Paradox effects of kynurenines on LTP induction in the Wistar rat. An in vivo study

被引:15
作者
Demeter, I. [1 ,2 ]
Nagy, K. [1 ]
Farkas, T. [1 ]
Kis, Zs. [1 ]
Kocsis, K. [1 ]
Knapp, L. [1 ]
Gellert, L. [1 ]
Fueloep, F. [3 ,4 ,5 ]
Vecsei, L. [2 ,6 ,7 ]
Toldi, J. [1 ,6 ,7 ]
机构
[1] Univ Szeged, Dept Physiol Anat & Neurosci, H-6726 Szeged, Hungary
[2] Univ Szeged, Dept Neurol, H-6726 Szeged, Hungary
[3] Hungarian Acad Sci, Inst Pharmaceut Chem, H-6720 Szeged, Hungary
[4] Hungarian Acad Sci, Res Grp Stereochem, H-6720 Szeged, Hungary
[5] Univ Szeged, H-6720 Szeged, Hungary
[6] Hungarian Acad Sci, Neurosci Res Grp, H-6725 Szeged, Hungary
[7] Univ Szeged, H-6725 Szeged, Hungary
关键词
Long-term potentiation; LTP; Hippocampus; Kynurenic acid; KYNA; Cognitive functions; LONG-TERM POTENTIATION; NMDA RECEPTORS; ACID; BRAIN; AMPA; MEMANTINE; NEUROPROTECTION; TRANSMISSION; DERIVATIVES; ANTAGONISTS;
D O I
10.1016/j.neulet.2013.08.028
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Kynurenic acid (KYNA), a neuroactive metabolite of tryptophan that acts on different receptors (e.g. those of N-methyl-D-aspartate (NMDA) and presynaptic alpha 7 nicotinic acetylcholine (nACh)), exerts fundamentally antiglutamatergic effects. In view of its antiglutamatergic properties, an elevation of the KYNA level within the brain might result in neuroprotection. However, the use of KYNA as a neuroprotective agent is rather limited, because it crosses the blood brain barrier (BBB) to only a poor extent. During recent years, new KYNA derivatives have been developed which can readily traverse the BBB and also exert neuroprotection. However, as KYNA and its derivatives are able to interfere with glutamatergic and cholinergic transmission, the potential risks of interfering with cognitive functions cannot be excluded. This in vivo study on anesthetized rats therefore tested the effects of the administration of KYNA and a KYNA derivative (SZR72) (in a dosage that exerted neuroprotection) on long-term potentiation (LTP) and pure field excitatory postsynaptic potentials induced by contralateral CA3 region stimulation and recorded in the pyramidal layer of the CA1 region of the hippocampus. Surprisingly, KYNA and this derivative did not reduce, but rather increased the induceability of LTP. The possible explanation is discussed in detail. In brief: an elevated KYNA level in the perisynaptic area produced, for example, by exogenous prodrug or derivative administration exerts preferential effects on the extrasynaptic NMDA receptors and the nACh receptors on presynaptic glutamatergic terminals, while sparing the currents mediated by synaptic NMDA and alpha-amino-3-hydroxy-5-methyl-4-isoxazoleproprionic acid receptors. This might be the explanation why the treatment with the prodrug of KYNA or the KYNA derivative in a dosage which induced neuroprotection did not reduce the cognitive functions or the LTP. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:138 / 141
页数:4
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