Hostname: page-component-78c5997874-94fs2 Total loading time: 0 Render date: 2024-11-10T13:17:22.620Z Has data issue: false hasContentIssue false

The effect of different dietary fats on gastrin levels in the pyloric antrum and plasma of weaner and adult Wistar rats

Published online by Cambridge University Press:  09 March 2007

N. U. Ekeke
Affiliation:
Department of Medicine, The Queen's University of Belfast, Grosvenor Road, Belfast BTI2 6BJ
C. Shaw
Affiliation:
Department of Medicine, The Queen's University of Belfast, Grosvenor Road, Belfast BTI2 6BJ
C. F. Johnston
Affiliation:
Department of Medicine, The Queen's University of Belfast, Grosvenor Road, Belfast BTI2 6BJ
K. D. Buchanan
Affiliation:
Department of Medicine, The Queen's University of Belfast, Grosvenor Road, Belfast BTI2 6BJ
A. H. G. Love
Affiliation:
Department of Medicine, The Queen's University of Belfast, Grosvenor Road, Belfast BTI2 6BJ
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

The effect of dietary fats on gastrin in the pyloric antrum and plasma of Wistar rats was examined. Two different age-groups of rats were fed on three different diets in which fat was in the form of menhadenoil (MO), hydrogenated coconut oil (CO) and safflower oil (SO) respectively. Control groups were fed on normal laboratory diet. Each diet was isoenergetic and no group showed significant differences in either food intake or weight gain during the experiment. Weaner rats fed on the MO diet exhibited significant reductions in both antral (P = 0.047) and plasma (P = 0.002) gastrin concentrations when compared with age-matched controls. Likewise, adult rats fed on the MO diet exhibited significant reductions in both antral (P = 0.008) and plasma (P = 0.002) gastrin concentrations. In addition, adult rats fed on the CO diet exhibited significant reductions in both antral (P = 0.047) and plasma gastrin(P = 0.002) concentrations. Rats from both age-groups fed on the SO diet exhibited no significant differences in gastrin concentrations when compared with their respective control groups. These findings indicate that the composition of dietary fat can have profound effects on both tissue and plasma concentrations of gastrin in rats.

Type
Metabolic Effects of Fats
Copyright
Copyright © The Nutrition Society 1993

References

REFERENCES

Ardill, J. E. S. (1979). Radioimmunoassay of gastrointestinal hormones. Clinics in Endocrinology and Metabolism 8, 265280.CrossRefGoogle Scholar
Bank, S., Barbezat, G. O., Novis, B. H., Ou, T., Odes, H. S., Helman, C., Narunsky, L., Duys, P. J. & Marks, I. N. (1976). Histamine-H, receptor antagonists in the treatment of duodenal ulcers. South African Medical Journal 50, 17811784.Google Scholar
Black, J. W., Duncan, W. A. M., Durant, G. J., Ganellin, C. R. & Parson, E. M. (1972). Definitions and antagonism of histamine-H, receptors. Nature 236, 385390.CrossRefGoogle Scholar
Castell, D. O. & Harris, L. D. (1970). Hormonal control of gastroesophageal sphincter strength. New England Journal of Medicine 282, 886890.CrossRefGoogle ScholarPubMed
Channusot, F., Esnault-Dupuy, C., Matigne, M., Portugal, H., Lairon, D., Quingard, A., Alcindor, G. L., Pauli, A. M., Lafont, H. & Hauton, C. J. (1988). Metabolism of low- and high-density lipoprotein-free-cholesterol in rats fed high fat diets. Annals of Nutrition & Metabolism 32, 271281.CrossRefGoogle Scholar
Crean, G. P., Marshall, M. W. & Rumsey, R. D. G. (1969). Parietal cell hyperplasia induced by the administration of pentagastrin to rats. Gastroenterology 57, 147155.CrossRefGoogle ScholarPubMed
Dockray, G. J. (1978). Gastrin overview. In Gut Hormones, pp. 129139. [Bloom, S. R., editor]. Edinburgh, London and New York: Churchill Livingstone.Google Scholar
Dremer, J. M., Michalek, A. V., Lininger, L., Huych, C., Bigauoette, J., Timchalk, M. A., Rynes, R. I., Rieminski, J. & Bartholomew, L. E. (1985). Effects of manipulation of dietary fatty acid on clinical manifestations of rheumatoid arthritis. Lancet i, 184187.Google Scholar
Dyerberg, T., Bank, H. O., Stofferson, E., Moncada, S. & Vane, J. R. (1978). Eicosapentaenoic acid and prevention of thrombosis and atherosclerosis. Lancet ii, 117119.CrossRefGoogle Scholar
Edkin, J. S. (1905). On the chemical mechanism of gastric secretion. Proceedings ofthe Royal Society of Biology 16, 376.Google Scholar
Gillespie, I. E. & Grossman, M. I. (1962). Effect of acid in pyloric pouch on response of fundic pouch to injected gastrin. American Journal of Physiology 203, 557562.CrossRefGoogle ScholarPubMed
Gingel, J. C., Davies, M. W. & Shields, R. (1968). Effect of a synthetic gastrin-like pentapeptide upon the intestinal transport of sodium, potassium and water. Gut 5, 19111916.Google Scholar
Gregory, R. A., Davies, M. W. & Tracy, H. J. (1964). The constitution and properties of the two gastrins extracted from hog antral mucosa. Gut 5, 103117.CrossRefGoogle ScholarPubMed
Greider, M. H., Steinberg, V. & McGuigan, J. E. (1972). Electron microscope identification of the gastrin cell of the human antral mucosa by means of immunocytochemistry. Gastroenterology 63, 572582.CrossRefGoogle ScholarPubMed
Korman, M. G., Sorveny, C. & Hanky, J. (1971). Effect of food on serum gastrin evaluated by radioimmunoassay. Gut 12, 619624.CrossRefGoogle ScholarPubMed
Lichtenberger, L. M., Castro, G. A., Copeland, E. M., Dudrick, S. J. & Johnson, L. R. (1974). The effect of food on rat antral gastrin concentration. Gastroenterology 55, 220.Google Scholar
Lichtenberger, L. M. & Johnson, L. R. (1974). Gastrin in the ontogenic development of the small intestine. American Journal of Physiology 227, 390395.CrossRefGoogle ScholarPubMed
Lichtenberger, L. M., Welsh, J. D. & Johnson, L. R. (1976). Relationship between the exchanges in gastrin levels and intestinal properties in the starved rat. American Journal of Digestive Diseases 21, 33.CrossRefGoogle Scholar
Lin, T. M. & Spray, G. F. (1969). Effect of pentagastrin, cholecystokinin, caerulein and glucagon on the choledochal resistance and bile flow of the conscious dog. Gastroenterology 56, 1178.Google Scholar
Meyer, J. & Jones, R. (1974). Canine pancreatic responses to intestinally perfused fat and products of fat digestion. American Journal of Physiology 226, 11781187.CrossRefGoogle ScholarPubMed
Rand, L. M., Hennissen, A. H. M. & Hornstra, G. (1988). Effects of dietary palm oil on arterial thrombosis, platelet responses and platelet membrane fluidity in rats. Lipids 23, 10191023.CrossRefGoogle ScholarPubMed
Renny, A., Snape, W.. Sun, E., London, R. & Cohen, S. (1983). Role of cholecystokinin in the gastrocolonic response to a fat meal. Gastroenterology 85, 1721.CrossRefGoogle ScholarPubMed
Shinton, R. A., Dodson, P. M. & Beevers, D. G. (1989). Hypertension and dietary fat. Journal of Human Hypertension 3, 7378.Google ScholarPubMed
Sicar, B., Johnson, L. R. & Lichtenberger, L. M. (1980). Effect of chemically defined diets on antral and serum gastrin levels in rats. American Journal of Physiology 238, G376G383.Google Scholar
Strunz, U. T., Walsh, J. H. & Grossman, M. I. (1977). Stimulation of gastrin release and gastric acid secretion by various amino acids. Clinical Research 24, 113.Google Scholar