دورية أكاديمية

Sex-Specific Differences in Fat Storage, Development of Non-Alcoholic Fatty Liver Disease and Brain Structure in Juvenile HFD-Induced Obese Ldlr-/-.Leiden Mice.

التفاصيل البيبلوغرافية
العنوان: Sex-Specific Differences in Fat Storage, Development of Non-Alcoholic Fatty Liver Disease and Brain Structure in Juvenile HFD-Induced Obese Ldlr-/-.Leiden Mice.
المؤلفون: Jacobs SAH; Department of Anatomy, Radboud university medical center, Donders Institute for Brain, Cognition and Behaviour, Preclinical Imaging Center PRIME, 6500 HB Nijmegen, The Netherlands., Gart E; Department of Metabolic Health Research, Netherlands Organisation for Applied Scientific Research (TNO), 2333 CK Leiden, The Netherlands.; Human and Animal Physiology, Wageningen University, 6700 AH Wageningen, The Netherlands., Vreeken D; Department of Anatomy, Radboud university medical center, Donders Institute for Brain, Cognition and Behaviour, Preclinical Imaging Center PRIME, 6500 HB Nijmegen, The Netherlands., Franx BAA; Department of Anatomy, Radboud university medical center, Donders Institute for Brain, Cognition and Behaviour, Preclinical Imaging Center PRIME, 6500 HB Nijmegen, The Netherlands., Wekking L; Department of Anatomy, Radboud university medical center, Donders Institute for Brain, Cognition and Behaviour, Preclinical Imaging Center PRIME, 6500 HB Nijmegen, The Netherlands., Verweij VGM; Department of Anatomy, Radboud university medical center, Donders Institute for Brain, Cognition and Behaviour, Preclinical Imaging Center PRIME, 6500 HB Nijmegen, The Netherlands., Worms N; Department of Metabolic Health Research, Netherlands Organisation for Applied Scientific Research (TNO), 2333 CK Leiden, The Netherlands., Schoemaker MH; Reckitt Benckiser Health, Mead Johnson Pediatric Nutrition Institute, 6545 CJ Nijmegen, The Netherlands., Gross G; Reckitt Benckiser Health, Mead Johnson Pediatric Nutrition Institute, 6545 CJ Nijmegen, The Netherlands., Morrison MC; Department of Metabolic Health Research, Netherlands Organisation for Applied Scientific Research (TNO), 2333 CK Leiden, The Netherlands.; Human and Animal Physiology, Wageningen University, 6700 AH Wageningen, The Netherlands., Kleemann R; Department of Metabolic Health Research, Netherlands Organisation for Applied Scientific Research (TNO), 2333 CK Leiden, The Netherlands.; Department of Vascular Surgery, Leiden University Medical Center, 2300 RC Leiden, The Netherlands., Arnoldussen IAC; Department of Anatomy, Radboud university medical center, Donders Institute for Brain, Cognition and Behaviour, Preclinical Imaging Center PRIME, 6500 HB Nijmegen, The Netherlands., Kiliaan AJ; Department of Anatomy, Radboud university medical center, Donders Institute for Brain, Cognition and Behaviour, Preclinical Imaging Center PRIME, 6500 HB Nijmegen, The Netherlands. amanda.kiliaan@radboudumc.nl.
المصدر: Nutrients [Nutrients] 2019 Aug 10; Vol. 11 (8). Date of Electronic Publication: 2019 Aug 10.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: MDPI Publishing Country of Publication: Switzerland NLM ID: 101521595 Publication Model: Electronic Cited Medium: Internet ISSN: 2072-6643 (Electronic) Linking ISSN: 20726643 NLM ISO Abbreviation: Nutrients Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Basel, Switzerland : MDPI Publishing
مواضيع طبية MeSH: Sex Factors*, Diet, High-Fat/*adverse effects , Non-alcoholic Fatty Liver Disease/*etiology , Obesity/*metabolism , Obesity/*pathology, Adipose Tissue/metabolism ; Animals ; Brain/pathology ; Female ; Lipid Metabolism ; Liver/pathology ; Male ; Mice ; Mice, Obese ; Obesity/complications ; Receptors, LDL/deficiency
مستخلص: Background: Sex-specific differences play a role in metabolism, fat storage in adipose tissue, and brain structure. At juvenile age, brain function is susceptible to the effects of obesity; little is known about sex-specific differences in juvenile obesity. Therefore, this study examined sex-specific differences in adipose tissue and liver of high-fat diet (HFD)-induced obese mice, and putative alterations between male and female mice in brain structure in relation to behavioral changes during the development of juvenile obesity.
Methods: In six-week-old male and female Ldlr-/-.Leiden mice (n = 48), the impact of 18 weeks of HFD-feeding was examined. Fat distribution, liver pathology and brain structure and function were analyzed imunohisto- and biochemically, in cognitive tasks and with MRI.
Results: HFD-fed female mice were characterized by an increased perigonadal fat mass, pronounced macrovesicular hepatic steatosis and liver inflammation. Male mice on HFD displayed an increased mesenteric fat mass, pronounced adipose tissue inflammation and microvesicular hepatic steatosis. Only male HFD-fed mice showed decreased cerebral blood flow and reduced white matter integrity.
Conclusions: At young age, male mice are more susceptible to the detrimental effects of HFD than female mice. This study emphasizes the importance of sex-specific differences in obesity, liver pathology, and brain function.
References: Proc Natl Acad Sci U S A. 2000 Nov 7;97(23):12735-40. (PMID: 11070087)
Metabolism. 2001 Aug;50(8):976-82. (PMID: 11474488)
Arterioscler Thromb Vasc Biol. 2001 Oct;21(10):1630-5. (PMID: 11597937)
Neuroscience. 2002;113(3):607-15. (PMID: 12150780)
J Endocrinol. 2003 Feb;176(2):237-46. (PMID: 12553872)
Horm Metab Res. 2003 Mar;35(3):142-6. (PMID: 12734773)
Arch Intern Med. 2003 Jul 14;163(13):1524-8. (PMID: 12860573)
Neuroscience. 2003;120(2):535-9. (PMID: 12890522)
Neurobiol Dis. 2004 Apr;15(3):640-7. (PMID: 15056472)
FASEB J. 2005 Jan;19(1):136-8. (PMID: 15522905)
Behav Brain Res. 2005 Feb 28;157(2):219-34. (PMID: 15639173)
Nat Rev Neurosci. 2006 Jun;7(6):477-84. (PMID: 16688123)
Arterioscler Thromb Vasc Biol. 2007 May;27(5):996-1003. (PMID: 17303782)
Arterioscler Thromb Vasc Biol. 2007 Aug;27(8):1706-21. (PMID: 17541027)
Gend Med. 2007;4 Suppl B:S75-95. (PMID: 18156105)
Obes Surg. 2009 Jun;19(6):745-50. (PMID: 18629594)
Clin Auton Res. 2008 Dec;18(6):331-8. (PMID: 18726054)
Neurobiol Dis. 2009 Mar;33(3):482-98. (PMID: 19130883)
Physiol Behav. 2009 May 25;97(2):199-204. (PMID: 19250944)
Obesity (Silver Spring). 2010 Mar;18(3):463-9. (PMID: 19730425)
Clin Liver Dis. 2009 Nov;13(4):533-44. (PMID: 19818303)
Nat Rev Neurosci. 2010 Jan;11(1):9-17. (PMID: 20019686)
Int J Obes (Lond). 2010 Jun;34(6):989-1000. (PMID: 20157318)
J Neurochem. 2010 Sep;114(6):1581-9. (PMID: 20557430)
PLoS Biol. 2010 Jun 29;8(6):e1000412. (PMID: 20613859)
Neurosci Biobehav Rev. 2011 Jan;35(3):565-72. (PMID: 20620164)
Acta Clin Belg. 1990;45(5):311-26. (PMID: 2177300)
PLoS One. 2011;6(7):e21374. (PMID: 21799735)
J Hepatol. 2012 Mar;56(3):515-7. (PMID: 22108387)
Hippocampus. 2012 Nov;22(11):2095-100. (PMID: 22593080)
Mol Nutr Food Res. 2012 Jul;56(7):1081-9. (PMID: 22611002)
Nat Methods. 2012 Jun 28;9(7):676-82. (PMID: 22743772)
Nat Methods. 2012 Jul;9(7):671-5. (PMID: 22930834)
J Lipid Res. 2012 Dec;53(12):2791-6. (PMID: 22993232)
Neurol Sci. 2013 Jul;34(7):1215-21. (PMID: 23109096)
Chromosome Res. 2013 Mar;21(1):15-26. (PMID: 23359013)
Dev Cogn Neurosci. 2013 Jul;5:106-18. (PMID: 23500670)
Biochim Biophys Acta. 2014 Mar;1842(3):377-92. (PMID: 23684841)
Obesity (Silver Spring). 2013 Jul;21(7):1313-20. (PMID: 23687103)
J Pharmacol Exp Ther. 2013 Dec;347(3):635-44. (PMID: 24049060)
Neurobiol Aging. 2014 Mar;35(3):600-13. (PMID: 24210253)
Cell. 2013 Dec 19;155(7):1464-78. (PMID: 24360271)
Brain Behav Immun. 2014 Aug;40:9-17. (PMID: 24662056)
Biomed Rep. 2014 Sep;2(5):633-636. (PMID: 25054002)
J Neurosci. 2014 Oct 15;34(42):13963-75. (PMID: 25319693)
J Nutr Biochem. 2015 Jan;26(1):24-35. (PMID: 25444517)
PLoS One. 2014 Dec 23;9(12):e115922. (PMID: 25535951)
J Neurosci. 2015 Mar 4;35(9):4092-103. (PMID: 25740536)
Br J Pharmacol. 2015 Nov;172(22):5293-305. (PMID: 26292849)
Int J Obes (Lond). 2016 Apr;40(4):675-84. (PMID: 26499443)
Int J Obes (Lond). 2016 Sep;40(9):1416-23. (PMID: 27121255)
Circ J. 2016 Jul 25;80(8):1773-80. (PMID: 27295999)
Sci Rep. 2016 Aug 22;6:31542. (PMID: 27545964)
Res Dev Disabil. 2016 Dec;59:410-416. (PMID: 27728872)
J Neurosci Res. 2017 Jan 2;95(1-2):40-49. (PMID: 27870404)
Biosci Rep. 2017 Feb 3;37(1):. (PMID: 28073971)
PLoS One. 2017 Jan 11;12(1):e0169740. (PMID: 28076416)
BMC Genomics. 2017 Jan 17;18(1):89. (PMID: 28095800)
Int J Obes (Lond). 2017 Jun;41(6):935-944. (PMID: 28220041)
Sci Rep. 2017 Mar 03;7:43261. (PMID: 28256596)
N Engl J Med. 2017 Jul 20;377(3):211-221. (PMID: 28538136)
PLoS One. 2017 Jul 5;12(7):e0180648. (PMID: 28678821)
J Nutr Biochem. 2017 Oct;48:128-137. (PMID: 28825992)
Neuroimage. 2017 Dec;163:197-205. (PMID: 28923275)
Neurosci Lett. 2018 Mar 23;670:36-40. (PMID: 29355696)
Hepatol Commun. 2017 May 12;1(4):311-325. (PMID: 29404461)
Front Physiol. 2018 Feb 23;9:132. (PMID: 29527177)
Trends Mol Med. 2018 May;24(5):458-471. (PMID: 29665983)
J Am Assoc Lab Anim Sci. 2018 Apr 18;:. (PMID: 29669621)
Hepatol Commun. 2018 Oct 29;2(12):1513-1532. (PMID: 30556039)
Int J Mol Sci. 2018 Dec 20;20(1):null. (PMID: 30577415)
Acta Physiol (Oxf). 2019 Jun;226(2):e13270. (PMID: 30830722)
Pharmacol Ther. 1995;67(1):101-54. (PMID: 7494860)
J Nutr. 1993 Nov;123(11):1939-51. (PMID: 8229312)
Pathology. 1995 Jul;27(3):221-3. (PMID: 8532386)
J Hepatol. 1997;26 Suppl 1:13-22. (PMID: 9138124)
فهرسة مساهمة: Keywords: juvenile; obesity; sex
المشرفين على المادة: 0 (Receptors, LDL)
تواريخ الأحداث: Date Created: 20190814 Date Completed: 20200204 Latest Revision: 20200225
رمز التحديث: 20231215
مُعرف محوري في PubMed: PMC6723313
DOI: 10.3390/nu11081861
PMID: 31405127
قاعدة البيانات: MEDLINE
الوصف
تدمد:2072-6643
DOI:10.3390/nu11081861