Literature DB >> 2720960

Sexually dimorphic behavioral and brain asymmetries in neonatal rats: effects of prenatal alcohol exposure.

B Zimmerberg1, J M Reuter.   

Abstract

Behavioral and neuroanatomical asymmetries were assessed in 3-day-old male and female rat pups chosen from litters whose dams had received one of 3 prenatal treatments: 35% ethanol-derived calories, pair-fed control, or lab chow control. Behavioral laterality was assessed by observing the preferred tail bias on postnatal (PN) day 1. On PN day 3, brains were sectioned and morphometric analyses conducted for total brain volume, left and right neocortical volumes, and left and right hippocampal volumes. Prenatal alcohol exposure altered the population proportions of left, right and neutral tail biases in male pups on PN day 1. Female pups were affected by both prenatal alcohol exposure and maternal undernutrition/stress of pair-feeding. Prenatal alcohol exposure decreased body weight and total brain volume, but increased the brain volume/body weight ratio compared to both control groups. Prenatal alcohol exposure also reduced the volumes of the hippocampus and neocortex, with the greatest proportional reduction found in the volume of the anterior neocortex. A left-right anterior neocortical asymmetry was observed, with tail bias, prenatal treatment and sex all significant factors. Alcohol-exposed males showed a 'feminized' asymmetry. These results demonstrate that a sexually dimorphic cerebral asymmetry can be detected at birth in rats; this asymmetry appears to be related to a postural position bias. The reversal of normal interhemispheric relations by prenatal alcohol exposure in male offspring suggested that the in utero hormonal milieu modulates the development of cerebral lateralization.

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Year:  1989        PMID: 2720960     DOI: 10.1016/0165-3806(89)90291-5

Source DB:  PubMed          Journal:  Brain Res Dev Brain Res        ISSN: 0165-3806


  8 in total

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4.  Acute alcohol exposure during neurulation: Behavioral and brain structural consequences in adolescent C57BL/6J mice.

Authors:  E W Fish; H T Holloway; A Rumple; L K Baker; L A Wieczorek; S S Moy; B Paniagua; S E Parnell
Journal:  Behav Brain Res       Date:  2016-05-13       Impact factor: 3.332

5.  The mouse-equivalent of the human BDNF VAL66MET polymorphism increases dorsal hippocampal volume and does not interact with developmental ethanol exposure.

Authors:  Clark W Bird; Megan J Barber; Jack Martin; Jacob J Mayfield; C Fernando Valenzuela
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7.  Reduced and delayed myelination and volume of corpus callosum in an animal model of Fetal Alcohol Spectrum Disorders partially benefit from voluntary exercise.

Authors:  Katrina A Milbocker; Gillian L LeBlanc; Eric K Brengel; Khan S Hekmatyar; Praveen Kulkarni; Craig F Ferris; Anna Y Klintsova
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8.  Sexual dimorphism of volume reduction but not cognitive deficit in fetal alcohol spectrum disorders: A combined diffusion tensor imaging, cortical thickness and brain volume study.

Authors:  Sarah Treit; Zhang Chen; Dongming Zhou; Lauren Baugh; Carmen Rasmussen; Gail Andrew; Jacqueline Pei; Christian Beaulieu
Journal:  Neuroimage Clin       Date:  2017-05-10       Impact factor: 4.881

  8 in total

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