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Exceptional endocrine profiles characterise the meerkat: sex, status, and reproductive patterns
In vertebrates, reproductive endocrine concentrations are strongly differentiated by sex, with androgen biases typifying males and estrogen biases typifying females. These sex differences can be reduced in female-dominant species; however, even the most masculinised of females have less testosterone...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5067592/ https://www.ncbi.nlm.nih.gov/pubmed/27752129 http://dx.doi.org/10.1038/srep35492 |
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author | Davies, Charli S. Smyth, Kendra N. Greene, Lydia K. Walsh, Debbie A. Mitchell, Jessica Clutton-Brock, Tim Drea, Christine M. |
author_facet | Davies, Charli S. Smyth, Kendra N. Greene, Lydia K. Walsh, Debbie A. Mitchell, Jessica Clutton-Brock, Tim Drea, Christine M. |
author_sort | Davies, Charli S. |
collection | PubMed |
description | In vertebrates, reproductive endocrine concentrations are strongly differentiated by sex, with androgen biases typifying males and estrogen biases typifying females. These sex differences can be reduced in female-dominant species; however, even the most masculinised of females have less testosterone (T) than do conspecific males. To test if aggressively dominant, female meerkats (Suricata suricatta) may be hormonally masculinised, we measured serum androstenedione (A(4)), T and estradiol (E(2)) in both sexes and social classes, during both ‘baseline’ and reproductive events. Relative to resident males, dominant females had greater A(4), equivalent T and greater E(2) concentrations. Males, whose endocrine values did not vary by social status, experienced increased T during reproductive forays, linking T to sexual behaviour, but not social status. Moreover, substantial E(2) concentrations in male meerkats may facilitate their role as helpers. In females, dominance status and pregnancy magnified the unusual concentrations of measured sex steroids. Lastly, faecal androgen metabolites replicated the findings derived from serum, highlighting the female bias in total androgens. Female meerkats are thus strongly hormonally masculinised, possibly via A(4)’s bioavailability for conversion to T. These raised androgen concentrations may explain female aggressiveness in this species and give dominant breeders a heritable mechanism for their daughters’ competitive edge. |
format | Online Article Text |
id | pubmed-5067592 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50675922016-10-26 Exceptional endocrine profiles characterise the meerkat: sex, status, and reproductive patterns Davies, Charli S. Smyth, Kendra N. Greene, Lydia K. Walsh, Debbie A. Mitchell, Jessica Clutton-Brock, Tim Drea, Christine M. Sci Rep Article In vertebrates, reproductive endocrine concentrations are strongly differentiated by sex, with androgen biases typifying males and estrogen biases typifying females. These sex differences can be reduced in female-dominant species; however, even the most masculinised of females have less testosterone (T) than do conspecific males. To test if aggressively dominant, female meerkats (Suricata suricatta) may be hormonally masculinised, we measured serum androstenedione (A(4)), T and estradiol (E(2)) in both sexes and social classes, during both ‘baseline’ and reproductive events. Relative to resident males, dominant females had greater A(4), equivalent T and greater E(2) concentrations. Males, whose endocrine values did not vary by social status, experienced increased T during reproductive forays, linking T to sexual behaviour, but not social status. Moreover, substantial E(2) concentrations in male meerkats may facilitate their role as helpers. In females, dominance status and pregnancy magnified the unusual concentrations of measured sex steroids. Lastly, faecal androgen metabolites replicated the findings derived from serum, highlighting the female bias in total androgens. Female meerkats are thus strongly hormonally masculinised, possibly via A(4)’s bioavailability for conversion to T. These raised androgen concentrations may explain female aggressiveness in this species and give dominant breeders a heritable mechanism for their daughters’ competitive edge. Nature Publishing Group 2016-10-18 /pmc/articles/PMC5067592/ /pubmed/27752129 http://dx.doi.org/10.1038/srep35492 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Davies, Charli S. Smyth, Kendra N. Greene, Lydia K. Walsh, Debbie A. Mitchell, Jessica Clutton-Brock, Tim Drea, Christine M. Exceptional endocrine profiles characterise the meerkat: sex, status, and reproductive patterns |
title | Exceptional endocrine profiles characterise the meerkat: sex, status, and reproductive patterns |
title_full | Exceptional endocrine profiles characterise the meerkat: sex, status, and reproductive patterns |
title_fullStr | Exceptional endocrine profiles characterise the meerkat: sex, status, and reproductive patterns |
title_full_unstemmed | Exceptional endocrine profiles characterise the meerkat: sex, status, and reproductive patterns |
title_short | Exceptional endocrine profiles characterise the meerkat: sex, status, and reproductive patterns |
title_sort | exceptional endocrine profiles characterise the meerkat: sex, status, and reproductive patterns |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5067592/ https://www.ncbi.nlm.nih.gov/pubmed/27752129 http://dx.doi.org/10.1038/srep35492 |
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