Evidence map›Paper›PMID 24739881›Full record

ArticlePloS one2014

Subchronic toxicological study of two artemisinin derivatives in dogs.

Ji-ye Yin, He-mei Wang, Quan-jun Wang, Yan-sheng Dong, Gang Han, Yong-biao Guan, Ke-yong Zhao, Wen-sheng Qu, Ye Yuan, Xiao-xin Gao and 2 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Clinical Efficacy and Safety of MalaroneAnimals : an open access journal from MDPI · 2022
    Article
  5. Article
  6. Article
  7. Antitumor Research on Artemisinin and Its Bioactive Derivatives.Natural products and bioprospecting · 2018
    Review
  8. Article
  9. Article
  10. 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

12 authors.

Ji-ye YinBeijing Institute of Pharmacology and Toxicology, Beijing, China.
He-mei WangBeijing Institute of Pharmacology and Toxicology, Beijing, China.
Quan-jun WangBeijing Institute of Pharmacology and Toxicology, Beijing, China.
Yan-sheng DongBeijing Institute of Pharmacology and Toxicology, Beijing, China.
Gang HanBeijing Institute of Pharmacology and Toxicology, Beijing, China.
Yong-biao GuanBeijing Institute of Pharmacology and Toxicology, Beijing, China.
Ke-yong ZhaoBeijing Institute of Pharmacology and Toxicology, Beijing, China.
Wen-sheng QuBeijing Institute of Pharmacology and Toxicology, Beijing, China.
Ye YuanBeijing Institute of Pharmacology and Toxicology, Beijing, China.
Xiao-xin GaoBeijing Institute of Pharmacology and Toxicology, Beijing, China.
Shu-fang JingBeijing Institute of Pharmacology and Toxicology, Beijing, China.
Ri-gao DingBeijing Institute of Pharmacology and Toxicology, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The objective of our study was to profile and compare the systematic changes between orally administered artesunate and intramuscularly injected artemether at a low dose over a 3-month period (92 consecutive days) in dogs. Intramuscular administration of 6 mg kg-1 artemether induced a decreased red blood cell (RBC) count (anemia), concurrent extramedullary hematopoiesis in the spleen and inhibition of erythropoiesis in the bone marrow. We also observed a prolonged QT interval and neuropathic changes in the central nervous system, which demonstrated the cortex and motor neuron vulnerability, but no behavioral changes. Following treatment with artesunate, we observed a decreased heart rate, which was most likely due to cardiac conduction system damage, as well as a deceased RBC count, extramedullary hematopoiesis in the spleen and inhibition of erythropoiesis in the bone marrow. However, in contrast to treatment with artemether, neurotoxicity was not observed following treatment with artesunate. In addition, ultra-structural examination by transmission electron microscopy showed mitochondrial damage following treatment with artesunate. These findings demonstrated the spectrum of toxic changes that result upon treatment with artesunate and artemether and show that the prolonged administration of low doses of these derivatives result in diverse toxicity profiles.

Indexed as

Administration, OralAnimalsArrhythmias, CardiacArtemetherArtemisininsArtesunateDogsErythrocyte CountErythropoiesisFemaleHematopoiesis, ExtramedullaryInjections, IntramuscularMaleMicroscopy, Electron, TransmissionMitochondriaToxicity TestsArtemetherArtemisininsArtesunate

Identifiers

PMID24739881
PMCPMC3989207
OpenAlexW2010299301

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.