Evidence map›Paper›PMID 34357584›Full record

ArticleActa parasitologica2021

The Metabolomic Profiles of Sera of Mice Infected with Plasmodium berghei and Treated by Effective Fraction of Naja naja oxiana Using

Fateme Hajialiani, Delavar Shahbazzadeh, Fatemeh Maleki, Taher Elmi, Fatemeh Tabatabaie, Zahra Zamani

Abstract read
PubMed Publisher
In one paragraph

Article in Acta parasitologica, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Serum metabolomic profiles in BALB/c mice induced byFrontiers in cellular and infection microbiology · 2023
    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 3 institutions in 1 country.

Fateme HajialianiDepartment of Medical Parasitology, School of Medicine-International Campus, Iran University of Medical Sciences, Tehran, Iran.
Delavar ShahbazzadehDepartment of Medical Biotechnology, Laboratory of Venom and Bio Therapeutics Molecules, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.
Fatemeh MalekiDepartment of Parasitology, Faculty of Para Medical Sciences, Iran University of Medical Sciences, Tehran, Iran.
Taher ElmiDepartment of Laboratory Science, Islamic Azad University, Babol Branch, Babol, Iran.
Fatemeh TabatabaieDepartment of Parasitology and Mycology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran. tabatabaei.f@iums.ac.ir.ORCID http://orcid.org/0000-0001-9189-4190
Zahra ZamaniBiochemistry Department, Pasteur Institute of Iran, Pasteur Avenue, Tehran, Iran. zamani@pasteur.ac.ir.ORCID http://orcid.org/0000-0003-3701-0854
Iran University of Medical Sciences · IRPasteur Institute of Iran · IRIslamic Azad University, Babol

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe use of venom fractions from the Iranian cobra could be useful adjunct treatments of malaria with chloroquine. A metabolomic investigation with PURPOSE: We sought to ascertain both safety and anti-parasitic effects of experimental therapies.

methodsAfter purification of the venom fractions, 25 mice were infected, then treated for 4 days with 0.2 ml of 5 mg/kg, 2.5 mg/kg and 1 mg/kg of the effective fraction, chloroquine, and a drug vehicle. An ED50 was obtained using Giemsa staining and real-time PCR analysis. The toxicity tests inspecting both liver and kidney tissues were performed.

resultsA clear inhibitory effect on parasitaemia was observed (with 75% inhibition with 5 mg/kg and 50% reduction when 2.5 mg/kg dosage used). ED50 obtained 2.5 mg/kg. The metabolomics were identified as differentiation of aminoacyl-t-RNA biosynthesis, valine, leucine, isoleucine biosynthesis and degradation pathways were observed.

conclusionUpon therapeutic effects of cobra venom fraction, further optimization of dose-dependent response of pharmacokinetics would be worthwhile for further exploration in adjunct experimental venom therapies.

Indexed as

Naja najaPlasmodium bergheiAnimalsIranMagnetic Resonance SpectroscopyMetabolomicsMiceMetabolomicsMiceNaja naja oxianaPlasmodium bergheiVenom

Identifiers

PMID34357584
OpenAlexW3189298919

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.