Evidence map›Paper›PMID 29732526›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2018

Neuroprotective evidence of alpha-lipoic acid and desvenlafaxine on memory deficit in a neuroendocrine model of depression.

Caren Nádia Soares de Sousa, Lucas Nascimento Meneses, Germana Silva Vasconcelos, Ingridy da Silva Medeiros, Márcia Calheiros Chaves Silva, Fayçal Mouaffak, Oussama Kebir, Cláudio Manuel Gonçalves da Silva Leite, Manoel Cláudio Azevedo Patrocinio, Danielle Macedo and 1 more

Abstract read
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In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

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  9. Anxiolytic Effect of Carvedilol in Chronic Unpredictable Stress Model.Oxidative medicine and cellular longevity · 2022
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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

11 authors at 4 institutions in 2 countries.

Caren Nádia Soares de SousaNeuropsychopharmacology Laboratory, Drug Research and Development Center, Department of Physiology and Pharmacology, Faculty of Medicine, Federal University of Ceará, Cel. Nunes de Melo Street, 1127, Fortaleza, CE, 60431-270, Brazil.
Lucas Nascimento MenesesNeuropsychopharmacology Laboratory, Drug Research and Development Center, Department of Physiology and Pharmacology, Faculty of Medicine, Federal University of Ceará, Cel. Nunes de Melo Street, 1127, Fortaleza, CE, 60431-270, Brazil.
Germana Silva VasconcelosNeuropsychopharmacology Laboratory, Drug Research and Development Center, Department of Physiology and Pharmacology, Faculty of Medicine, Federal University of Ceará, Cel. Nunes de Melo Street, 1127, Fortaleza, CE, 60431-270, Brazil.
Ingridy da Silva MedeirosNeuropsychopharmacology Laboratory, Drug Research and Development Center, Department of Physiology and Pharmacology, Faculty of Medicine, Federal University of Ceará, Cel. Nunes de Melo Street, 1127, Fortaleza, CE, 60431-270, Brazil.
Márcia Calheiros Chaves SilvaNeuropsychopharmacology Laboratory, Drug Research and Development Center, Department of Physiology and Pharmacology, Faculty of Medicine, Federal University of Ceará, Cel. Nunes de Melo Street, 1127, Fortaleza, CE, 60431-270, Brazil.
Fayçal MouaffakDepartment of Seine Saint Denis, Ville Evrard Psychiatric Hospital, Paris, France.
Oussama KebirLaboratory of Pathophysiology of Psychiatric Diseases, Center for Psychiatry and Neurosciences, University Paris Descartes, Paris, France.
Cláudio Manuel Gonçalves da Silva LeiteDepartment of Physiology and Pharmacology, Faculty of Medicine, Federal University of Ceará, Fortaleza, Ceará, Brazil.
Manoel Cláudio Azevedo PatrocinioUniversity Center Christus-Unichristus, Fortaleza, Ceará, Brazil.
Danielle MacedoNeuropsychopharmacology Laboratory, Drug Research and Development Center, Department of Physiology and Pharmacology, Faculty of Medicine, Federal University of Ceará, Cel. Nunes de Melo Street, 1127, Fortaleza, CE, 60431-270, Brazil.
Silvânia Maria Mendes VasconcelosNeuropsychopharmacology Laboratory, Drug Research and Development Center, Department of Physiology and Pharmacology, Faculty of Medicine, Federal University of Ceará, Cel. Nunes de Melo Street, 1127, Fortaleza, CE, 60431-270, Brazil. silvania_vasconcelos@yahoo.com.br.
Universidade Federal do Ceará · BRHôpital de Ville-Évrard · FRInstitut de Psychiatrie et Neurosciences de Paris · FRUnichristus · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cognitive impairment is present in patients with depression. We hypothesized that alpha-lipoic acid (ALA) can reduce cognitive impairment, especially when combined to antidepressants. Female mice received vehicle or corticosterone (CORT) 20 mg/kg, s.c. for 14 days. From the 15th to 21st day, the animals were divided in groups: vehicle, CORT, CORT+desvenlafaxine (DVS) 10 or 20 mg/kg, ALA 100 or 200 mg/kg, DVS10+ALA100, DVS20+ALA100, DVS10+ALA200, or DVS20+ALA200. Tail suspension (TST), social interaction (SIT), novel object recognition (NOR), and Y-maze tests were conducted. Acetylcholinesterase activity (AChE) was measured in the prefrontal cortex (PFC), hippocampus (HC), and striatum (ST). CORT caused depressive-like behavior, impairment in SIT, and cognitive deficits. Alpha-lipoic acid and DVS, alone or combined, reversed CORT effect on TST. In the NOR, ALA200 alone, DVS10+ALA100, or DVS10+ALA200 reversed the deficits in short-term memory, while DVS20 alone or DVS20+ALA200 reversed the deficits in long-term memory. In the Y-maze test, ALA200 alone, DVS20+ALA100, or DVS20+ALA200 reversed the deficits caused by CORT in the working memory. CORT increased AChE in the PFC, HC, and ST. ALA200 alone or DVS20+ALA200 reversed this effect in the PFC, while DVS20 or DVS20+ALA100 reversed this effect in the HC. In the ST, DVS10 or 20, alone or combined, and ALA100 reversed the effects of CORT. These results suggest that DVS+ALA, by reversing CORT-induced memory and social deficits, seems to be a promising therapy for the treatment of depression and reversal of cognitive impairment observed in this disorder.

Indexed as

AcetylcholinesteraseAnimalsAntidepressive AgentsBehavior, AnimalBrainCorticosteroneDepressionDesvenlafaxine SuccinateDrug SynergismFemaleMemory DisordersMemory, Short-TermMiceNeuroprotective AgentsSocial BehaviorThioctic AcidAcetylcholinesteraseAntidepressive AgentsCorticosteroneDesvenlafaxine SuccinateNeuroprotective AgentsThioctic AcidAcetylcholinesteraseAlpha-lipoic acidCognitive impairmentCorticosterone model of depressionDesvenlafaxineMajor depressive disorder

Identifiers

PMID29732526
OpenAlexW2802507999

What OpenQuestion holds

Textmetadata
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.