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Author(s): Delaney KZ, Dam V, Murphy J, Morais JA, Denis R, Atlas H, Pescarus R, Garneau PY, Santosa S...
The ability to accurately identify and quantify immune cell populations within adipose tissue is important in understanding the role of immune cells in metabolic disease risk. Flow cytometry is the...
Article GUID: 32926866
Author(s): Tam BT, Murphy J, Khor N, Morais JA, Santosa S
Although childhood-onset obesity (CO) and adult-onset obesity (AO) are known to lead to distinctive clinical manifestations and disease risks, the fundamental differences between them are largely unclear. The aim of the current study is to investigate the f...
Article GUID: 32808657
Author(s): Tam BT, Morais JA, Santosa S
Obes Rev. 2020 Feb 05;: Authors: Tam BT, Morais JA, Santosa S
Article GUID: 32020741
Author(s): Santosa S, Bush NC, Jensen MD
J Clin Endocrinol Metab. 2017 08 01;102(8):3056-3064 Authors: Santosa S, Bush NC, Jensen MD
Article GUID: 28641384
Author(s): Murphy J, Bacon SL, Morais JA, Tsoukas MA, Santosa S
Obesity (Silver Spring). 2019 May 27;: Authors: Murphy J, Bacon SL, Morais JA, Tsoukas MA, Santosa S
Article GUID: 31131996
Author(s): Varady KA, Dam VT, Klempel MC, Horne M, Cruz R, Kroeger CM, Santosa S
Sci Rep. 2015 Jan 05;5:7561 Authors: Varady KA, Dam VT, Klempel MC, Horne M, Cruz R, Kroeger CM, Santosa S
Article GUID: 25557754
Author(s): Santosa S, Jensen MD
Front Endocrinol (Lausanne). 2015;6:103 Authors: Santosa S, Jensen MD
Article GUID: 26191040
Author(s): Dam V, Sikder T, Santosa S
Obes Rev. 2016 Jan;17(1):1-17 Authors: Dam V, Sikder T, Santosa S
Article GUID: 26667065
Author(s): Santosa S, Bonnes SL, Jensen MD
J Clin Endocrinol Metab. 2016 05;101(5):2089-98 Authors: Santosa S, Bonnes SL, Jensen MD
Article GUID: 27003301
Author(s): Yang SQ, DeGuire JR, Lavery P, Mak IL, Weiler HA, Santosa S
Nutr Res. 2016 May;36(5):408-17 Authors: Yang SQ, DeGuire JR, Lavery P, Mak IL, Weiler HA, Santosa S
Article GUID: 27101759
Author(s): Murphy J, Moullec G, Santosa S
Metabolism. 2017 Feb;67:31-40 Authors: Murphy J, Moullec G, Santosa S
Article GUID: 28081776
Author(s): Delaney KZ, Vanstone CA, Weiler HA, Santosa S
Sci Rep. 2018 Oct 12;8(1):15204 Authors: Delaney KZ, Vanstone CA, Weiler HA, Santosa S
Article GUID: 30315178
Title: | Acetyl-CoA regulation, OXPHOS integrity and leptin level are different in females with different onsets of obesity. |
Authors: | Tam BT, Murphy J, Khor N, Morais JA, Santosa S |
Link: | https://www.ncbi.nlm.nih.gov/pubmed/32808657 |
DOI: | 10.1210/endocr/bqaa142 |
Category: | Endocrinology |
PMID: | 32808657 |
Dept Affiliation: | PERFORM
1 Department of Health, Kinesiology, and Applied Physiology, Concordia University, Montreal, Quebec, Canada. 2 Metabolism, Obesity, Nutrition Lab, PERFORM Centre, Concordia University, Montreal, Quebec, Canada. 3 Division of Geriatric Medicine and Research Institute of McGill University Health Centre, Montreal, Quebec, Canada. |
Description: |
Although childhood-onset obesity (CO) and adult-onset obesity (AO) are known to lead to distinctive clinical manifestations and disease risks, the fundamental differences between them are largely unclear. The aim of the current study is to investigate the fundamental differences between subcutaneous adipose tissue from CO and AO and identify metabolic differences between abdominal (abSAT) and femoral subcutaneous adipose tissues (feSAT). Total and regional body composition was assessed using DXA and computed tomography. Level of acetyl-CoA, NAD+/NADH, acetyl-CoA network genes, mitochondrial complex abundance, H3 acetylation were determined in biopsied abSAT and feSAT. Serum leptin and adiponectin were measured. Our results showed that acetyl-CoA was higher in subcutaneous adipose tissue from subjects with AO compared to CO. Multiple linear regression revealed that ATP citrate lyase was the only main effect affecting the level of acetyl-CoA. Circulating leptin was higher in AO. The increased level of acetyl-CoA was strongly associated with histone H3 acetylation, LEPTIN expression in adipose tissue and circulating leptin in AO. NAD+/NADH was higher in CO, however, mitochondrial complexes abundance, complex II: complex V and complex IV: complex V ratio were lower in CO, reflecting compromised mitochondrial function in adipose tissue from CO. Moreover, we identified differences in the level of acetyl-CoA and NAD+/NADH ratio between abSAT and feSAT, suggesting that these fat depots may possess different metabolic properties. The fundamental difference in the important metabolic intermediate, acetyl-CoA, between CO and AO may help us better understand the development of obesity and the pathogenesis of different obesity-related diseases in human. PMID: 32808657 [PubMed - as supplied by publisher] |