Differential effect of weight loss with low-fat diet or high-fat diet restriction on inflammation in the liver and adipose tissue of mice with diet-induced obesity.
Differential effect of weight loss with low-fat diet or high-fat diet restriction on inflammation in the liver and adipose tissue of mice with diet-induced obesity.
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DOI:
10.1016/j.atherosclerosis.2011.07.025
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发表时间:
2011-11
期刊:
影响因子:
5.3
通讯作者:
Wu, Huaizhu
中科院分区:
文献类型:
--
作者:
Wang, Qun;Perrard, Xiaoyuan Dai;Perrard, Jerry L.;Mansoori, Amir;Raya, Joe L.;Hoogeveen, Ron;Smith, C. Wayne;Ballantyne, Christie M.;Wu, Huaizhu
We studied the effects of weight loss induced by either a low-fat normal diet (ND) or restriction of high-fat diet (HFD) on hepatic steatosis, inflammation in the liver and adipose tissue (AT), and blood monocytes of obese mice. In mice with HFD-induced obesity, weight loss was achieved by switching from HFD to ND and maintaining on ND ad libitum or by restricting HFD intake to match body weight of mice with ND-induced weight loss. After diet interventions for 4 weeks, hepatic steatosis, hepatic and AT inflammation, and blood CD11c+ monocytes were examined. At 4 weeks after switching diets, body weight was reduced by 23% from baseline. To achieve the same reduced body weight required restricting calorie intake from HFD. Weight loss with either ND or HFD restriction decreased body fat mass and ameliorated liver steatosis; both effects were greater with ND-induced weight loss than HFD restriction–induced weight loss. Weight loss with ND but not HFD restriction normalized blood CD11c+ monocytes and attenuated hepatic inflammation assessed by chemokine and CD11c expression. In contrast, weight loss with HFD restriction significantly reduced chemokine levels and CD11c+ cells in AT compared to obese controls, and tended to reduce AT chemokines and CD11c+ cells more than ND-induced weight loss. In mice with diet-induced obesity, weight loss with ND was superior in alleviating hepatic inflammation and steatosis, whereas weight loss with HFD calorie restriction provided greater amelioration of AT inflammation.
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影响因子:
24
作者:
Owan, Theophilus;Avelar, Erick;Litwin, Sheldon E.
通讯作者:
Litwin, Sheldon E.
影响因子:
8.2
作者:
Flachs, P;Mohamed-Ali, V;Kopecky, J
通讯作者:
Kopecky, J
影响因子:
6.5
作者:
Attie, AD;Krauss, RM;Ntambi, JM
通讯作者:
Ntambi, JM
DOI:
10.1056/nejmoa0804748
发表时间:
2009-02-26
期刊:
The New England journal of medicine
影响因子:
--
作者:
Sacks FM;Bray GA;Carey VJ;Smith SR;Ryan DH;Anton SD;McManus K;Champagne CM;Bishop LM;Laranjo N;Leboff MS;Rood JC;de Jonge L;Greenway FL;Loria CM;Obarzanek E;Williamson DA
通讯作者:
Williamson DA
影响因子:
82.9
作者:
Berg, AH;Combs, TP;Scherer, PE
通讯作者:
Scherer, PE