Soluble epoxide hydrolase inhibitor can protect the femoral head against tobacco smoke exposure-induced osteonecrosis in spontaneously hypertensive rats

Toxicology. 2022 Jan 15:465:153045. doi: 10.1016/j.tox.2021.153045. Epub 2021 Nov 18.

Abstract

Exposure to tobacco smoke (TS) has been considered a risk factor for osteonecrosis of the femoral head (ONFH). Soluble epoxide hydrolase inhibitors (sEHIs) have been found to reduce inflammation and oxidative stress in a variety of pathologies. This study was designed to assess the effect of sEHI on the development of ONFH phenotypes induced by TS exposure in spontaneously hypertensive (SH) rats. SH and normotensive Wistar Kyoto (WKY) rats were exposed to filtered air (FA) or TS (80 mg/m3 particulate concentration) 6 h/day, 3 days/week for 8 weeks. During this period, sEHI was delivered through drinking water at a concentration of 6 mg/L. Histology, immunohistochemistry, and micro-CT morphometry were performed for phenotypic evaluation. As results, TS exposure induced significant increases in adipocyte area, bone specific surface (BS/BV), and trabecular separation (Tb.SP), as well as significant decreases in bone mineral density (BMD), percent trabecular area (Tb.Ar), HIF-1a expression, bone volume fraction (BV/TV), trabecular numbers (Tb.N), and trabecular thickness (Tb.Th) in both SH and WKY rats. However, the protective effects of sEHI were mainly observed in TS-exposed SH rats, specifically in the density of osteocytes, BMD, Tb.Ar, HIF-1a expression, BV/TV, BS/BV, Tb.N, and Tb.SP. Our study confirms that TS exposure can induce ONFH especially in SH rats, and suggests that sEHI therapy may protect against TS exposure-induced osteonecrotic changes in the femoral head.

Keywords: Osteonecrosis the femoral head; Soluble epoxide hydrolase inhibitors; Spontaneously hypertensive rats; Tobacco smoke.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Disease Models, Animal
  • Enzyme Inhibitors / pharmacology*
  • Epoxide Hydrolases / antagonists & inhibitors*
  • Epoxide Hydrolases / metabolism
  • Femur Head / drug effects*
  • Femur Head / enzymology
  • Femur Head / pathology
  • Femur Head Necrosis / enzymology
  • Femur Head Necrosis / etiology
  • Femur Head Necrosis / pathology
  • Femur Head Necrosis / prevention & control*
  • Hypertension / complications*
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism
  • Male
  • Nicotiana*
  • Osteocytes / drug effects*
  • Osteocytes / enzymology
  • Osteocytes / pathology
  • Phenylurea Compounds / pharmacology*
  • Piperidines / pharmacology*
  • Rats
  • Rats, Inbred SHR
  • Rats, Inbred WKY
  • Smoke*
  • Vascular Endothelial Growth Factor A / metabolism

Substances

  • 1-trifluoromethoxyphenyl-3-(1-propionylpiperidine-4-yl)urea
  • Enzyme Inhibitors
  • Hif1a protein, rat
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Phenylurea Compounds
  • Piperidines
  • Smoke
  • Vascular Endothelial Growth Factor A
  • vascular endothelial growth factor A, rat
  • Epoxide Hydrolases
  • EPHX2 protein, rat