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J Physiol Volume 544, Number 2, 477-486, October 15, 2002 DOI: 10.1113/jphysiol.2002.024703
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Journal of Physiology (2002), 544.2, pp. 477-486
© Copyright 2002 The Physiological Society
DOI: 10.1113/jphysiol.2002.024703

Paired pulse facilitation of corticogeniculate EPSCs in the dorsal lateral geniculate nucleus of the rat investigated in vitro

Björn Granseth, Erik Ahlstrand and Sivert Lindström

Department of Biomedicine and Surgery, Faculty of Health Sciences, Linköpings universitet, SE-581 85 Linköping, Sweden

To investigate paired pulse facilitation of corticogeniculate EPSCs, whole-cell patch-clamp recordings were made from principal cells in the rat dorsal lateral geniculate nucleus (dLGN) in vitro. Thalamic slices, oriented so that both corticogeniculate and retinogeniculate axons could be stimulated, were cut from young (16- to 37-day-old) DA-HAN rats. Corticogeniculate EPSCs displayed pronounced paired pulse facilitation at stimulus intervals up to 400 ms. The facilitation had a fast and a slow component of decay with time constants of 12 ± 7 and 164 ± 47 ms (means ± S.D.), respectively. Maximum paired pulse ratio (EPSC2 times EPSC1-1) was 3.7 ± 1.1 at the 20-30 ms interval. Similar to other systems, the facilitation was presynaptic. Retinogeniculate EPSCs recorded in the same dLGN cells displayed paired pulse depression at intervals up to at least 700 ms. The two types of EPSCs differed in their calcium response curves. At normal [Ca2+]o, the corticogeniculate synapse functioned over the early rising part of a Hill function, while the retinogeniculate synapse operated over the middle and upper parts of the curve. The paired pulse ratio of corticogeniculate EPSCs was maximal at physiological [Ca2+]o. The facilitation is proposed to have an important role in the function of the corticogeniculate circuit as a neuronal amplifier.



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