Korthals J K, Korthals M A
James A. Haley Veterans Hospital, Tampa, FL.
Acta Neuropathol. 1990;81(1):20-4. doi: 10.1007/BF00662633.
We have developed a new model of an acute ischemic nerve injury in rat produced by the combined effects of right femoral artery ligation and intraperitoneal injection of serotonin. Light microscopic studies were performed on the right sciatic, tibial, plantar and sural nerves dissected from rats 7 days to 6 months after serotonin injection. Ischemic lesions occurred mostly in the middle tibial nerve and involved either a part or the whole transverse nerve section. Partial tibial nerve lesions appeared mainly as small subperineurial or large wedge-shaped areas of fiber loss or regeneration. No well-delineated central fascicular lesions were seen. Sural nerves were less damaged than tibial nerves. The predominantly subperineurial fascicular distribution of ischemic lesions seen in the present model differs from the central fascicular distribution found in previous experimental studies on nerve ischemia. The different distribution of lesions is probably related to the small fascicular size and local microvascular architecture of the affected nerve segment, as well as to the method of producing ischemia.
我们通过右股动脉结扎和腹腔注射血清素的联合作用,建立了一种新的大鼠急性缺血性神经损伤模型。在注射血清素后7天至6个月,对从大鼠身上解剖出的右侧坐骨神经、胫神经、足底神经和腓肠神经进行了光镜研究。缺血性病变主要发生在胫神经中部,累及部分或整个神经横切面。部分胫神经病变主要表现为神经束膜下小面积或大面积楔形纤维丢失或再生区域。未见界限清楚的中央束状病变。腓肠神经的损伤程度低于胫神经。在本模型中观察到的缺血性病变主要呈神经束膜下束状分布,这与先前关于神经缺血的实验研究中发现的中央束状分布不同。病变分布的差异可能与受影响神经段的神经束较小、局部微血管结构以及产生缺血的方法有关。