Evidence map›Paper›PMID 32801713›Full record

ArticleNeuropsychiatric disease and treatment2020

Protective Effects of

Nasroallah Moradi-Kor, Masoomeh Dadkhah, Ali Ghanbari, Hadi Rashidipour, Ahmad Reza Bandegi, Mehdi Barati, Parviz Kokhaei, Ali Rashidy-Pour

Open access · goldAbstract read
In one paragraph

Article in Neuropsychiatric disease and treatment, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 20% 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

23 citing papers in PubMed, 2 syntheses or guidelines pooled it, 32 citations in OpenAlex.

  1. Pooled it
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  8. Developmental and Early-Life Stress-Induced Effects on 5-HTbioRxiv : the preprint server for biology · 2025
    Article
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  11. Indian journal of clinical biochemistry : IJCB · 2025
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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 4 institutions in 1 country.

Nasroallah Moradi-KorStudent Research Committee, Semnan University of Medical Sciences, Semnan, Iran.ORCID 0000-0001-9905-6845
Masoomeh DadkhahPharmaceutical Sciences Research Center, Ardabil University of Medical Sciences, Ardabil, Iran.ORCID 0000-0003-0274-1075
Ali GhanbariResearch Center of Physiology, Semnan University of Medical Sciences, Semnan, Iran.ORCID 0000-0002-7568-3681
Hadi RashidipourSchool of Veterinary Medicine, Islamic Azad University, Garmsar, Iran.
Ahmad Reza BandegiLaboratory of Endocrine Research, Research Center of Physiology, School of Medicine, Semnan University of Medical Sciences, Semnan, Iran.
Mehdi BaratiDepartment of Immunology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.ORCID 0000-0002-5715-1948
Parviz KokhaeiCancer Research Center, Semnan University of Medical Sciences, Semnan, Iran.
Ali Rashidy-PourResearch Center of Physiology, Semnan University of Medical Sciences, Semnan, Iran.
Semnan University of Medical Sciences · IRArdabil University of Medical Sciences · IRIslamic Azad University of Garmsar · IRMashhad University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeAmple evidence indicates that chronic adolescence stress is associated with an increased risk of developing neuropsychiatric disorders in adulthood. Given the importance of the effective therapeutic ways to overcome adolescent stress-related deficits, the present study investigated the effects of

methodsDuring the adolescent period (PNDs30-40), rats were subjected to restraint stress. Then, the animals were subjected to SP treatment (200 mg/kg/day), EX, EE, and the combined treatments (SP+EX, and SP+EE) for 15 days between PNDs41-55. Subsequently, anxiety or depression-like behaviors, BDNF levels, oxidative stress markers and mRNA expression of BDNF and 5HT

resultsStressed rats demonstrated enhanced anxiety levels and depression-like behaviors in adulthood. Regarding the oxidative stress markers, stressed rats exhibited significantly higher levels of malondialdehyde, a lipid peroxidation product, higher activities of antioxidant enzymes (glutathione peroxidase and superoxide dismutase) and significantly lower total antioxidant reactivity capacity in the PFC. Additionally, adolescent stress significantly increased 5HT3 receptor mRNA expression and decreased BDNF content and its mRNA expression in the PFC. Treatments with SP, EX, EE, and the combined interventions alleviated these deficits.

conclusionOur findings indicate that appropriate interventions during the adolescent period can protect against adolescent stress-induced behavioral, and biochemical defects and oxidative stress damage in adulthood.

Indexed as

adolescent stressanxietydepressionenvironmental enrichmentoxidative stressphysical activity spirulina

Identifiers

PMID32801713
PMCPMC7387863
OpenAlexW3044174297

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.