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HERO ID
7354840
Reference Type
Journal Article
Title
Examining sources of variation in HPG axis function among individuals and populations of the dark-eyed junco
Author(s)
Bergeon Burns, CM; Rosvall, KA; Hahn, TP; Demas, GE; Ketterson, ED
Year
2014
Is Peer Reviewed?
Yes
Journal
Hormones and Behavior
ISSN:
0018-506X
EISSN:
1095-6867
Volume
65
Issue
2
Page Numbers
179-187
Language
English
PMID
24140626
DOI
10.1016/j.yhbeh.2013.10.006
Web of Science Id
WOS:000332056800013
Abstract
Gonadal steroids are important mediators of traits relevant to fitness, and thus may be targets of selection. However, more knowledge is needed about sources of variation along the endocrine axes that may contribute to functional variation in steroid levels. In a controlled captive environment, we studied males of two closely related subspecies of the dark-eyed junco (Junco hyemalis) that differ in testosterone-related phenotype, asking whether they also differ in testosterone (T), and assessing the contribution of the sequential links of the hypothalamic-pituitary-gonadal axis. When males of both subspecies were challenged with gonadotropin-releasing hormone (GnRH), they were similar in circulating luteinizing hormone (LH) and T responses. When challenged with exogenous LH, they again produced levels of T similar to one another, and to the levels produced in response to GnRH. However, the smaller, less ornamented, and less aggressive subspecies had greater abundance of mRNA for LH receptor in the testes and for androgen receptor in the rostral hypothalamus, suggesting potential differences in regulatory feedback. We suggest that circulating hormone levels may be less prone to evolutionary change than the responsiveness of individual hormone targets. Among individuals, T titers were highly repeatable whether males were challenged with GnRH or with LH, but LH produced in response to GnRH did not covary with T produced in response to LH. Testis mass, but not LH receptor transcript abundance, predicted individual variation in T responses. These data implicate the gonad, but not the pituitary, as an important source of individual variation in T production.
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