کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
4337463 1614777 2015 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Sex-specific restoration of MK-801-induced sensorimotor gating deficit by environmental enrichment
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب (عمومی)
پیش نمایش صفحه اول مقاله
Sex-specific restoration of MK-801-induced sensorimotor gating deficit by environmental enrichment
چکیده انگلیسی


• Postnatal MK-801 led to a significant deficit in prepulse inhibition (PPI).
• PPI deficit by MK-801 was observed in both sexes on postnatal days 28–30.
• Enriched environment was applied from birth up to the time of PPI testing.
• Enriched environment restored MK-801-induced PPI deficit only in male rats.
• Enriched environment per se had no significant effect on PPI.

Despite ample evidence of N-methyl-d-aspartate (NMDA) receptor dysfunction in schizophrenia, no study has addressed the effects of enriched environment (EE) on sensorimotor gating deficits induced by postnatal NMDA receptor blockade. We evaluated the effect of EE on sensorimotor gating (measured by prepulse inhibition, PPI), or on sensorimotor gating deficit induced by the NMDA receptor antagonist (+)-5-methyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5,10-imine maleate (MK-801) in both sexes of Wistar rats. Rats were injected with MK-801 (1 mg/kg) on postnatal days (P) 6–10. EE was provided from birth up to the time of experiments on P28–30 or P58–60. PPI data were collected at three prepulse intensities and then averaged to yield global PPI.MK-801 treatment reduced PPI significantly in both sexes. While EE per se had no significant effect on PPI, it restored MK-801-induced PPI deficit only in male rats. An extended period of EE did not influence PPI deficit in female rats. Our results indicate that postnatal exposure to MK-801 may exert long-lasting effects on neuronal circuits underlying sensorimotor gating. Sex-specific modulation of such effects by EE suggests sexually dimorphic mechanisms are involved.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neuroscience - Volume 299, 23 July 2015, Pages 28–34
نویسندگان
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