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Estrogen receptors involvement in intervertebral discogenic pain of the elderly women: colocalization and correlation with the expression of Substance P in nucleus pulposus.

Abstract
Estrogenic modulation of pain is an exceedingly complex phenomenon. However, whether estrogen is involved in discogenic low back pain still remains unclear. Here, immunoreactivity staining technique was used to examine the expression level of the estrogen receptors (ERα and ERβ) and a pain related neuropeptide, Substance P in the lumbar intervertebral discs to analyze the relationship between the ERs and Substance P. Nucleus pulposus tissues of 23 elderly female patients were harvested during spinal surgeries and made to detect the immunoreactivity staining of ERα, ERβ and Substance P. The colocalization and intensities of ERs and Substance P were explored and evaluated respectively. The correlations between changes of ERα, ERβ and Substance P were also assessed.Our results revealed that Substance P colocalized with ERα and ERβ both in cytoplasm and nucleus of the nucleus pulposus cells. HSCORE analysis indicated that Substance P negatively correlated with both ERα and ERβ expression. Collectively, the crosstalk between ERs and Substance P might exist in the disc tissue. Estrogen-dependent pain mechanism might partly be mediated through ERs and Substance P in the nucleus pulposus of the elderly females. Estrogen and its receptors might be drug targets in discogenic low back pain diseases.
AuthorsXiao-Xing Song, Sheng Shi, Zhen Guo, Xin-Feng Li, Bu-Wei Yu
JournalOncotarget (Oncotarget) Vol. 8 Issue 24 Pg. 38136-38144 (Jun 13 2017) ISSN: 1949-2553 [Electronic] United States
PMID28430617 (Publication Type: Journal Article)
Chemical References
  • Receptors, Estrogen
  • Substance P
Topics
  • Aged
  • Female
  • Humans
  • Intervertebral Disc Degeneration (complications, metabolism)
  • Intervertebral Disc Displacement (complications, metabolism)
  • Low Back Pain (etiology, metabolism)
  • Nucleus Pulposus (metabolism)
  • Receptors, Estrogen (metabolism)
  • Substance P (metabolism)

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