Lin L, Chen J, York D A
Pennington Biomedical Research Center, Baton Rouge, LA 70808, USA.
Peptides. 1997;18(5):657-61. doi: 10.1016/s0196-9781(97)00128-9.
The pancreatic peptide enterostatin will acutely reduce fat intake in rats provided a choice of diets. Chronic ICV infusions of enterostatin suppress the intake of high fat diet. However, the effects of chronic ICV enterostatin on diet choice has not previously been studied. To investigate this, enterostatin (0.5 microgram/h) or artificial cerebrospinal fluid (CSF) was infused for 9 days into the lateral ventricle of rats adapted to a two-choice high-fat (HF) and low-fat (LF) diet regime. Enterostatin reduced intake of HF diet with the maximum depression at day 4, but there was no compensatory increase in LF intake. The body weight of enterostatin-infused rats declined. This was associated with a reduction in fat pad and liver weights compared to the CSF-infused control rats. Serum triglycerides and insulin were decreased and corticosterone was elevated in enterostatin-infused rats. The data show that enterostatin will chronically reduce fat intake and body weight and suggest that enterostatin may attenuate the appetite for fat.
若给大鼠提供多种饮食选择,胰腺肽肠抑素会迅速减少其脂肪摄入量。长期脑室内注射肠抑素可抑制高脂饮食的摄入。然而,此前尚未研究过长期脑室内注射肠抑素对饮食选择的影响。为对此进行研究,将肠抑素(0.5微克/小时)或人工脑脊液(CSF)注入适应了高脂(HF)和低脂(LF)两种饮食选择模式的大鼠侧脑室,持续9天。肠抑素减少了高脂饮食的摄入量,在第4天抑制作用最大,但低脂饮食的摄入量没有相应增加。注射肠抑素的大鼠体重下降。与注射脑脊液的对照大鼠相比,这与脂肪垫和肝脏重量的减少有关。注射肠抑素的大鼠血清甘油三酯和胰岛素水平降低,皮质酮水平升高。数据表明,肠抑素会长期减少脂肪摄入量和体重,并提示肠抑素可能会减弱对脂肪的食欲。