Evidence map›Paper›PMID 40377688›Full record

ArticlePsychopharmacology2025

The interaction between finasteride and corticosterone levels: implications for depression-, and anxiety-like behavior and hippocampal synaptic plasticity in male rats.

Jose Nayana, Byrathnahalli S Shankaranarayana Rao, Bettadapura N Srikumar

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Article in Psychopharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Jose NayanaDepartment of Neurophysiology, National Institute of Mental Health and Neuro Sciences (NIMHANS), Hosur Road, Bengaluru, 560029, India.ORCID http://orcid.org/0000-0002-4772-5354
Byrathnahalli S Shankaranarayana RaoDepartment of Neurophysiology, National Institute of Mental Health and Neuro Sciences (NIMHANS), Hosur Road, Bengaluru, 560029, India.ORCID http://orcid.org/0000-0002-8323-8211
Bettadapura N SrikumarDepartment of Neurophysiology, National Institute of Mental Health and Neuro Sciences (NIMHANS), Hosur Road, Bengaluru, 560029, India. kumarasri@nimhans.ac.in.ORCID http://orcid.org/0000-0001-9162-0990

Funding

Human Resource Development Group 09/490(0102)/2019-EMR-INIMHANS NIMH/Proj/BNS/00555Science and Engineering Research Board CRG/2020/005229; ECR/2015/000545
6 · The paper itself

Abstract

rationaleFinasteride is FDA-approved for the treatment of hair loss and in older men for benign prostatic hyperplasia. However, some patients treated with finasteride reported suicidal ideation, depression, and anxiety. The neurobiological mechanisms underlying this are not clearly understood. Previously, we showed that short-term finasteride administration results in depression- and anxiety-like behaviour. Since finasteride treatment is long-term in the clinic, we examine the effects of chronic finasteride administration in the current study.

objectiveThis study aims to understand the behavioral, cellular, and molecular changes in male rats following 21 days of finasteride (3 mg, 10 mg, and 30 mg/Kg) administration.

methodsDepression-like behavior was evaluated using forced swim (FST), sucrose preference (SPT), and splash tests. Anxiety-like behavior was assessed using elevated plus maze (EPM), open field (OFT), light-dark (LDT), Vogel's conflict (VCT), and home cage emergence (HCET), and depression-related anxiety in novelty-suppressed feeding task (NSFT) tests. Hippocampal synaptic plasticity was assessed by field excitatory post-synaptic potentials (fEPSP) recordings in the Schaffer-collateral-CA1 synapses, and plasma corticosterone levels were estimated using ELISA.

resultsChronic finasteride administration induced depression-like and anxiety-like behavior in SPT and EPM, respectively, but not in the other paradigms. There was a modest decrease in long-term potentiation in the hippocampus. Interestingly, there was an increase in the plasma corticosterone levels with 6 days of finasteride administration, but not after 14 or 21 days of administration.

conclusionsChronic administration of finasteride did not induce a robust depression- and anxiety-like behavior and modestly affected synaptic plasticity. This could be potentially because of the adaptive response observed in the plasma corticosterone levels.

Indexed as

5-alpha Reductase InhibitorsAnxietyCorticosteroneDepressionFinasterideHippocampusNeuronal PlasticityAnimalsBehavior, AnimalDisease Models, AnimalDose-Response Relationship, DrugMaleRatsRats, Sprague-Dawley5-alpha Reductase InhibitorsCorticosteroneFinasteride5α-reductase inhibitorAnxietyCorticosteroneDepressionSynaptic plasticity

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.