c-Kit mutant mouse behavioral phenotype: altered meal patterns and CCK sensitivity but normal daily food intake and body weight
- 1 November 2003
- journal article
- Published by American Physiological Society in American Journal of Physiology-Regulatory, Integrative and Comparative Physiology
- Vol. 285 (5) , R1170-R1183
- https://doi.org/10.1152/ajpregu.00015.2003
Abstract
The mouse W/Wv mutation of the c-Kit receptor causes extensive loss of gastrointestinal interstitial cells of Cajal and vagal intramuscular arrays (IMAs; one of the two putative mechanoreceptors in gastrointestinal smooth muscle). To characterize the behavioral phenotype of the c-Kit mouse and to evaluate the roles of these mechanoreceptors in controlling food intake, meal patterns and daily intakes of W/Wv mice and controls were examined using solid (20-mg pellets) and liquid (Isocal) maintenance diets. After the meal pattern experiments, CCK (0.5, 1, 2, 4, 8, and 16 μg/kg ip) was administered to examine the role of the interstitial cells and vagal IMA mechanoreceptors in relaying peripheral signals of satiety activated by CCK-A receptors, whereas the specificity of the response was assessed with the antagonist devazepide (300 μg/kg ip). On both diets, the W/Wv mice ate smaller meals for shorter durations, with a compensatory increase in meal number, resulting in daily intakes and body weights similar to the controls. After CCK injections, the mutant mice consistently suppressed intake more (∼2×) in 30-min tests, regardless of the test diet (12.5% glucose, chow, pellets, and Isocal). The increased sensitivity of W/Wv mice to CCK reflected an increased potency of the hormone (c-Kit mouse ED50 = 2.4 μg/kg; control ED50 = 6.4 μg/kg) and a shift of the dose-response curve to the left. Devazepide blocked the CCK suppression of ingestion. These results indicate that the selective loss of the interstitial cells and IMAs disrupts short-term feeding of the W/Wv mice by inducing an earlier satiety, possibly by altering gastric accommodation and/or emptying, without affecting the long-term mechanisms controlling overall intake or body weight. The results also suggest that the reduction of interstitial cells and IMAs augments the sensitivity to or increases the efficiency of exogenous CCK.Keywords
This publication has 33 references indexed in Scilit:
- Attenuated satiation response to intestinal nutrients in rats that do not express CCK-A receptorsPeptides, 2001
- C-Kit mutant mice have a selective loss of vagal intramuscular mechanoreceptors in the forestomach.Brain Structure and Function, 2001
- Selective knockout of intramuscular interstitial cells reveals their role in the generation of slow waves in mouse stomachThe Journal of Physiology, 2001
- Cholecystokinin satiety involves CCKA receptors perfused by the superior pancreaticoduodenal arteryAmerican Journal of Physiology-Regulatory, Integrative and Comparative Physiology, 1998
- Little and often: Ingestive behavior patterns following hippocampal lesions in rats.Behavioral Neuroscience, 1998
- Interstitial cells of Cajal mediate inhibitory neurotransmission in the stomach.Proceedings of the National Academy of Sciences, 1996
- Abdominal vagotomy alters the structure of the ingestive behavior of rats ingesting liquid diets.Behavioral Neuroscience, 1994
- A system for studying the microstructure of ingestive behavior in micePhysiology & Behavior, 1992
- Mechanical properties and sensitivity to CCK of vagal gastric slowly adapting mechanoreceptorsAmerican Journal of Physiology-Gastrointestinal and Liver Physiology, 1988
- Cholecystokinin octapeptide and gastric mechanoreceptor activity in rat brainAmerican Journal of Physiology-Gastrointestinal and Liver Physiology, 1983