sincalide and Feeding-and-Eating-Disorders

sincalide has been researched along with Feeding-and-Eating-Disorders* in 2 studies

Other Studies

2 other study(ies) available for sincalide and Feeding-and-Eating-Disorders

ArticleYear
Facilitation of cancer-associated anorexia by cholecystokinin.
    Regulatory peptides, 1988, Volume: 20, Issue:2

    Cholecystokinin octapeptide (CCK-8, 5 micrograms/kg) was injected i.p. into male Sprague-Dawley rats bearing the Walker 256-carcinosarcoma, or into non-tumour bearing controls, on a 20-h food deprivation schedule. Food and water intake and body weight maintenance were monitored for 15 days after tumour implantation and compared to that of tumour-bearing animals not injected with CCK-8. Food intake was significantly reduced for the duration of the two 4-day periods of CCK-8 injection, indicating that behavioural tolerance to this peptide did not occur. The severity of anorexia and body weight loss in tumour-bearing animals was significantly greater than that observed in non-tumour bearing controls, for the first 13 days of observation. These results indicate that endogenous peptides, such as CCK, may function in tumour-bearing animals to enhance the anorexia and wasting which typifies the anorexia cachexia syndrome.

    Topics: Animals; Anorexia; Body Weight; Cachexia; Carcinoma 256, Walker; Drinking; Eating; Feeding and Eating Disorders; Male; Rats; Rats, Inbred Strains; Satiation; Sincalide

1988
Hyperphagia during lactation: satiety response to CCK and growth of the pancreas.
    The American journal of physiology, 1983, Volume: 244, Issue:1

    Cholecystokinin (CCK) secreted from the duodenum during feeding has been shown to elicit satiety and stimulate growth of the pancreas in addition to affecting gastrointestinal function. In previous experiments hyperphagic Zucker obese rats were less sensitive to the effects of CCK on satiety and had a smaller pancreas than normal-weight rats. In the present experiments with hyperphagic lactating Zucker rats, the food intake response to exogenously administered CCK and the size and composition of the pancreas were measured. Food intakes after a 2-h fast were not decreased by 4.0 or 8.0 micrograms/kg CCK-8 during wk 1, 2, or 3 of lactation. However, in the same rats 2 wk after pups were weaned, 4.0 and 8.0 micrograms/kg CCK-8 decreased food intake 32% (2.1 +/- 0.4 vs. 3.1 +/- 0.3 g, paired t = 2.33, P less than 0.03) and 52% (1.5 +/- 0.2 vs. 3.1 +/- 0.5 g, paired t = 3.48, P less than 0.006). On day 18 of lactation, pancreas weight was increased 41% (1.38 +/- 0.05 vs. 0.98 +/- 0.02 g, paired t = 2.68, P less than 0.02) and contents of DNA, RNA, and protein were increased 57, 57, and 73%, respectively. Thus, hyperphagia in lactating female rats was associated with 1) decreased sensitivity to the satiety effect of CCK similar to that in hyperphagic obese rats and 2) hypertrophy of the pancreas in contrast to decreased pancreas size in obese rats.

    Topics: Animals; Cholecystokinin; DNA; Dose-Response Relationship, Drug; Eating; Feeding and Eating Disorders; Female; Humans; Hyperphagia; Lactation; Organ Size; Pancreas; Peptide Fragments; Pregnancy; Proteins; Rats; Rats, Zucker; RNA; Sincalide

1983