Mattingly G E, Fischer V W
Acta Neuropathol. 1985;68(2):149-54. doi: 10.1007/BF00688637.
Axons of the peripheral nervous system (PNS) are reduced in caliber in response to the experimental diabetic state. The cause of this reduced axonal size is disputed. Various theories include (a) axonal dwindling, (b) inhibition of growth, and (c) shrinkage due to serum hyperosmolarity. This study was designed to directly address these conflicting theories and to provide additional information on the character of the peripheral neuropathy resulting from an experimentally induced diabetic state. Four weeks, 6 and 12 months after establishing a streptozotocin-induced diabetic condition in rats, a morphometric evaluation of randomly selected cross sections of myelinated nerve fibers in the common peroneal nerve was performed on diabetic and age and weight-matched control animals. A reduction in the cross-sectional area of axons with a concomitant increase in the width of myelin sheaths was detected following 6 months of exposure to the diabetic state. Axons in rats diabetic for 12 months showed smaller cross-sectional areas than those seen in rats diabetic for only 6 months; hence, a dwindling in axonal caliber had occurred during this period. These findings indicate the presence of an axonopathy, associated with a myelin sheath alteration in the common peroneal nerve of the chronically diabetic rat.
在实验性糖尿病状态下,外周神经系统(PNS)的轴突直径会减小。轴突尺寸减小的原因存在争议。各种理论包括:(a)轴突萎缩;(b)生长抑制;(c)血清高渗导致的萎缩。本研究旨在直接探讨这些相互矛盾的理论,并提供关于实验性诱导糖尿病状态导致的周围神经病变特征的更多信息。在给大鼠建立链脲佐菌素诱导的糖尿病状态后的4周、6个月和12个月,对糖尿病大鼠以及年龄和体重匹配的对照动物的腓总神经中随机选择的有髓神经纤维横切面进行形态计量学评估。在暴露于糖尿病状态6个月后,检测到轴突横截面积减小,同时髓鞘宽度增加。糖尿病12个月的大鼠轴突横截面积比仅糖尿病6个月的大鼠小;因此,在此期间轴突直径发生了萎缩。这些发现表明存在一种轴突病,与慢性糖尿病大鼠腓总神经的髓鞘改变有关。