Hostname: page-component-586b7cd67f-rdxmf Total loading time: 0 Render date: 2024-11-26T05:05:31.296Z Has data issue: false hasContentIssue false

Pancreatic and extra-pancreatic effects of the traditional anti-diabetic plant, Medicago sativa (lucerne)

Published online by Cambridge University Press:  09 March 2007

Alison M Gray
Affiliation:
School of Biomedical Sciences, University of Ulster, Coleraine BT52 1SA
Peter R Flatt
Affiliation:
School of Biomedical Sciences, University of Ulster, Coleraine BT52 1SA
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.

Medicago sativa (lucerne) is used as a traditional plant treatment of diabetes. In the present study, administration of lucerne in the diet (62·5 g/kg) and drinking water (2·5 g/l) reduced the hyperglycaemia of streptozotocin-diabetic mice. An aqueous extract of lucerne (1 mg/ml) stimulated 2-deoxy-glucose transport (1·8-fold), glucose oxidation (1·7-fold) and incorporation of glucose into glycogen (l·6-fold) in mouse abdominal muscle. In acute 20 min tests, 0·25–1 mg/ml aqueous extract of lucerne evoked a stepwise 2·5–6·3-fold stimulation of insulin secretion from the BRIN-BD11 pancreatic B-cell line. This effect was abolished by 0·5 mM-diazoxide, and prior exposure to extract did not affect subsequent stimulation of insulin secretion by 10 mM-L-alanine, thereby negating a detrimental effect on cell viability. The effect of extract was potentiated by 16·7 mM-glucose and by 1 mM-3-isobutyl-1-methylxanthine. L-Alanine (10 mM) and a depolarizing concentration of KCI (25 mM) did not augment the insulin-releasing activity of lucerne. Activity of the extract was found to be heat stable and largely acetone insoluble, and was enhanced by exposure to acid and alkali (0·1 M-HCI and NaOH) but decreased 25% with dialysis to remove components with molecular mass <2000 Da. Sequential extraction with solvents revealed insulin-releasing activity in both methanol and water fractions indicating a cumulative effect of more than one extract constituent. The results demonstrate the presence of antihyperglycaemic, insulin-releasing and insulin-like activity in the traditional antidiabetic plant, Medicago sativu.

Type
General Nutrition
Copyright
Copyright © The Nutrition Society 1997

References

REFERENCES

Bailey, C. J. & Day, C. (1989). Traditional treatments for diabetes. Diabetes Care 12, 553564.CrossRefGoogle ScholarPubMed
Bailey, C. J. & Puah, J. A. (1986). Effect of metformin on glucose metabolism in mouse soleus muscle. Diabète et Metabolisme 12, 212218.Google ScholarPubMed
Flatt, P. R. & Bailey, C. J. (1981). Abnormal plasma glucose and insulin responses in heterozygous lean (ob/ + ) mice. Diabetologia 20, 573577.CrossRefGoogle ScholarPubMed
Hunt, S. M., Chrzanowska, C., Barnett, C. R., Brand, H. N. & Fawell, J. K. (1987). A comparison of in vitro cytotoxicity assays and their application to water samples. Alternatives to Laboratory Animals 15, 2029.CrossRefGoogle Scholar
Lewis, J. J. (1949). Diabetes and the insulin administration problem. Physiological Reviews 29, 7590.CrossRefGoogle ScholarPubMed
Lust, J. (1986). The Herb Book. London: Bantam Books.Google Scholar
McClenaghan, N. H., Barnett, C. R., Ah-Sing, E., Abdelwahab, Y. H. A., O'Harte, F. P. M., Yoon, T.-W., Swanston-Flatt, S. K. & Flatt, P. R. (1996). Characterization of a novel glucose-responsive insulin-secreting cell line, BRIN-BDll, produced by electrofusion. Diabetes 45, 11321140.CrossRefGoogle ScholarPubMed
Prager, R., Schernthaser, G. & Graf, H. (1986). Effect of metformin on peripheral insulin sensitivity in non-insulin dependent diabetes mellitus. Diabète Metabolisme 12, 346350.Google ScholarPubMed
Rubenstein, A. H., Levin, N. W. & Elliott, G. A. (1962 a). Manganese-induced hypoglycaemia. Lancet ii, 13481351.CrossRefGoogle Scholar
Rubenstein, A. H., Levin, N. W. & Elliott, G. A. (1962 b). Hypoglycaemia induced by manganese. Nature 194, 188199.CrossRefGoogle ScholarPubMed
Schwanstecher, C. & Panten, U. (1994). Interactive control by sulphonylureas and cytosolic nucleotides of the ATP-sensitive K+ channel in pancreatic B-cells. In Frontiers of Insulin Secretion and Pancreatic B-cell Research, pp. 161166 [Flatt, P. R. and Lenzen, S., editors]. London: Smith-Gordon.Google Scholar
Sharp, G. W. G. (1979). The adenylate cyclase-cylic AMP system in islets of Langerhans and its role in the control of insulin releases. Diabetologia 16, 287297.CrossRefGoogle Scholar
Stevens, J. F. (1971). Determination of glucose by automatic analyser. Clinica Chimica Acta 32, 199201.CrossRefGoogle ScholarPubMed
Swanston-Flatt, S. K., Day, C., Bailey, C. J. & Flatt, P. R. (1990). Traditional plant treatments for diabetes. Studies in normal and streptozotocin diabetic mice. Diabetologia 33, 462464.CrossRefGoogle ScholarPubMed
Trube, G., Rorsman, P. & Ohno-Shosaku, T. (1986). Opposite effects of tolbutamide and diazoxide on ATP-dependent K+ channel in mouse pancreatic B-cells. Pflugers Archives 407, 493499.CrossRefGoogle Scholar
World Health Organization (1980). Second Report of the WHO Expert Committee on Diabetes Mellitus. Technical Report Series 646, p.66. Geneva: World Health Organization.Google Scholar
Yada, T. (1994). Action mechanisms of amino acids in pancreatic B-cells. In Frontiers of lnsulin Secretion and Pancreatic B-cell Research, pp. 129135 [Flatt, P. R. and Lenzen, S., editors]. London: Smith-Gordon.Google Scholar