Evidence map›Paper›PMID 32468451›Full record

ReviewAdvances in experimental medicine and biology2020

In Silico and In Vivo Studies on Quercetin as Potential Anti-Parkinson Agent.

Hemanth Kumar Boyina, Sree Lakshmi Geethakhrishnan, Swetha Panuganti, Kiran Gangarapu, Krishna Prasad Devarakonda, Vasudha Bakshi, Sandhya Rani Guggilla

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances in experimental medicine and biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
27.0field-weighted citation impact, top 1% 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

18 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Review
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  5. Lead Phytomolecules for Treating Parkinson's Disease.Central nervous system agents in medicinal chemistry · 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

7 authors at 2 institutions in 1 country.

Hemanth Kumar BoyinaSchool of Pharmacy, Anurag Group of Institutions, Hyderabad, Telangana, India. hemanthboyina6@outlook.com.
Sree Lakshmi GeethakhrishnanSchool of Pharmacy, Anurag Group of Institutions, Hyderabad, Telangana, India.
Swetha PanugantiSchool of Pharmacy, Anurag Group of Institutions, Hyderabad, Telangana, India.
Kiran GangarapuSchool of Pharmacy, Anurag Group of Institutions, Hyderabad, Telangana, India.
Krishna Prasad DevarakondaSchool of Pharmacy, Anurag Group of Institutions, Hyderabad, Telangana, India.
Vasudha BakshiSchool of Pharmacy, Anurag Group of Institutions, Hyderabad, Telangana, India.
Sandhya Rani GuggillaUniversity College of Pharmaceutical Sciences, Kakatiya University, Warangal, Telangana, India.
Advanced Numerical Research and Analysis Group · INKakatiya University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD) is a major cause of morbidity and mortality among older individuals. Several researchers have suggested that iron chelators which cross the blood-brain barrier (BBB) might have clinical efficacy in treating PD. Therefore, efforts are made not only in order to improve the effect of L-dopa but also to introduce drugs which provide anti-parkinsonian and neuroprotective effects. In this study, quercetin, a flavonoid, exhibited noticeable neuroprotective effects via iron induced-oxidative stress-dependent apoptotic pathways. Our results suggested that quercetin significantly decreased the catalepsy and exhibited neuroprotective effects in rotenone-induced Parkinson. A model of rotenone-induced Parkinsonism in rats produced the decrease in glutathione, SOD, catalase, and serum iron concentration and the increase in H2O2 and lipid peroxidation activity. Quercetin efficiently halted the deleterious toxic effects of L-dopa, revealing normalization of catalepsy and rotarod score, in addition to amelioration of neurochemical parameters, indicating benefit of both symptomatic and neuroprotective therapies. In silico molecular docking studies have also shown that quercetin could be an ideal potential drug target for aromatic L-amino acid decarboxylase and human catechol-O-methyltransferase. In conclusion, quercetin possesses strong iron-chelating abilities and could be recommended as a disease-modifying therapy when administered in combination with L-dopa, early on in the course of Parkinson's disease.

Indexed as

AnimalsAntiparkinson AgentsAromatic-L-Amino-Acid DecarboxylasesCatechol O-MethyltransferaseHumansLevodopaMolecular Docking SimulationParkinson DiseaseQuercetinAntiparkinson AgentsAromatic-L-Amino-Acid DecarboxylasesCatechol O-MethyltransferaseLevodopaQuercetinCarbidopaCatalepsyCOMTLevodopaMolecular dockingParkinson’s diseaseQuercetin

Identifiers

PMID32468451
OpenAlexW3032246776

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.