Anesthetics Rapidly Promote Synaptogenesis during a Critical Period of Brain Development

被引:122
作者
De Roo, Mathias
Klauser, Paul
Briner, Adrian
Nikonenko, Irina
Mendez, Pablo
Dayer, Alexandre
Kiss, Jozsef Z.
Muller, Dominique
Vutskits, Laszlo
机构
[1] Department of Neuroscience, Faculty of Medicine, University of Geneva, Geneva
[2] Department of Anesthesiology, Pharmacology and Intensive Care, University Hospital of Geneva, Geneva
[3] Department of Adult Psychiatry, University Hospital of Geneva, Geneva
关键词
D O I
10.1371/journal.pone.0007043
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Experience-driven activity plays an essential role in the development of brain circuitry during critical periods of early postnatal life, a process that depends upon a dynamic balance between excitatory and inhibitory signals. Since general anesthetics are powerful pharmacological modulators of neuronal activity, an important question is whether and how these drugs can affect the development of synaptic networks. To address this issue, we examined here the impact of anesthetics on synapse growth and dynamics. We show that exposure of young rodents to anesthetics that either enhance GABAergic inhibition or block NMDA receptors rapidly induce a significant increase in dendritic spine density in the somatosensory cortex and hippocampus. This effect is developmentally regulated; it is transient but lasts for several days and is also reproduced by selective antagonists of excitatory receptors. Analyses of spine dynamics in hippocampal slice cultures reveals that this effect is mediated through an increased rate of protrusions formation, a better stabilization of newly formed spines, and leads to the formation of functional synapses. Altogether, these findings point to anesthesia as an important modulator of spine dynamics in the developing brain and suggest the existence of a homeostatic process regulating spine formation as a function of neural activity. Importantly, they also raise concern about the potential impact of these drugs on human practice, when applied during critical periods of development in infants.
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页数:9
相关论文
共 39 条
[1]
NMDA receptors inhibit synapse unsilencing during brain development [J].
Adesnik, Hillel ;
Li, Guangnan ;
During, Matthew J. ;
Pleasure, Samuel J. ;
Nicoll, Roger A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (14) :5597-5602
[2]
Refining the roles of GABAergic signaling during neural circuit formation [J].
Akerman, Colin J. ;
Cline, Hollis T. .
TRENDS IN NEUROSCIENCES, 2007, 30 (08) :382-389
[3]
Growth and neurodevelopmental outcome in extremely-low-birth-weight infants after laparotomy [J].
Chacko, J ;
Ford, WDA ;
Haslam, R .
PEDIATRIC SURGERY INTERNATIONAL, 1999, 15 (07) :496-499
[4]
Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett Syndrome [J].
Dani, VS ;
Chang, Q ;
Maffei, A ;
Turrigiano, GG ;
Jaenisch, R ;
Nelson, SB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (35) :12560-12565
[5]
Activity-dependent PSD formation and stabilization of newly formed spines in hippocampal slice cultures [J].
De Roo, Mathias ;
Klauser, Paul ;
Mendez, Pablo ;
Poglia, Lorenzo ;
Muller, Dominique .
CEREBRAL CORTEX, 2008, 18 (01) :151-161
[6]
Inhibitory synaptogenesis in mouse somatosensory cortex [J].
DeFelipe, J ;
Marco, P ;
Fairen, A ;
Jones, EG .
CEREBRAL CORTEX, 1997, 7 (07) :619-634
[7]
Specific GABAA circuits for visual cortical plasticity [J].
Fagiolini, M ;
Fritschy, JM ;
Löw, K ;
Möhler, H ;
Rudolph, U ;
Hensch, TK .
SCIENCE, 2004, 303 (5664) :1681-1683
[8]
Imaging neuronal subsets in transgenic mice expressing multiple spectral variants of GFP [J].
Feng, GP ;
Mellor, RH ;
Bernstein, M ;
Keller-Peck, C ;
Nguyen, QT ;
Wallace, M ;
Nerbonne, JM ;
Lichtman, JW ;
Sanes, JR .
NEURON, 2000, 28 (01) :41-51
[9]
Critical period plasticity in local cortical circuits [J].
Hensch, TK .
NATURE REVIEWS NEUROSCIENCE, 2005, 6 (11) :877-888
[10]
Critical period regulation [J].
Hensch, TK .
ANNUAL REVIEW OF NEUROSCIENCE, 2004, 27 :549-579