Affiliation:
1. Neuroscience Research Center Institute of Neuropharmacology Kerman University of Medical Sciences Kerman Iran
2. Cognitive Neuroscience Research Center Institute of Neuropharmacology Kerman University of Medical Sciences Kerman Iran
3. Department of Anatomy School of Medicine Dezful University of Medical Sciences Dezful Iran
Abstract
AbstractIntroductionAutism spectrum disorder is a developmental disorder that can affect sensory‐motor behaviors in the valproic acid (Val) rodent model of autism. Although whisker deprivation (WD) induces plastic changes in the cortical neurons, tactile stimulation (TS) during the neonatal period may reverse it. Here, we investigate the interaction effects of TS and WD on behavioral and histologic features of barrel cortex neurons in juvenile Val‐treated.MethodsControl (CTL, CTL–TS, CTL–WD, and CTL–TS–WD groups) and Val‐treated (Val, Val–TS, Val–WD, and Val–TS–WD groups) rats of both sexes were subjected to behavioral tests of social interaction, and novel texture recognition, and Nissl staining. The TS groups were exposed to sensory stimulation for 15 min, three times/day; moreover, all whiskers in the WD groups were trimmed every other day from postnatal days 1 to 21.ResultsBoth prenatal valproic acid administration and postnatal WD decreased the rats’ performance percentage of the Val and CTL–WD groups of both sexes compared with the CTL groups in the social interaction and texture discrimination tests. Following TS, the performance of the Val–TS–WD group increased significantly compared to the Val group (p < .05), whereas the performance of the CTL–TS–WD group rescued to the CTL group. Nissl staining results also revealed the neuron degeneration percentage in the barrel field area of the Val and CTL–WD groups was increased significantly (p < .05) compared with the CTL group. In this regard, TS decreased the neuron degeneration percentage of the Val–TS–WD and the CTL–TS–WD groups, compared with the CTL group, significantly (p < .05).ConclusionTS in juvenile male and female rats can act as a modulator and compensate for the behavioral and histological consequences of WD and prenatal valproic acid exposure.
Funder
Kerman University of Medical Sciences
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1 articles.
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