Behavioral Effects of Gut Hormones in Neonatal Rats: II. Cholecystokinin Administration During the First Postnatal Week

References

• Allin J. T., Banks E. M. Functional aspects of ultrasound production by infant albino rats (Rattus Norvegicus). Animal Behaviour 1972; 20: 175–185
   PubMed Web of Science ®Google Scholar
• Beach F. A., Jaynes J. Studies of maternal retrieving in rats I: Recognition of young. Journal of Mammalogy 1956; 37: 177–180
   Google Scholar
• Birke L. I. A., Sadler D. Progestin-induced changes in play behavior of the prepubertal rat. Physiology and Behavior 1983; 30: 341–347
   PubMed Web of Science ®Google Scholar
• Birke L. I. A., Sadler D. Differences in maternal behavior of rats and the sociosexual development of the offspring. Developmental Psychobiology 1987; 20: 85–99
   PubMed Web of Science ®Google Scholar
• Brants F., Morisset J. Trophic effects of cholecystokinin-pancreozymin on pancreatic acinar cells from rats of different ages. Proceedings of the Society for Experimental Biology & Medicine 1976; 153: 523–527
   PubMedGoogle Scholar
• Dockray G. J. Cholecystokinin. Gut hormones, S. R. Bloom, J. M. Polack. Churchill Livingstone., Edinburgh 1981; 228–239
   Google Scholar
• Greenberg D., Smith G. P., Gibbs J. Infusion of CCK-8 into hepatic portal vein fails to reduce food intake in rats. American Journal of Physiology 1987; 252: R1015–R1018
   PubMed Web of Science ®Google Scholar
• Hill J. M., Gozes I., Hill J. L., Fridkin M., Brenneman D. E. Vasoactive intestinal peptide antagonist retards the development of neonatal behaviors in the rat. Peptides 1991; 12: 187–192
   PubMed Web of Science ®Google Scholar
• Johnson L. R., Guthrie P. D. Effect of cholecystokinin and 16, 16-dimethyl PGE2 on RNA and DNA of gastric and duodenal mucosa. Gastroenterology 1976; 67: 601–606
   Google Scholar
• Leigh H., Hofer M. Behavioral and physiological effects of litter-mate removal on the remaining single pup and mother during the pre-weaning period in rats. Psychosomatic Medicine 1973; 35: 497–508
   PubMedGoogle Scholar
• Liddle R. A. Integrated actions of cholecystokinin on the gastrointestinal tract: Use of the cholecystokinin bioassay. Gastroenterological Clinics of North America 1989; 18: 735–756
   PubMed Web of Science ®Google Scholar
• Meaney M. J., Stewart J. A descriptive study of social development in the rat (Rattus norvegicus). Animal Behaviour 1981; 29: 34–45
   Web of Science ®Google Scholar
• Moore C. L. An olfactory basis for maternal discrimination of sex of offspring in rat (Rattus norvegicus). Animal Behaviour 1981; 29: 383–386
   Google Scholar
• Moore C. L. Maternal behavior of rats is affected by hormonal condition of pups. Journal of Comparative and Physiological Psychology 1982; 96: 123–129
   PubMed Web of Science ®Google Scholar
• Moore C. L. Maternal contributions to the development of masculine sexual behavior in laboratory rats. Developmental Psychobiology 1984; 17: 347–356
   PubMed Web of Science ®Google Scholar
• Moore C. L., Morelli G. A. Mother rats interact differentially with male and female offspring. Journal of Comparative and Physiological psychology 1979; 93: 677–684
   PubMed Web of Science ®Google Scholar
• Naito H., Tonoue T. Sex difference in ultrasound distress calls by rat pups. Behavioral Brain Research 1987; 25: 13–21
   PubMedGoogle Scholar
• Noirot E. Ultrasounds and maternal behavior in small rodents. Developmental Psychobiology 1972; 5: 371–387
   PubMedGoogle Scholar
• Papp M., Dobronyi I., Varga G. Excessive doses of cerulein stimulate pancreatic growth in suckling rats but damage the pancreas of weaned rats. Biology of the Neonate 1988; 54: 339–346
   PubMedGoogle Scholar
• Papp M., Varga G., Dobronyi I. Caerulein stimulates pancreatic growth and somatic growth in suckling rats. International Journal of Pancreatology 1987; 2: 171–181
   PubMedGoogle Scholar
• Richmond G., Sachs B. D. Maternal discrimination of pup sex in rats. Developmental Psychobiology 1983; 17: 347–350
   Google Scholar
• Robinson P. H., Moran T. H., McHugh P. R. Gastric cholecystokinin receptors and the effect of cholecystokinin on feeding and gastric emptying in the neonatal rat. Annals of the New York Academy of Sciences 1985; 448: 627–619
   Google Scholar
• Robinson P. H., Moran T. H., McHugh P. R. Cholecystokinin inhibits independent ingestion in neonatal rats. American Journal of Physiology 1988; 255: R14–R20
   PubMed Web of Science ®Google Scholar
• Sharpe R. M., Wyatt A. C. The influence of the sex of litter mates on subsequent maternal behavior in Rattus norvegicus. Animal Behaviour 1975; 23: 551–559
   PubMedGoogle Scholar
• Smith G. P., Gibbs J., Schneider L., Greenberg D., Murphy R., Corp E., Corwin R. The satiating effect of cholecystokinin. Progress in Obesity Research, Y. Oomura, S. Tarui, S. Inoue, T. Shamazu. John Libbey & Company., London 1991; 25–28
   Google Scholar
• Uvnäs-Moberg K. The gastrointestinal tract in growth and reproduction. Scientific American 1989a; 261: 60–65
   Google Scholar
• Uvnäs-Moberg K. Gastrointestinal hormones in mother and infant. Acta Paediatrica Scandinavica (Suppl.) 1989b; 351: 88–93
   PubMedGoogle Scholar
• Uvnäs-Moberg K. Endocrinological control of food intake. Nutrition Review 1990; 48: 57–63
   PubMed Web of Science ®Google Scholar
• Uvnäs-Moberg K., Widström A. M., Marchini G., Winberg J. Release of GI hormones in mother and infant by sensory stimulation. Acta Paediatrica Scandinavia 1987; 76: 851–860
   PubMedGoogle Scholar
• Wager-Srdar S. A., Levine A. S. The effect of cholecystokinin octapeptide on food intake and consummatory behavior in lactating rats. Physiology and Behavior 1991; 50: 331–336
   PubMedGoogle Scholar
• Weller A., Blass E. M. Behavioral evidence for cholecystokinin-opiate interactions in neonatal rats. American Journal of Physiology 1988; 255: R901–R907
   Google Scholar
• Weller A., Biass E. M. Cholecystokinin conditioning in rats: Ontogenetic determinants. Behavioral Neuroscience 1990; 104: 199–206
   PubMedGoogle Scholar
• Weller A., Corp E. C., Tyrka A., Ritter R. C., Brenner L., Gibbs J., Smith G. P. Trypsin inhibitor and maternal reunion increase plasma cholecystokinin in neonatal rats. Peptides 1991, in press
   Google Scholar
• Weller A., Rozin A. Behavioral effects of gut hormones in neonatal rats: I. Somatostatin administration during the first postnatal week. International Journal of Neuroscience 1992, in press
   PubMedGoogle Scholar
• Weller A., Smith G. P., Gibbs J. Endogenous cholecystokinin reduces feeding in young rats. Science 1990; 247: 1589–1591
   PubMedGoogle Scholar
• Zadina J. E., Kastin A. J., Coy D. H., Adinoff B. A. Developmental, behavioral, and opiate receptor changes after prenatal or postnatal β-endorphin, CRF, or Tyr-MIF-1. Psychoneuroendocrinology 1985; 4: 367–383
   Google Scholar
• Zagon I. S., McLaughlin P. J. Perinatal methadone exposure and its influence on the behavioral ontogeny of rats. Pharmacology, Biochemistry and Behavior 1978; 9: 665–671
   PubMed Web of Science ®Google Scholar