Mohammad Reza Afarinesh , Bi Bi Marzieh Ahmadi , Mansoureh Sabzalizadeh , Vahid Sheibani
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引用次数: 0
Abstract
The barrel cortex is a specialized region of the primary somatosensory cortex that processes tactile information from whiskers. This study investigates how tactile stimulation (TS) affects excitatory receptive fields and surrounds suppression in barrel cortex neurons of male and female autistic-like rats, using various whisker displacement protocols. The animals were categorized into control, Valproic acid pre-treated (Val), and Val-TS treatment groups. In male Val-TS rats, TS reduced layer IV ON/OFF amplitudes for principal and adjacent whisker displacements, while only OFF response latency to principal whisker displacement decreased. In females, Val group showed increased ON/OFF amplitudes, which decreased in Val-TS, returning to control levels. ON/OFF response latency to principal whisker displacement increased in Val-TS, returning to control. Tactile stimulation more effectively remodeled receptive fields and temporal timing in female barrel cortex. In layer V, male Val-TS rats showed no significant amplitude differences but decreased ON/OFF latencies to principal whisker displacement. Adjacent whisker responses were largely unchanged. In females, Val-TS rats had increased ON/OFF amplitudes to principal whisker displacement, but no latency changes. Adjacent whisker responses showed amplitude and latency differences, suggesting receptive-field expansion and remodeling. In terms of inhibitory responses, conditioning test (CT) ratio analysis indicated significant group effects for both ON and OFF responses in layer IV, with the Val-TS group showing higher CT-ratios than the Val and control groups for both sexes. Layer V responses indicated similar trends, with elevated CT-ratios in male rats under Val-TS conditions, whereas females did not show significant differences. Overall, these findings reveal distinct variations in responses of the barrel cortex neurons based on sex and treatment conditions, emphasizing the nuanced impact of interventions on neuronal responsiveness. This research enhances our understanding of sex-dependent neural adaptations and their implications for sensory processing and neuroplasticity in response to external stimuli.
期刊介绍:
Physiology & Behavior is aimed at the causal physiological mechanisms of behavior and its modulation by environmental factors. The journal invites original reports in the broad area of behavioral and cognitive neuroscience, in which at least one variable is physiological and the primary emphasis and theoretical context are behavioral. The range of subjects includes behavioral neuroendocrinology, psychoneuroimmunology, learning and memory, ingestion, social behavior, and studies related to the mechanisms of psychopathology. Contemporary reviews and theoretical articles are welcomed and the Editors invite such proposals from interested authors.