4.7 Article

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

Journal

NUTRIENTS
Volume 13, Issue 10, Pages -

Publisher

MDPI
DOI: 10.3390/nu13103599

Keywords

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

Funding

  1. Counter ACT Program, National Institute of Health Office of the Director (NIH OD)
  2. National Institute of Enivronmental Science (NIEHS) [UO1ES030674]

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This study found that dietary phytoestrogens can protect against experimentally induced pulmonary fibrosis. Compared to mice on a regular diet, mice on a phytoestrogen-free diet showed more severe signs of chronic lung injury and pulmonary fibrosis.
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.

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