Tucek S, Hanzlíková V, Stráníková D
J Neurol Sci. 1978 Apr;36(2):237-46. doi: 10.1016/0022-510x(78)90084-9.
Axonal transport of acetylcholinesterase (AChE) and choline acetyltransferase (ChAc) and ultrastructural degenerative changes were compared in isolated nerve segments of rabbit peroneal nerves kept in vivo for 22 h, either with preserved blood supply (control segments) or under conditions of ischemia (ischemic segments). Ischemia abolished the proximo-distal and disto-proximal axonal transport of AChE and the proximo-distal transport of ChAc which, in control segments, were revealed by accumulations of the enzymes at corresponding ends of the segments. Total activities of AChE and ChAc recovered in isolated segments with intact blood supply corresponded to the activities in normal nerves; in ischemic segments, 50% of ChAc activity was lost in 22 h, whereas all AChE activity was preserved. Ultrastructural changes were found in few fibres in control segments and in many fibres in ischemic segments 22 h after nerve interruption. The early changes in control segments correspond to those described in the literature for peripheral stump of severed nerves. The microtubules, neurofilaments and mitochondria were not affected. In ischemic segments, various stages of axoplasmic disintegration occurred in the myelinated and unmyelinated axons:flocculation and clumping of axoplasmic material, decomposition of neurofilaments and microtubules, swelling, formation of amorphous densities and breakdown of mitochondrial cristae. Swelling, amorphous densities, clumping of nuclear chromatin and necrotic mitochondrial changes appeared also in Schwann cells. It is concluded that ischemia blocks axonal transport and brings about, within 22 h, ultrastructural changes both in nerve fibres and in Schwann cells. Cytoplasmic ChAc is affected earlier by necrotic degeneration of the axons than membrane-bound AChE.
在体内保存22小时的兔腓神经孤立节段中,比较了乙酰胆碱酯酶(AChE)和胆碱乙酰转移酶(ChAc)的轴突运输以及超微结构退行性变化。这些节段要么具有保留的血液供应(对照节段),要么处于缺血状态(缺血节段)。缺血消除了AChE的近端到远端和远端到近端的轴突运输以及ChAc的近端到远端运输,在对照节段中,通过酶在节段相应末端的积累显示出这些运输。具有完整血液供应的孤立节段中AChE和ChAc的总活性与正常神经中的活性相对应;在缺血节段中,22小时内ChAc活性损失了50%,而所有AChE活性均得以保留。在神经中断22小时后,对照节段中少数纤维出现超微结构变化,缺血节段中许多纤维出现超微结构变化。对照节段中的早期变化与文献中描述的切断神经外周残端的变化一致。微管、神经丝和线粒体未受影响。在缺血节段中,有髓和无髓轴突发生了不同阶段的轴浆崩解:轴浆物质的絮凝和聚集、神经丝和微管的分解、肿胀、无定形密度的形成以及线粒体嵴的破坏。施万细胞中也出现了肿胀、无定形密度、核染色质聚集和坏死性线粒体变化。结论是,缺血阻断轴突运输,并在22小时内导致神经纤维和施万细胞出现超微结构变化。细胞质中的ChAc比膜结合的AChE更早受到轴突坏死性变性的影响。