IGF-1 facilitates extinction of conditioned fear

被引:20
作者
Maglio, Laura E. [1 ,2 ,3 ]
Noriega-Prieto, Jose A. [1 ,4 ]
Maroto, Irene B. [1 ,5 ,6 ]
Martin-Cortecero, Jesus [1 ,7 ]
Munoz-Callejas, Antonio [1 ]
Callejo-Mostoles, Marta [1 ]
Fernandez de Sevilla, David [1 ]
机构
[1] Univ Autonoma Madrid, Fac Med, Dept Anat Histol & Neurociencia, Madrid, Spain
[2] Univ La Laguna, Dept Ciencias Med Basicas Fisiol, Tenerife, Spain
[3] Univ La Laguna, Inst Tecnol Biomed ITB, Tenerife, Spain
[4] Univ Minnesota, Dept Neurosci, Minneapolis, MN USA
[5] Univ Complutense Madrid, Inst Univ Invest Neuroquim IUIN, Inst Ramon Y Cajal Invest Sanitaria IRYCIS, Ctr Invest Biomed Red Enfermedades Neurodegenerat, Madrid, Spain
[6] Univ Complutense Madrid, Fac Quim, Dept Bioquim & Biol Mol, Madrid, Spain
[7] Heidelberg Univ, Inst Physiol & Pathophysiol, Med Biophys, Heidelberg, Germany
关键词
GROWTH-FACTOR-I; MEDIAL PREFRONTAL CORTEX; PAIRED-PULSE FACILITATION; INTRINSIC EXCITABILITY; INFRALIMBIC CORTEX; PROTEIN-SYNTHESIS; NMDA RECEPTORS; GLIAL-CELLS; CA1; REGION; RAT-BRAIN;
D O I
10.7554/eLife.67267
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Insulin-like growth factor-1 (IGF-1) plays a key role in synaptic plasticity, spatial learning, and anxiety-like behavioral processes. While IGF-1 regulates neuronal firing and synaptic transmission in many areas of the central nervous system, its signaling and consequences on excitability, synaptic plasticity, and animal behavior dependent on the prefrontal cortex remain unexplored. Here, we show that IGF-1 induces a long-lasting depression of the medium and slow post-spike afterhyperpolarization (mAH P and sAHP), increasing the excitability of layer 5 pyramidal neurons of the rat infralimbic cortex. Besides, IGF-1 mediates a presynaptic long-term depression of both inhibitory and excitatory synaptic transmission in these neurons. The net effect of this IGF-1-mediated synaptic plasticity is a long-term potentiation of the postsynaptic potentials. Moreover, we demonstrate that IGF-1 favors the fear extinction memory. These results show novel functional consequences of IGF-1 signaling, revealing IGF-1 as a key element in the control of the fear extinction memory.
引用
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页数:20
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