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Histopathological nerve and skeletal muscle changes in rats subjected to persistent insulin-induced hypoglycemia. | LitMetric

AI Article Synopsis

  • * The study developed a rat model to explore persistent hypoglycemia caused by human insulin, distinguishing between effects of insulin vs. the new analogues, which could minimize animal use in testing.
  • * Findings revealed that long-term insulin infusion led to significant nerve and muscle tissue degeneration, marking a breakthrough in understanding the impact of chronic hypoglycemia.

Article Abstract

New insulin analogues with a longer duration of action and a flatter pharmacodynamic profile are developed to improve convenience and safety for diabetic patients. During the nonclinical development of such analogues, safety studies must be conducted in nondiabetic rats, which consequently are rendered chronically hypoglycemic. A rat comparator model using human insulin would be valuable, as it would enable differentiation between effects related to either persistent insulin-induced hypoglycemia (IIH) or a new analogue per se. Such a model could alleviate the need for an in-study-comparator and thereby reduce the number of animals used during development. Thus, the aims of the present study were i) to develop a preclinical animal model of persistent hypoglycemia in rats using human insulin infusion for four weeks and ii) to investigate histopathological changes in sciatic nerves and quadriceps femoris muscle tissue, as little is known about the response to persistent hypoglycemia in these tissues. Histopathologic changes in insulin-infused animals included axonal degeneration and myofibre degeneration. To our knowledge, this is the first study to show that persistent IIH provokes peripheral nerve and skeletal myofiber degeneration within the same animals. This suggests that the model can serve as a nonclinical comparator model during development of long-acting insulin analogues.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766526PMC
http://dx.doi.org/10.1293/tox.2015-0041DOI Listing

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