The prenatal environment, including prenatal stress, has been extensively studied in laboratory animals and humans. However, studies of the prenatal environment usually directly stress pregnant females, but stress may come ‘indirectly’, through stress to a cage-mate. The current study used indirect prenatal bystander stress and investigated the effects on the gross morphology, pre-weaning behavior, and epigenome of rat offspring. Pregnant Long-Evans rats were housed with another female rat that underwent elevated platform stress from gestational days 12 to 16. We found that ultrasonic vocalizations of female cage-mates were disrupted following the stress procedure. After birth, offspring were tested on two behavioral tasks and sacrificed at postnatal day 21 (p21). Frontal cortex and hippocampal tissue was used to measure global DNA methylation and gene expression changes. At p21, bystander-stressed female offspring exhibited increased body weight. Offspring behavior on the negative geotaxis task was altered by prenatal bystander stress, and locomotor behavior was reduced in female offspring. Global DNA methylation increased in the frontal cortex and hippocampus of bystander-stressed offspring. Microarray analysis revealed significant gene expression level changes in 558 different genes, of which only 10 exhibited overlap between males and females or brain areas. These alterations in gene expression were associated with overrepresentation of 36 biological processes and 34 canonical pathways. Prenatal stress thus does not have to be experienced by the mother herself to influence offspring brain development. Furthermore, this type of ‘indirect’ prenatal stress alters offspring DNA methylation patterns, gene expression profiles, and behavior.

1.
Lemaire V, et al: Prenatal stress produces learning deficits associated with an inhibition of neurogenesis in the hippocampus. Proc Natl Acad Sci 2000;97:11032–11037.
2.
Seckl J: Prenatal glucocorticoids and long-term programming. Eur J Endocrinol 2004;151:U49–U62.
3.
Kapoor A, et al: Fetal programming of hypothalamo-pituitary-adrenal function: prenatal stress and glucocorticoids. J Physiol 2006;572:31–44.
4.
Jaenisch R, Bird A: Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals. Nat Genet 2003;33:245–254.
5.
Bernstein B, Meissner A, Lander E: The mammalian epigenome. Cell 2007;128:669–681.
6.
Bird A: Perceptions of epigenetics. Nature 2007;447:396–398.
7.
Weber M, Schubeler D: Genomic patterns of DNA methylation: targets and function of an epigenetic mark. Curr Opin Cell Biol 2007;19:273–280.
8.
Weber M, et al: Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome. Nat Genet 2007;39:457–466.
9.
Feinberg AP, Tycko B: The history of cancer epigenetics. Nat Rev Cancer 2004;4:143–153.
10.
Nuyt AM, Szyf M: Developmental programming through epigenetic changes. Circ Res 2007;100:452–455.
11.
Goel N, Bale TL: Examining the intersection of sex and stress in modelling neuropsychiatric disorders. J Neuroendocrinol 2009;21:415–420.
12.
Kofman O: The role of prenatal stress in the etiology of developmental behavioral disorders. Neurosci Biobehav Rev 2002;26:457–470.
13.
Mueller B, Bale T: Sex-specific programming of offspring emotionality after stress early in pregnancy. J Neurosci 2008;28:9055–9065.
14.
McCormick CM, et al: Sex-specific effects of prenatal stress on hypothalamic-pituitary-adrenal responses to stress and brain glucocorticoid receptor density in adult rats. Dev Brain Res 1995;84:55–61.
15.
Barbazanges A, et al: Maternal glucocorticoid secretion mediates long-term effects of prenatal stress. J Neurosci 1996;16:3943–3949.
16.
Weaver I, et al: Epigenetic programming by maternal behavior. Nat Neurosci 2004;7:847–854.
17.
Weinstock M: Gender differences in the effects of prenatal stress on brain development and behavior. Neurochem Res 2007;32:1730–1740.
18.
Wong TP, et al: Hippocampal long-term depression mediates acute stress-induced spatial memory retrieval impairment. Proc Natl Acad Sci 2007;104:11471–11476.
19.
Qiagen: AllPrep DNA/RNA Mini Handbook. Valencia, Qiagen, 2005.
20.
Pogribny I, Yi P, James SJ: A sensitive new method for rapid detection of abnormal methylation patterns in global DNA and within CpG islands. Biochem Biophys Res Commun 1999;262:624–628.
21.
Pogribny IP, et al: Genomic hypomethylation is specific for preneoplastic liver in folate/methyl deficient rats and does not occur in non-target tissues. Mutat Res 2004;548:53–59.
22.
Koturbash I, et al: Role of epigenetic effectors in maintenance of the long-term persistent bystander effect in spleen in vivo. Carcinogenesis 2007;28:1831–1838.
23.
Affymetrix: Data sheet: GeneChip Gene 1.0 ST array system for human, mouse and rat. Santa Clara, Affymetrix, 2007.
24.
Blazejczyk M, Miron M, Nadon R: FlexArray: a statistical data analysis software for gene expression microarrays. 2007. http://genomequebec.mcgill.ca/FlexArray.
25.
Irizarry RA, et al: Exploration, normalization, and summaries of high density oligonucleotide array probe level data. Biostatistics 2003;4:249–264.
26.
Benjamini Y, Hochberg Y: Controlling the false discovery rate: a practical and powerful approach to multiple testing. J R Stat Soc Series B Stat Methodol 1995;57:289–300.
27.
NCBI (National Center for Biotechnology Information). www.ncbi.nlm.nih.gov/genomeprj/10621 (accessed March 22, 2011).
28.
Knuston B, Burgdorf J, Panksepp J: Ultrasonic vocalizations as indices of affective states in rats. Psychol Bull 2002;128:961–977.
29.
Blanchard RJ, et al: Twenty-two kHz alarm cries to presentation of a predator, by laboratory rats living in visible burrow systems. Physiol Behav 1991;50:967–972.
30.
Taylor S, et al: Biobehavioral responses to stress in females: tend-and-befriend, not fight-or-flight. Psychol Rev 2000;107:411–429.
31.
Langford D, et al: Social modulation of pain as evidence for empathy in mice. Science 2006;312:1967–1970.
32.
Van Den Hove D, et al: Prenatal stress and neonatal rat brain development. Neuroscience 2006;137:145–155.
33.
Drago F, Di Leo D, Giardina L: Prenatal stress induces body weight deficit and behavioral alteration in rats: the effect of diazepam. Eur Neuropsychopharmacol 1999;9:239–245.
34.
Gue M, et al: Sex differences in learning deficits induced by prenatal stress in juvenile rats. Behav Brain Res 2004;150:149–157.
35.
Alberts JR, Motz BA, Schank JC: Positive geotaxis in infant rats (Rattus norvegicus): a natural behavior and a historical correction. J Comp Psychol 2004;118:123–132.
36.
Patin V, Lordi B, Caston J: Does prenatal stress affect the motoric development of rat pups? Dev Brain Res 2004;149:85–92.
37.
Vallee M, et al: Prenatal stress induces high anxiety and postnatal handling induces low anxiety in adult offspring: correlation with stress-induced corticosterone secretion. J Neurosci 1997;17:2626–2636.
38.
Andrus B, et al: Gene expression patterns in the hippocampus and amygdala of endogenous depression and chronic stress models. Mol Psychiatry 2010, E-pub ahead of print.
39.
Mychasiuk R, Gibb R, Kolb B: Prenatal bystander stress induces neuroanatomical changes in the prefrontal cortex and hippocampus of developing rat offspring. Synapse, in submission.
40.
Chen G, Nunez G: Sterile inflammation: sensing and reacting to damage. Nat Rev Immunol 2010;10:826–837.
41.
Hirunsatit R, et al: Twenty-one-base-pair insertion polymorphism creates an enhancer element and potentiates SLC6A1 GABA transporter promoter activity. Pharmacogenet Genomics 2009;19:53–65.
42.
Kolb B, Whishaw I: Fundamentals of Human Neuropsychology, ed 6. New York, Worth, 2008.
43.
Foster A, Kemp J: Glutamate- and GABA-based CNS therapeutics. Curr Opin Pharmacol 2006;6:7–17.
44.
Das R, Hampton D, Jirtle R: Imprinting evolution and human health. Mamm Genome 2009;20:563–572.
45.
Rakyan V, et al: Metastable epialleles in mammals. Trends Genet 2002;18:348–351.
46.
Weaver I, et al: Reversal of maternal programming of stress response in adult offspring through methyl supplementation: altering epigenetic marking later in life. J Neurosci 2005;25:11045–11054.
47.
Meaney M, et al: Early environmental regulation of forebrain glucocorticoid receptor gene expression: implications for adrenocortical response to stress. Dev Neurosci 1996;18:49–72.
48.
Meaney M, et al: Postnatal handling increases the expression of cAMP-inducible transcription factors in the rat hippocampus: the effects of thyroid hormones and serotonin. J Neurosci 2000;20:3926–3935.
Copyright / Drug Dosage / Disclaimer
Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher.
Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.
You do not currently have access to this content.