Deficiency in Nrf2 transcription factor decreases adipose tissue mass and hepatic lipid accumulation in leptin‐deficient mice. (29th November 2014)
- Record Type:
- Journal Article
- Title:
- Deficiency in Nrf2 transcription factor decreases adipose tissue mass and hepatic lipid accumulation in leptin‐deficient mice. (29th November 2014)
- Main Title:
- Deficiency in Nrf2 transcription factor decreases adipose tissue mass and hepatic lipid accumulation in leptin‐deficient mice
- Authors:
- Xu, Jialin
Donepudi, Ajay C.
More, Vijay R.
Kulkarni, Supriya R.
Li, Liya
Guo, Liangran
Yan, Bingfang
Chatterjee, Tapan
Weintraub, Neal
Slitt, Angela L. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="oby20929-sec-0001" sec-type="section"> <title>Objective</title> <p>To evaluate whether Nrf2 deficiency impacts insulin resistance and lipid accumulation in liver and white adipose tissue.</p> </sec> <sec id="oby20929-sec-0002" sec-type="section"> <title>Methods</title> <p>Lep<sup>ob/ob</sup> mice (OB) with targeted Nrf2 deletion (OB‐Nrf2KO) were generated. Pathogenesis of obesity and type 2 diabetes was measured in C57BL/6J, Nrf2KO, OB, and OB‐Nrf2KO mice. Hepatic lipid content, lipid clearance, and very low‐density lipoprotein (VLDL) secretion were determined between OB and OB‐Nrf2KO mice.</p> </sec> <sec id="oby20929-sec-0003" sec-type="section"> <title>Results</title> <p>OB‐Nrf2KO mice exhibited decreased white adipose tissue mass and decreased adipogenic and lipogenic gene expression compared with OB mice. Nrf2 deficiency prolonged hyperglycemia in response to glucose challenge, which was paralleled by reduced insulin‐stimulated Akt phosphorylation. In OB mice, Nrf2 deficiency decreased hepatic lipid accumulation, decreased peroxisome proliferator‐activated receptor γ expression and nicotinamide adenine dinucleotide phosphate (NADPH) content, and enhanced VLDL secretion. However, this observation was opposite in lean mice. Additionally, OB‐Nrf2KO mice exhibited increased plasma triglyceride content, decreased HDL‐cholesterol content, and enhanced apolipoprotein B expression,<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="oby20929-sec-0001" sec-type="section"> <title>Objective</title> <p>To evaluate whether Nrf2 deficiency impacts insulin resistance and lipid accumulation in liver and white adipose tissue.</p> </sec> <sec id="oby20929-sec-0002" sec-type="section"> <title>Methods</title> <p>Lep<sup>ob/ob</sup> mice (OB) with targeted Nrf2 deletion (OB‐Nrf2KO) were generated. Pathogenesis of obesity and type 2 diabetes was measured in C57BL/6J, Nrf2KO, OB, and OB‐Nrf2KO mice. Hepatic lipid content, lipid clearance, and very low‐density lipoprotein (VLDL) secretion were determined between OB and OB‐Nrf2KO mice.</p> </sec> <sec id="oby20929-sec-0003" sec-type="section"> <title>Results</title> <p>OB‐Nrf2KO mice exhibited decreased white adipose tissue mass and decreased adipogenic and lipogenic gene expression compared with OB mice. Nrf2 deficiency prolonged hyperglycemia in response to glucose challenge, which was paralleled by reduced insulin‐stimulated Akt phosphorylation. In OB mice, Nrf2 deficiency decreased hepatic lipid accumulation, decreased peroxisome proliferator‐activated receptor γ expression and nicotinamide adenine dinucleotide phosphate (NADPH) content, and enhanced VLDL secretion. However, this observation was opposite in lean mice. Additionally, OB‐Nrf2KO mice exhibited increased plasma triglyceride content, decreased HDL‐cholesterol content, and enhanced apolipoprotein B expression, suggesting Nrf2 deficiency caused dyslipidemia in these mice.</p> </sec> <sec id="oby20929-sec-0004" sec-type="section"> <title>Conclusions</title> <p>Nrf2 deficiency in Lep<sup>ob/ob</sup> mice reduced white adipose tissue mass and prevented hepatic lipid accumulation but induced insulin resistance and dyslipidemia. This study indicates a dual role of Nrf2 during metabolic dysregulation—increasing lipid accumulation in liver and white adipose tissue but preventing lipid accumulation in obese mice.</p> </sec> </abstract> … (more)
- Is Part Of:
- Obesity. Volume 23:Number 2(2015:Feb.)
- Journal:
- Obesity
- Issue:
- Volume 23:Number 2(2015:Feb.)
- Issue Display:
- Volume 23, Issue 2 (2015)
- Year:
- 2015
- Volume:
- 23
- Issue:
- 2
- Issue Sort Value:
- 2015-0023-0002-0000
- Page Start:
- 335
- Page End:
- 344
- Publication Date:
- 2014-11-29
- Subjects:
- Obesity -- Periodicals
616.398005 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1930-739X ↗
http://www.obesityresearch.org ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/oby.20929 ↗
- Languages:
- English
- ISSNs:
- 1930-7381
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6196.929955
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4092.xml