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. Author manuscript; available in PMC: 2023 Nov 1.
Published in final edited form as: Toxicol Appl Pharmacol. 2022 Aug 23;454:116208. doi: 10.1016/j.taap.2022.116208

Table 1. Summary of effects of loss of FXR on NM-induced lung histopathology.

Sections were prepared 3 d, 14 d and 28 d after administration of PBS (CTL) or nitrogen mustard (NM) to male wild-type (WT) and FXR−/− mice. Histopathologic changes were quantified in H&E and Masson’s trichrome stained sections as described in the Materials and Methods. Values are mean ± SE, n = 4–5 mice/treatment/time point.

Histopathology WT
FXR−/−
CTL NM CTL NM
3 d Epithelial hyperplasia
Perivascular inflammation 1.4 ± 0.2 1.75 ± 0.3
Perivascular edema 1.4 ± 0.2 2.0 ± 0.0#
Neutrophils (alveolar) 1.0 ± 0.3 1.5 ± 0.3
Foamy alveolar macrophages
Alveolar wall thickening
Fibrosis 0.4 ± 0.2 0.5 ± 0.3
14 d Epithelial hyperplasia 0.2 ± 0.2 0.8 ± 0.2#
Perivascular inflammation 0.8 ± 0.2 1.2 ± 0.4
Perivascular edema 0.8 ± 0.4
Neutrophils (alveolar) 0.4 ± 0.2 0.8 ± 0.2
Foamy alveolar macrophages 1.4 ± 0.2 1.8 ± 0.2
Alveolar wall thickening 1.6 ± 0.7 3.8 ± 0.7#
Fibrosis 0.2 ± 0.2 1.0 ± 0.3 0.2 ± 0.2 2.2 ± 0.4*#
28 d Epithelial hyperplasia
Perivascular inflammation 1.0 ± 0.0 0.2 ± 0.0 1.0 ± 0.0
Perivascular edema
Neutrophils (alveolar)
Foamy alveolar macrophages 1.0 ± 0.0 1.0 ± 0.0
Alveolar wall thickening 1.0 ± 0.0 1.0 ± 0.0
Fibrosis 1.0 ± 0.0 0.4 ± 0.2 0.8 ± 0.2
*

Significantly different (p ≤ 0.05) from CTL mice.

#

Significantly different (p ≤ 0.05) from WT mice.