Evidence map›Paper›PMID 40498164›Full record

ArticleMolecular biology reports2025

Antidepressant effects of fluoxetine: upregulation of connexin 36 and 43 in the hippocampus, prefrontal cortex, and amygdala.

Saeidreza Hosseinirezaabad, Sahel Motaghi, Manijeh Dogani, Masoud Teimouri

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Article in Molecular biology reports, 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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1 · What the graph read from it

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3 · Its place in the literature

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2 citing papers in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Saeidreza HosseinirezaabadDepartment of Basic Sciences, Faculty of Veterinary Medicine, Shahid Bahonar University of Kerman, Kerman, Iran.
Sahel MotaghiDepartment of Basic Sciences, Faculty of Veterinary Medicine, Shahid Bahonar University of Kerman, Kerman, Iran. sahelmotaghi@uk.ac.ir.ORCID http://orcid.org/0000-0002-2159-6195
Manijeh DoganiDepartment of Biology, Faculty of Sciences, Shahid Bahonar University of Kerman, Kerman, Iran.
Masoud TeimouriDepartment of Basic Sciences, Faculty of Veterinary Medicine, Shahid Bahonar University of Kerman, Kerman, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMajor depressive disorder is a prevalent and debilitating psychiatric condition. Understanding its molecular mechanisms can aid in the development of more effective treatments. Gap junctions (GJs), composed of connexin (CX) proteins, facilitate direct intercellular communication and have been implicated in the pathophysiology of depression. In particular, connexin 36 (CX36) and connexin 43 (CX43) play key roles in neuronal and glial interactions, respectively. This study aimed to investigate whether fluoxetine modulates the expression of CX36 and CX43 in specific limbic regions, including the ventral hippocampus (v Hip), medial prefrontal cortex (m PC), and basolateral amygdala (BLA) of rats subjected to chronic unpredictable stress (CUS). METHODS AND

resultsAdult male Wistar rats (n = 7 per group) were assigned to control, CUS, and CUS + fluoxetine groups. Our results revealed that CX36 expression was significantly reduced in the v Hip and m PC of CUS rats (P < 0.05), while CX43 expression was significantly lower in all examined brain regions compared to controls (P < 0.05, P < 0.001). Fluoxetine administration significantly upregulated both CX36 and CX43 expression across all regions compared to the CUS group (P < 0.05).

conclusionsThese findings suggest that fluoxetine may exert part of its antidepressant effects by modulating gap junction communication, highlighting a potential novel mechanism for fluoxetine action in depression.

Indexed as

Antidepressive AgentsConnexin 43ConnexinsFluoxetineAmygdalaAnimalsDepressionGap Junction delta-2 ProteinGap JunctionsHippocampusMalePrefrontal CortexRatsRats, WistarStress, PsychologicalUp-RegulationAntidepressive AgentsConnexin 43ConnexinsFluoxetineGap Junction delta-2 ProteinConnexinDepressionFluoxetineStress

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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 Socratic graph.