Tnfα, Cox2 and AdipoQ adipokine gene expression levels are modulated in murine adipose tissues by both nicotine and nACh receptors containing the β2 subunit

Mol Genet Metab. 2012 Nov;107(3):561-70. doi: 10.1016/j.ymgme.2012.08.012. Epub 2012 Aug 18.

Abstract

Studies have provided evidences for the effects of nicotine on adipose tissues, as well as in inflammatory response. We hypothesized that nicotine affects adipokine gene expression in adipose tissues via specific neuronal nicotinic acetylcholine receptors (nAChRs). First, we described the expression of multiple nAChR subunit genes in mouse white and brown adipose tissues (WAT and BAT), and detected differential expression in WAT and BAT (α2>α5>β2 and α2>β2>β4, respectively). Additionally, when nicotine was administered to wild-type mice, it significantly affected the expression of adipokine genes, such as Tnfα, AdipoQ, Haptoglobin and Mcp1 in WAT. Next, we demonstrated that in mice deficient for the β2 nAChR subunit (β2-/- mice), the expression levels of Cox2 and Ngfβ genes in WAT, and Leptin, Cox2, AdipoQ and Haptoglobin in BAT, were significantly altered. Furthermore, interactions between mouse β2 subunit and nicotine treatment affected the expression levels of the adipokine genes Tnfα, Cox2 and AdipoQ in WAT and of AdipoQ in BAT. Finally, analysis of a cellular model of cultured adipocytes demonstrated that application of nicotine after silencing of the β2 nAChR subunit significantly elevated the expression level of Cox2 gene. Together, our data suggest a molecular link between the β2 nACh receptor subunit and the expression levels of specific adipokines, which is also affected by nicotine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / cytology
  • Adipocytes / drug effects
  • Adipocytes / metabolism
  • Adiponectin / genetics*
  • Adiponectin / metabolism
  • Adipose Tissue, Brown / drug effects*
  • Adipose Tissue, Brown / metabolism
  • Adipose Tissue, White / drug effects*
  • Adipose Tissue, White / metabolism
  • Animals
  • Cells, Cultured
  • Cyclooxygenase 2 / genetics*
  • Cyclooxygenase 2 / metabolism
  • Gene Expression / drug effects
  • Gene Silencing
  • Male
  • Mice
  • Mice, Knockout
  • Nicotine / pharmacology*
  • Organ Specificity
  • RNA, Small Interfering / genetics
  • Receptors, Nicotinic / genetics
  • Receptors, Nicotinic / metabolism*
  • Signal Transduction / drug effects
  • Tumor Necrosis Factor-alpha / genetics*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Adiponectin
  • Adipoq protein, mouse
  • RNA, Small Interfering
  • Receptors, Nicotinic
  • Tumor Necrosis Factor-alpha
  • nicotinic receptor beta2
  • Nicotine
  • Ptgs2 protein, mouse
  • Cyclooxygenase 2