Cited by 21Endometriosis Research and TreatmentPain Mechanisms and TreatmentsNeuropeptides and Animal Physiology

Endometriosis Is Associated With a Shift in MU Opioid and NMDA Receptor Expression in the Brain Periaqueductal Gray

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Torres-Reverón, Annelyn, Palermo, Karylane, Hernández-López, Anixa, Hernández, Siomara, Cruz, Myrella L., Thompson, Kenira J., Flores, Idhaliz, Appleyard, Caroline B.·2016·Reproductive Sciences

Abstract

Studies have examined how endometriosis interacts with the nervous system, but little attention has been paid to opioidergic systems, which are relevant to pain signaling. We used the autotransplantation rat model of endometriosis and allowed to progress for 60 days. The brain was collected and examined for changes in endogenous opioid peptides, mu opioid receptors (MORs), and the N-methyl-d-aspartate subunit receptor (NR1) in the periaqueductal gray (PAG), since both of these receptors can regulate PAG activity. No changes in endogenous opioid peptides in met- and leu-enkephalin or β-endorphin levels were observed within the PAG. However, MOR immunoreactivity was significantly decreased in the ventral PAG in the endometriosis group. Endometriosis reduced by 20% the number of neuronal profiles expressing MOR and reduced by 40% the NR1 profiles. Our results suggest that endometriosis is associated with subtle variations in opioidergic and glutamatergic activity within the PAG, which may have implications for pain processing.

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Crossref · 10.1177/1933719116630410

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  • Experimental induction of endometriosis in rats reduced opioid receptor expression by 20%, suggesting that the presence of endometriosis interferes with analgesia.

    “Experimental induction of endometriosis in rats reduced opioid receptor expression by 20%, suggesting that the presence of endometriosis interferes with analgesia (Torres‐Reverón et al., 2016).”

    From Endometriosis and polycystic ovary syndrome are diametric disorders (2021) · cites this paper as Torres‐Reverón et al., 2016

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Authors
Torres-Reverón, A., Palermo, K., Hernández-López, A., Hernández, S., Cruz, M. L., Thompson, K. J., Flores, I., & Appleyard, C. B.
Affiliations
Ponce Health Sciences University (PR)
Corresponding author
Torres-Reverón, Annelyn
Venue
Reproductive Sciences
Published
2016-09
Volume
23
Issue
9
Pages
1158-1167
ISSN
  • 1933-7191 (ISSN-L)
  • 1933-7205
OpenAlex
W2340224778
Cited by
21
References
9
Citations by year
2026: 1 · 2025: 3 · 2024: 2 · 2023: 2 · 2022: 2 · 2021: 1 · 2020: 3 · 2018: 3 · 2017: 4
FWCI
3.10
Type
journal article
Language
en
Open access
Locations
  • Reproductive Sciences (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institute of General Medical Sciences (R25GM082406)
  • National Institute on Minority Health and Health Disparities (G12MD007579, U54MD007579)
  • National Center for Complementary and Integrative Health (K07AT008027, R15AT006373)
Topics
  • Health Sciences › Medicine › Reproductive Medicine › Endometriosis Research and Treatment
  • Health Sciences › Medicine › Physiology › Pain Mechanisms and Treatments
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
Keywords
endometriosis, mu-opioid receptor, NMDA receptor, NR1 subunit, periaqueductal gray, endogenous opioids, enkephalin, beta-endorphin, pain processing, glutamatergic activity
MeSH terms
Animals, beta-Endorphin, Endometriosis, Enkephalin, Leucine, Enkephalin, Methionine, Female, Periaqueductal Gray, Receptors, N-Methyl-D-Aspartate, Rats, Sprague-Dawley, Receptors, Opioid, mu, Rats

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