Determinants of vitamin D receptor gene expression in visceral and subcutaneous adipose tissue in non-obese, obese, and morbidly obese subjects

被引:20
|
作者
Yuzbashian, Emad [1 ]
Asghari, Golaleh [1 ,2 ]
Hedayati, Mehdi [3 ]
Zarkesh, Maryam [3 ]
Mirmiran, Parvin [1 ,2 ]
Khalaj, Alireza [4 ]
机构
[1] Shahid Beheshti Univ Med Sci, Res Inst Endocrine Sci, Nutr & Endocrine Res Ctr, POB 19395-4763, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Natl Nutr & Food Technol Res Inst, Fac Nutr Sci & Food Technol, Dept Clin Nutr & Dietet, Tehran, Iran
[3] Shahid Beheshti Univ Med Sci, Res Inst Endocrine Sci, Cellular & Mol Endocrine Res Ctr, POB 19395-4763, Tehran, Iran
[4] Shahed Univ, Tehran Obes Treatment Ctr, Dept Surg, Tehran, Iran
关键词
VDR; 25(OH)D; Dietary intake; SERUM 25-HYDROXYVITAMIN D; D DEFICIENCY; INFLAMMATION; RELIABILITY; METABOLISM; VALIDITY; ENERGY; TARGET; DELTA; FAT;
D O I
10.1016/j.jsbmb.2018.11.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We aimed to illustrate determinants of VDR gene expression in visceral and subcutaneous adipose tissue among individuals without diabetes. We gathered visceral and subcutaneous adipose tissues during an elective abdominal surgery form 33 morbidly obese (BMI > 40 kg/m(2)), 23 obese (BMI = 30-40 kg/m(2)), and 35 non-obese (BMI < 30 kg/m(2)) participants who were free of diabetes. Participants were classified according to their degree of obesity. Before the surgery, habitual dietary intake, physical activity, 25(OH)D, body mass index (BMI), waist circumference (WC), and HOMA-IR was gathered. Non-obese participants had significantly lower mean VDR gene expression in visceral adipose tissues than both the obese and morbidly obese ones and had also lower expression in subcutaneous adipose tissues than the morbidly obese participants. In multiple linear regression models, BMI and HOMA-IR were the independent positive predictors of VDR gene expression in subcutaneous fat. Among non-obese subjects, WC and 25(OH)D were the positive and negative independent predictors of visceral adipose tissue VDR gene expression, respectively. Among obese participants, 25(OH)D was negatively, and BMI and HOMA-IR were positively associated with VDR mRNA levels in visceral adipose tissue. In morbidly obese participants, the independent positive predictors of VDR gene expression in visceral fat were BMI and HOMA-IR, and negative predictors were 25(OH)D and calcium intake. Our findings suggested that 25(OH)D concentrations are the fundamental elements to determine VDR gene expression in visceral fat which by increasing fat depots, the subsequent insulin resistance became another predictor of VDR gene expression.
引用
收藏
页码:82 / 87
页数:6
相关论文
共 50 条
  • [1] Global gene expression profiles of subcutaneous adipose tissue in obese and non-obese young men
    French, C
    Martin, G
    Roebothan, B
    Peng, YW
    Fitzpatrick, D
    Pace, D
    Sun, G
    OBESITY RESEARCH, 2005, 13 : A31 - A31
  • [2] HABITUAL PHYSICAL ACTIVITY AND APELIN GENE EXPRESSION IN VISCERAL AND SUBCUTANEOUS ADIPOSE TISSUES AMONG MORBID OBESE AND NON-OBESE SUBJECTS
    Mahmoodi, Behnaz
    Shemshaki, Afsaneh
    Yuzbashian, Emad
    Zarkesh, Maryam
    Asghari, Golaleh
    Mirmiran, Parvin
    Hedayati, Mehdi
    Safarian, Mohammad
    ANNALS OF NUTRITION AND METABOLISM, 2017, 71 : 281 - 282
  • [3] Gene expression in visceral and subcutaneous adipose tissue of morbidly obese subjects: an insight into the new Adipokines and inflammatory mediators
    Zahiragic, Samra
    Svehlikova, Eva
    Schweighofer, Natascha
    Tuca, Alexandru
    Schultes, Bernd
    Thurnheer, Martin
    Obermayer-Pietsch, Barbara
    Freisinger, Oana
    Tadler, Friedrich
    Pieber, Thomas R.
    WIENER KLINISCHE WOCHENSCHRIFT, 2011, 123 : S15 - S15
  • [4] GLUCOSE UTILIZATION AND INSULIN RESPONSIVENESS OF HUMAN SUBCUTANEOUS ADIPOSE TISSUE IN OBESE AND NON-OBESE SUBJECTS
    ENGLHARDT, A
    KASPEREK, R
    LIEBERMEISTER, H
    JAHNKE, K
    HORMONE AND METABOLIC RESEARCH, 1971, 3 (04) : 266 - +
  • [5] Inflammatory gene expression in adipose tissue according to diagnosis of anxiety and mood disorders in obese and non-obese subjects
    Coin-Araguez, Leticia
    Javier Pavon, Francisco
    Contreras, Alba
    Gentile, Adriana-Mariel
    Lhamyani, Said
    De Diego-Otero, Yolanda
    Casado, Yolanda
    Oliva Olivera, Wilfredo
    Olveira, Gabriel
    Tinahones, Francisco J.
    Perez Costillas, Lucia
    El Bekay, Rajaa
    SCIENTIFIC REPORTS, 2018, 8
  • [6] Inflammatory gene expression in adipose tissue according to diagnosis of anxiety and mood disorders in obese and non-obese subjects
    Leticia Coín-Aragüez
    Francisco Javier Pavón
    Alba Contreras
    Adriana-Mariel Gentile
    Said Lhamyani
    Yolanda De Diego-Otero
    Yolanda Casado
    Wilfredo Oliva Olivera
    Gabriel Olveira
    Francisco J. Tinahones
    Lucía Pérez Costillas
    Rajaa El Bekay
    Scientific Reports, 8
  • [7] Gene expression differences in non-obese, obese and previously obese subjects.
    Tessarech, M.
    Mileti, E.
    Kwok, K.
    Arner, P.
    Bonneau, D.
    Colin, E.
    Ryden, M.
    Daub, C.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 226 - 226
  • [8] EXPRESSION OF RESISTIN IN VISCERAL AND SUBCUTANEOUS ADIPOSE TISSUE OF CENTRALLY OBESE POSTMORTEM SUBJECTS
    Noorjamal, N. A.
    Omar, E.
    Mahmood, M. S.
    Hasmi, A. H.
    Nawawi, H. Mohd
    ATHEROSCLEROSIS, 2019, 287 : E273 - E273
  • [9] Different expression of the adipocytokines in subcutaneous and visceral adipose tissue of extremely obese subjects
    Gasperikova, D.
    Stencl, J.
    Skopkova, M.
    Vlcek, M.
    Pechan, J.
    Radikova, Z.
    Imrich, R.
    Ukropcova, B.
    Ukropec, J.
    Klimes, I.
    Penesova, A.
    DIABETOLOGIA, 2007, 50 : S308 - S308
  • [10] Differential circulating and visceral fat microRNA expression of non-obese and obese subjects
    Kim, Nan Hee
    Ahn, Jiyun
    Choi, Yong Min
    Son, Hyo Jung
    Choi, Won Hee
    Cho, Hyun Joo
    Yu, Ji Hee
    Seo, Ji A.
    Jang, Young Jin
    Jung, Chang Hwa
    Ha, Tae Youl
    CLINICAL NUTRITION, 2020, 39 (03) : 910 - 916