Prostaglandin F<sub>2α</sub> exacerbates ovalbumin-induced chronic pneumonia and attenuates depression in mice

Prolonged lung inflammation leads to the development of asthma and approximately 27.8% of adult patients with asthma suffer from depression. We examined the effect of the prostaglandin F<sub>2α</sub> (PGF<sub>2α</sub>) receptor (FP receptor) agonist, fluprostenol, on ovalbumin (OVA)-induced asthma and asthma-related depression in mice. Repeated fluprostenol+OVA administration increased OVA-induced inflammatory cell infiltration and mRNA expression of inflammatory mediators in the lung. In contrast, in the tail suspension and forced swim tests, fluprostenol+OVA administration significantly reduced the immobile time compared with saline+OVA-administered mice. Fluprostenol+OVA treatment significantly upregulated serotonin 1A receptor and tryptophan hydroxylase in the hippocampus compared with the expression in saline+OVA mice. These results suggest that PGF receptor (FP receptor) stimulation promotes lung inflammation but attenuates depression, possibly via the serotonin pathway.

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Publication Details

Journal
Journal of Veterinary Medical Science
Published
2025-01-01
DOI
https://doi.org/10.1292/jvms.25-0196
Primary Topic
Pneumonia and Respiratory Infections
Type
article
Field-Weighted Citation Impact
0.00

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article

Prostaglandin F2α exacerbates ovalbumin-induced chronic pneumonia and attenuates depression in mice

Satoshi Inoue, Atsushi Fujimura, Hiroshi Satoh, Toko Maehara et al.
Journal of Veterinary Medical Science
Pneumonia and Respiratory Infections
article

Prostaglandin F2α exacerbates ovalbumin-induced chronic pneumonia and attenuates depression in mice

Satoshi Inoue, Atsushi Fujimura, Hiroshi Satoh, Toko Maehara, Rin SEGAWA
article en

Abstract

Prolonged lung inflammation leads to the development of asthma and approximately 27.8% of adult patients with asthma suffer from depression. We examined the effect of the prostaglandin F<sub>2α</sub> (PGF<sub>2α</sub>) receptor (FP receptor) agonist, fluprostenol, on ovalbumin (OVA)-induced asthma and asthma-related depression in mice. Repeated fluprostenol+OVA administration increased OVA-induced inflammatory cell infiltration and mRNA expression of inflammatory mediators in the lung. In contrast, in the tail suspension and forced swim tests, fluprostenol+OVA administration significantly reduced the immobile time compared with saline+OVA-administered mice. Fluprostenol+OVA treatment significantly upregulated serotonin 1A receptor and tryptophan hydroxylase in the hippocampus compared with the expression in saline+OVA mice. These results suggest that PGF receptor (FP receptor) stimulation promotes lung inflammation but attenuates depression, possibly via the serotonin pathway.

Journal of Veterinary Medical ScienceVol. 87(10)
Iwate University (JP)
Ono Medical Research Foundation, Japan Society for the Promotion of Science
Good health and well-being
Openalex Percentile: Top 73%
Pneumonia and Respiratory Infections
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