RESUMEN
Accumulating evidence suggests that neuronal nicotinic acetylcholine receptors (nAChRs) may play a key role in the pathophysiology of some neurological diseases such as epilepsy. Based on genetic studies in patients with epileptic disorders worldwide and animal models of seizure, it has been demonstrated that nAChR activity is altered in some specific types of epilepsy, including autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) and juvenile myoclonic epilepsy (JME). Neuronal nAChR antagonists also have antiepileptic effects in pre-clinical studies. There is some evidence that conventional antiepileptic drugs may affect neuronal nAChR function. In this review, we re-examine the evidence for the involvement of nAChRs in the pathophysiology of some epileptic disorders, especially ADNFLE and JME, and provide an overview of nAChR antagonists that have been evaluated in animal models of seizure.
Asunto(s)
Anticonvulsivantes/farmacología , Epilepsia/metabolismo , Neuronas/metabolismo , Antagonistas Nicotínicos/farmacología , Receptores Nicotínicos/metabolismo , Animales , Anticonvulsivantes/uso terapéutico , Epilepsia/tratamiento farmacológico , Epilepsia/genética , Epilepsia/fisiopatología , Humanos , Neuronas/efectos de los fármacos , Neuronas/fisiología , Antagonistas Nicotínicos/uso terapéutico , Receptores Nicotínicos/química , Receptores Nicotínicos/genéticaRESUMEN
According to traditional models of the basal ganglia-thalamocortical network of connections, dopamine exerts D2-like receptor (D2LR)-mediated effects through actions on striatal neurons that give rise to the "indirect" pathway, secondarily affecting the activity in the internal and external pallidal segments (GPi and GPe, respectively) and the substantia nigra pars reticulata (SNr). However, accumulating evidence from the rodent literature suggests that D2LR activation also directly influences synaptic transmission in these nuclei. To further examine this issue in primates, we combined in vivo electrophysiological recordings and local intracerebral microinjections of drugs with electron microscopic immunocytochemistry to study D2LR-mediated modulation of neuronal activities in GPe, GPi, and SNr of normal and MPTP-treated (parkinsonian) monkeys. D2LR activation with quinpirole increased firing in most GPe neurons, likely due to a reduction of striatopallidal GABAergic inputs. In contrast, local application of quinpirole reduced firing in GPi and SNr, possibly through D2LR-mediated effects on glutamatergic inputs. Injections of the D2LR antagonist sulpiride resulted in effects opposite to those of quinpirole in GPe and GPi. D2 receptor immunoreactivity was most prevalent in putative striatal-like GABAergic terminals and unmyelinated axons in GPe, GPi, and SNr, but a significant proportion of immunoreactive boutons also displayed ultrastructural features of glutamatergic terminals. Postsynaptic labeling was minimal in all nuclei. The D2LR-mediated effects and pattern of distribution of D2 receptor immunoreactivity were maintained in the parkinsonian state. Thus, in addition to their preferential effects on indirect pathway striatal neurons, extrastriatal D2LR activation in GPi and SNr also influences direct pathway elements in the primate basal ganglia under normal and parkinsonian conditions.
Asunto(s)
Ganglios Basales/fisiología , Cuerpo Estriado/fisiología , Trastornos Parkinsonianos/metabolismo , Receptores de Dopamina D2/fisiología , Animales , Ganglios Basales/efectos de los fármacos , Cuerpo Estriado/efectos de los fármacos , Agonistas de Dopamina/farmacología , Antagonistas de Dopamina/farmacología , Antagonistas de los Receptores de Dopamina D2 , Macaca mulatta , Vías Nerviosas/efectos de los fármacos , Vías Nerviosas/fisiología , Trastornos Parkinsonianos/fisiopatología , Receptores de Dopamina D2/agonistasRESUMEN
Learning a visuomotor skill involves a distributed network which includes the primary motor cortex (M1). Despite multiple lines of evidence supporting the role of M1 in motor learning and memory, it is unclear whether M1 plays distinct roles in different aspects of learning such as acquisition and retention. Here, we investigated the nature and chronometry of that processing through a temporally specific disruption of M1 activity using single-pulse transcranial magnetic stimulation (TMS). We applied single-pulse TMS to M1 or dorsal premotor cortex (PMd) during adaptation of rapid arm movements (approximately 150 ms duration) to a visuomotor rotation. When M1 was stimulated either immediately after the end of each trial or with a 700 ms delay, subjects exhibited normal adaptation. However, whereas the memory of the subjects who received delayed-TMS showed normal rates of forgetting during deadaptation, the memory of those who received immediate TMS was more fragile: in the deadaptation period, they showed a faster rate of forgetting. Stimulation of PMd with adjusted (reduced) intensity to rule out the possibility of coactivation of this structure caused by the current spread from M1 stimulation did not affect adaptation or retention. The data suggest that, during the short time window after detection of movement errors, neural processing in M1 plays a crucial role in formation of motor memories. This processing in M1 may represent a slow component of motor memory which plays a significant role in retention.
Asunto(s)
Corteza Motora/fisiología , Desempeño Psicomotor/fisiología , Tiempo de Reacción/fisiología , Retención en Psicología/fisiología , Adolescente , Adulto , Femenino , Humanos , Masculino , Destreza Motora/fisiología , Estimulación Luminosa/métodosRESUMEN
In Parkinson's disease, neurons of the internal segment of the globus pallidus (GPi) display the low-frequency tremor-related oscillations. These oscillatory activities are transmitted to the thalamic relay nuclei. Computer models of the interacting thalamocortical (TC) and thalamic reticular (RE) neurons were used to explore how the TC-RE network processes the low-frequency oscillations of the GPi neurons. The simulation results show that, by an interaction between the TC and RE neurons, the TC-RE network transforms a low-frequency oscillatory activity of the GPi neurons to a higher frequency of oscillatory activity of the TC neurons (the superharmonic frequency transformation). In addition to the interaction between the TC and RE neurons, the low-threshold calcium current in the RE and TC neurons and the hyperpolarization-activated cation current (I (h)) in the TC neurons have significant roles in the superharmonic frequency transformation property of the TC-RE network. The external globus pallidus (GPe) oscillatory activity, which is directly transmitted to the RE nucleus also displays a significant modulatory effect on the superharmonic frequency transformation property of the TC-RE network.
Asunto(s)
Relojes Biológicos/fisiología , Corteza Cerebral/fisiología , Globo Pálido/fisiología , Núcleos Talámicos Intralaminares/fisiología , Vías Nerviosas/fisiología , Tálamo/fisiología , Potenciales de Acción/fisiología , Animales , Calcio/metabolismo , Señalización del Calcio/fisiología , Humanos , Canales Iónicos/fisiología , Modelos Neurológicos , Red Nerviosa/fisiología , Inhibición Neural/fisiología , Redes Neurales de la Computación , Neuronas/fisiología , Enfermedad de Parkinson/fisiopatología , Transmisión Sináptica/fisiología , Temblor/fisiopatologíaRESUMEN
Resting tremor is the most specific sign for idiopathic Parkinson' disease. It has been proposed that parkinsonian tremor results from the activity of the central oscillators. One of the hypotheses, which have been proposed about the possible principles underlying such central oscillations, is the subthalamic nucleus (STN)-external globus pallidus (GPe)-pacemaker hypothesis. Activity from the central oscillator is proposed to be transmitted via trans-cortical pathways to the periphery. A computational model of the basal ganglia (BG) is proposed for simulating the effects of the internal globus pallidus (GPi)-pedunculopontine (PPN) loop activity on the transmission of the STN-GPe-pacemaker oscillatory activities to the cortex, based on known anatomy and physiology of the BG. According to the result of the simulation, the GPi-PPN loop activity can suppress the transmission of the STN-GPe-pacemaker oscillatory activities to the cortex. This suppressive effect is controlled by various factors such as the strength of the synaptic connection from the PPN to the GPi, the strength of the synaptic connection from the GPi to the PPN, the spontaneous tonic activities of the GPi and PPN, the direct excitatory projections from the STN to the PPN, the frequency of the STN oscillatory burst activity, the duration of the STN burst, and the maximum T-type calcium channel conductance in the type-I PPN neurons.
Asunto(s)
Relojes Biológicos/fisiología , Corteza Cerebral/fisiología , Globo Pálido/fisiología , Vías Nerviosas/fisiología , Núcleo Subtalámico/fisiología , Animales , Ganglios Basales/fisiología , Simulación por Computador , Modelos Neurológicos , Inhibición Neural/fisiología , Enfermedad de Parkinson/fisiopatología , Transmisión SinápticaRESUMEN
Up to now a number of models have been proposed to underlie memory formation in the central nervous system. Two of these models are the reverberatory circuit model and the other one the self-feedback loop model. This paper considers these two models regarding their ability to preserve neural activity and to hold information. In the self-feedback loop model, the activity level of the loop output is computed regarding the short lasting initial input. In the reverberatory circuit model, the activity levels of the proposed two-layer network outputs were computed regarding the short lasting initial inputs of the network. In the self-feedback loop model, the activity level of the loop output changes with each reverberation until it reaches a specific limit and then remains at that level. In the reverberatory circuit model, the activity levels of the proposed two-layer network outputs display an oscillatory behavior. These models can preserve the input activity, but they change its level with each reverberation. Information carried by a single neuron is related to its activity level. Therefore these models change the information during the reverberation. Short-term memory must hold the information for a certain period of time, so these models cannot be proposed to underlie short-term memory formation.
Asunto(s)
Memoria a Corto Plazo , Modelos Biológicos , Modelos Neurológicos , Redes Neurales de la Computación , HumanosRESUMEN
Parkinsonian tremor is most likely due to oscillatory neuronal activities of central oscillators such as the subthalamic nucleus (STN)-external segment of the globus pallidus (GPe) pacemaker within the basal ganglia (BG). Activity from the central oscillator is proposed to be transmitted via transcortical pathways to the periphery. A computational model of the BG is proposed for simulating the transmission of the STN oscillatory activity to the cortex, based closely on known anatomy and physiology of the BG. According to the results of the simulation, for transmission of the STN oscillatory activity to the cortex, the STN oscillatory activity has to be transmitted simultaneously to the thalamus via STN-internal segment of the globus pallidus (GPi)-thalamus and STN-GPe-GPi-thalamus pathways. This transmission is controlled by the various factors such as the phase between the STN and GPe oscillatory activities, the STN oscillatory activity frequency, the low-threshold calcium spike bursts of the thalamus and the GPi spontaneous activity.