Original Article

Neuropsychopharmacology (2004) 29, 1344–1352, advance online publication, 7 April 2004; doi:10.1038/sj.npp.1300436

Maternal Behavior Regulates Benzodiazepine/GABAA Receptor Subunit Expression in Brain Regions Associated with Fear in BALB/c and C57BL/6 Mice

Christian Caldji1, Josie Diorio1, Hymie Anisman2 and Michael J Meaney1

  1. 1Developmental Neuroendocrinology Laboratory, Douglas Hospital Research Centre, McGill University, Montréal, Canada
  2. 2Institute of Neuroscience, Carleton University, Ottawa, Ontario, Canada

Correspondence: MJ Meaney, Developmental Neuroendocrinology Laboratory, Douglas Hospital Research Centre, 6875 Boul. LaSalle, Montreal, Quebec, Canada H4H 1R3. Tel: +514 761 6131 ext.3938; Fax: +514 762 3034, E-mail: michael.meaney@mcgill.ca

Received 31 July 2003; Revised 5 February 2004; Accepted 5 February 2004; Published online 7 April 2004.

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Abstract

Inbred strains of mice, such as BALB/cByJ and C57BL/6ByJ, have been used repeatedly to study genotype–phenotype relations. These strains differ on behavioral measures of fear. In novel environments, for example, BALB/c mice are substantially more neophobic than C57BL/6 animals. The benzodiazepine (BZ)/GABAA receptor system has been proposed as a regulator of behavioral responses to stress, and BALB/c and C57BL/6 mice differ in BZ/GABAA receptor binding. In the present study, we found increased BZ receptor levels in C57BL/6 mice in the central and basolateral nuclei of the amygdala as well as the locus coeruleus using either flunitrazepam (nonselective) or zolpidem (alpha1 subtype selective) as radioligands. Differences in receptor binding were most pronounced in the amygdala and locus coeruleus using [3H]zolpidem. C57BL/6 mice showed increased alpha1 mRNA levels in the locus coeuruleus compared to BALB/c mice. In addition, italic gamma2 mRNA expression in BALB/c mice was decreased in the central nucleus of the amygdala to levels that were 2–2.5-fold lower than those of C57BL/6 mice. The results of an adoption study revealed that the biological offspring of C57BL/6 mothers fostered after birth to BALB/c dams showed decreased levels of italic gamma2 mRNA expression in the central nucleus of the amygdala in comparison to peers fostered to other C57BL/6 mothers (the reverse was found for the biological offspring of BALB/c mothers). In a step-down exploration paradigm, BALB/cByJ mice crossfostered onto a C57BL/6ByJ dam expressed reduced anxiety responses. However, among C57BL/6ByJ mice, the relatively low levels of anxiety ordinarily evident were not increased when mice of this strain were reared by a BALB/cByJ dam. These preliminary findings suggest that the strain differences in the BZ/GABAA receptor system occur, at least in part, as a function of parental care. Such findings may reflect a mammalian example of an indirect genetic effect mediated by maternal care.

Keywords:

amygdala, mouse, gene expression, benzodiazepine/GABAA receptor, fear/anxiety

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