Dietary Phytoestrogens Ameliorate Hydrochloric Acid-Induced Chronic Lung Injury and Pulmonary Fibrosis in Mice

Nutrients. 2021 Oct 14;13(10):3599. doi: 10.3390/nu13103599.

Abstract

We previously reported that female mice exhibit protection against chemically induced pulmonary fibrosis and suggested a potential role of estrogen. Phytoestrogens act, at least in part, via stimulation of estrogen receptors; furthermore, compared to residents of Western countries, residents of East Asian countries consume higher amounts of phytoestrogens and exhibit lower rates of pulmonary fibrosis. Therefore, we tested the hypothesis that dietary phytoestrogens ameliorate the severity of experimentally induced pulmonary fibrosis. Male mice placed on either regular soybean diet or phytoestrogen-free diet were instilled with 0.1 N HCl to provoke pulmonary fibrosis. Thirty days later, lung mechanics were measured as indices of lung function and bronchoalveolar lavage fluid (BALF) and lung tissue were analyzed for biomarkers of fibrosis. Mice on phytoestrogen-free diet demonstrated increased mortality and stronger signs of chronic lung injury and pulmonary fibrosis, as reflected in the expression of collagen, extracellular matrix deposition, histology, and lung mechanics, compared to mice on regular diet. We conclude that dietary phytoestrogens play an important role in the pathogenesis of pulmonary fibrosis and suggest that phytoestrogens (e.g., genistein) may be useful as part of a therapeutic regimen against hydrochloric acid-induced lung fibrosis and chronic lung dysfunction.

Keywords: gender differences; genistein; hydrochloric acid; idiopathic pulmonary fibrosis (IPF); isoflavones; mice; phytoestrogens.

MeSH terms

  • Animals
  • Chronic Disease
  • Diet*
  • Extracellular Matrix Proteins / metabolism
  • Hydrochloric Acid
  • Inflammation / pathology
  • Leukocyte Count
  • Lung / physiopathology
  • Lung Injury / chemically induced*
  • Lung Injury / complications
  • Lung Injury / drug therapy*
  • Lung Injury / mortality
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Models, Biological
  • Phytoestrogens / pharmacology
  • Phytoestrogens / therapeutic use*
  • Pulmonary Fibrosis / complications
  • Pulmonary Fibrosis / drug therapy*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Signal Transduction
  • Transforming Growth Factor beta / metabolism

Substances

  • Extracellular Matrix Proteins
  • Phytoestrogens
  • RNA, Messenger
  • Transforming Growth Factor beta
  • Hydrochloric Acid