WldS protects against peripheral neuropathy and retinopathy in an experimental model of diabetes in mice

• Published in: Diabetologia 2011, Vol.54 (9), p.2440-2450
• Main Authors: Zhu, S. S., Ren, Y., Zhang, M., Cao, J. Q., Yang, Q., Li, X. Y., Bai, H., Jiang, L., Jiang, Q., He, Z. G., Chen, Q.
• Format: Article
• Language: English
• Subjects: Biological and medical sciences; Cranial nerves. Spinal roots. Peripheral nerves. Autonomic nervous system. Gustation. Olfaction; Diabetes. Impaired glucose tolerance; Endocrine pancreas. Apud cells (diseases); Endocrinopathies; Etiopathogenesis. Screening. Investigations. Target tissue resistance; Human Physiology; Internal Medicine; Medical sciences; Medicine; Medicine & Public Health; Metabolic Diseases; Nervous system (semeiology, syndromes); Neurology; Ophthalmology; Retinopathies
• ISSN: 0012-186X; 1432-0428
• DOI: 10.1007/s00125-011-2226-1

Aims/hypothesis We aimed to evaluate the effect of the mutant Wld S (slow Wallerian degeneration; also known as Wld ) gene in experimental diabetes on early experimental peripheral diabetic neuropathy and diabetic retinopathy. Methods The experiments were performed in four groups of mice: wild-type (WT), streptozotocin (STZ)-induced diabetic WT, C57BL/ Wld S and STZ-induced diabetic C57BL/ Wld S . In each group, intraperitoneal glucose and insulin tolerance tests were performed; blood glucose, glycated haemoglobin and serum insulin were monitored. These mice were also subjected to the following behavioural tests: grasping test, hot-plate test and von Frey aesthesiometer test. For some animals, sciatic–tibial motor nerve conduction velocity, tail sensory nerve conduction velocity and eye pattern electroretinogram were measured. At the end of the experiments, islets were isolated to detect glucose-stimulated insulin secretion, ATP content and extent of apoptosis. The NAD/NADH ratio in islets and retinas was evaluated. Surviving retinal ganglion cells were estimated by immunohistochemistry. Results We found that the Wld S gene is expressed in islets and protects beta cells against multiple low doses of STZ by increasing the NAD/NADH ratio, maintaining the ATP concentration, and reducing apoptosis. Consistently, significantly higher insulin concentrations, lower blood glucose concentrations, and better glucose tolerance were observed in Wld S mice compared with WT mice after STZ treatment. Furthermore, Wld S alleviated abnormal sensory responses, nerve conduction, retina dysfunction and reduction of surviving retinal ganglion cells in STZ-induced diabetic models. Conclusions/interpretation We provide the first evidence that expression of the Wld S gene decreases beta cell destruction and preserves islet function in STZ-induced diabetes, thus revealing a novel protective strategy for diabetic models.