Evidence map›Paper›PMID 36990664›Full record

ArticlePsychiatry investigation2023

Atomoxetine and Fluoxetine Activate AMPK-ACC-CPT1 Pathway in Human SH-SY5Y and U-87 MG Cells.

Songhee Jeon, Jeong-Eun Park, Young Ho Do, Renata Santos, Seong Mi Lee, Bung-Nyun Kim, Jae Hoon Cheong, Yeni Kim

Open access · diamondAbstract read
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Article in Psychiatry investigation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 6 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 6 institutions in 2 countries.

Songhee JeonCenter for Glocal Future Biomedical Scientists at Chonnam National University, Gwangju, Republic of Korea.
Jeong-Eun ParkDepartment of Otorhinolaryngology Head and Neck Surgery, Dongtan Sacred Heart Hospital, Hallym University College of Medicine, Hwaseong, Republic of Korea.
Young Ho DoDepartment of Child and Adolescent Psychiatry, National Center for Mental Health, Seoul, Republic of Korea.
Renata SantosINSERM U1266, Institute of Psychiatry and Neuroscience of Paris (IPNP), Laboratory of Dynamics of Neuronal Structure in Health and Disease, Université Paris Cité, Paris, France.
Seong Mi LeeDepartment of Child and Adolescent Psychiatry, National Center for Mental Health, Seoul, Republic of Korea.
Bung-Nyun KimDivision of Child & Adolescent Psychiatry, Department of Psychiatry and Institute of Human Behavioral Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
Jae Hoon CheongInstitute for New Drug Development, School of Pharmacy, Jeonbuk National University, Jeonju, Republic of Korea.
Yeni KimDepartment of Child and Adolescent Psychiatry, National Center for Mental Health, Seoul, Republic of Korea.
Chonnam National University · KRDongguk University · KRHallym University Dongtan Sacred Heart Hospital · KRInserm · FRJeonbuk National University · KRSeoul National University · KR

Funding

Dongguk UniversityKorea Health Industry Development InstituteMinistry of Health and Welfare A120013Ministry of Health and Welfare HI18C1077National Research Foundation of Korea 2018R1A2B003640
6 · The paper itself

Abstract

objectiveAtomoxetine and fluoxetine are psychopharmacologic agents associated with loss of appetite and weight. Adenosine monophosphate-activated protein kinase (AMPK) is the cellular energy sensor that regulate metabolism and energy, being activated by fasting and inhibited by feeding in the hypothalamus.

methodsHuman brain cell lines (SH-SY5Y and U-87 MG cells) were used to study the outcome of atomoxetine and fluoxetine treatment in the activity of AMPK-acetyl-CoA carboxylase (ACC)- carnitine palmitoyl transferase 1 (CPT1) pathway and upstream regulation by calcium/calmodulin-dependent kinase kinase β (CaMKKβ) using immunoblotting and CPT1 enzymatic activity measures.

resultsPhosphorylation of AMPK and ACC increased significantly after atomoxetine and fluoxetine treatment in the first 30-60 minutes of treatment in the two cell lines. Activation of AMPK and inhibition of ACC was associated with an increase by 5-fold of mitochondrial CPT1 activity. Although the neuronal isoform CPT1C could be detected by immunoblotting, activity was not changed by the drug treatments. In addition, the increase in phospho-AMPK and phospho-ACC expression induced by atomoxetine was abolished by treatment with STO-609, a CaMKKβ inhibitor, indicating that AMPK-ACC-CPT1 pathway is activated through CaMKKβ phosphorylation.

conclusionThese findings indicate that at the cellular level atomoxetine and fluoxetine treatments may activate AMPK-ACC-CPT1 pathways through CaMKKβ in human SH-SY5Y and U-87 MG cells.

Indexed as

Adenosine monophosphate-activated protein kinaseAtomoxetineCalcium/calmodulin-dependent kinase kinase β.Carnitine palmitoyl transferaseFluoxetine

Identifiers

PMID36990664
PMCPMC10064201
OpenAlexW4353031513

What OpenQuestion holds

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Registered trials

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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.