Abstract
The oxidation of alanine, arginine, leucine, glucose, and pyruvate was studied in microdissected pancreatic islets of obese–hyperglycaemic mice. The following main observations were made. The oxidation of glucose was enhanced severalfold when its concentration was raised from 3 to 20mm. At the latter concentration the rate was about 65mmol/h per kg dry wt. The oxidation of 17mm-pyruvate amounted to 20mmol/h per kg dry wt. indicating a significant entry of this compound into the β-cells. Leucine oxidation was little affected by concentration changes above 5mm, the rate at 20mm corresponding to about 25% of that obtained with 20mm-glucose. In the absence of glucose, the oxidation of alanine or arginine was barely significant. Glucose stimulated the oxidation of alanine but depressed that of leucine. These effects of glucose were blocked by mannoheptulose or iodoacetamide but were not influenced by adrenaline, diazoxide, dibutyryl 3′:5′-cyclic AMP, or glibenclamide. The rate of alanine oxidation was doubled in the presence of 17mm-pyruvate but was unaffected by citrate or succinate. Succinate depressed the oxidation of leucine. Neither alanine nor leucine significantly affected the oxidation of glucose. It is suggested that the effects of glucose on the oxidation of alanine and leucine were mediated by metabolism of the sugar, and that amino acids do not act as insulin secretagogues by serving as fuels for the β-cells. The results are consistent with the existence of mechanisms auxiliary to glucose metabolism for control of insulin release.
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Selected References
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- Ashcroft S. J., Hedeskov C. J., Randle P. J. Glucose metabolism in mouse pancreatic islets. Biochem J. 1970 Jun;118(1):143–154. doi: 10.1042/bj1180143. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Christensen H. N., Cullen A. M. Behavior in the rat of a transport-specific, bicyclic amino acid. Hypoglycemic action. J Biol Chem. 1969 Mar 25;244(6):1521–1526. [PubMed] [Google Scholar]
- Cory H. T., Rose S. P. Alanine metabolism in rat cortex in vitro. J Neurochem. 1970 Oct;17(10):1477–1484. doi: 10.1111/j.1471-4159.1970.tb00514.x. [DOI] [PubMed] [Google Scholar]
- Danielsson A., Hellman B., Idahl L. A. Levels of -ketoglutarate and glutamate in stimulated pancreatic -cells. Horm Metab Res. 1970 Jan;2(1):28–31. doi: 10.1055/s-0028-1095123. [DOI] [PubMed] [Google Scholar]
- Edgar P., Rabinowitz D., Merimee T. J., Almogela E. Effect of arginine on insulin release in vitro. Metabolism. 1969 Feb;18(2):84–86. doi: 10.1016/0026-0495(69)90100-0. [DOI] [PubMed] [Google Scholar]
- Fajans S. S., Floyd J. C., Jr, Knopf R. F., Conn F. W. Effect of amino acids and proteins on insulin secretion in man. Recent Prog Horm Res. 1967;23:617–662. doi: 10.1016/b978-1-4831-9826-2.50017-9. [DOI] [PubMed] [Google Scholar]
- HUMBEL R. E., RENOLD A. E. Studies on isolated islets of Langerhans (Brockmann bodies) of teleost fishes. I. Metabolic activity in vitro. Biochim Biophys Acta. 1963 Jul 2;74:84–95. doi: 10.1016/0006-3002(63)91332-5. [DOI] [PubMed] [Google Scholar]
- Hellman B. Methodological approaches to studies on the pancreatic islets. Diabetologia. 1970 Apr;6(2):110–120. doi: 10.1007/BF00421438. [DOI] [PubMed] [Google Scholar]
- Hellman B. Studies in obese-hyperglycemic mice. Ann N Y Acad Sci. 1965 Oct 8;131(1):541–558. doi: 10.1111/j.1749-6632.1965.tb34819.x. [DOI] [PubMed] [Google Scholar]
- Ihle R., Schultze M., Rosenthal S. Wechselwirkungen zwischen Glukose- und Aminosäurestoffwechsel in embryonalen Rattenamnionzellen. Der Einfluss von Glukose auf die CO2-Bildung aus Alanin und Glyzin. Acta Biol Med Ger. 1966;17(4):375–382. [PubMed] [Google Scholar]
- KEEN H., FIELD J. B., PASTAN I. H. A simple method for in vitro metabolic studies using small volumes of tissue and medium. Metabolism. 1963 Feb;12:143–147. [PubMed] [Google Scholar]
- LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
- LOWRY O. H. The quantitative histochemistry of the brain; histological sampling. J Histochem Cytochem. 1953 Nov;1(6):420–428. doi: 10.1177/1.6.420. [DOI] [PubMed] [Google Scholar]
- Lambert A. E., Jeanrenaud B., Junod A., Renold A. E. Organ culture of fetal rat pancreas. II. Insulin release induced by amino and organic acids, by hormonal peptides, by cationic alterations of the medium and by other agents. Biochim Biophys Acta. 1969 Sep 2;184(3):540–553. doi: 10.1016/0304-4165(69)90268-2. [DOI] [PubMed] [Google Scholar]
- Milner R. D., Hales C. N. The role of calcium and magnesium in insulin secretion from rabbit pancreas studied in vitro. Diabetologia. 1967 Mar;3(1):47–49. doi: 10.1007/BF01269910. [DOI] [PubMed] [Google Scholar]
- Milner R. D. Stimulation of insulin secretion in vitro by essential aminoacids. Lancet. 1969 May 31;1(7605):1075–1076. doi: 10.1016/s0140-6736(69)91709-7. [DOI] [PubMed] [Google Scholar]
- SCHEPARTZ B. OXIDATION OF L-AMINO ACIDS AND INCORPORATION INTO PROTEIN IN HOMOGENATES OF BRAIN AT TWO STAGES OF DEVELOPMENT. J Neurochem. 1963 Dec;10:825–829. doi: 10.1111/j.1471-4159.1963.tb11907.x. [DOI] [PubMed] [Google Scholar]
- SWAIMAN K. F., MILSTEIN J. M. OXIDATIVE DECARBOXYLATION OF ASPARTATE, ALANINE AND GLYCINE IN DEVELOPING RABBIT BRAIN. Biochim Biophys Acta. 1964 Oct 9;93:64–70. doi: 10.1016/0304-4165(64)90260-0. [DOI] [PubMed] [Google Scholar]
- Sadasivudu B., Lajtha A. Metabolism of amino acids in incubated slices of mouse brain. J Neurochem. 1970 Aug;17(8):1299–1311. doi: 10.1111/j.1471-4159.1970.tb03379.x. [DOI] [PubMed] [Google Scholar]
