Abstract
Cell, animal and human studies dealing with carotenoids and carotenoid derivatives as nutritional regulators of adipose tissue biology with implications for the etiology and management of obesity and obesity-related metabolic diseases are reviewed. Most studied carotenoids in this context are β-carotene, cryptoxanthin, astaxanthin and fucoxanthin, together with β-carotene-derived retinoids and some other apocarotenoids. Studies indicate an impact of these compounds on essential aspects of adipose tissue biology including the control of adipocyte differentiation (adipogenesis), adipocyte metabolism, oxidative stress and the production of adipose tissue-derived regulatory signals and inflammatory mediators. Specific carotenoids and carotenoid derivatives restrain adipogenesis and adipocyte hypertrophy while enhancing fat oxidation and energy dissipation in brown and white adipocytes, and counteract obesity in animal models. Intake, blood levels and adipocyte content of carotenoids are reduced in human obesity. Specifically designed human intervention studies in the field, though still sparse, indicate a beneficial effect of carotenoid supplementation in the accrual of abdominal adiposity. In summary, studies support a role of specific carotenoids and carotenoid derivatives in the prevention of excess adiposity, and suggest that carotenoid requirements may be dependent on body composition.
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- ADH:
-
alcohol dehydrogenase
- ALDH:
-
aldehyde dehydrogenase
- AMPK:
-
AMP-dependent protein kinase
- atRA:
-
all trans retinoic acid
- BAT:
-
brown adipose tissue
- BC:
-
β-carotene
- BCO1:
-
β-carotene-15,15′-oxygenase
- BCO2:
-
β-carotene-9’,10′-oxygenase
- BMI:
-
body mass index
- bw:
-
body weight
- C/EBP:
-
CCAAT-enhancer binding protein
- CD36:
-
cluster of differentiation 36
- CRABP:
-
cellular retinoic acid binding protein
- CRBP:
-
cellular retinol binding protein
- FABP:
-
fatty acid binding protein
- ISX:
-
intestine-specific homeobox
- LRAT:
-
lecithin: retinol acyltransferase
- LDLr:
-
low density lipoprotein receptor
- LPL:
-
lipoprotein lipase
- NF-κB:
-
nuclear factor κB
- Nrf2:
-
nuclear factor erythroid 2-related factor 2
- PPAR:
-
peroxisome proliferator activated receptor
- Rald:
-
retinaldehyde
- RAR:
-
retinoic acid receptor
- RBP (or RBP4):
-
retinol binding protein
- RBPR2:
-
RBP receptor 2
- RDH:
-
retinol dehydrogenase
- REH:
-
retinyl ester hydrolase
- ROS:
-
reactive oxygen species
- RXR:
-
retinoid X receptor
- SR-B1:
-
scavenger receptor class B, member 1
- STRA6:
-
stimulated retinoic acid 6
- UCP1:
-
uncoupling protein 1
- WAT:
-
white adipose.
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Acknowledgements
The authors acknowledge funding support from the European Union’s Seventh Framework Programme FP7 under grant agreements n. 244995 (BIOCLAIMS Project) and n. 278373 (DIABAT project), the Spanish Government (grant AGL2012-33692), Fundación Ramón Areces, and the Instituto de Salud Carlos III, Centro de Investigación Biomédica en Red Fisiopatología de la Obesidad y Nutrición, CIBERobn. The authors are also grateful to The Nemours Research Foundation and The Players Center for Child Health at Wolfson Children’s Hospital in Jacksonville, Florida for their generous support. The UIB group is a member of the European Nutrigenomics Organization and the network IBERCAROT (CYTED, Spanish Government, n° 112RT0445).
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Bonet, M.L., Canas, J.A., Ribot, J., Palou, A. (2016). Carotenoids in Adipose Tissue Biology and Obesity. In: Stange, C. (eds) Carotenoids in Nature. Subcellular Biochemistry, vol 79. Springer, Cham. https://doi.org/10.1007/978-3-319-39126-7_15
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