Evaluation of alloxan on induction of diabetes in albino rats

Authors

  • Soni . Department of Pharmacology, MGM Medical College, Jamshedpur
  • A. N. Mishra Department of Pharmacology, MGM Medical College, Jamshedpur

DOI:

https://doi.org/10.18203/2319-2003.ijbcp20195290

Keywords:

Alloxan, Alopecia, Diabetes

Abstract

Background: Alloxan-induced diabetes model is used as a “study tool” to elucidate the pathophysiology of the disease and much more as a “search engine” for antidiabetic compounds with better therapeutic characteristics. It was the first agent used in the category of chemically induced diabetes to create a model of insulin dependent diabetes mellitus. Other chemicals being streptozocin, dexamethasone, insulin antibodies-induced diabetes.

Methods: Albino rats were divided into four groups with ten rats in each group. Alloxan monohydrate 2%, solution which was dissolved in 0.9% of sodium chloride (normal saline) as a diluent and given intraperitoneally to rats and blood glucose estimation made by using glucometer. Total 40 albino rats were taken and divided into 4 groups. 10 rats receiving normal saline were grouped as Group A, 10 rats received alloxan at a dose of 150 mg/kg as Group B, 10 rats received alloxan at a dose of 160 mg/kg as Group C and 10 rats received alloxan at a dose of 170 mg/kg as Group D.

Results: Highest rate of mortality and alopecia were noted in group D receiving alloxan at a dose of 170 mg/kg whereas highest percentage of fluctuation in fasting blood glucose range was seen in group C receiving alloxan at a dose of 160 mg/kg.

Conclusions: Such unpredictable response shows that alloxan is not ideal drug for induction of diabetes in experimental animal. Mortality, fasting blood glucose returning to non-diabetic range and alopecia are the chief drawbacks.

Author Biography

Soni ., Department of Pharmacology, MGM Medical College, Jamshedpur

senior resident

department of pharmacology

References

Lumelsky N, Blondel O, Laeng P, Velasco I, Ravin R, McKay R. Differentiation of embryonic stem cells to insulin-secreting structures similar to pancreatic islets. Science. 2001;292(5520):1389-94.

Muoio DM, Newgard CB. Molecular and metabolic mechanisms of insulin resistance and β-cell failure in type 2 diabetes. Nature Reviews Molecul Cell Biol. 2008;9(3):193.

Busnardo AC, DiDio LJ, Tidrick RT, Thomford NR. History of the pancreas. Am J Surg. 1983;146(5):539-50.

Rees DA, Alcolado JC. Animal models of diabetes mellitus. Diabetic Med. 2005;22(4):359-70.

Liebig LJ, Wohler F. A History of Chemistry. Palgrave, London: 1964: 294-336.

Black HE, Rosenblum IY, Capen CC. Chemically induced (streptozotocin-alloxan) diabetes mellitus in the dog: biochemical and ultrastructural studies. Am J Pathol. 1980;98(2):295.

Ahmed SK, Sunil M, Cheekavolu C, Alasyam N. Evaluation of antidiabetic effect of Murrayakoenigii leaves chloroform extract (MKLCE) in alloxan induced diabetic albino rats. 20187;11(6):474-7.

Care V. CPCSEA guidelines for laboratory animal facility. Indian J Pharmacol. 2003;35:257-74.

Ighodaro MO, Adeosun MA, Akinloye AO. Alloxan-induced diabetes, a common model for evaluating the glycemic-control potential of therapeutic compounds and plants extracts in experimental studies. Medicina. 2017;53(6):365-74.

Gerich JE, Charles MA, Grodsky GM. Regulation of pancreatic insulin and glucagon secretion. Annual Review Physiol. 1976;38(1):353-88.

Szkudelski T. Streptozotocin–nicotinamide-induced diabetes in the rat. Characteristics of the experimental model. Exp BiolMed. 2012;237(5):481-90.

Downloads

Published

2019-11-25

How to Cite

., S., & Mishra, A. N. (2019). Evaluation of alloxan on induction of diabetes in albino rats. International Journal of Basic & Clinical Pharmacology, 8(12), 2748–2750. https://doi.org/10.18203/2319-2003.ijbcp20195290

Issue

Section

Original Research Articles