کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2844805 1166365 2010 4 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Cholecystokinin-8 increases the satiety ratio in diabetic rats more than cholecystokinin-33
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی فیزیولوژی
پیش نمایش صفحه اول مقاله
Cholecystokinin-8 increases the satiety ratio in diabetic rats more than cholecystokinin-33
چکیده انگلیسی

Cholecystokinin (CCK) is a satiety peptide and a potential anti-diabetic agent, which exists in different forms (e.g. CCK-8 and CCK-33). In normal rats, CCK-8 and 33 stimulate insulin secretion similarly but their satiety effects vary. In diabetic rats, those effects require testing. Here, we compared size of the first meal (10% sucrose test diet), intermeal interval (IMI, time between first and second meal) and satiety ratio (SR, amount of satiation produced by every unit of food consumed in the first meal) by CCK-8 or 33 (0, 1, 3, 5 nmol/kg) intraperitoneally in streptozotocin-injected (diabetic) and citrate buffer-injected (control) rats. We found that both peptides reduce meal size in diabetic and control rats with no difference between groups, CCK-33 (5 nmol) prolonged IMI in diabetic rats and CCK-8 and CCK-33 increased satiety ratio in control rats, but only CCK-8 increased it in the diabetic group. Therefore, CCK-8 increases the satiety ratio in diabetic rats more than CCK-33.

Research highlights
► Satiety effects by CCK-8 and 33 were tested in diabetic rats
► We measured size of the first meal, intermeal interval (IMI) and satiety ratio (SR)
► Both peptides reduced meal size but only CCK-8 increased SR it diabetic rats
► Therefore, in diabetic rats CCK-8 is a more powerful satiety peptide than CCK-33.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Physiology & Behavior - Volume 101, Issue 5, 2 December 2010, Pages 649–652
نویسندگان
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