scholarly journals Molecular Basis of White Adipose Tissue Remodeling That Precedes and Coincides With Hibernation in the Syrian Hamster, a Food-Storing Hibernator

2019 ◽  
Vol 9 ◽  
Author(s):  
Yuichi Chayama ◽  
Lisa Ando ◽  
Yuya Sato ◽  
Shuji Shigenobu ◽  
Daisuke Anegawa ◽  
...  
Keyword(s):  
Adipose Tissue ◽  
White Adipose Tissue ◽  
Syrian Hamster ◽  
Molecular Basis ◽  
Tissue Remodeling ◽  
Food Storing ◽  
Adipose Tissue Remodeling

scholarly journals Oral Ang-(1-7) treatment improves white adipose tissue remodeling and hypertension in rats with metabolic syndrome

Nutrition: X ◽  
2019 ◽  
Vol 1 ◽  
pp. 100004 ◽  
Author(s):  
Maria Andréa Barbosa ◽  
Graziele Galdino de Sousa ◽  
Uberdan Guilherme Mendes de Castro ◽  
Cláudia Martins Carneiro ◽  
Vivian Paulino Figueiredo ◽  
...  
Keyword(s):  
Metabolic Syndrome ◽  
Adipose Tissue ◽  
White Adipose Tissue ◽  
Tissue Remodeling ◽  
Adipose Tissue Remodeling

scholarly journals Protein kinase Cβ deficiency attenuates obesity syndrome ofob/obmice by promoting white adipose tissue remodeling

2011 ◽  
Vol 53 (3) ◽  
pp. 368-378 ◽  
Author(s):  
Wei Huang ◽  
Rishipal R. Bansode ◽  
Naresh C. Bal ◽  
Madhu Mehta ◽  
Kamal D. Mehta
Keyword(s):  
Adipose Tissue ◽  
Protein Kinase ◽  
White Adipose Tissue ◽  
Tissue Remodeling ◽  
Adipose Tissue Remodeling ◽  
Obesity Syndrome

scholarly journals Adipose Tissue Remodeling in Children: The Link between Collagen Deposition and Age-Related Adipocyte Growth

2012 ◽  
Vol 97 (4) ◽  
pp. 1320-1327 ◽  
Author(s):  
Charmaine S. Tam ◽  
Joan Tordjman ◽  
Adeline Divoux ◽  
Louise A. Baur ◽  
Karine Clément
Keyword(s):  
Adipose Tissue ◽  
Tissue Remodeling ◽  
Collagen Deposition ◽  
Age Related ◽  
Adipose Tissue Remodeling

scholarly journals Evidence for the Regulatory Role of Lipocalin 2 in High-Fat Diet-Induced Adipose Tissue Remodeling in Male Mice

Endocrinology ◽  
2013 ◽  
Vol 154 (10) ◽  
pp. 3525-3538 ◽  
Author(s):  
Hong Guo ◽  
Merlijn Bazuine ◽  
Daozhong Jin ◽  
Merry M. Huang ◽  
Samuel W. Cushman ◽  
...  
Keyword(s):  
Adipose Tissue ◽  
High Fat Diet ◽  
Adipocyte Differentiation ◽  
Tissue Remodeling ◽  
Peroxisome Proliferator ◽  
Lipocalin 2 ◽  
Peroxisome Proliferator Activated Receptor ◽  
Adipose Tissue Remodeling ◽  
Fat Depot

Lipocalin 2 (Lcn2) has previously been characterized as an adipokine/cytokine playing a role in glucose and lipid homeostasis. In this study, we investigate the role of Lcn2 in adipose tissue remodeling during high-fat diet (HFD)-induced obesity. We find that Lcn2 protein is highly abundant selectively in inguinal adipose tissue. During 16 weeks of HFD feeding, the inguinal fat depot expanded continuously, whereas the expansion of the epididymal fat depot was reduced in both wild-type (WT) and Lcn2−/− mice. Interestingly, the depot-specific effect of HFD on fat mass was exacerbated and appeared more pronounced and faster in Lcn2−/− mice than in WT mice. In Lcn2−/− mice, adipocyte hypertrophy in both inguinal and epididymal adipose tissue was more profoundly induced by age and HFD when compared with WT mice. The expression of peroxisome proliferator-activated receptor-γ protein was significantly down-regulated, whereas the gene expression of extracellular matrix proteins was up-regulated selectively in epididymal adipocytes of Lcn2−/− mice. Consistent with these observations, collagen deposition was selectively higher in the epididymal, but not in the inguinal adipose depot of Lcn2−/− mice. Administration of the peroxisome proliferator-activated receptor-γ agonist rosiglitazone (Rosi) restored adipogenic gene expression. However, Lcn2 deficiency did not alter the responsiveness of adipose tissue to Rosi effects on the extracellular matrix expression. Rosi treatment led to the further enlargement of adipocytes with improved metabolic activity in Lcn2−/− mice, which may be associated with a more pronounced effect of Rosi treatment in reducing TGF-β in Lcn2−/− adipose tissue. Consistent with these in vivo observations, Lcn2 deficiency reduces the adipocyte differentiation capacity of stromal-vascular cells isolated from HFD-fed mice in these cells. Herein Rosi treatment was again able to stimulate adipocyte differentiation to a similar extent in WT and Lcn2−/− inguinal and epididymal stromal-vascular cells. Thus, combined, our data indicate that Lcn2 has a depot-specific role in HFD-induced adipose tissue remodeling.

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