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Increased paternal corticosterone exposure influences offspring behaviour and expression of urinary pheromones

Abstract:
Abstract Background Studies have shown that paternal stress prior to conception can influence the innate behaviours of their offspring. The evolutionary impacts of such intergenerational effects are therefore of considerable interest. Our group previously showed in a model of daily stress that glucocorticoid treatment of adult male mouse breeders prior to conception leads to increased anxiety-related behaviours in male offspring. Here, we aimed to understand the transgenerational effects of paternal stress exposure on the social behaviour of progeny and its potential influence on reproductive success. Results We assessed social parameters including social reward, male attractiveness and social dominance, in the offspring (F1) and grand-offspring (F2). We report that paternal corticosterone treatment was associated with increased display of subordination towards other male mice. Those mice were unexpectedly more attractive to female mice while expressing reduced levels of the key rodent pheromone Darcin, contrary to its conventional role in driving female attraction. We investigated the epigenetic regulation of major urinary protein (Mup) expression by performing the first Oxford Nanopore direct methylation of sperm DNA in a mouse model of stress, but found no differences in Mup genes that could be attributed to corticosterone-treatment. Furthermore, no overt differences of the prefrontal cortex transcriptome were found in F1 offspring, implying that peripheral mechanisms are likely contributing to the phenotypic differences. Interestingly, no phenotypic differences were observed in the F2 grand-offspring. Conclusions Overall, our findings highlight the potential of moderate paternal stress to affect intergenerational (mal)adaptive responses, informing future studies of adaptiveness in rodents, humans and other species
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1186/s12915-023-01678-z

Authors

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Role:
Author
ORCID:
0000-0003-1466-2948
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Role:
Author
ORCID:
0000-0002-2648-7828
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-2903-9537



Publisher:
BioMed Central
Journal:
BMC Biology More from this journal
Volume:
21
Issue:
1
Pages:
186-186
Article number:
186
Publication date:
2023-09-04
DOI:
EISSN:
1741-7007
ISSN:
1741-7007


Language:
English
Keywords:
Pubs id:
1525820
Local pid:
pubs:1525820
Source identifiers:
W4386424630
Deposit date:
2026-05-17
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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