Involvement of cholecystokinin receptor in the inhibition of gastrointestinal motility by oxytocin in ovariectomized rats
Abstract
The effects of oxytocin on gastric emptying, gastrointestinal transit, and plasma levels of cholecystokinin (CCK) were studied in ovariectomized rats. Gastrointestinal motility was assessed in rats 15 min after intragastric instillation of a test meal containing charcoal and Na2 51CrO4. Gastric emptying was determined by measuring the amount of radiolabeled chromium contained in the small intestine as a percentage of the initial amount received. Gastrointestinal transit was evaluated by calculating the geometric center of distribution of the radiolabeled marker. Blood samples were collected for CCK radioimmunoassay. After administration of oxytocin (0.2-0.8 mg/kg), gastric emptying and gastrointestinal transit were inhibited, whereas plasma concentration of CCK was increased in a dose-dependent manner. Atosiban, an oxytocin receptor antagonist, effectively attenuated the oxytocin-induced inhibition of gastric emptying and gastrointestinal transit. However, administration of atosiban alone had no effect on gastric emptying and gastrointestinal transit. The selective CCK1 receptor antagonists, devazepide and lorglumide, effectively attenuated the oxytocin-induced inhibition of gastric emptying and gastrointestinal transit. L-365, 260, a selective CCK2 receptor antagonist, did not alter the oxytocin-induced inhibition of gastric emptying and gastrointestinal transit. These results suggest that oxytocin inhibits gastric emptying and gastrointestinal transit in ovariectomized rats via a mechanism involving the stimulation of CCK release and CCK1 receptor activation.
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Studies in rats demonstrate that intraperitoneal oxytocin increases levels of the peripheral satiety hormone CCK and inhibits gastric emptying; these effects are blocked by administration of a CCK-1 receptor antagonist.
“Studies in rats demonstrate that intraperitoneal oxytocin increases levels of the peripheral satiety hormone CCK and inhibits gastric emptying; these effects are blocked by administration of a CCK-1 receptor antagonist(29, 30).”
From Oxytocin reduces caloric intake in men (2015) · cites this paper as [30]
Oxytocin may reduce food intake by inhibiting gastric emptying.
“Oxytocin may also reduce food intake by inhibiting gastric emptying.”
From Oxytocin reduces caloric intake in men (2015) · cites this paper as [30]
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Vitali, M., Fontana, M., Giorgi, A. D., Marotta, D., Crucianelli, S., Antonucci, A., & Protano, C. (2023) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph20085527 · Cited by 4 · see citing works
Intranasal oxytocin as a treatment for obesity: safety and efficacy
Balestrino, R., Losa, M., Albano, L., Barzaghi, L. R., & Mortini, P. (2023) · Expert Review of Endocrinology & Metabolism · doi:10.1080/17446651.2023.2216794 · Cited by 2 · see citing works
Actions of appetite regulating peptides on supraoptic nucleus (SON) oxytocin neurones
Velmurugan, S. (2009) · ERA · Cited by 1 · see citing works
ABOZAID, M. D. N. A. A. E. R. (2018) · The Medical Journal of Cairo University/The Medical Journal of Cairo University · doi:10.21608/mjcu.2018.59872
- Authors
- Wu, C.-L., Doong, M.-L., & Wang, P. S.
- Affiliations
- Hungkuang University (TW)
- National Yang Ming University (TW)
- Corresponding author
- Wu, Chiu-Lung
- ORCID
- Wang, Paulus S.
- Venue
- European Journal of Pharmacology
- Publisher
- Elsevier BV
- Published
- 2008-02
- Volume
- 580
- Issue
- 3
- Pages
- 407-415
- ISSN
- 0014-2999 (ISSN-L)
- OpenAlex
- W2045003744
- Cited by
- 27
- References
- 78
- Citations by year
- 2023: 2 · 2022: 2 · 2021: 3 · 2019: 1 · 2018: 1 · 2017: 3 · 2016: 1 · 2015: 2 · 2014: 2 · 2013: 1 · 2012: 3
- FWCI
- 1.50
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- European Journal of Pharmacology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
- Keywords
- oxytocin, cholecystokinin, CCK-A receptor, gastrointestinal motility, gastric emptying, gastrointestinal transit, ovariectomy, atosiban, devazepide, lorglumide, CCK2 receptor, plasma CCK levels, postprandial motility
- MeSH terms
- Animals, Benzodiazepinones, Cholecystokinin, Dose-Response Relationship, Drug, Eating, Female, Gastric Emptying, Gastrointestinal Motility, Gastrointestinal Transit, Ovariectomy, Oxytocin, Phenylurea Compounds, Proglumide, Radioimmunoassay, Receptors, Cholecystokinin, Sincalide, Vasotocin, Rats, Sprague-Dawley, Receptors, Oxytocin, Devazepide, Receptor, Cholecystokinin A, Rats
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