Brain nicotinic receptors:: structure and regulation, role in learning and reinforcement

被引:245
作者
Changeux, JP [1 ]
Bertrand, D [1 ]
Corringer, PJ [1 ]
Dehaene, S [1 ]
Edelstein, S [1 ]
Léna, C [1 ]
Le Novère, N [1 ]
Marubio, L [1 ]
Picciotto, M [1 ]
Zoli, M [1 ]
机构
[1] Inst Pasteur, CNRS URA 1284, F-75724 Paris 15, France
关键词
nicotinic receptor; structure; learning; reinforcement;
D O I
10.1016/S0165-0173(97)00040-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The introduction, in the late sixties, of the concepts and methods of molecular biology to the study of the nervous system had a profound impact on the field, primarily through the identification of its basic molecular components. These structures include, for example, the elementary units of the synapse: neurotransmitters, neuropeptides and their receptors, but also ionic channels, intracellular second messengers and the relevant enzymes, cell surface adhesion molecules, or growth and trophic factors [21,78,81,52,79]. Attempts to establish appropriate causal relationships between these molecular components, the actual organisation of neural networks, and a defined behavior, nevertheless, still must overcome many difficulties. A first problem is the recognition of the minimum levels of organisation, from the molecular, cellular, or multicellular (circuit) to the higher cognitive levels, that determine the given physiological and/or behavioral performance under investigation. A common difficulty (and potential source of errors of interpretation) is to relate a cognitive function to a network organization which does not possess the required structural complexity and vice-versa. Another problem is to distinguish, among the components of the system, those which are actually necessary and those which, taken together, suffice for a given behavior to take place. Identification of such a minimal set of building blocks may receive decisive insights from the elaboration of neurally plausible formal models that bring together, within a single and coherent 'artificial organism', the neuronal network, the circulating activity, and the behavior they determine (see [42,43,45,72,30]). In this communication, we shall attempt, still in a preliminary fashion, to bring together: (1) our recent knowledge on the molecular biology of brain nicotinic receptors (nAChRs) and their allosteric properties and (2) integrated behaviors, such as cognitive learning, investigated for instance with delayed-response or passive avoidance tasks that are likely to involve nAChRs in particular at the level of reinforcement (or reward) mechanisms (see [18,29,135]). (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:198 / 216
页数:19
相关论文
共 167 条
[1]   INTERCELLULAR COMMUNICATION IN THE BRAIN - WIRING VERSUS VOLUME TRANSMISSION [J].
AGNATI, LF ;
ZOLI, M ;
STROMBERG, I ;
FUXE, K .
NEUROSCIENCE, 1995, 69 (03) :711-726
[2]   Nicotinic acetylcholine receptors on hippocampal neurons: Distribution on the neuronal surface and modulation of receptor activity [J].
Albuquerque, EX ;
Pereira, EFR ;
Alkondon, M ;
Schrattenholz, A ;
Maelicke, A .
JOURNAL OF RECEPTOR AND SIGNAL TRANSDUCTION RESEARCH, 1997, 17 (1-3) :243-266
[3]   The biological, social and clinical bases of drug addiction: Commentary and debate [J].
Altman, J ;
Everitt, BJ ;
Glautier, S ;
Markou, A ;
Nutt, D ;
Oretti, R ;
Phillips, GD ;
Robbins, TW .
PSYCHOPHARMACOLOGY, 1996, 125 (04) :285-345
[4]  
AMADOR M, 1995, J NEUROSCI, V15, P4525
[5]  
ANDERSEN P, 1993, MEMORY CONCEPTS BASI
[6]   THE ALLOSTERIC TRANSITION OF GLYCOGEN-PHOSPHORYLASE [J].
BARFORD, D ;
JOHNSON, LN .
NATURE, 1989, 340 (6235) :609-616
[7]   STEROIDS INHIBIT NICOTINIC ACETYLCHOLINE-RECEPTORS [J].
BERTRAND, D ;
VALERA, S ;
BERTRAND, S ;
BALLIVET, M ;
RUNGGER, D .
NEUROREPORT, 1991, 2 (05) :277-280
[8]   MUTATIONS AT 2 DISTINCT SITES WITHIN THE CHANNEL DOMAIN M2 ALTER CALCIUM PERMEABILITY OF NEURONAL ALPHA-7 NICOTINIC RECEPTOR [J].
BERTRAND, D ;
GALZI, JL ;
DEVILLERSTHIERY, A ;
BERTRAND, S ;
CHANGEUX, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (15) :6971-6975
[9]   UNCONVENTIONAL PHARMACOLOGY OF A NEURONAL NICOTINIC RECEPTOR MUTATED IN THE CHANNEL DOMAIN [J].
BERTRAND, D ;
DEVILLERSTHIERY, A ;
REVAH, F ;
GALZI, JL ;
HUSSY, N ;
MULLE, C ;
BERTRAND, S ;
BALLIVET, M ;
CHANGEUX, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (04) :1261-1265
[10]   ACTIVATION AND BLOCKING OF NEURONAL NICOTINIC ACETYLCHOLINE-RECEPTOR RECONSTITUTED IN XENOPUS OOCYTES [J].
BERTRAND, D ;
BALLIVET, M ;
RUNGGER, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (05) :1993-1997