The use of alloxan to induce diabetes in rabbits and some of the changes it causes in the body
DOI:
https://doi.org/10.31210/spi2025.28.04.31Keywords:
alloxan, diabetes, rabbit, blood glucose, histopathologyAbstract
Alloxan is frequently used to induce experimental diabetes in animals. Furthermore, by altering the dosage of administered alloxan, it has been extensively utilized to cause experimental diabetes with varying degrees of the disease severity in animals, including dogs, rats, mice, and rabbits. Alloxan significantly and dose-dependently increased blood glucose levels in rabbits. The study’s objectives are to examine the effects of alloxan time effect, changes in pancreatic histopathology, and blood glucose monitoring, administer the preparation to a diabetic rabbit model. Adult local breed rabbits were provided by the College of Kerbala Veterinary Medicine Laboratory Animal Center, where the experiment was conducted. To investigate the animals, they were divided into 2 groups. The rabbits of the first (experimental) group (n=5) received an injection of alloxan monohydrate at a dose of 150 mg/kg body weight. The rabbits from the second group, the control group (n=5), were given an injection of the same volume of isotonic saline. The studies showed that before the start of the experiment, the blood glucose levels of the first and second groups were practically the same, 108.2±146 and 113.0±7.5 mg/dl, respectively. A week after the administration of alloxan monohydrate, the rabbits from the first group showed a sharp increase in glucose levels by 2.9 times (P<0.05) compared to the same indicator before the start of the experiment, which was also 2.8 times higher (P<0.05) than the indicator in the control group of rabbits. It was found that the glucose level in rabbits from the first experimental group during 2, 3, and 4 weeks of the study remained quite high, above 261 mg/dl, which was significantly higher (P<0.05) compared to the indicator before the start of the experiment and compared to the similar indicators in the control group. According to histological pancreas studies from the rabbits treated with alloxan monohydrate, characteristic changes were observed, indicating a negative effect of the administered drug on the cells of the studied organ. In particular, a month after the administration of alloxan monohydrate, dystrophic changes in the population of β-cells were detected in the study of pancreatic islets of Langerhans, characterized by vacuolization of the cytoplasm, pyknosis and karyolysis of the nuclei.
References
Definition, diagnosis and classification of diabetes mellitus and its complications : report of a WHO consultation. Part 1, Diagnosis and classification of diabetes mellitus. (1999). World Health Organization. Geneva: World Health Organization, WHO Department of Non Communicable Disease Surveillance. Retrieved from: https://iris.who.int/handle/10665/66040
Patel, D., Kumar, R., Prasad, S., Sairam, K., & Hemalatha, S. (2011). Antidiabetic and in vitro antioxidant potential of Hybanthus enneaspermus (Linn) F. Muell in streptozotocin-induced diabetic rats. Asian Pacific Journal of Tropical Biomedicine, 1 (4), 316–322. https://doi.org/10.1016/s2221-1691(11)60051-8
Hernandez-Galicia, E., Aguilar-Contreras, A., Aguilar-Santamaria, L., Roman-Ramos, R., Chavez-Miranda, A. A., Garcia-Vega, L. M., Flores-Saenz, J. L., & Alarcon-Aguilar, F. J. (2002). Studies on hypoglycemic activity of Mexican medicinal plants. Proceedings of the Western Pharmacology Society, 45, 118–124.
Szkudelski, T. (2001). The mechanism of alloxan and streptozotocin action in B cells of the rat pancreas. Physiological Research, 50 (6), 537–546.
Iranloye, B. O., Arikawe, A. P., Rotimi, G., & Sogbade, A. O. (2011). Anti-diabetic and anti-oxidant effects of Zingiber officinale on alloxan-induced and insulin-resistant diabetic male rats. Nigerian Journal of Physiological Sciences, 26 (1), 89–96.
Zaman, R. (2006). High prevalence of diabetes mellitus and promoting factors among human urban population of Bahawalpur-district, Pakistan: cross-sectional study. Research Journal of Medical Sciences, 3 (2), 62–69.
Wang, T. J., Larson, M. G., Vasan, R. S., Cheng, S., Rhee, E. P., McCabe, E., Lewis, G. D., Fox, C. S., Jacques, P. F., Fernandez, C., O’Donnell, C. J., Carr, S. A., Mootha, V. K., Florez, J. C., Souza, A., Melander, O., Clish, C. B., & Gerszten, R. E. (2011). Metabolite profiles and the risk of developing diabetes. Nature Medicine, 17 (4), 448–453. https://doi.org/10.1038/nm.2307
Bacha, F., Lee, S., Gungor, N., & Arslanian, S. A. (2010). From pre-diabetes to type 2 diabetes in obese youth. Diabetes Care, 33 (10), 2225–2231. https://doi.org/10.2337/dc10-0004
Tripathi, V., & Verma, J. J. (2024). Current updates of Indian antidiabetic medicinal plants. International Journal of Research in Pharmacy and Chemistry, 4 91), 114–118. Retrieved from: https://www.ijrpc.com/files/19-431.pdf
Standring, S., Borley, N. R., Collins, P., & Gray, H. (2008). Gray’s anatomy. The anatomical basis of clinical practice. (40th ed.). London: Churchill Livingstone.
Wöhler, F., & Liebig, J. (1838). Untersuchungen über die Natur der Harnsäure. Annalen Der Pharmacie, 26 (3), 241–336. https://doi.org/10.1002/jlac.18380260302
Lenzen, S., Tiedge, M., Jörns, A., & Munday, R. (1996). Alloxan derivatives as a tool for the elucidation of the mechanism of the diabetogenic action of alloxan. In: E. Shafrir (Ed.). Lessons from Animal Diabetes VI, (pp. 113–122). Boston: Birkhäuser. https://doi.org/10.1007/978-1-4612-4112-6_8
Shaw Dunn, J., & Mcletchie, N. G. B. (1943). Experimental alloxan diabetes in the rat. The Lancet, 242 (6265), 384–387. https://doi.org/10.1016/s0140-6736(00)87397-3
Jorns, A., Munday, R., Tiedge, M., & Lenzen, S. (1997). Comparative toxicity of alloxan, N-alkylalloxans and ninhydrin to isolated pancreatic islets in vitro. Journal of Endocrinology, 155 (2), 283–293. https://doi.org/10.1677/joe.0.1550283
Brückmann, G., & Wertheimer, E. (1947). Alloxan studies: the action of alloxan homologues and related compounds. Journal of Biological Chemistry, 168 (1), 241–256. https://doi.org/10.1016/s0021-9258(17)35111-6
Lenzen, S. (2007). The mechanisms of alloxan- and streptozotocin-induced diabetes. Diabetologia, 51 (2), 216–226. https://doi.org/10.1007/s00125-007-0886-7
Boquist, L., Nelson, L., & Lorentzon, R. (1983). Uptake of labeled alloxan in mouse organs and mitochondria in vivo and in vitro. Endocrinology, 113 (3), 943–948. https://doi.org/10.1210/endo-113-3-943
Heikkila, R. E., Winston, B., Cohen, G., & Barden, H. (1976). Alloxan-induced diabetes – evidence for hydroxyl radical as a cytotoxic intermediate. Biochemical Pharmacology, 25 (9), 1085–1092. https://doi.org/10.1016/0006-2952(76)90502-5
Tiedge, M., Lortz, S., Drinkgern, J., & Lenzen, S. (1997). Relation between antioxidant enzyme gene expression and antioxidative defense status of insulin-producing cells. Diabetes, 46 (11), 1733–1742. https://doi.org/10.2337/diab.46.11.1733
Lenzen, S., Tiedge, M., & Panten, U. (1987). Glucokinase in pancreatic B-cells and its inhibition by alloxan. Acta Endocrinologica, 115 (1), 21–29. https://doi.org/10.1530/acta.0.1150021
Lenzen, S., & Mirzaie-Petri, M. (1991). Inhibition of glucokinase and hexokinase from pancreatic β-cells and liver by alloxan, alloxantin, dialuric acid, and t-butylhydroperoxide. Biomedical Research, 12 (5), 297–307. https://doi.org/10.2220/biomedres.12.297
Lenzen, S., & Munday, R. (1991). Thiol-group reactivity, hydrophilicity and stability of alloxan, its reduction products and its N-methyl derivatives and a comparison with ninhydrin. Biochemical Pharmacology, 42 (7), 1385–1391. https://doi.org/10.1016/0006-2952(91)90449-f
Khushk, I., Dahot, M. U., Baloach, S. A., & Bhutto, M. A. (2010). The evaluation of soybean extracts in alloxan-induced diabetic rabbits. World Applied Sciences Journal (Special Issue of Biotechnology & Genetic Engineering), 8, 22–25.
Schiller, N. K., & McNamara, D. B. (1999). Balloon catheter vascular injury of the alloxan-induced diabetic rabbit: The role of insulin-like growth factor. Molecular and Cellular Biochemistry, 202 (1–2), 159–167. https://doi.org/10.1023/a:1007005919319
Im Walde, S. S., Dohle, C., Schott-Ohly, P., & Gleichmann, H. (2002). Molecular target structures in alloxan-induced diabetes in mice. Life Sciences, 71 (14), 1681–1694. https://doi.org/10.1016/s0024-3205(02)01918-5
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2025 Scientific Progress & Innovations

This work is licensed under a Creative Commons Attribution 4.0 International License.
Creative Commons Attribution 4.0 International Licens