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Phenotyping animal models of diabetic peripheral neuropathy in rats: advantages and limitations

https://doi.org/10.14341/probl9284

Abstract

Diabetic polyneuropathy is one of the most common late complications of diabetes mellitus, as well as the main cause of ulcerative foot defects. The prevalence of neuropathy among people with diabetes varies from 28 to 65%, depending on the disease duration and diagnostic features. Initial signs of damage are detected as early as in prediabetes. To date, there is a fairly limited knowledge of the mechanisms of nerve fiber damage in diabetes. Also, it is unclear which type of nerve fibers is involved in damage first and how the nervous system regulates repair of tissues and local immunity. Animal models of diabetic peripheral neuropathy enable studying new aspects of the pathogenesis of this common diabetes complication and open prospects for the search and development of new drugs.

About the Authors

Zera N. Abdulvapova

Endocrinology Research Centre


Russian Federation

MD



Ekaterina V. Artemova

Endocrinology Research Centre


Russian Federation

MD



Anna M. Gorbacheva

Lomonosov Moscow State University


Russian Federation

MD



Gagik R. Galstyan

Endocrinology Research Centre


Russian Federation

PhD, professor



Alla Yu. Tokmakova

Endocrinology Research Centre


Russian Federation

PhD



Svetlana A. Gavrilova

Lomonosov Moscow State University


Russian Federation

PhD



References

1. Gordois A, Scuffham P, Shearer A, et al. The health care costs of diabetic peripheral neuropathy in the U.S. Diabetes Care. 2003;26(6):1790-1795. doi: 10.2337/diacare.26.6.1790

2. Ziegler D, Strom A, Lobmann R, et al. High prevalence of diagnosed and undiagnosed polyneuropathy in subjects with and without diabetes participating in a nationwide educational initiative (PROTECT study). J Diabetes Complications. 2015; 29(8):998-1002. doi: 10.1016/j.jdiacomp.2015.09.008

3. Biessels GJ, Bril V, Calcutt NA, et al. Phenotyping animal models of diabetic neuropathy: a consensus statement of the diabetic neuropathy study group of the EASD (Neurodiab). J Peripher Nerv Syst. 2014;19(2):77-87. doi: 10.1111/jns5.12072

4. Davidson E, Coppey L, Lu B, et al. The roles of streptozotocin neurotoxicity and neutral endopeptidase in murine experimental diabetic neuropathy. Exp Diabetes Res. 2009;2009:431980. doi: 10.1155/2009/431980

5. Lenzen S. The mechanisms of alloxan- and streptozotocin-induced diabetes. Diabetologia. 2008;51(2):216-226. doi: 10.1007/s00125-007-0886-7

6. Sima AA, Zhang W, Xu G, et al. A comparison of diabetic polyneuropathy in type II diabetic BBZDR/Wor rats and in type I diabetic BB/Wor rats. Diabetologia. 2000;43(6):786-793. doi: 10.1007/s00125005137

7. Sullivan KA, Hayes JM, Wiggin TD, et al. Mouse models of diabetic neuropathy. Neurobiol Dis. 2007;28(3):276-285. doi: 10.1016/j.nbd.2007.07.022

8. Choeiri C, Hewitt K, Durkin J, et al. Longitudinal evaluation of memory performance and peripheral neuropathy in the Ins2C96Y Akita mice. Behav Brain Res. 2005;157(1):31-38. doi: 10.1016/j.bbr.2004.06.005

9. Chang H-J, Gurley SB. Assessment of Diabetic Nephropathy in the Akita Mouse. In: Joost HG, Al-Hasani H, Schürmann A, editors. Animal Models in Diabetes Research. New York: Humana Press; 2012;17-29. doi: 10.1007/978-1-62703-068-7

10. Schmidt I. Metabolic diseases: the environment determines the Odds, even for genes. News Physiol Sci. 2002;17(3):115-121. doi: 10.1152/nips.01380.2001

11. Clark JB, Palmer CJ, Shaw WN. The Diabetic Zucker Fatty Rat. Proc Soc Exp Biol Med. 1983;173(1):68-75. doi: 10.3181/00379727-173-41611

12. Schmidt RE, Dorsey DA, Beaudet LN, Peterson RG. Analysis of the Zucker Diabetic Fatty (ZDF) type 2 diabetic rat model suggests a neurotrophic role for insulin/IGF-I in diabetic autonomic neuropathy. Am J Path. 2003;163(1):21-28. doi: 10.1016/s0002-9440(10)63626-7

13. Jaggi AS, Jain V, Singh N. Animal models of neuropathic pain. Fundam Clin Pharmacol. 2011;25(1):1-28. doi: 10.1111/j.1472-8206.2009.00801.x

14. Lirk P, Flatz M, Haller I, et al. In Zucker diabetic fatty rats, subclinical diabetic neuropathy increases in vivo lidocaine block duration but not in vitro neurotoxicity. Reg Anesth Pain Med. 2012;37(6):601-606. doi: 10.1097/AAP.0b013e3182664afb

15. Li F, Abatan OI, Kim H, et al. Taurine reverses neurological and neurovascular deficits in Zucker diabetic fatty rats. Neurobiol Dis. 2006;22(3):669-676. doi: 10.1016/j.nbd.2006.01.012

16. Lupachyk S, Watcho P, Hasanova N, et al. Triglyceride, nonesterified fatty acids, and prediabetic neuropathy: role for oxidative-nitrosative stress. Free Radic Biol Med. 2012;52(8):1255-1263. doi: 10.1016/j.freeradbiomed.2012.01.029

17. Lupachyk S, Watcho P, Obrosov AA, et al. Endoplasmic reticulum stress contributes to prediabetic peripheral neuropathy. Exp Neurol. 2013;247:342-348. doi: 10.1016/j.expneurol.2012.11.001

18. Oltman CL, Davidson EP, Coppey LJ, et al. Vascular and neural dysfunction in Zucker diabetic fatty rats: a difficult condition to reverse. Diabetes Obes Metab. 2008;10(1):64-74. doi: 10.1111/j.1463-1326.2007.00814.x

19. Oltman CL, Davidson EP, Coppey LJ, et al. Treatment of Zucker diabetic fatty rats with AVE7688 improves vascular and neural dysfunction. Diabetes Obes Metab. 2009;11(3):223-233. doi: 10.1111/j.1463-1326.2008.00924.x

20. Sasase T, Ohta T, Masuyama T, et al. The spontaneously diabetic torii rat: an animal model of nonobese type 2 diabetes with severe diabetic complications. J Diabetes Res. 2013;2013:976209. doi: 10.1155/2013/976209

21. Shinohara M, Masuyama T, Shoda T, et al. A new spontaneously diabetic non-obese Torii rat strain with severe ocular complications. Int J Exp Diabetes Res. 2000;1(2):89-100. doi: 10.1155/edr.2000.89

22. Masuyama T, Komeda K, Hara A, et al. Chronological characterization of diabetes development in male spontaneously diabetic Torii rats. Biochem Biophys Res Commun. 2004;314(3):870-877. doi: 10.1016/j.bbrc.2003.12.18

23. Yamaguchi T, Sasase T, Mera Y, et al. Diabetic peripheral neuropathy in spontaneously diabetic Torii-Leprfa (SDT Fatty) rats. J Vet Med Sci. 2012;74(12):1669-1673. doi: 10.1292/jvms.12-0149

24. Matsumoto T, Ono Y, Kuromiya A, et al. Long-term treatment with ranirestat (AS-3201), a potent aldose reductase inhibitor, suppresses diabetic neuropathy and cataract formation in rats. J Pharmacol Sci. 2008;107(3):340-348. doi: 10.1254/jphs.08071FP

25. Yamada K, Hosokawa M, Fujimoto S, et al. The spontaneously diabetic Torii rat with gastroenteropathy. Diabetes Res Clin Pract. 2007;75(2):127-134. doi: 10.1016/j.diabres.2006.06.034

26. Sasase T, Morinaga H, Yamamoto H, et al. Increased fat absorption and impaired fat clearance cause postprandial hypertriglyceridemia in spontaneously diabetic Torii rat. Diabetes Res Clin Pract. 2007;78(1):8-15. doi: 10.1016/j.diabres.2007.02.020

27. Davidson EP, Coppey LJ, Holmes A, et al. Characterization of diabetic neuropathy in the Zucker diabetic Sprague-Dawley rat: a new animal model for type 2 diabetes. J Diabetes Res. 2014;2014:714273. doi: 10.1155/2014/714273

28. Gonzalez AD, Gallant MA, Burr DB, Wallace JM. Multiscale analysis of morphology and mechanics in tail tendon from the ZDSD rat model of type 2 diabetes. J Biomech. 2014;47(3):681-686. doi: 10.1016/j.jbiomech.2013.11.045

29. Coppey L, Davidson E, Lu B, et al. Vasopeptidase inhibitor ilepatril (AVE7688) prevents obesity- and diabetes-induced neuropathy in C57Bl/6J mice. Neuropharmacology. 2011;60(2-3):259-266. doi: 10.1016/j.neuropharm.2010.09.008

30. Coppey LJ, Gellett JS, Davidson EP, et al. Changes in endoneurial blood flow, motor nerve conduction velocity and vascular relaxation of epineurial arterioles of the sciatic nerve in ZDF-obese diabetic rats. Diabetes Metab Res Rev. 2002;18(1):49-56. doi:10.1002/dmrr.257

31. Davidson EP, Coppey LJ, Calcutt NA, et al. Diet-induced obesity in Sprague-Dawley rats causes microvascular and neural dysfunction.Diabetes Metab Res Rev. 2010;26(4):306-318. doi: 10.1002/dmrr.1088

32. Oltman CL, Coppey LJ, Gellett JS, et al. Progression of vascular and neural dysfunction in sciatic nerves of Zucker diabetic fatty and Zucker rats. Am J Physiol Endocrinol Metab. 2005;289(1):E113-E122. doi: 10.1152/ajpendo.00594.2004

33. Akash M, Rehman K, Chen S. Goto-kakizaki rats: its suitability as non-obese diabetic animal model for spontaneous type 2 diabetes mellitus.Curr Diabetes Rev. 2013;9(5):387-396. doi: 10.2174/15733998113099990069

34. Wang F, Gao N, Yin J, Yu FS. Reduced innervation and delayed re-innervation after epithelial wounding in type 2 diabetic Goto-Kakizaki rats. Am J Pathol. 2012;181(6):2058-2066. doi: 10.1016/j.ajpath.2012.08.029

35. Tirabassi RS, Flanagan JF, Wu T, et al. The BBZDR/Wor Rat Model for investigating the complications of type 2 diabetes mellitus. ILAR Journal. 2004;45(3):292-302. doi: 10.1093/ilar.45.3.292

36. Kamenov Z, Higashino H, Todorova M, et al. Physiological characteristics of diabetic neuropathy in sucrose-fed Otsuka long-evans Tokushima fatty rats. Methods Find Exp Clin Pharmacol. 2006;28(1):13-18. doi: 10.1358/mf.2006.28.1.962772

37. Nakamura J, Hamada Y, Sakakibara F, et al. Physiological and morphometric analyses of neuropathy in sucrose-fed OLETF rats. Diabetes Res Clin Pract. 2001;51(1):9-20. doi: 10.1016/s0168-8227(00)00205-9


Supplementary files

Review

For citations:


Abdulvapova Z.N., Artemova E.V., Gorbacheva A.M., Galstyan G.R., Tokmakova A.Yu., Gavrilova S.A. Phenotyping animal models of diabetic peripheral neuropathy in rats: advantages and limitations. Problems of Endocrinology. 2018;64(3):188-193. https://doi.org/10.14341/probl9284

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