Evidence map›Paper›PMID 42511760›Full record

ArticleInternational journal of molecular sciences2026

Amifostine Attenuates Doxorubicin-Induced Subacute Hepatic and Renal Toxicity in Rats.

Vesna Jaćević, Viktorija Dragojević-Simić, Jelica Grujić-Milanović, Silva Dobrić, Dubravko Bokonjić, Zoran Milovanović, Sladjan Milanović, Radoje Simić

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Vesna JaćevićDepartment of Experimental Toxicology and Pharmacology, National Poison Control Centre, Military Medical Academy, Crnotravska 17, 11000 Belgrade, Serbia.ORCID 0000-0001-5137-2638
Viktorija Dragojević-SimićDepartment for Pharmacological Science, Medical Faculty of the Military Medical Academy, University of Defence in Belgrade, Crnotravska 17, 11000 Belgrade, Serbia.ORCID 0000-0003-1979-0762
Jelica Grujić-MilanovićDepartment of Cardiovascular Research, Institute for Medical Research, National Institute of the Republic of Serbia, University of Belgrade, 11129 Belgrade, Serbia.ORCID 0000-0001-8014-3121
Silva DobrićVojnosanitetski Pregled, Medical Faculty of the Military Medical Academy, University of Defence in Belgrade, Crnotravska 17, 11000 Belgrade, Serbia.ORCID 0000-0003-0493-8525
Dubravko BokonjićDepartment of Experimental Toxicology and Pharmacology, National Poison Control Centre, Military Medical Academy, Crnotravska 17, 11000 Belgrade, Serbia.
Zoran MilovanovićSpecial Police Unit, Police Department of the City of Belgrade, Ministry of Interior, Trebevićka 12/A, 11030 Belgrade, Serbia.
Sladjan MilanovićDepartment for Biomechanics, Biomedical Engineering and Physics of Complex Systems, Institute for Medical Research, National Institute of the Republic of Serbia, University of Belgrade, 11129 Belgrade, Serbia.ORCID 0000-0001-7688-1201
Radoje SimićInstitute of Mother and Child Health Care of Serbia "Dr Vukan Čupić", University of Belgrade, Radoja Dakića 6-8, 11000 Belgrade, Serbia.ORCID 0009-0008-0824-951X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to evaluate the general, hepatoprotective and renoprotective effects of amifostine (AMI) in rats treated with a large, single dose of doxorubicin (DOX), assessed at 7 and 56 days after administration. Rats were divided into six experimental groups: Control (0.9% NaCl intraperitoneally (ip)), amifostine (AMI300, 300 mg/kg (ip)), doxorubicin (DOX6, 6 mg/kg (ip)), doxorubicin (DOX10, 10 mg/kg (ip)), doxorubicin (DOX6, 6 mg/kg (ip)) + amifostine (AMI300, 300 mg/kg (ip) 30 min before DOX6), and doxorubicin (DOX10, 10 mg/kg (ip)) + amifostine (AMI300, 300 mg/kg (ip) 30 min before DOX10). Absolute liver and kidney weights were significantly increased in AMI300 + DOX6-treated animals compared to DOX6 only on day 56. In the group of DOX10-treated rats, AMI300 significantly prevented changes in the number of white blood cells during the four weeks after treatment. The severity of hepatic and renal injuries in the DOX6-treated groups was also significantly less in rats pretreated with AMI300 on day 56 (

Indexed as

AmifostineChemical and Drug Induced Liver InjuryDoxorubicinKidneyLiverAnimalsMaleOrgan SizeRatsRats, WistarAmifostineDoxorubicinamifostinedoxorubicinhepatotoxicitynephrotoxicityratssubacute toxicity

Identifiers

PMID42511760
PMCPMC13410120

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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.