Polychlorinated biphenyl-77 induces adipocyte differentiation and proinflammatory adipokines and promotes obesity and atherosclerosis

Environ Health Perspect. 2008 Jun;116(6):761-8. doi: 10.1289/ehp.10554.

Abstract

Background: Obesity, an inflammatory condition linked to cardiovascular disease, is associated with expansion of adipose tissue. Highly prevalent coplanar polychlorinated biphenyls (PCBs) such as 3,3',4,4'-tetrachlorobiphenyl (PCB-77) accumulate in adipose tissue because of their lipophilicity and increase with obesity. However, the effects of PCBs on adipocytes, obesity, and obesity-associated cardiovascular disease are unknown.

Objectives: In this study we examined in vitro and in vivo effects of PCB-77 on adipocyte differentiation, proinflammatory adipokines, adipocyte morphology, body weight, serum lipids, and atherosclerosis.

Methods: PCB-77 or 2,2',4,4,5,5'-hexachlorobiphenyl (PCB-153) was incubated with 3T3-L1 adipocytes either during differentiation or in mature adipocytes. Concentration-dependent effects of PCB-77 were contrasted with those of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). For in vivo studies, we treated C57BL/6 wild-type (WT) or aryl hydrocarbon receptor (AhR)(-/-) mice with vehicle or PCB-77 (49 mg/kg, by intraperitoneal injection) and examined body weight gain. In separate studies, we injected ApoE(-/-) mice with vehicle or PCB-77 over a 6-week period and examined body weight, adipocyte size, serum lipids, and atherosclerosis.

Results: Low concentrations of PCB-77 or TCDD increased adipocyte differentiation, glycerol-3-phosphate dehydrogenase activity, and expression of peroxisome proliferator-activated receptor gamma, whereas higher concentrations inhibited adipocyte differentiation. Effects of PCB-77 were abolished by the AhR antagonist alpha-naphthoflavone. PCB-77 promoted the expression and release of various proinflammatory cytokines from 3T3-L1 adipocytes. Administration of PCB-77 increased body weight gain in WT but not AhR(-/-) mice. ApoE(-/-) mice injected with PCB-77 exhibited greater body weight, adipocyte hypertrophy, serum dyslipidemia, and augmented atherosclerosis.

Conclusions: Our findings suggest that PCB-77 may contribute to the development of obesity and obesity-associated atherosclerosis.

Keywords: adipocyte differentiation; aryl hydrocarbon receptor; ectopic lipid deposition; obesity; polychlorinated biphenyl.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / cytology
  • Adipocytes / drug effects*
  • Adipokines / metabolism*
  • Animals
  • Atherosclerosis / chemically induced*
  • Atherosclerosis / pathology
  • Body Weight / drug effects
  • Body Weight / physiology
  • Cell Differentiation / drug effects*
  • Cytokines / metabolism
  • Gene Expression / drug effects
  • Glycerolphosphate Dehydrogenase / metabolism
  • Inflammation Mediators / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Obesity / chemically induced*
  • Obesity / pathology
  • PPAR gamma / metabolism
  • Polychlorinated Biphenyls / toxicity*
  • Receptors, Aryl Hydrocarbon / genetics
  • Receptors, Aryl Hydrocarbon / physiology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Weight Gain / drug effects
  • Weight Gain / physiology

Substances

  • Adipokines
  • Cytokines
  • Inflammation Mediators
  • PPAR gamma
  • Receptors, Aryl Hydrocarbon
  • Polychlorinated Biphenyls
  • Glycerolphosphate Dehydrogenase
  • 3,4,3',4'-tetrachlorobiphenyl
  • 2,4,5,2',4',5'-hexachlorobiphenyl