Glucose-dependent insulinotropic polypeptide monoclonal antibodies prevent and treat obesity in wild-type and hyperphagic mice

被引:1
|
作者
Wolfe, M. Michael [1 ]
Apovian, Caroline M. M. [2 ]
Boylan, Michael O. O. [1 ]
机构
[1] Case Western Reserve Univ, Dept Physiol & Biophys, 10900 Euclid Ave, Cleveland, OH 44106 USA
[2] Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA USA
关键词
Y GASTRIC BYPASS; EXPRESSION; SURGERY; WEIGHT; GIP;
D O I
10.1002/oby.23758
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ObjectiveThis study aimed to investigate whether a glucose-dependent insulinotropic polypeptide (GIP) monoclonal antibody (mAb) will promote weight loss in wild-type mice and to determine effects of this mAb in preventing weight gain in ob/ob mice. MethodsPhosphate-buffered saline (PBS) or GIP mAb was injected intraperitoneally to wild-type mice fed a 60% high-fat diet (HFD). After 12 weeks, mice that received PBS were divided into two groups and were fed a 37% HFD for 5 weeks; one group received PBS, and one group received GIP mAb. In a separate study, PBS or GIP mAb was injected intraperitoneally to ob/ob mice fed normal mouse chow for 8 weeks. ResultsPBS-treated mice gained significantly more than those treated with GIP mAb, with no difference in food consumption detected. Obese mice fed a 37% HFD and PBS continued to gain weight (+2.1% +/- 0.9%), whereas mice administered GIP mAb lost 4.1% +/- 1.4% body weight (p < 0.01). Leptin-deficient mice consumed similar amounts of chow, and, after 8 weeks, the PBS- and GIP mAb-treated mice gained 250.4% +/- 9.1% and 192.4% +/- 7.3%, respectively (p < 0.01). ConclusionsThese studies support the hypothesis that a reduction in GIP signaling appears to affect body weight without suppressing food intake and might provide a novel, useful method for the treatment and prevention of obesity.
引用
收藏
页码:1499 / 1504
页数:6
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