4.2 Article

Androgen and estrogen (α) receptor localization on periaqueductal gray neurons projecting to the rostral ventromedial medulla in the male and female rat

期刊

JOURNAL OF CHEMICAL NEUROANATOMY
卷 36, 期 3-4, 页码 216-226

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jchemneu.2008.08.001

关键词

Gonadal steroid receptor; Hormone; Immunohistochemistry; Sex differences; Descending modulatory pathway; Pain; Antinociception

资金

  1. NIH [DA16272, P50 AR49555]

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The periaqueductal gray (PAG) is involved in many gonadal steroid-sensitive behaviors, including responsiveness to pain. The PAG projects to the rostral ventromedial medulla (RVM), comprising the primary circuit driving pain inhibition. Morphine administered systemically or directly into the PAG produces greater analgesia in male compared to female rats, while manipulation of gonadal hormones alters morphine potency in both sexes. It is unknown if these alterations are due to steroidal actions on PAG neurons projecting to the RVM. The expression of androgen (AR) and estrogen (ER alpha) receptors in the PAG of female rats and within this descending inhibitory pathway in both sexes is unknown. The present study used immunohistochemical techniques (1) to map the distribution of AR and ER alpha across the rostrocaudal axis of the PAG: and (2) to determine whether AR and/or ER alpha were colocalized on PAG neurons projecting to the RVM in male and female rats. AR and ER alpha immunoreactive neurons (AR-IR, ER alpha-IR) were densely distributed within the caudal PAG of male rats, with the majority localized in the lateral/ventrolateral PAG. Females had significantly fewer AR-IR neurons, while the quantity of ER alpha was comparable between the sexes. In both sexes, approximately 25-50% of AR-IR neurons and 20-50% of ER alpha-IR neurons were retrogradely labeled. This study provides direct evidence of the expression of steroid receptors in the PAG and the descending pathway driving pain inhibition in both male and female rats and may provide a mechanism whereby gonadal steroids modulate pain and morphine potency. (C) 2008 Elsevier B.V. All rights reserved.

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