Silicosis decreases bone mineral density in rats

Toxicol Appl Pharmacol. 2018 Jun 1:348:117-122. doi: 10.1016/j.taap.2018.04.023. Epub 2018 Apr 19.

Abstract

Silicosis is the most common occupational lung disease in China, and is associated with a variety of complications, many of which are poorly understood. For example, recent data indicate that silicosis associates with the development of osteopenia, and in some cases this bone loss is severe, meeting criteria for osteoporosis. Although many factors are likely to contribute to this relationship, including a sedentary lifestyle in patients with advanced silicotic lung disease, we hypothesized that silica might directly reduce bone mineral density. In the present study, six Wistar rats were exposed to silica for 24 weeks in order to induce pulmonary silicosis and examine the relationship to bone mineral density. As expected, all rats exposed to silica developed severe pulmonary fibrosis, as manifested by the formation of innumerable silicotic nodules and the deposition of large amounts of interstitial collagen. Moreover, micro-CT results showed that bone mineral density (BMD) was also significantly reduced in rats exposed to silica when compared control animals and this associated with a modest reduction in serum calcium and 25-hydroxyvitamin D levels. In addition, we found that decreased BMD was also linked to increased osteoclast activity as well as fibrosis-like changes, and to the deposition of silica within bone marrow. In summary, our findings support the hypothesis that silicosis reduces bone mineral density and provide support for ongoing investigations into the mechanisms causing osteopenia in silicosis patients.

Keywords: Bone mineral density; Osteoclast; Osteoporosis; Silicosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Density*
  • Calcium / blood
  • Collagen / metabolism
  • Disease Models, Animal
  • Femur / diagnostic imaging
  • Femur / pathology*
  • Lung / metabolism
  • Lung / pathology*
  • Male
  • Osteoclasts / drug effects
  • Osteoclasts / metabolism
  • Osteoclasts / pathology
  • Osteoporosis / blood
  • Osteoporosis / chemically induced*
  • Osteoporosis / diagnostic imaging
  • Osteoporosis / pathology
  • Pulmonary Fibrosis / chemically induced*
  • Pulmonary Fibrosis / metabolism
  • Pulmonary Fibrosis / pathology
  • Rats, Wistar
  • Risk Assessment
  • Severity of Illness Index
  • Silicon Dioxide*
  • Silicosis / etiology*
  • Silicosis / metabolism
  • Silicosis / pathology
  • Tibia / diagnostic imaging
  • Tibia / pathology*
  • Time Factors
  • Vitamin D / analogs & derivatives
  • Vitamin D / blood
  • X-Ray Microtomography

Substances

  • Vitamin D
  • Silicon Dioxide
  • Collagen
  • 25-hydroxyvitamin D
  • Calcium