Sabel B A, Schneider G E
Institute of Medical Psychology, University of Munich Medical School, Federal Republic of Germany.
Exp Brain Res. 1988;73(3):505-18. doi: 10.1007/BF00406608.
Unilateral lesions of the right superior colliculus (SC) were made in hamsters on the day after birth. In order to quantify the extent of abnormal innervation by left eye fibers in the diencephalon and midbrain, the left eye was removed on postnatal day 12 or 36, and after an appropriate survival time, the brains were stained for degenerating axons and axon terminals with the Fink-Heimer method. In additional cases, anterograde transport of 3H proline-leucine or horseradish peroxidase was used to assess left eye connectivity. In agreement with previous reports we found abnormal projections in the ventral nucleus of the lateral geniculate body (LGv), in the lateral posterior nucleus (LP) of the thalamus, and in the left SC (the 'recrossing' pathway). We also noted areas of abnormally heavy terminal fields arranged in patches in coronal sections in the dorsal nucleus of the lateral geniculate body (LGd). These patches arise from columns of dense innervation that are oriented along a rostral-to-caudal axis. If the right SC lesion was made large enough to diminish the recrossing pathway, retinofugal axons establish a significantly smaller distal terminal field in the left SC. In these cases, a corresponding increase in the size of terminal fields in all major proximal structures (LGd, LGv, LP, DTN) was observed. The sum of abnormal proximal growth ("compensatory sprouting") was found to truly compensate for the distal loss of terminals. The evaluation of hamsters in which left eye connectivity was assessed at the age of 12 days revealed that lesion-induced patches of abnormal growth have already reached their full size by that time. These findings provide evidence for the 'pruning-effect' and demonstrate that retinofugal axons support a fixed number of terminal arborizations (the principle of 'conservation of total axonal arborizations').
在出生后第二天对仓鼠进行右侧上丘(SC)的单侧损伤。为了量化间脑和中脑左侧眼纤维异常支配的程度,在出生后第12天或36天摘除左眼,经过适当的存活时间后,用芬克 - 海默法对大脑进行变性轴突和轴突终末染色。在其他病例中,使用³H - 脯氨酸 - 亮氨酸或辣根过氧化物酶的顺行运输来评估左眼的连接性。与先前的报道一致,我们发现在外侧膝状体腹侧核(LGv)、丘脑外侧后核(LP)以及左侧上丘(“重新交叉”通路)存在异常投射。我们还注意到在外侧膝状体背侧核(LGd)的冠状切片中,终末场异常密集的区域呈斑块状分布。这些斑块源于沿头尾轴排列的密集神经支配柱。如果右侧上丘损伤足够大以减少重新交叉通路,视网膜传出轴突在左侧上丘建立的远端终末场会显著变小。在这些情况下,观察到所有主要近端结构(LGd、LGv、LP、DTN)终末场大小相应增加。发现异常近端生长的总和(“代偿性发芽”)确实补偿了终末的远端损失。对12天大时评估左眼连接性的仓鼠的评估表明,损伤诱导的异常生长斑块在那时已经达到其最大尺寸。这些发现为“修剪效应”提供了证据,并证明视网膜传出轴突支持固定数量的终末分支(“总轴突分支守恒”原则)。