, Grenoble, F-38000, France.; Inserm, U1216, Grenoble, F-38000, France., Thomas A; Université Grenoble Alpes, Laboratoire HP2, Grenoble, F-38042, France.; Inserm U1042, Laboratoire HP2, Grenoble, F-38042, France., Borel AL; Université Grenoble Alpes, Laboratoire HP2, Grenoble, F-38042, France.; Inserm U1042, Laboratoire HP2, Grenoble, F-38042, France., Remy C; Université Grenoble Alpes, IRMaGe, Grenoble, F-38000, France.; Inserm, US017, Grenoble, F-38043, France.; CNRS, UMS 3552, Grenoble, F-38043, France.; CHU Grenoble-Alpes, IRMaGe, Grenoble, F-38000, France.; Inserm, U1216, Grenoble, F-38000, France., Levy P; Université Grenoble Alpes, Laboratoire HP2, Grenoble, F-38042, France.; Inserm U1042, Laboratoire HP2, Grenoble, F-38042, France.; CHU Grenoble-Alpes, Laboratoires du Sommeil et EFCR, Grenoble, F-38043, France., Arnaud C; Université Grenoble Alpes, Laboratoire HP2, Grenoble, F-38042, France. claire.arnaud@univ-grenoble-alpes.fr.; Inserm U1042, Laboratoire HP2, Grenoble, F-38042, France. claire.arnaud@univ-grenoble-alpes.fr., Dematteis M; Université Grenoble Alpes, Laboratoire HP2, Grenoble, F-38042, France. maurice.dematteis@univ-grenoble-alpes.fr.; Inserm U1042, Laboratoire HP2, Grenoble, F-38042, France. maurice.dematteis@univ-grenoble-alpes.fr.; CHU Grenoble-Alpes, Service d'Addictologie, Grenoble, F-38043, France. maurice.dematteis@univ-grenoble-alpes.fr.
المصدر: Scientific reports [Sci Rep] 2017 Sep 11; Vol. 7 (1), pp. 11180. Date of Electronic Publication: 2017 Sep 11.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE
أسماء مطبوعة: Original Publication: London : Nature Publishing Group, copyright 2011-
مواضيع طبية MeSH: Body Fat Distribution* , Insulin Resistance*, Adipose Tissue, White/*anatomy & histology , Hypoxia/*pathology , Sleep Apnea Syndromes/*pathology, Animals ; Disease Models, Animal ; Epididymis/pathology ; Male ; Mice, Inbred C57BL ; Peritoneum/pathology ; Skin/pathology
مستخلص: Sleep apnea syndrome is characterized by repetitive upper airway collapses during night leading to intermittent hypoxia (IH). The latter is responsible for metabolic disturbances that rely, at least in part, on abdominal white fat inflammation. Besides qualitative alterations, we hypothesized that IH could also modify body fat distribution, a key factor for metabolic complications. C57BL6 mice exposed to IH (21-5% FiO 2 , 60 s cycle, 8 h/day) or air for 6 weeks were investigated for topographic fat alterations (whole-body MRI). Specific role of epididymal fat in IH-induced metabolic dysfunctions was assessed in lipectomized or sham-operated mice exposed to IH or air. Whereas total white fat volume was unchanged, IH induced epididymal adipose tissue (AT) loss with non-significant increase in subcutaneous and mesenteric fat. This was associated with impaired insulin sensitivity and secretion. Epididymal lipectomy led to increased subcutaneous fat in the perineal compartment and prevented IH-induced metabolic disturbances. IH led to reduced epididymal AT and impaired glucose regulation. This suggests that, rather than epididymal AT volume, qualitative fat alterations (i.e. inflammation) could represent the main determinant of metabolic dysfunction. This deterioration of glucose regulation was prevented in epididymal-lipectomized mice, possibly through prevention of IH-induced epididymal AT alterations and compensatory increase in subcutaneous AT.
References: Neurosci Biobehav Rev. 2001 Jan;25(1):15-28. (PMID: 11166075)
Int J Obes (Lond). 2005 Jul;29(7):778-84. (PMID: 15917857)
J Am Coll Cardiol. 2013 Aug 13;62(7):569-76. (PMID: 23770180)
Horm Metab Res. 2006 Oct;38(10):631-8. (PMID: 17075771)
J Mol Med (Berl). 2012 Apr;90(4):435-45. (PMID: 22086141)
J Clin Invest. 2011 Jun;121(6):2094-101. (PMID: 21633177)
ILAR J. 2009;50(3):262-81. (PMID: 19506313)
Am J Physiol Regul Integr Comp Physiol. 2000 Sep;279(3):R936-43. (PMID: 10956251)
Am J Respir Crit Care Med. 2013 Jul 15;188(2):240-8. (PMID: 23328524)
Mediators Inflamm. 2015 ;2015 :620258. (PMID: 25873766)
J Lipid Res. 2013 Apr;54(4):1058-65. (PMID: 23386706)
Am J Physiol Regul Integr Comp Physiol. 2012 Oct 1;303(7):R700-9. (PMID: 22895743)
Sci Rep. 2017 Mar 03;7:43663. (PMID: 28255159)
Eur Respir J. 2017 Apr 19;49(4):null. (PMID: 28424360)
Diabetes. 2002 Oct;51(10):2951-8. (PMID: 12351432)
J Am Coll Cardiol. 2008 Aug 19;52(8):686-717. (PMID: 18702977)
Eur Respir J. 2014 Feb;43(2):513-22. (PMID: 24072212)
J Appl Physiol (1985). 2009 May;106(5):1538-44. (PMID: 19265062)
Am J Physiol Endocrinol Metab. 2008 Jan;294(1):E15-26. (PMID: 17957034)
Am J Respir Crit Care Med. 2007 Apr 15;175(8):851-7. (PMID: 17272786)
Biochem Biophys Res Commun. 2014 May 16;447(4):660-5. (PMID: 24755071)
Obesity (Silver Spring). 2011 Nov;19(11):2167-74. (PMID: 21799478)
J Appl Physiol (1985). 2005 Nov;99(5):1643-8. (PMID: 16037401)
J Appl Physiol (1985). 2012 Oct 15;113(8):1304-10. (PMID: 22723632)
J Appl Physiol (1985). 2011 Sep;111(3):881-90. (PMID: 21737828)
J Clin Invest. 1995 Jul;96(1):88-98. (PMID: 7615840)
Diabetes Care. 2012 Nov;35(11):2384-9. (PMID: 22912423)
Physiol Rep. 2013 Aug;1(2):null. (PMID: 23914298)
Life Sci. 2016 Apr 1;150:1-7. (PMID: 26883978)
Br J Nutr. 2008 Aug;100(2):227-35. (PMID: 18397542)
Eur Respir J. 2011 Jun;37(6):1418-23. (PMID: 21177837)
J Appl Physiol (1985). 2017 Jul 20;:jap.00630.2017. (PMID: 28729392)
Diabetes Care. 2012 Sep;35(9):1902-6. (PMID: 22688546)
Circ Res. 2005 May 13;96(9):939-49. (PMID: 15890981)
Eur Respir J. 2012 Mar;39(3):746-67. (PMID: 21920888)
Curr Opin Clin Nutr Metab Care. 2010 Jul;13(4):377-81. (PMID: 20531174)
J Clin Endocrinol Metab. 2011 Nov;96(11):E1756-60. (PMID: 21865361)
Am J Physiol. 1997 Dec;273(6 Pt 2):R2117-23. (PMID: 9435669)
Cell Stress Chaperones. 2016 May;21(3):515-22. (PMID: 26902078)
Physiol Rev. 2013 Jan;93(1):359-404. (PMID: 23303913)
تواريخ الأحداث: Date Created: 20170913 Date Completed: 20190612 Latest Revision: 20190613
رمز التحديث: 20240829
مُعرف محوري في PubMed: PMC5593960
DOI: 10.1038/s41598-017-11782-0
PMID: 28894286
قاعدة البيانات: MEDLINE
الوصف
تدمد:2045-2322
DOI:10.1038/s41598-017-11782-0