Evidence map›Paper›PMID 36433759›Full record

ArticleThe international journal of neuropsychopharmacology2023

Antidepressant and Neuroprotective Effects of 3-Hydroxy Paroxetine, an Analog of Paroxetine in Rats.

Pedro Efraín Hernández-Arrambide, Alan Carrasco-Carballo, Irving Parra, Delfino Chamorro-Arenas, Isabel Martínez, Félix Luna, Fernando Sartillo-Piscil, Yousef Tizabi, Liliana Mendieta

Open access · goldAbstract read
In one paragraph

Article in The international journal of neuropsychopharmacology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 61% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
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

9 authors at 2 institutions in 2 countries.

Pedro Efraín Hernández-ArrambideLaboratorio de Neuroquímica, Facultad de Ciencias Químicas Benemérita Universidad Autónoma de Puebla, Puebla, Mexico.
Alan Carrasco-CarballoLaboratorio de Elucidación y Síntesis en Química Orgánica, Facultad de Ciencias Químicas, Benemérita Universidad Autónoma de Puebla, Puebla, Mexico.
Irving ParraLaboratorio de Neuroquímica, Facultad de Ciencias Químicas Benemérita Universidad Autónoma de Puebla, Puebla, Mexico.
Delfino Chamorro-ArenasLaboratorio de Síntesis Orgánica, Facultad de Ciencias Químicas, Benemérita Universidad Autónoma de Puebla, Puebla, Mexico.
Isabel MartínezLaboratorio de Neuroquímica, Facultad de Ciencias Químicas Benemérita Universidad Autónoma de Puebla, Puebla, Mexico.
Félix LunaLaboratorio de Neuroendocrinología, Facultad de Ciencias Químicas, Benemérita Universidad Autónoma de Puebla, Puebla, Mexico.
Fernando Sartillo-PiscilLaboratorio de Síntesis Orgánica, Facultad de Ciencias Químicas, Benemérita Universidad Autónoma de Puebla, Puebla, Mexico.
Yousef TizabiDepartment of Pharmacology, Howard University College of Medicine, Washington DC, USA.
Liliana MendietaLaboratorio de Neuroquímica, Facultad de Ciencias Químicas Benemérita Universidad Autónoma de Puebla, Puebla, Mexico.ORCID 0000-0001-6049-2770
Benemérita Universidad Autónoma de Puebla · MXHoward University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundParoxetine (PX) is a widely used antidepressant with side effects such as weakness, dizziness, and trouble sleeping. In search of novel compounds with better efficacy and fewer side effects, we synthesized 3HPX, a hydroxylated analog of PX, and compared the 2 in silico for their pharmacokinetic and binding properties and in vivo for their antidepressant and potential neuroprotective effects.

methodsIn silico studies compared pharmacological properties as well as interactions of PX and 3HPX with the serotonin transporter. In vivo studies utilized an animal model of comorbid depression-Parkinson disease. Adult male Wistar rats were injected (sterotaxically) with lipopolysaccharide in the striatum (unilaterally), followed by 14 days of once-daily injections (i.p.) of 10 mg/kg PX or 3HPX. Animals were tested for motor asymmetry and locomotor activity as well as indices of anhedonia and helplessness using sucrose preference and forced swim tests, respectively. Brains of these animals were collected after the last test, and tyrosine hydroxylase-positive neurons in substantia nigra pars compacta and Iba-1-positive stained microglia in ipsilateral striatum were measured.

resultsIn silico findings indicated that 3HPX could bind stronger to serotonin transporter and also have a better clearance and hence less toxicity compared with PX. In vivo results revealed a more effective reversal of immobility in the swim test, substantial increase in tyrosine hydroxylase-positive cells in the substantia nigra pars compacta, and more ramified Iba-1+ cells by 3HPX compared with PX.

conclusionThe findings suggest superior effectiveness of 3HPX as an antidepressant and neuroprotectant compared with PX and hence potential utility in Parkinson disease depression co-morbidity.

Indexed as

Neuroprotective AgentsParkinson DiseaseAnimalsAntidepressive AgentsDisease Models, AnimalMaleParoxetineRatsRats, WistarSerotonin Plasma Membrane Transport ProteinsSubstantia NigraTyrosine 3-MonooxygenaseAntidepressive AgentsNeuroprotective AgentsParoxetineSerotonin Plasma Membrane Transport ProteinsTyrosine 3-Monooxygenasedepressionlipopolysaccharidemotor activityneuroinflammationParkinson’s diseaseParoxetine

Identifiers

PMID36433759
PMCPMC10032298
OpenAlexW4310297834

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.