Résumé
Les relations entre adipocytes et polluants ne se limiteraient pas à un simple stockage moléculaire, les polluants suivant les mouvements des acides gras au gré des alternances des états de lipolyse et de lipogenèse: l’étude menée in vitro sur des souris confirme que la présence de faibles quantités de benzo(a)pyrène (B[a]P) dans l’alimentation ou dans l’environnement de l’animal induit une prise de poids significative dès les premiers jours de l’exposition. L’étude in vitro sur des adipocytes isolés de souris montre que le phénomène est en lien avec un dysfonctionnement de récepteurs transmembranaires (β-récepteurs, récepteurs MC2-R). De récents résultats mettent en cause l’accumulation des polluants dans la membrane cellulaire, provoquant une modification de l’intégrité de ces récepteurs spécifiques. Le caractère ubiquitaire du phénomène est par ailleurs souligné.
Abstract
The relationship between adipocytes and pollutants does not appear to be limited to molecular storage only, as pollutants follow the movements of fatty acids as they alternate between lipolysis and lipogenesis: an in vitro study in mice confirms that the presence of small quantities of benzoapyrene in the animal’s food or environment gives rise to significant weight gain from the very first days of exposure. An in vitro study of isolated mouse adipocytes shows that the phenomenon is linked to a malfunction of transmembrane receptors (β receptors, MC2-R receptors). Recent results suggest that an accumulation of pollutants in the cell membrane might affect the integrity of these particular receptors. The phenomenon’s ubiquitous nature is also emphasised.
Références
Grova N, Valley A, Turner JD, et al. (2007) Modulation of behavior and NMDA-R1 gene mRNA expression in adult female mice after sub-acute administration of benzo(a) pyrene. Neurotoxicology 28: 630–636
Irigaray P, Mejean L, Laurent F (2005) Behavior of dioxin in pig adipocytes. Food Chem Toxicol 43: 457–460
Rodbell M (1964) Metabolism of isolated fat cells. I. Effects of hormones on glucose. Metabolism and Lipolysis. J Biol Chem 239: 375–380
Zalatan F, Krause JA, Blask DE (2001) Inhibition of isoproterenol-induced lipolysis in rat inguinal adipocytes in vitro by physiological melatonin via a receptor-mediated mechanism. Endocrinology 142: 3783–3790
Irigaray P, Ogier V, Jacquenet S, et al. (2006) Benzo[a] pyrene impairs β-adrenergic stimulation of adipose tissue lipolysis and causes weight gain in mice. A novel molecular mechanism of toxicity for a common food pollutant. FEBS J 273: 1362–1372
Litosch I, Hudson TH, Mills I, et al. (1982) Forskolin as an activator of cyclic AMP accumulation and lipolysis in rat adipocytes. Mol Pharmacol 22: 109–115
Peterson MJ, Patterson C, Ashmore J (1968) Effects of antilipolytic agents on dibutyryl cyclic AMP-induced lipolysis in adipose tissue. Life Sci 7: 551–560
Sikkema J, de Bont JA, Poolman B (1994) Interactions of cyclic hydrocarbons with biological membranes. J Biol Chem 18: 8022–8028
Sikkema J, Poolman B, Konings WN, de Bont JA (1992) Effects of the membrane action of tetralin on the functional and structural properties of artificial and bacterial membranes. J Bacteriol 174: 2986–2992
Plant AL, Benson DM, Smith LC (1985) Cellular uptake and intracellular localization of benzo[a]pyrene by digital fluorescence imaging microscopy. J Cell Biol 100: 1295–1308
Plant AL, Knapp RD, Smith LC (1987) Mechanism and rate of permeation of cells by polycyclic aromatic hydrocarbons. J Biol Chem 25: 2514–2519
Jimenez M, Aranda FJ, Teruel JA, Ortiz A (2002) The chemical toxic benzo[a]pyrene perturbs the physical organization of phosphatidylcholine membranes. Environ Toxicol Chem 21: 787–793
Anderson PA, Alster JM, Clinton SK, et al. (1985) Plasma amino acids and excretion of protein end products by mice fed 10 or 40 % soybean protein diets with or without dietary benzo[a]pyrene or 1,2-dimethylhydrazine. J Nutr 115: 1515–1527
Sydnor KL, Allen C, Higgins B (1972) Effect of an aqueous extract of cigarette-smoke condensate on benzo[a]pyrene-induced sarcoma and body weight in the rat. Natl Cancer Inst 48: 893–909
Rigdon RH, Neal J (1966) Effect of feeding benzo[a]pyrene on growth of young mice. Tex Rep Biol Med 24: 473–478
Saunders CR, Shockley DC, Knuckles ME (2001) Behavioral effects induced by acute exposure to benzo(a)pyrene in F-344 rats. Neurotox Res 3: 557–579
Brunette DM, Katz M (1975) The interactions of benzo(a) pyrene with cell membranes: uptake into Chinese hamster ovary (CHO) cells and fluorescence studies with isolated membranes. Chem Biol Interact 11: 1–14
Imbeault P, Chevrier J, Dewailly E, et al. (2001) Increase in plasma pollutant levels in response to weight loss in humans is related to in vitro subcutaneous adipocyte basal lipolysis. Int J Obes 25: 1585–1591
Irigaray P, Newby JA, Lacomme S, Belpomme D (2007) Overweight/obesity and cancer genesis: more than a biological link. Biomed Pharmacother 61: 665–678
Hutcheon DE, Kantrowitz J, Van Gelder RN, Flynn E (1983) Factors affecting plasma benzo[a]pyrene levels in environmental studies. Environ Res 32: 104–110
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Amoussou, B., Guivarch, Y., Heidi, H. et al. Les 10es Entretiens de nutrition, institut Pasteur de Lille L’obésité, une maladie nutritionnelle. Obes 3, 128–132 (2008). https://doi.org/10.1007/s11690-008-0147-z
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DOI: https://doi.org/10.1007/s11690-008-0147-z