Identification of neurokinin B-expressing neurons as an highly estrogen-receptive, sexually dimorphic cell group in the ovine arcuate nucleus

被引:120
作者
Goubillon, ML
Forsdike, RA
Robinson, JE
Ciofi, P
Caraty, A
Herbison, AE [1 ]
机构
[1] Babraham Inst, Neuroendocrinol Lab, Cambridge CB2 4AT, England
[2] Inst Francois Magendie, INSERM, U378, F-33077 Bordeaux, France
[3] INRA, Physiol Reprod Stn, F-37380 Nouzilly, France
关键词
D O I
10.1210/en.141.11.4218
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Studies were undertaken to examine the hypothesis that neurons expressing neurokinin B (NKB) may represent an estrogen-receptive input to GnRH neurons in the sheep. Cells immunoreactive for NKB were located almost exclusively within the arcuate nucleus of the ovine hypothalamus. Dual labeling experiments revealed that essentially all NKB neurons (97%) were immunoreactive for estrogen receptor ru and that NKB-immunoreactive fibers were found in close proximity to approximately 40% of GnRH neurons located in the rostral preoptic area as well as intermingled with GnRH fibers in the median eminence. The analysis of male and female brains revealed a marked female-dominant sex difference in the numbers of NKB neurons, and sections obtained from in utero androgen-treated females indicated that this sex difference resulted from an organizational influence of testosterone during neural development. Tn adult ovariectomized awes, in situ hybridization studies failed to detect any significant effect of 8- to 26-h exposure of estrogen on cellular NKB messenger RNA levels. Together, these studies identify the first sexually differentiated neuronal cell population in the ovine hypothalamus and, remarkably, show that essentially all of these female-dominant NKB neurons express estrogen receptors. Although these neurons may be involved in any number of steroid-dependent, sexually differentiated functions in the sheep, the neuroanatomical evidence for potential NKB inputs to GnRH neurons suggests a role for this novel population in the regulation of reproductive function.
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页码:4218 / 4225
页数:8
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