Evidence map›Paper›PMID 42089890›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2026

Effects of exposure to lisdexamfetamine dimesylate on hepatic parameters of pubertal rats.

João Vinícius Honório da Silva, Letícia Cavalcante Santos, Rafaela Pires Erthal, Dayane Priscila Dos Santos, Camila Rodrigues Ferraz, Camila Franciele de Souza, Luís Eduardo Duarte Gonçalves, Waldiceu Aparecido Verri, Niels Olsen Saraiva Câmara, Ernane Torres Uchôa and 2 more

Abstract read
In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 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

12 authors.

João Vinícius Honório da SilvaDepartment of General Biology, Biological Sciences Center, State University of Londrina - UEL, Londrina, Paraná, Brazil.
Letícia Cavalcante SantosDepartment of Histology, Biological Sciences Center, State University of Londrina - UEL, Londrina, Paraná, Brazil.
Rafaela Pires ErthalDepartment of General Biology, Biological Sciences Center, State University of Londrina - UEL, Londrina, Paraná, Brazil.
Dayane Priscila Dos SantosDepartment of General Biology, Biological Sciences Center, State University of Londrina - UEL, Londrina, Paraná, Brazil.
Camila Rodrigues FerrazDepartment of Pathology, Biological Sciences Center, State University of Londrina - UEL, Londrina, Paraná, Brazil.
Camila Franciele de SouzaDepartment of Physiological Sciences, Biological Sciences Center, State University of Londrina - UEL, Londrina, Paraná, Brazil.
Luís Eduardo Duarte GonçalvesDepartment of Immunology, Biomedical Sciences Institute, University of São Paulo - USP, São Paulo, Brazil.
Waldiceu Aparecido VerriDepartment of Pathology, Biological Sciences Center, State University of Londrina - UEL, Londrina, Paraná, Brazil.
Niels Olsen Saraiva CâmaraDepartment of Immunology, Biomedical Sciences Institute, University of São Paulo - USP, São Paulo, Brazil.
Ernane Torres UchôaDepartment of Physiological Sciences, Biological Sciences Center, State University of Londrina - UEL, Londrina, Paraná, Brazil.
Glaura Scantamburlo Alves FernandesDepartment of General Biology, Biological Sciences Center, State University of Londrina - UEL, Londrina, Paraná, Brazil.
Fábio Goulart de AndradeDepartment of Histology, Biological Sciences Center, State University of Londrina - UEL, Londrina, Paraná, Brazil. andrade@uel.br.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico #309633/2021-4Conselho Nacional de Desenvolvimento Científico e Tecnológico #313704/2021Fundação de Amparo à Pesquisa do Estado de São Paulo 17/05264-7
6 · The paper itself

Abstract

Lisdexamfetamine dimesylate (LDX) is a psychostimulant, that has been widely recommended in recent years for the treatment of Attention-Deficit/Hyperactivity Disorder. The present study aims to evaluate the effects of LDX administration on the hepatic morphophysiology of pubertal Wistar rats, since the liver plays a central role in systemic metabolism. Male Wistar rats were randomly distributed into two experimental groups: LDX group (LDX) - received 11.3 mg/kg/day of LDX diluted in tap water; and the Control group (C) - received tap water only. Animals were treated by gavage during puberty, from postnatal day (PND) 25 to PND 65. The results showed that administration of LDX decreased white adipose tissue weight without altering overall body weight gain. Plasma biochemical analysis demonstrated an increase in plasma total cholesterol and in the concentration of hepatic transaminases in LDX rats. In addition, LDX animals exhibited an increase in N-acetyl-β-D-glucosaminidase activity, indirectly indicating macrophage recruitment to the liver. This study shows that daily exposure to LDX during puberty causes early liver inflammation and damage due, in part, to increased hepatic transaminases and associated with indirect signs of macrophage recruitment. This finding highlights the importance of monitoring the indiscriminate use of amphetamines and alerting patients to possible liver disorders.

Indexed as

Central Nervous System StimulantsChemical and Drug Induced Liver InjuryLisdexamfetamine DimesylateLiverAcetylglucosaminidaseAdipose Tissue, WhiteAnimalsCholesterolMacrophagesMaleOrgan SizeRatsRats, WistarSexual MaturationAcetylglucosaminidaseCentral Nervous System StimulantsCholesterolLisdexamfetamine DimesylateAmphetamineHepatotoxicityInflammationInjury

Identifiers

PMID42089890
PMCPMC13391714

What Socratic 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 Socratic graph.