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1.
Neurosci Lett ; 422(3): 181-6, 2007 Jul 18.
Artigo em Inglês | MEDLINE | ID: mdl-17629403

RESUMO

Long-term potentiation (LTP) is a form of activity-dependent synaptic plasticity that is a candidate cellular mechanism for some forms of learning and memory. Although GABAergic synaptic inhibition plays a critical role in regulating of synaptic plasticity, there is still little known about the GABAergic modulation on LTP induction in chronic preparation. In the present study we examined the effect of GABA(A) agonist, diazepam (DZM), and antagonist, picrotoxin (PTX) on the induction of LTP in the somatosensory cortex of freely moving rats for a long-term period. In adult rats a bipolar stimulating and recording electrode were implanted into corpus callusom and somatosensory cortex, respectively. Two weeks after the surgery, evoked field potential responses were recorded before, during (12 days), and after (1 month) induction period of LTP by high-frequency stimulation. The LTP characteristics were compared between control, DZM and PTX groups during the time course of recording in each rat. Administration of DZM prior to train, blocked the induction of neocortical LTP, while the PTX increased the development of LTP making the highest differential levels of LTP about 12 days after the initiation of LTP induction. Our findings suggest that the augmentation of LTP by PTX can be explained by an interaction between excitatory and inhibitory pathways. Suppression of neocortical inhibitory inputs by PTX causes enhancement in LTP induction. These results suggest that GABAergic system has an important role in synaptic plasticity and long-term modification of somatosensory cortex in freely moving rat.


Assuntos
Potenciais Evocados/fisiologia , Potenciação de Longa Duração/fisiologia , Neocórtex/fisiologia , Ácido gama-Aminobutírico/metabolismo , Animais , Eletrodos Implantados , Potenciais Evocados/efeitos dos fármacos , Moduladores GABAérgicos/farmacologia , Potenciação de Longa Duração/efeitos dos fármacos , Masculino , Neocórtex/efeitos dos fármacos , Ratos , Ratos Sprague-Dawley , Ácido gama-Aminobutírico/efeitos dos fármacos
2.
Brain Res Bull ; 74(1-3): 29-36, 2007 Sep 14.
Artigo em Inglês | MEDLINE | ID: mdl-17683786

RESUMO

Neonatal single whisker experience changes the response properties of spared barrel neurons to deflections of principal and adjacent whiskers. However little is known about the temporal characteristics of the paired whisker inputs. To address this issue we used computer controlled mechanical displacement of paired whiskers in control and plucked animals (plucking of all whiskers but D2 started at 0, 5 and 8 postnatal days). The principal whisker (PW) and its caudal adjacent whisker (AW) were deflected simultaneously or serially at different inter-stimulus intervals (10, 20, 30, 50 and 100 ms). Neuronal responses were recorded in D2 spared barrel both in layers IV and V. In the control group, combined deflection of AW prior to PW led to suppression of ON and OFF responses to PW deflection both in layers IV and V. The magnitude of this suppression was strongly dependent on the inter-stimulus intervals (ISIs). At almost all tested ISIs, whisker plucking from P0, P5 and P8 weakened suppressive interactions in layers IV and V barrel neurons for both ON and OFF responses. The most decrease in inhibitory interactions was observed in P5 plucked animals. Principal whisker-evoked ON responses were increased only in P0 plucked animals both in layers IV and V. AW-evoked ON responses are decreased in P5 plucked animals in layer IV. The available data suggest that sensory experience can modulate temporal aspects of response integration and receptive field properties of layers IV and V neurons in barrel cortex. These changes have different critical periods.


Assuntos
Plasticidade Neuronal/fisiologia , Neurônios/fisiologia , Córtex Somatossensorial/citologia , Córtex Somatossensorial/crescimento & desenvolvimento , Vibrissas/inervação , Potenciais de Ação/fisiologia , Fatores Etários , Animais , Animais Recém-Nascidos , Condicionamento Psicológico , Masculino , Inibição Neural/fisiologia , Estimulação Física/métodos , Ratos , Ratos Wistar , Privação Sensorial/fisiologia , Estatísticas não Paramétricas , Fatores de Tempo
3.
Brain Res ; 1015(1-2): 129-35, 2004 Jul 23.
Artigo em Inglês | MEDLINE | ID: mdl-15223376

RESUMO

Controlled mechanical displacement was used to stimulate single whiskers in normal and C-fiber depleted rats to quantitatively examine the role of C-fibers in the response properties of barrel cortical cells. C-fiber depletion using neonatal capsaicin treatment increased the barrel single-unit response magnitude to deflection of both principal and adjacent whiskers while there was not any significant difference in the barrel cells' spontaneous activity. Capsaicin treatment increased the neural response duration of adjacent whisker stimulation but did not change that to the principal whisker deflection. There was no difference in response latencies of principal or adjacent whisker displacement between the normal and C-fiber-depleted groups. The efficiency of neural code for differentiation of principal and adjacent whiskers was measured by ROC analysis, which reflects the performance of an ideal observer in this discrimination using cells' firing rate. No significant difference was found in the performance of neurons in capsaicin-treated and control groups in distinguishing principal and adjacent whisker deflections from each other. These results suggest that neonatal C-fiber depletion causes an expansion of barrel cells receptive field but it does not affect the discrimination of individual whisker stimulation by the barrel cells.


Assuntos
Discriminação Psicológica/fisiologia , Potenciais Somatossensoriais Evocados/fisiologia , Fibras Nervosas Amielínicas/metabolismo , Córtex Somatossensorial/fisiologia , Tato/fisiologia , Vibrissas/inervação , Análise de Variância , Animais , Animais Recém-Nascidos , Capsaicina , Denervação/métodos , Masculino , Neurônios/fisiologia , Estimulação Física , Curva ROC , Ratos , Ratos Sprague-Dawley , Tempo de Reação/fisiologia , Transdução de Sinais/fisiologia , Córtex Somatossensorial/citologia , Vibrissas/fisiologia
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