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Synergistic effect of CART (cocaine- and amphetamine-regulated transcript) peptide and cholecystokinin on food intake regulation in lean mice
L Maletinska, J Maixnerova, R Matyskova, R Haugvicova, Z Pirnik, A Kiss, B Zelezna
Language English Country Great Britain
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BioMedCentral
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- MeSH
- Hormone Antagonists pharmacology MeSH
- Benzodiazepinones pharmacology MeSH
- Devazepide pharmacology MeSH
- Phenylurea Compounds pharmacology MeSH
- Financing, Organized MeSH
- Thinness MeSH
- Injections, Intraperitoneal MeSH
- Injections, Intraventricular MeSH
- Mice, Inbred C57BL MeSH
- Mice MeSH
- Neurons metabolism drug effects MeSH
- Dorsomedial Hypothalamic Nucleus physiology drug effects MeSH
- Paraventricular Hypothalamic Nucleus physiology drug effects MeSH
- Solitary Nucleus physiology drug effects MeSH
- Exploratory Behavior physiology drug effects MeSH
- Peptide Fragments pharmacology MeSH
- Nerve Tissue Proteins pharmacology MeSH
- Proto-Oncogene Proteins c-fos metabolism MeSH
- Receptor, Cholecystokinin A antagonists & inhibitors MeSH
- Receptor, Cholecystokinin B antagonists & inhibitors MeSH
- Appetite Regulation physiology drug effects MeSH
- Sincalide pharmacology MeSH
- Drug Synergism MeSH
- Dose-Response Relationship, Drug MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Animals MeSH
BACKGROUND: CART (cocaine- and amphetamine-regulated transcript) peptide and cholecystokinin (CCK) are neuromodulators involved in feeding behavior. This study is based on previously found synergistic effect of leptin and CCK on food intake and our hypothesis on a co-operation of the CART peptide and CCK in food intake regulation and Fos activation in their common targets, the nucleus tractus solitarii of the brainstem (NTS), the paraventricular nucleus (PVN), and the dorsomedial nucleus (DMH) of the hypothalamus. RESULTS: In fasted C57BL/6 mice, the anorexigenic effect of CART(61-102) in the doses of 0.1 or 0.5 microg/mouse was significantly enhanced by low doses of CCK-8 of 0.4 or 4 microg/kg, while 1 mg/kg dose of CCK-A receptor antagonist devazepide blocked the effect of CART(61-102) on food intake. After simultaneous administration of 0.1 microg/mouse CART(61-102) and of 4 microg/kg of CCK-8, the number of Fos-positive neurons in NTS, PVN, and DMH was significantly higher than after administration of each particular peptide. Besides, CART(61-102) and CCK-8 showed an additive effect on inhibition of the locomotor activity of mice in an open field test. CONCLUSION: The synergistic and long-lasting effect of the CART peptide and CCK on food intake and their additive effect on Fos immunoreactivity in their common targets suggest a co-operative action of CART peptide and CCK which could be related to synergistic effect of leptin on CCK satiety
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- $a Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Flemingovo nam, 2, 16610 Prague 6, Czech Republic. maletin@uochb.cas.cz
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- $a BACKGROUND: CART (cocaine- and amphetamine-regulated transcript) peptide and cholecystokinin (CCK) are neuromodulators involved in feeding behavior. This study is based on previously found synergistic effect of leptin and CCK on food intake and our hypothesis on a co-operation of the CART peptide and CCK in food intake regulation and Fos activation in their common targets, the nucleus tractus solitarii of the brainstem (NTS), the paraventricular nucleus (PVN), and the dorsomedial nucleus (DMH) of the hypothalamus. RESULTS: In fasted C57BL/6 mice, the anorexigenic effect of CART(61-102) in the doses of 0.1 or 0.5 microg/mouse was significantly enhanced by low doses of CCK-8 of 0.4 or 4 microg/kg, while 1 mg/kg dose of CCK-A receptor antagonist devazepide blocked the effect of CART(61-102) on food intake. After simultaneous administration of 0.1 microg/mouse CART(61-102) and of 4 microg/kg of CCK-8, the number of Fos-positive neurons in NTS, PVN, and DMH was significantly higher than after administration of each particular peptide. Besides, CART(61-102) and CCK-8 showed an additive effect on inhibition of the locomotor activity of mice in an open field test. CONCLUSION: The synergistic and long-lasting effect of the CART peptide and CCK on food intake and their additive effect on Fos immunoreactivity in their common targets suggest a co-operative action of CART peptide and CCK which could be related to synergistic effect of leptin on CCK satiety
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