Urinary phenotyping indicates weight loss-independent metabolic effects of Roux-en-Y gastric bypass in mice.
Urinary phenotyping indicates weight loss-independent metabolic effects of Roux-en-Y gastric bypass in mice.
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尿液表型分析表明 Roux-en-Y 胃绕道手术对小鼠的代谢影响与体重减轻无关
DOI:
10.1021/pr300909v
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发表时间:
2013
影响因子:
4.4
通讯作者:
Holmes E.
中科院分区:
文献类型:
--
作者:
Seyfried F;Miras AD;Cluny NL; Lannoo M;Fenske WK;Sharkey KA;Nicholson JK;Le Roux CW;Holmes E.
Patients with a body mass index (BMI) above 35 kg/m2with metabolic diseases benefit from Roux-en-Y gastric bypass (RYGB) independently of their final BMI and the amount of body weight lost. However, the weight loss independent metabolic effects induced by RYGB remain less well understood. To elucidate metabolic changes after RYGB,1H NMR spectroscopy-based urine metabolic profiles from RYGB (n= 7), ad libitum-fed sham (AL,n= 5), and body-weight-matched sham (BWM,n= 5) operated mice were obtained. Gut morphometry and fecal energy content were analyzed. Food intake and body weight of RYGB mice were significantly reduced (p= 0.001) compared to sham-AL. There was a strong tendency that BWM-shams required less food to maintain the same body weight as RYGB mice (p= 0.05). No differences were found in fecal energy content between the groups, excluding malabsorption in RYGB animals. Unlike RYGB-operated rats, gut hypertrophy was not observed in RYGB-operated mice. Urinary tricarboxylic acid cycle intermediates were higher in the sham groups, suggesting altered mitochondrial metabolism after RYGB surgery. Higher urinary levels of trimethylamine, hippurate and trigonelline in RYGB mice indicate that the RYGB operation caused microbial disturbance. Taken together, we demonstrate for the first time that there are RYGB specific metabolic effects, which are independent of food intake and body weight loss. Increased utilization of TCA cycle intermediates and altered gut microbial-host co-metabolites might indicate increased energy expenditure and microbial changes in the gut, respectively.
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影响因子:
4.4
作者:
McClay, Joseph L.;Adkins, Daniel E.;van den Oord, Edwin J. C. G.
通讯作者:
van den Oord, Edwin J. C. G.
影响因子:
9
作者:
Rubino, Francesco;Kaplan, Lee M.;Cummings, David E.
通讯作者:
Cummings, David E.
影响因子:
3.7
作者:
Mutch DM;Fuhrmann JC;Rein D;Wiemer JC;Bouillot JL;Poitou C;Clément K
通讯作者:
Clément K
影响因子:
158.5
作者:
Adams, Ted D.;Gress, Richard E.;Hunt, Steven C.
通讯作者:
Hunt, Steven C.
影响因子:
14.8
作者:
Beckonert, Olaf;Keun, Hector C.;Nicholson, Jeremy K.
通讯作者:
Nicholson, Jeremy K.