Lo Fu-Sun, Mize R Ranney
Department of Cell Biology and Anatomy, Louisiana State University Health Sciences Center, New Orleans, Louisiana 70112, USA.
Eur J Neurosci. 2002 May;15(9):1421-32. doi: 10.1046/j.1460-9568.2002.01979.x.
The developing retinocollicular pathway undergoes synaptic refinement in order to form the precise retinotopic pattern seen in adults. To study the mechanisms which underlie refinement, we investigated long-term changes in retinocollicular transmission in rats aged P0-P25. Field potentials (FPs) in the superior colliculus (SC) were evoked by stimulation of optic tract fibers in an in vitro isolated brainstem preparation. High intensity stimulation induced long-term depression (LTD) in the SC after both low (1000 stimuli at 1 Hz) and higher (1000 stimuli at 50 Hz) frequency stimulation. The induction of LTD was independent of activation of NMDA and GABA(A) receptors, because D-APV (100 microM) and bicuculline (10 microM) did not block LTD. Induction of LTD was dependent upon activation of L-type Ca(2+) channels as 10 microM nitrendipine, an L-type Ca(2+) channel blocker, significantly decreased the magnitude of LTD. LTD was down-regulated during development. LTD magnitude was greatest in rats aged P0-P9 and significantly less in rats aged P10-P25. Long-term potentiation (LTP) was induced by low intensity stimulation and only after high frequency tetanus (1000 stimuli at 50 Hz). LTP was NMDA receptor dependent because d-APV (100 microM) completely abolished it. LTP induction was also blocked by the L-type Ca2+ channel blocker nitrendipine. The magnitude of LTP first increased with age, being significantly greater at P7-P13 than at P0-3 and then decreased at P23-25. In summary, both LTD and LTP are present during retinocollicular pathway refinement, but have different transmitter and ionic mechanisms and time courses of expression.
发育中的视网膜-视皮质通路会经历突触精细化过程,以形成在成人中可见的精确视网膜拓扑模式。为了研究精细化背后的机制,我们调查了P0-P25大鼠视网膜-视皮质传递的长期变化。在体外分离的脑干标本中,通过刺激视束纤维诱发上丘(SC)的场电位(FPs)。高强度刺激在低频(1Hz的1000次刺激)和高频(50Hz的1000次刺激)刺激后均能在上丘诱导出长时程抑制(LTD)。LTD的诱导不依赖于NMDA和GABAA受体的激活,因为D-APV(100μM)和荷包牡丹碱(10μM)不能阻断LTD。LTD的诱导依赖于L型钙通道的激活,因为L型钙通道阻滞剂尼群地平(10μM)能显著降低LTD的幅度。LTD在发育过程中被下调。LTD幅度在P0-P9大鼠中最大,而在P10-P25大鼠中显著减小。低强度刺激且仅在高频强直刺激(50Hz的1000次刺激)后可诱导出长时程增强(LTP)。LTP依赖于NMDA受体,因为d-APV(100μM)可完全消除它。L型钙通道阻滞剂尼群地平也可阻断LTP的诱导。LTP幅度首先随年龄增加,在P7-P13时显著大于P0-3时,然后在P23-25时下降。总之,在视网膜-视皮质通路精细化过程中同时存在LTD和LTP,但它们具有不同的递质和离子机制以及表达的时间进程。