The relationship of visfatin/pre-B-cell colony-enhancing factor/nicotinamide phosphoribosyltransferase in adipose tissue with inflammation, insulin resistance, and plasma lipids
Visfatin/pre-B-cell colony-enhancing factor (PBEF)/nicotinamide phosphoribosyltransferase (Nampt) has been proposed as an insulin-mimicking adipocytokine predominantly secreted from visceral adipose tissue (VAT) and correlated with obesity. However, recent evidence challenged this proposal and instead suggested visfatin/PBEF/Nampt as a proinflammatory cytokine. The study aimed to examine whether visfatin/PBEF/Nampt was predominantly expressed in VAT and was correlated with obesity. The relationship of visfatin/PBEF/Nampt gene expression in adipose tissues with proinfiammatory gene expression and metabolic phenotypes was also examined. The relative messenger RNA (mRNA) levels of visfatin/PBEF/Nampt, macrophage-specific marker CD68, and prointlammatory genes were measured in paired abdominal VAT and subcutaneous adipose tissues (SAT) and from 53 nondiabetic adults using quantitative real-time polymerase chain reaction. Fasting glucose, insulin, triglyceride, cholesterol, and uric acid levels were measured; and systemic insulin sensitivity was quantified with modified insulin suppression tests. There was no difference in visfatin/PBEF/Nampt mRNA levels between VAT and SAT, and neither was associated with measures of obesity. Visfatin/PBEF/Nampt mRNA levels were strongly correlated with proinflammatory gene expression including CD68 and tumor necrosis factor a gene in both VAT and SAT. The VAT and SAT visfatin/PBEF/Nampt mRNA expressions were positively correlated with steady-state plasma glucose concentrations measured with modified insulin suppression tests, a direct measurement of systemic insulin resistance (r = 0.42, P =.03 and r = 0.44, P =.03, respectively). The VAT visfatin/PBEF/Nampt mRNA expression was also positively correlated with fasting triglyceride (r = 0.42, P = .002) and total cholesterol levels (r = 0.37, P = .009). Visfatin/PBEF/Nampt is not predominantly secreted from VAT and is not correlated with obesity. Our findings suggest that visfatin/PBEF/ Nampt is a proinflammatory marker of adipose tissue associated with systemic insulin resistance and hyperlipidemia. (C) 2010 Elsevier Inc. All rights reserved.
机构:Univ Oslo, Internal Med Res Inst, Rikshosp, Radiumhosp Med Ctr, N-0027 Oslo, Norway
Dahl, Tuva B.
Yndestad, Arne
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Yndestad, Arne
Skjelland, Mona
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Skjelland, Mona
Oie, Erik
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Oie, Erik
Dahl, Arve
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Dahl, Arve
Michelsen, Annika
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Michelsen, Annika
Damas, Jan K.
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Damas, Jan K.
Tunheim, Siv H.
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Tunheim, Siv H.
Ueland, Thor
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Smith, Camilla
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Smith, Camilla
Bendz, Bjorn
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Bendz, Bjorn
Tonstad, Serena
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Tonstad, Serena
Gullestad, Lars
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Gullestad, Lars
Froland, Stig S.
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Krohg-Sorensen, Kirsten
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Russell, David
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Aukrust, Pal
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Aukrust, Pal
Halvorsen, Bente
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Univ Oslo, Internal Med Res Inst, Rikshosp, Radiumhosp Med Ctr, N-0027 Oslo, NorwayUniv Oslo, Internal Med Res Inst, Rikshosp, Radiumhosp Med Ctr, N-0027 Oslo, Norway
机构:Univ Oslo, Internal Med Res Inst, Rikshosp, Radiumhosp Med Ctr, N-0027 Oslo, Norway
Dahl, Tuva B.
Yndestad, Arne
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机构:Univ Oslo, Internal Med Res Inst, Rikshosp, Radiumhosp Med Ctr, N-0027 Oslo, Norway
Yndestad, Arne
Skjelland, Mona
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Skjelland, Mona
Oie, Erik
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Oie, Erik
Dahl, Arve
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Dahl, Arve
Michelsen, Annika
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Michelsen, Annika
Damas, Jan K.
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Damas, Jan K.
Tunheim, Siv H.
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Tunheim, Siv H.
Ueland, Thor
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Ueland, Thor
Smith, Camilla
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Smith, Camilla
Bendz, Bjorn
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Bendz, Bjorn
Tonstad, Serena
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Tonstad, Serena
Gullestad, Lars
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Gullestad, Lars
Froland, Stig S.
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Froland, Stig S.
Krohg-Sorensen, Kirsten
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Russell, David
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Russell, David
Aukrust, Pal
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Aukrust, Pal
Halvorsen, Bente
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Univ Oslo, Internal Med Res Inst, Rikshosp, Radiumhosp Med Ctr, N-0027 Oslo, NorwayUniv Oslo, Internal Med Res Inst, Rikshosp, Radiumhosp Med Ctr, N-0027 Oslo, Norway