Evidence map›Paper›PMID 32306722›Full record

ArticleIranian biomedical journal2020

Carvacrol and Thymol Attenuate Cytotoxicity Induced by Amyloid β25-35 via Activating Protein Kinase C and Inhibiting Oxidative Stress in PC12 Cells.

Zahra Azizi, Mona Salimi, Amir Amanzadeh, Nahid Majelssi, Nasser Naghdi

Open access · diamondAbstract read
In one paragraph

Article in Iranian biomedical journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Analysis of Pharmacological Properties ofLife (Basel, Switzerland) · 2025
    Review
  5. Article
  6. Review
  7. Review
  8. The effects of carvacrol and p-cymene on AβCNS neuroscience & therapeutics · 2024
    Article
  9. mFrontiers in cell and developmental biology · 2024
    Review
  10. Article
  11. Antioxidants (Basel, Switzerland) · 2023
    Article
  12. Review
  13. Article
  14. Pharmaceutical biology · 2021
    Article
  15. Antioxidants (Basel, Switzerland) · 2020
    Article
  16. Article
  17. 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

5 authors at 1 institution in 1 country.

Zahra AziziDepartment of Physiology and Pharmacology, Pasteur Institute of Iran, Tehran, Iran.
Mona SalimiDepartment of Physiology and Pharmacology, Pasteur Institute of Iran, Tehran, Iran.
Amir AmanzadehDepartment of Cell Bank, Pasteur Institute of Iran, Tehran, Iran.
Nahid MajelssiDepartment of Physiology and Pharmacology, Pasteur Institute of Iran, Tehran, Iran.
Nasser NaghdiDepartment of Physiology and Pharmacology, Pasteur Institute of Iran, Tehran, Iran.
Pasteur Institute of Iran · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Our previous findings indicated that carvacrol and thymol alleviate cognitive impairments caused by Aβ in rodent models of Alzheimer's disease (AD). In this study, the neuroprotective effects of carvacrol and thymol against Aβ25-35-induced cytotoxicity were evaluated, and the potential mechanisms were determined. Methods: PC12 cells were pretreated with Aβ25-35 for 2 h, followed by incubation with carvacrol or thymol for additional 48 h. Cell viability was measured by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide method. A flurospectrophotometer was employed to observe the intracellular reactive oxygen species (ROS) production. Protein kinase C (PKC) activity was analyzed using ELISA. Results: Our results indicated that carvacrol and thymol could significantly protect PC12 cells against Aβ25-35-induced cytotoxicity. Furthermore, Aβ25-35 could induce intracellular ROS production, while carvacrol and thymol could reverse this effect. Moreover, our findings showed that carvacrol and thymol elevate PKC activity similar to Bryostatin-1, as a PKC activator. Conclusion: This study provided the evidence regarding the protective effects of carvacrol and thymol against Aβ25–35-induced cytotoxicity in PC12 cells. The results suggested that the neuroprotective effects of these compounds against Aβ25-35 might be through attenuating oxidative damage and increasing the activity of PKC as a memory-related protein. Thus, carvacrol and thymol were found to have therapeutic potential in preventing or modulating AD.

Indexed as

Amyloid beta-PeptidesAnimalsApoptosisCell SurvivalCymenesEnzyme ActivationNeuroprotective AgentsOxidative StressPC12 CellsPeptide FragmentsProtein Kinase CRatsReactive Oxygen SpeciesThymolAmyloid beta-Peptidesamyloid beta-protein (25-35)carvacrolCymenesNeuroprotective AgentsPeptide FragmentsProtein Kinase CReactive Oxygen SpeciesThymolAlzheimer’s diseaseCarvacrolReactive oxygen speciesThymol

Identifiers

PMID32306722
PMCPMC7275817
OpenAlexW3020800114

What OpenQuestion holds

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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.