Evidence map›Paper›PMID 32420487›Full record

ArticleHeliyon2020

Devil's claw (

Rupasree Peruru, R Usha Rani, Jhansyrani Thatiparthi, Sunitha Sampathi, Sujatha Dodoala, K V S R G Prasad

Open access · goldAbstract read
In one paragraph

Article in Heliyon, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. The Therapeutic Potential ofPharmaceuticals (Basel, Switzerland) · 2024
    Review
  4. Neuroprotective effect of quercetin andFood science & nutrition · 2023
    Article
  5. Article
  6. Review
  7. The Fight against Infection and Pain: Devil's Claw (Molecules (Basel, Switzerland) · 2022
    Review
  8. Review
  9. Article
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

6 authors at 2 institutions in 1 country.

Rupasree PeruruInstitute of Pharmaceutical Technology, Sri Padmavati Mahila Visvavidyalayam, Tirupati, India.
R Usha RaniInstitute of Pharmaceutical Technology, Sri Padmavati Mahila Visvavidyalayam, Tirupati, India.
Jhansyrani ThatiparthiInstitute of Pharmaceutical Technology, Sri Padmavati Mahila Visvavidyalayam, Tirupati, India.
Sunitha SampathiNational Institute of Pharmaceutical Education and Research-Hyderabad, India.
Sujatha DodoalaInstitute of Pharmaceutical Technology, Sri Padmavati Mahila Visvavidyalayam, Tirupati, India.
K V S R G PrasadInstitute of Pharmaceutical Technology, Sri Padmavati Mahila Visvavidyalayam, Tirupati, India.
Sri Padmavati Mahila Visvavidyalayam · INNational Institute of Pharmaceutical Education and Research · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Over 200 million people are exposed to arsenic worldwide in their daily lives. Arsenic is a toxic ubiquitous metalloid distributed in the ground water. From the last few decades it is obtaining considerable attention for its severe neurotoxic properties. In this study the neuroprotective efficacy of devil's claw (DCW), a potent antioxidant has been investigated against arsenic induced neurotoxicity in female rats. Neurotoxicity was established by oral administration of 13 mg/kg sodium arsenite. The animals were divided into five groups (n = 6) including normal control, disease/arsenic control, standard treatment (Apocynin, 10 mg/kg), DCW treatment I (DCW, 200 mg/kg) and DCW treatment II (DCW, 400 mg/kg). Exploratory, anxiety and motor coordination related behavior of the animals was assessed using hole-board, forced swimming, beam walk and elevated plus maze tests. Findings revealed that DCW treatment ameliorated anxiety and motor in-coordination in the rats compared to the arsenic control group. In addition, arsenic induced a significant oxidative stress in arsenic only treated group, whereas co-administration with DCW the oxidative stress was reduced prominently. Arsenic control group produced gliosis and nuclear pyknosis of the brain cells which were prominently suppressed with the treatment of DCW for 21 days. The activity of DCW was in correlation with the concentration of harpagoside in the serum estimated by the HPLC method, supports that harpagoside was the active constituent responsible for neuroprotective effect. Further findings are required to understand the molecular mechanisms involved in neuroprotective effect of harpagoside and DCW.

Indexed as

ArsenicDevil's clawHarpagophytum procumbensHarpagosideNeurobehavior and neurotoxicityNeuroscience

Identifiers

PMID32420487
PMCPMC7218267
OpenAlexW3023164073

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.