May 2004
Volume 45, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2004
Effects of binocular form deprivation on the NMDA–EPSCs in rat visual cortex
Author Affiliations & Notes
  • Z.Q. Yin
    Southwest Eye Hospital, Southwest Hospital, Chongqing, China
  • W. Qin
    Southwest Eye Hospital, Southwest Hospital, Chongqing, China
  • S.J. Wang
    Southwest Eye Hospital, Southwest Hospital, Chongqing, China
  • Footnotes
    Commercial Relationships  Z.Q. Yin, None; W. Qin, None; S.J. Wang, None.
  • Footnotes
    Support  Chinese NSFC grant to Z. Q. Yin # 30025014, 39970252
Investigative Ophthalmology & Visual Science May 2004, Vol.45, 2561. doi:
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      Z.Q. Yin, W. Qin, S.J. Wang; Effects of binocular form deprivation on the NMDA–EPSCs in rat visual cortex . Invest. Ophthalmol. Vis. Sci. 2004;45(13):2561.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Abstract: : Purpose: To investigate the effects of binocular form deprivation (BFD) on the excitatory postsynaptic currents (EPSCs) mediated by the N–methyl–D–aspartate (NMDA) receptor (NMDA–EPSCs), and the proportion of NMDA–EPSCs relative to glutamate receptor currents (glutamate–EPSCs) during development in rat visual cortex. Methods: BFD was performed by suturing the eyelids of Wistar rats at postnatal day (PD) 14 (before eye–opening). Visual cortical slices (300 µm) were prepared from normal and BFD Wistar rats aged PD 14, 21 and 28. Recordings were obtained in slices from layer II to IV using the whole–cell patch–clamp technique. Glutamate–EPSCs were isolated in the presence of bicuculline methiodide (20 µM) in the bathing medium, and NMDA–EPSCs were isolated with a combination of bicuculline methiodide (20 µM) and 6–cyano–7–nitroquinoxaline–2,3–dione (CNQX, 20 µM). We also applied D,L–2–amino–5–phosphonovalerate (AP–5, 20 µM) to study the NMDA–only mediated currents. For each cell, the ratio of peak NMDA to glutamate currents was calculated. Results: In 66 cells, recorded from layers II to IV of rat visual cortex, isolation of glutamate–EPSCs and NMDA–EPSCs were achieved as described above. During visual development, the decay time constant of NMDA–EPSCs became shorter after eye–opening in normal rats (F = 5.949, P < 0.05; PD 28 Vs PD 14, P = 0.027), but not in rats with BFD (P > 0.05); the weighted time constant of NMDA–EPSCs in visual cortex became shorter after the rats’ eyes were opened in the normal group (F2, 37 =4.727, P =0.015; PD 28 Vs PD 14, P =0.035), but not in the BFD group (P >0.05); the rise time constant and peak value of NMDA–EPSCs showed no significant changes in normal and BFD groups (P > 0.05); the ratio of NMDA–EPSCs to glutamate–EPSCs became smaller gradually with age in the normal rats (F = 4.661, P < 0.05; PD 28 Vs PD 14, P = 0.025), but not in the BFD group (P > 0.05). Conclusions:These studies reveal that the proportion of NMDA–EPSCs relative to glutamate–EPSCs and the decay time constant of NMDA–EPSCs are influenced by BFD in critical period of visual development. These changes may reflect important experience–dependent modifications of neuronal synapses in visual cortex.

Keywords: visual development • visual cortex • electrophysiology: non–clinical 
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