LABORATORIES

Neurophysiology and Synaptic Plasticity

Neurophysiology and Synaptic Plasticity 

Research

Team

Publications

Contact

Others

Research

Our group is focused in the study of the cellular processes and molecular mechanisms underlying the regulation of synaptic transmission. We are particularly interested in the ability of neurons to regulate the synaptic strength over time, a process called synaptic plasticity, which is crucial both during physiological and pathological conditions of the Nervous System (NS).

Lines of investigation

Our goal is to investigate the properties, mechanisms and consequences of astrocyte signaling on neuronal excitability and synaptic transmission in the control of motor activity. The general aim of our work is elucidate whether activation of astrocytes regulates potassium conductances, glutamatergic and GABAergic synaptic transmission and, consequently, modulates motor network excitability in physiological and pathological conditions. We propose a multidisciplinary approach to study different aspects of neuron-astrocytes interaction, from changes in intracellular calcium signaling, effects on synaptic transmission, remodeling of synaptic structures, changes in intrinsic neuronal properties, excitability, integration of information into neural circuits and, finally, the consequences on behavior.

In our studies, we apply several functional and structural approaches to the experimental animal models, including:

  • Extra and intracellular (patch- clamp technics) recordings of neuronal electrical activity.
  • Simultaneous recordings of electrical activity and calcium imaging both in brain slices and in vivo.
  • Electrochemistry techniques (fast cyclic voltammetry at the carbon fiber microelectrode, amperometry, biosensors).
  • Optogenetic and chemogenic stimulation (ex vivo and in vivo).
  • Electrophysiology, calcium imaging and behavioral tests combined in freely moving animals.

AAV5-GFAP-hM3Dq-mCherry and AAV5-gfaABC1D-cyto-GCaMP6f expression in astrocytes in the CA1 region of the hippocampus. Scale bar, 50 μm.

Team

Eduardo Martín Montiel: Principal Investigator
Samuel Alberquilla Martínez: Postdoctoral researcher
Sara Expósito Reguero: Predoctoral researcher
Pablo Azón Espinar: Predoctoral researcher
Lucía García Carracedo: Research assistant, Comunidad Autónoma de Madrid
Alejandro Hernández Seco: Master Studen. Program JAE Intro, CSIC

Publications

Featured publications

  • Mellado S, Moreno-Ruiz B, Expósito S, Fernández M, Martín ED*. Prolactin Reduces Hippocampal Parvalbumin and GABAA Receptor Expression in Female Mice. Neuroendocrinology. 2021. doi: 10.1159/000520279.

  • Zamora-Moratalla A, Martín ED*. Prolactin enhances hippocampal synaptic plasticity in female mice of reproductive age. Hippocampus. 2021. 31(3):281-293. doi: 10.1002/hipo.23288.

  • Moreno-Ruiz B, Mellado S, Zamora-Moratalla A, Albarracín AL, Martín ED*. Increase in serum prolactin levels in females improves the performance of spatial learning by promoting changes in the circuital dynamics of the hippocampus. Psychoneuroendocrinology. 2021. 124:105048. DOI: 10.1016/j.psyneuen.2020.105048.

  • Lines J, Martín ED, Kofuji P, Aguilar J, Araque A. Astrocytes modulate sensory-evoked neuronal network activity. Nat Commun. 2020. 11:3689. DOI: 10.1038/s41467-020-17536-3.

  • Alberquilla S, Gonzalez-Granillo A, Martín ED**, Moratalla R**. Dopamine regulates spine density in striatal projection neurons in a concentration-dependent manner. Neurobiology of Disease. 2020. 134:104666. DOI: 10.1016/j.nbd.2019.104666.

  • Corkrum M, Covelo A, Lines J, Bellocchio L, Pisansky M, Loke K, Quintana R, Rothwell PE, Lujan R, Marsicano G, Martin ED, Thomas MJ, Kofuji P, Araque A (2020) Dopamine-Evoked Synaptic Regulation in the Nucleus Accumbens Requires Astrocyte Activity. Neuron. 18;105(6):1036-1047.e5. doi: 10.1016/j.neuron.2019.12.026.

  • Caffeine-mediated BDNF release regulates long-term synaptic plasticity through activation of IRS2 signaling. Lao-Peregrín C, Ballesteros JJ, Fernández M, Zamora-Moratalla A, Saavedra A, Gómez Lázaro M, Pérez-Navarro E, Burks D, Martín ED*. Addict Biol. 2017; 22:1706-1718. doi: 10.1111/adb.12433.

  • Synapse-specific astrocyte gating of amygdala-related behavior. Martin-Fernandez M, Jamison S, Robin LM, Zhao Z, Martin ED, Aguilar J, Benneyworth MA, Marsicano G, Araque A. Nat Neurosci. 2017 20(11):1540-1548. doi: 10.1038/nn.4649.

  • The insulin-like growth factor I receptor regulates glucose transport by astrocytes. Hernandez-Garzón E, Fernandez AM, Perez-Alvarez A, Genis L, Bascuñana P, Fernandez de la Rosa R, Delgado M, Angel Pozo M, Moreno E, McCormick PJ, Santi A, Trueba-Saiz A, Garcia-Caceres C, Tschöp MH, Araque A, Martin ED, Torres Aleman I. Glia. 2016; 64:1962-71. doi: 10.1002/glia.23035.

  • Structural and functional plasticity of astrocyte processes and dendritic spine interactions. Perez-Alvarez A, Navarrete M, Covelo A, Martin ED, Araque A. J Neurosci. 2014; 34:12738-44. doi: 10.1523/JNEUROSCI.2401-14.2014.

  • Dopamine release regulation by astrocytes during cerebral ischemia. Oliva I, Fernández M, Martín ED. Neurobiol Dis. 2013; 58:231-41. doi: 10.1016/j.nbd.2013.06.007.

  • Confocal microscopy for astrocyte in vivo imaging: Recycle and reuse in microscopy. Pérez-Alvarez A, Araque A, Martín ED. Front Cell Neurosci. 2013; 7:51. doi:10.3389/fncel.2013.00051.

  • Astrocytes mediate in vivo cholinergic-induced synaptic plasticity. Navarrete M, Perea G, Fernandez de Sevilla D, Gómez-Gonzalo M, Núñez A, Martín ED**, Araque A**. PLoS Biol. 2012; 10:e1001259. doi: 10.1371/journal.pbio.1001259.

  • IRS-2 Deficiency impairs NMDA receptor-dependent long-term potentiation. Martín ED, Sánchez-Perez A, Trejo JL, Martin-Aldana JA, Cano Jaimez M, Pons S, Acosta Umanzor C, Menes L, White MF, Burks DJ. Cereb Cortex. 2012; 22:1717-27. doi: 10.1093/cercor/bhr216.

  • Overexpression of Reelin prevents the manifestation of behavioral phenotypes related to schizophrenia and bipolar disorder. Teixeira CM, Martín ED, Sahún I, Masachs N, Pujadas L, Corvelo A, Bosch C, Rossi D, Martinez A, Maldonado R, Dierssen M, Soriano E. Neuropsychopharmacology. 2011; 36:2395-405. doi: 10.1038/npp.2011.153.

  • Flufenamic acid suppresses epileptiform activity in hippocampus by reducing excitatory synaptic transmission and neuronal excitability. Fernández M, Lao-Peregrín C, Martín ED. Epilepsia. 2010; 51:384-90. doi: 10.1111/j.1528-1167.2009.02279.x.

  • Adenosine released by astrocytes contributes to hypoxia-induced modulation of synaptic transmission. Martín ED, Fernández M, Perea G, Pascual O, Haydon PG, Araque A, Ceña V. Glia. 2007; 55:36-45

Contact

Where to find us

Laboratory of neurophysiology and synaptic plasticity

Instituto Cajal CSIC. Avda. Doctor Arce, 37. 28002. Madrid

Call us

Write us

Others 

Skip to content