Literature DB >> 17659594

Neonatal maternal separation alters adult eyeblink conditioning and glucocorticoid receptor expression in the interpositus nucleus of the cerebellum.

Aaron A Wilber1, Christopher J Southwood, Greta Sokoloff, Joseph E Steinmetz, Cara L Wellman.   

Abstract

Neonatal maternal separation alters learning and memory. Glucocorticoids also modulate adult learning and memory, and neonatal maternal separation alters forebrain glucocorticoid receptor (GR) concentrations. We used eyeblink classical conditioning to assess the effect of neonatal maternal separation on associative learning. We assessed delay eyeblink conditioning, GR expression, and total neuron number in the interpositus nucleus, a critical site of plasticity in eyeblink conditioning, in adult rats that had undergone either standard animal facilities rearing, handling for 15 min, or maternal separation for either 15 or 60 min per day on postnatal days 2-14. At 2-3 months of age, delay eyeblink classical conditioning was assessed. Brains were processed for GR immunohistochemistry, and GR expression in the interpositus nucleus was assessed using a computer-based densitometry system. Neuron counts and nuclear volumes were obtained from an alternate series of thionin-stained sections. Maternal separation significantly impaired eyeblink conditioning in male but not female rats. Handling and maternal separation did not significantly affect interpositus neuron number and volume. However, prolonged maternal separation significantly increased GR expression in the posterior interpositus in males, and increases were correlated with eyeblink conditioning. In female rats, maternal separation and handling did not significantly alter interpositus neuron number, volume, or GR protein expression, and GR expression did not correlate with eyeblink conditioning. Thus, neonatal maternal separation produces adult deficits in eyeblink conditioning and alterations in GR expression in its neural substrate in a sex-dependent manner. 2007 Wiley Periodicals, Inc

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Year:  2007        PMID: 17659594     DOI: 10.1002/dneu.20549

Source DB:  PubMed          Journal:  Dev Neurobiol        ISSN: 1932-8451            Impact factor:   3.964


  22 in total

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3.  MK-801 administration during neonatal ethanol withdrawal attenuates interpositus cell loss and juvenile eyeblink conditioning deficits.

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Review 4.  Reconceptualizing sex, brain and psychopathology: interaction, interaction, interaction.

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5.  Neonatal corticosterone administration impairs adult eyeblink conditioning and decreases glucocorticoid receptor expression in the cerebellar interpositus nucleus.

Authors:  A A Wilber; G L Lin; C L Wellman
Journal:  Neuroscience       Date:  2011-01-09       Impact factor: 3.590

Review 6.  Neonatal handling: an overview of the positive and negative effects.

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9.  Ethanol-exposed neonatal rats are impaired as adults in classical eyeblink conditioning at multiple unconditioned stimulus intensities.

Authors:  Derick H Lindquist; Greta Sokoloff; Joseph E Steinmetz
Journal:  Brain Res       Date:  2007-03-06       Impact factor: 3.252

10.  Litter and sex effects on maternal behavior and DNA methylation of the Nr3c1 exon 17 promoter gene in hippocampus and cerebellum.

Authors:  Therese A Kosten; David A Nielsen
Journal:  Int J Dev Neurosci       Date:  2014-04-08       Impact factor: 2.457

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