Calcutt Nigel A
Department of Pathology, University of California San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0612, USA.
Curr Diab Rep. 2002 Dec;2(6):482-8. doi: 10.1007/s11892-002-0117-z.
Neuropathy remains a major complication of diabetes and there is no approved treatment that prevents its progression or alleviates the associated symptoms. Animal models of diabetic neuropathy are hampered by their short life span, which precludes the development of overt structural pathology, and they are best viewed as exhibiting early metabolic, neurochemical, and functional indices of nerve disorders that may predict progression to overt diabetic neuropathy. In this context, diabetic animals have use in both establishing potential etiologic mechanisms and for screening novel therapeutic agents. Treatment strategies are evolving in concert with a developing understanding of how hyperglycemia causes nerve dysfunction and recent or ongoing clinical trials are investigating this rational approach to drug design. It is only by the successful demonstration of clinical efficacy of a compound developed by this approach that the use of animal models of diabetic neuropathy can be validated.
神经病变仍然是糖尿病的主要并发症,目前尚无经批准的可预防其进展或缓解相关症状的治疗方法。糖尿病神经病变的动物模型因其寿命短而受到限制,这使得明显的结构病理学变化难以发展,它们最好被视为表现出神经紊乱的早期代谢、神经化学和功能指标,这些指标可能预测向明显糖尿病神经病变的进展。在这种情况下,糖尿病动物在建立潜在病因机制和筛选新型治疗药物方面都有应用价值。随着对高血糖如何导致神经功能障碍的认识不断发展,治疗策略也在不断演变,近期或正在进行的临床试验正在研究这种合理的药物设计方法。只有通过成功证明通过这种方法开发的化合物的临床疗效,糖尿病神经病变动物模型的应用才能得到验证。