# Finasteride withdrawal induces anxiety‐like behavior and novelty avoidance in adult male rats

**Authors:** Lucia Cioffi, Silvia Diviccaro, Gabriela Chrostek, Francesco Paolo Ulloa Severino, Silvia Giatti, Diego Scheggia, Roberto Cosimo Melcangi

PMC · DOI: 10.1111/jne.70150 · Journal of Neuroendocrinology · 2026-02-27

## TL;DR

Finasteride withdrawal in rats causes anxiety-like behavior and avoidance of new experiences, aligning with reported human side effects.

## Contribution

The study reveals delayed behavioral effects of finasteride withdrawal in rats, supporting the relevance of post-finasteride syndrome.

## Key findings

- Finasteride withdrawal caused anxiety-like behavior and novelty avoidance in rats.
- Behavioral changes were more pronounced after drug discontinuation than during treatment.
- Results align with clinical reports of post-finasteride syndrome in humans.

## Abstract

Finasteride, an inhibitor of the enzyme 5alpha‐reductase, prescribed for benign prostatic hyperplasia and androgenetic alopecia, induces a wide variety of side effects during treatment and upon withdrawal, like sexual dysfunction and cognitive and psychological disorders, inducing the so‐called post‐finasteride syndrome (PFS). Here, we explored the behavioral effects of this drug in adult male rats after subchronic finasteride treatment (20 days) and at drug discontinuation (1 month). We employed multiple behavioral paradigms, including the open field test and elevated plus maze to assess locomotor activity and anxiety, and a novelty‐seeking test to evaluate exploratory behavior and approach‐avoidance tendencies. Our results revealed a dichotomy between immediate and delayed finasteride effects. While effects after subchronic treatment were mild, significant behavioral alterations emerged at the withdrawal. In particular, pronounced hyperactivity, decreased center exploration in the open field, and marked avoidance of novel stimuli, collectively indicating an anxiety‐like behavioral phenotype, were revealed. These results, showing a picture of increased vulnerability, are in agreement with clinical reports in PFS, highlighting the relevance of our model for this condition. Moreover, the data here described strengthen the importance of monitoring patients not only during treatment but also following discontinuation of finasteride therapy.

## Linked entities

- **Chemicals:** finasteride (PubChem CID 57363)
- **Diseases:** benign prostatic hyperplasia (MONDO:0010811), androgenetic alopecia (MONDO:0005339)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Slc6a3 (solute carrier family 6 member 3) [NCBI Gene 24898] {aka Dat1}
- **Diseases:** sleep problems (MESH:D012893), loss of (MESH:D016388), neurodegenerative and psychiatric disorders (MESH:D019636), Anxiety (MESH:D001007), sexual dysfunction (MESH:D012735), behavioral alterations (MESH:D001523), confusion (MESH:D003221), AGA (MESH:D000505), difficulty in concentration (MESH:C567712), hyperactivity (MESH:D006948), BPH (MESH:D011470), PFS (MESH:D000094025), neuropsychiatric (MESH:C000631768), mental cloudiness (MESH:C563262), agitation (MESH:D011595), Depression (MESH:D003866), brain fog (MESH:D005222), cognitive alterations (MESH:D003072), panic attacks (MESH:D016584)
- **Chemicals:** 5alpha-androstane-3alpha,17beta-diol (MESH:D015113), T (MESH:D014316), testosterone (MESH:D013739), ethanol (MESH:D000431), dihydroprogesterone (MESH:D004092), PROG (MESH:D011374), Finasteride (MESH:D018120), 5alpha-reduced (-), corn oil (MESH:D003314), allopregnanolone (MESH:D011280), steroid (MESH:D013256), dihydrotestosterone (MESH:D013196)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12949371/full.md

## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12949371/full.md

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Source: https://tomesphere.com/paper/PMC12949371