Evidence map›Paper›PMID 40672662›Full record

ArticleACS pharmacology & translational science2025

Alpha-Lipoic Acid Reduces Methemoglobin and Oxidative Imbalance in the Blood and Liver Induced by Dapsone in Mice: Molecular Mechanism of Antioxidant Action.

Savio Monteiro Dos Santos, Joni Tetsuo Sakai, Bruno Alexandre Quadros Gomes, Lisa Maria Mendes de Almeida Souza, Roseane Guimarães Ferreira, Kaio Murilo Monteiro Espíndola, Ana Flávia Oliveira Pampolha, Kelly Davis, Pamela Suelen da S Seabra, Larissa de N da Paz Lopes and 4 more

Abstract read
In one paragraph

Article in ACS pharmacology & translational science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

14 authors.

Savio Monteiro Dos SantosPostgraduate Program in Neuroscience and Cell Biology, Federal University of Pará/UFPA, Rua Augusto Corrêa, 01, Bairro Guamá, 66075-110 Belém, Pará, Brazil.ORCID https://orcid.org/0000-0002-0927-9680
Joni Tetsuo SakaiPostgraduate Program in Pharmaceutical Sciences, Faculty of Pharmacy, Federal University of Pará/UFPA, Rua Augusto Corrêa, 01, Bairro Guamá, 66075-110 Belém, Pará, Brazil.
Bruno Alexandre Quadros GomesPostgraduate Program in Neuroscience and Cell Biology, Federal University of Pará/UFPA, Rua Augusto Corrêa, 01, Bairro Guamá, 66075-110 Belém, Pará, Brazil.
Lisa Maria Mendes de Almeida SouzaPostgraduate Program in Pharmaceutical Sciences, Faculty of Pharmacy, Federal University of Pará/UFPA, Rua Augusto Corrêa, 01, Bairro Guamá, 66075-110 Belém, Pará, Brazil.
Roseane Guimarães FerreiraPostgraduate Program in Neuroscience and Cell Biology, Federal University of Pará/UFPA, Rua Augusto Corrêa, 01, Bairro Guamá, 66075-110 Belém, Pará, Brazil.
Kaio Murilo Monteiro EspíndolaPostgraduate Program in Pharmacology and Biochemistry, Faculty of Pharmacy, Federal University of Pará/UFPA, Rua Augusto Corrêa, 01, Bairro Guamá, 66075-110 Belém, Pará, Brazil.
Ana Flávia Oliveira PampolhaPostgraduate Program in Pharmacology and Biochemistry, Faculty of Pharmacy, Federal University of Pará/UFPA, Rua Augusto Corrêa, 01, Bairro Guamá, 66075-110 Belém, Pará, Brazil.
Kelly DavisPostgraduate Program in Pharmacology and Biochemistry, Faculty of Pharmacy, Federal University of Pará/UFPA, Rua Augusto Corrêa, 01, Bairro Guamá, 66075-110 Belém, Pará, Brazil.
Pamela Suelen da S SeabraLaboratory Immunology, Microbiology, and In Vitro Assays (LABEIM), Faculty of Pharmacy, Federal University of Pará/UFPA, 66075-110 Belém, Pará, Brazil.
Larissa de N da Paz LopesLaboratory Immunology, Microbiology, and In Vitro Assays (LABEIM), Faculty of Pharmacy, Federal University of Pará/UFPA, 66075-110 Belém, Pará, Brazil.
Fabricia de Jesus Paiva da Fonseca SizoPostgraduate in Biology of Infectious and Parasitic Agents, Federal University of Pará/UFPA, Rua Augusto Corrêa, 01, Bairro Guamá, 66075-110 Belém, Pará, Brazil.
Agnaldo da Silva CarneiroPostgraduate Program in Medicinal Chemistry and Molecular Modeling, Faculty of Pharmacy, Federal University of Pará/UFPA, 66075-110 Belém, Pará, Brazil.
Michael D ColemanCollege of Health and Life Sciences, Aston University, Aston Triangle, Birmingham B4 7ET, U.K.
Marta Chagas MonteiroPostgraduate Program in Pharmaceutical Sciences, Faculty of Pharmacy, Federal University of Pará/UFPA, Rua Augusto Corrêa, 01, Bairro Guamá, 66075-110 Belém, Pará, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dapsone (DDS) is a sulfone clinically used in the treatment of dermatological disorders, such as dermatitis herpetiformis and psoriasis, besides , , and infections. However, the chronic use of DDS can lead to adverse effects involving all organ systems, such as dapsone hypersensitivity syndrome, methemoglobinemia, hemolytic anemia, and liver injury. These effects probably occur due to the presence of its toxic metabolite DDS-NOH, which can generate reactive oxygen species (ROS), and iron overload, causing oxidative stress. In this sense, antioxidant compounds with chelating properties such as Alpha-lipoic acid (ALA) may be an interesting adjuvant therapy strategy in treating or preventing oxidative stress and adverse reactions related to DDS. This study showed that DDS 40 mg/kg increased the methemoglobin and induced oxidative stress in the erythrocytes and liver of mice. However, post-treatment with ALA 12.5 mg/kg was able to restore redox status and hepatic biomarkers in DDS-intoxicated animals. Thus, inhibiting the formation of methemoglobin and lipid peroxidation in the blood, as well as reducing iron accumulation and production of hepatic enzymes stimulated by DDS metabolism. In addition, the molecular docking shows that ALA in its oxidized form can inhibit DDS-NOH. These findings highlight the potential of ALA and its thiol derivatives as antioxidants in counteracting the harmful effects of DDS metabolites. However, further investigations are necessary to understand the therapeutic potential and antioxidant mechanisms of ALA and its derivatives for the development of new strategies to prevent or alleviate oxidative damage associated with DDS treatment.

Indexed as

alpha lipoic aciddapsonehepatotoxicitymethemoglobinoxidative stress

Identifiers

PMID40672662
PMCPMC12260938

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