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视网膜感受器丧失后上丘的代谢变化——非活动视觉系统中的神经营养相互作用

Metabolic changes in the superior colliculus after retinal receptor loss--neurotrophic interactions in the inactive visual system.

作者信息

Thurlow G A, Cooper R M

机构信息

Psychology Department, University of Calgary, Alberta, Canada.

出版信息

Exp Neurol. 1988 Jun;100(3):563-77. doi: 10.1016/0014-4886(88)90040-4.

Abstract

In the mature rat, direct denervation by means of eye enucleation resulted in a temporary metabolic depression followed by "recovery" in primary visual centers as determined by the 2-deoxyglucose technique (4). After unilateral destruction of the retinal receptor layer by means of intense light, the superior colliculus (SC) demonstrated this same depression-recovery process. Because receptor destruction is believed to silence ongoing ganglion cell activity, and because the SC changes occurred whether or not ganglion cells sustained damage, it appeared that direct denervation of colliculus neurons was not necessary to initiate the depression-recovery sequence and that lack of activity or "disuse" was the critical factor. The silencing effect of the receptor destruction was confirmed when tetrodotoxin (TTX) injections into the damaged eye 2 months after damaging light exposure only slightly affected metabolic activity in the recovered colliculus. Binocular TTX injections in unilaterally light-damaged rats after 2 months of recovery resulted in greater depression in the normal colliculus than in the "recovered" colliculus, again suggesting that increases in glucose metabolism over time reflected physiological adjustments in the SC to loss of afferent activity. The strong depression in the SC fed by the normal eye after TTX injection confirmed that tonic retinal afferent activity was important to the metabolic integrity of the SC and that cessation of such activity could lead to at least to depression in the system. In a final group of 2-month recovery animals the light-damaged eye was enucleated. Presumably, if withdrawal of afferent activity is solely responsible for initiating the depression-recovery sequence, the destruction of already silenced retinal ganglion cells would have no effect on the recovered SC. This was not found to be the case. In fact, enucleation reinstated the metabolic depression in the recovered SC and demonstrated that denervation per se resulted in depression of glucose metabolism in postsynaptic neurons. Even in the absence of impulse activity, visual system neurons maintained trophic interactions.

摘要

在成年大鼠中,通过眼球摘除进行直接去神经支配会导致短暂的代谢抑制,随后通过2-脱氧葡萄糖技术(4)测定,初级视觉中枢会出现“恢复”。在通过强光单侧破坏视网膜受体层后,上丘(SC)也表现出同样的抑制-恢复过程。由于受体破坏被认为会使正在进行的神经节细胞活动沉默,并且由于无论神经节细胞是否受到损伤,SC都会发生变化,因此似乎去神经支配丘神经元并非启动抑制-恢复序列所必需,而缺乏活动或“废用”才是关键因素。当在损伤性光照2个月后向受损眼注射河豚毒素(TTX)时,仅轻微影响恢复后的上丘的代谢活动,这证实了受体破坏的沉默效应。在恢复2个月后的单侧光损伤大鼠中进行双眼TTX注射,正常上丘的抑制程度比“恢复”的上丘更大,这再次表明随着时间的推移葡萄糖代谢的增加反映了上丘对传入活动丧失的生理调节。TTX注射后由正常眼供血的上丘出现强烈抑制,这证实了视网膜传入的紧张性活动对上丘代谢完整性很重要,这种活动的停止至少会导致系统抑制。在最后一组恢复2个月的动物中,摘除了光损伤的眼睛。据推测,如果传入活动的撤回是启动抑制-恢复序列的唯一原因,那么已经沉默的视网膜神经节细胞的破坏对恢复后的上丘不会有影响。但事实并非如此。实际上,摘除眼球使恢复后的上丘再次出现代谢抑制,并表明去神经支配本身会导致突触后神经元葡萄糖代谢降低。即使在没有冲动活动的情况下,视觉系统神经元仍维持着营养相互作用。

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