Changes in fat mass influence SREBP-1c and UCP-2 gene expression in formerly obese subjects

Donatella Gniuli, Giuseppina Rosa, Melania Manco, Antonino Scarfone, Nathalie Vega, Aldo V. Greco, Marco Castagneto, Hubert Vidal, Geltrude Mingrone

Research output: Contribution to journalArticle

Abstract

Objective: To investigate the effect of fat mass (FM) reduction on adipose tissue gene expression in terms of lipid synthesis [sterol regulatory binding protein 1c (SREBP-1c)] and lipid oxidation [uncoupling protein 2 (UCP-2)] 2 years after lipid malabsorption and to assess the influence of lipid malabsorption on fat-free mass (FFM) maintenance evaluating the expression of genes related to glycolysis [hexokinase (HKII)] and glucose storage [glycogen synthase (GS)]. Research Method and Procedures: SREBP-1c, UCP-2, HKII, and GS mRNA expression were studied by reverse transcriptase-competitive polymerase chain reaction in 10 massively obese subjects before and 2 years after biliopancreatic diversion (BPD). Body composition was assessed by isotopic dilution method and insulin sensitivity by euglycemic-hyperinsulinemic clamp. Results: FM decrease was ∼60%, whereas FFM remained at normal physiological levels. In adipose tissue, SREBP-1c mRNA reduction (-39%, p <0.005) was related only to FM changes after BPD, and UCP-2 decrease (-37%, p <0.05) was dependent on free fatty acid (FFA) changes. No significant variations were observed in HKII and GS gene expression in skeletal muscle. Discussion: Lipid malabsorption induced by BPD altered the expression of genes involved in glucose and lipid metabolism, with different consequences on FM and FFM. The degree of FM loss seems to interfere with SREBP-1c gene suppression to preserve an adequate amount of fat storage, in accordance with the thrifty genotype hypothesis. The reduction of FFAs induced by BPD acts in inhibiting FFA transportation to the mitochondria (UCP-2), contributing to the decreased lipid oxidation inside the adipose tissue.

Original languageEnglish
Pages (from-to)567-573
Number of pages7
JournalObesity Research
Volume13
Issue number3
Publication statusPublished - 2005

Fingerprint

regulatory proteins
Sterols
sterols
binding proteins
Carrier Proteins
Fats
Biliopancreatic Diversion
Gene Expression
gene expression
lipids
Lipids
Glycogen Synthase
glycogen (starch) synthase
proteins
Adipose Tissue
malabsorption
Nonesterified Fatty Acids
adipose tissue
Uncoupling Protein 2
Glucose

Keywords

  • Bilio-pancreatic diversion
  • Fat free mass
  • Fat mass
  • Sterol regulatory binding protein 1c
  • Uncoupling protein 2

ASJC Scopus subject areas

  • Medicine (miscellaneous)
  • Public Health, Environmental and Occupational Health
  • Endocrinology
  • Food Science
  • Endocrinology, Diabetes and Metabolism

Cite this

Gniuli, D., Rosa, G., Manco, M., Scarfone, A., Vega, N., Greco, A. V., ... Mingrone, G. (2005). Changes in fat mass influence SREBP-1c and UCP-2 gene expression in formerly obese subjects. Obesity Research, 13(3), 567-573.

Changes in fat mass influence SREBP-1c and UCP-2 gene expression in formerly obese subjects. / Gniuli, Donatella; Rosa, Giuseppina; Manco, Melania; Scarfone, Antonino; Vega, Nathalie; Greco, Aldo V.; Castagneto, Marco; Vidal, Hubert; Mingrone, Geltrude.

In: Obesity Research, Vol. 13, No. 3, 2005, p. 567-573.

Research output: Contribution to journalArticle

Gniuli, D, Rosa, G, Manco, M, Scarfone, A, Vega, N, Greco, AV, Castagneto, M, Vidal, H & Mingrone, G 2005, 'Changes in fat mass influence SREBP-1c and UCP-2 gene expression in formerly obese subjects', Obesity Research, vol. 13, no. 3, pp. 567-573.
Gniuli, Donatella ; Rosa, Giuseppina ; Manco, Melania ; Scarfone, Antonino ; Vega, Nathalie ; Greco, Aldo V. ; Castagneto, Marco ; Vidal, Hubert ; Mingrone, Geltrude. / Changes in fat mass influence SREBP-1c and UCP-2 gene expression in formerly obese subjects. In: Obesity Research. 2005 ; Vol. 13, No. 3. pp. 567-573.
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abstract = "Objective: To investigate the effect of fat mass (FM) reduction on adipose tissue gene expression in terms of lipid synthesis [sterol regulatory binding protein 1c (SREBP-1c)] and lipid oxidation [uncoupling protein 2 (UCP-2)] 2 years after lipid malabsorption and to assess the influence of lipid malabsorption on fat-free mass (FFM) maintenance evaluating the expression of genes related to glycolysis [hexokinase (HKII)] and glucose storage [glycogen synthase (GS)]. Research Method and Procedures: SREBP-1c, UCP-2, HKII, and GS mRNA expression were studied by reverse transcriptase-competitive polymerase chain reaction in 10 massively obese subjects before and 2 years after biliopancreatic diversion (BPD). Body composition was assessed by isotopic dilution method and insulin sensitivity by euglycemic-hyperinsulinemic clamp. Results: FM decrease was ∼60{\%}, whereas FFM remained at normal physiological levels. In adipose tissue, SREBP-1c mRNA reduction (-39{\%}, p <0.005) was related only to FM changes after BPD, and UCP-2 decrease (-37{\%}, p <0.05) was dependent on free fatty acid (FFA) changes. No significant variations were observed in HKII and GS gene expression in skeletal muscle. Discussion: Lipid malabsorption induced by BPD altered the expression of genes involved in glucose and lipid metabolism, with different consequences on FM and FFM. The degree of FM loss seems to interfere with SREBP-1c gene suppression to preserve an adequate amount of fat storage, in accordance with the thrifty genotype hypothesis. The reduction of FFAs induced by BPD acts in inhibiting FFA transportation to the mitochondria (UCP-2), contributing to the decreased lipid oxidation inside the adipose tissue.",
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AU - Rosa, Giuseppina

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AU - Scarfone, Antonino

AU - Vega, Nathalie

AU - Greco, Aldo V.

AU - Castagneto, Marco

AU - Vidal, Hubert

AU - Mingrone, Geltrude

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AB - Objective: To investigate the effect of fat mass (FM) reduction on adipose tissue gene expression in terms of lipid synthesis [sterol regulatory binding protein 1c (SREBP-1c)] and lipid oxidation [uncoupling protein 2 (UCP-2)] 2 years after lipid malabsorption and to assess the influence of lipid malabsorption on fat-free mass (FFM) maintenance evaluating the expression of genes related to glycolysis [hexokinase (HKII)] and glucose storage [glycogen synthase (GS)]. Research Method and Procedures: SREBP-1c, UCP-2, HKII, and GS mRNA expression were studied by reverse transcriptase-competitive polymerase chain reaction in 10 massively obese subjects before and 2 years after biliopancreatic diversion (BPD). Body composition was assessed by isotopic dilution method and insulin sensitivity by euglycemic-hyperinsulinemic clamp. Results: FM decrease was ∼60%, whereas FFM remained at normal physiological levels. In adipose tissue, SREBP-1c mRNA reduction (-39%, p <0.005) was related only to FM changes after BPD, and UCP-2 decrease (-37%, p <0.05) was dependent on free fatty acid (FFA) changes. No significant variations were observed in HKII and GS gene expression in skeletal muscle. Discussion: Lipid malabsorption induced by BPD altered the expression of genes involved in glucose and lipid metabolism, with different consequences on FM and FFM. The degree of FM loss seems to interfere with SREBP-1c gene suppression to preserve an adequate amount of fat storage, in accordance with the thrifty genotype hypothesis. The reduction of FFAs induced by BPD acts in inhibiting FFA transportation to the mitochondria (UCP-2), contributing to the decreased lipid oxidation inside the adipose tissue.

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