Therapeutic actions of methyl eugenol in acute lung inflammation induced in rats

被引:0
|
作者
de Sousa, Maria Alana Rocha [1 ]
Teixeira, Guilherme dos Santos [2 ]
Marquesa, Rosemarie Brandim [4 ]
de Sousa, Luciana Mendes Ribeiro [3 ]
Ramos, Ricardo Martins [8 ]
Bento, Ricardo Rodrigues de Franca [5 ]
Neto, Bartolomeu Cruz Viana [3 ,6 ]
Gusmao, Suziete Batista Soares [6 ]
Sa, Jose Luiz Silva [1 ]
Maia Filho, Antonionio Luiz Martins [1 ,4 ]
Lobo, Anderson Oliveira [3 ]
Gusma, Gustavo Oliveira de Meira [1 ,7 ]
机构
[1] Univ Estadual Piaui, Dept Chem, Chem Grad Program PPGQ, BR-64002150 Teresina, PI, Brazil
[2] Univ Estadual Piaui, Dept Chem, BR-64002150 Teresina, PI, Brazil
[3] Fed Univ Piaui UFPI, Mat Sci & Engn Grad Program PPGCM, Interdisciplinary Lab Adv Mat LIMAV, BR-64049550 Teresina, PI, Brazil
[4] Univ Estadual Piaui, Biotechnol Res Ctr, BR-64003120 Teresina, PI, Brazil
[5] Univ Fed Mato Grosso, Inst Phys, BR-78060900 Mato Grosso, MT, Brazil
[6] Fed Univ Piaui UFPI, Dept Phys, BR-64049550 Teresina, PI, Brazil
[7] Univ Estadual Piaui, Dept Phys, BR-64002150 Teresina, PI, Brazil
[8] Fed Inst Educ Sci & Technol Piaui, Lab Mol Biol & Epidemiol LaBME, Campus Teresina Cent, BR-64000040 Teresina, PI, Brazil
关键词
Therapeutic approach; Methyl eugenol; Molecular docking; Ischemia-reperfusion injury; INTESTINAL ISCHEMIA; INJURY; PERMEABILITY; REPERFUSION; DAMAGE; LIVER; MODEL; METHYLEUGENOL; ANTIOXIDANT; SOLUBILITY;
D O I
10.1016/j.sajb.2024.04.023
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Acute respiratory distress syndrome (ARDS) is an inflammatory disease that affects the lungs with rupture of the alveolar-capillary barrier and loss of lung compliance, orchestrated by an intense inflammatory process mediated by neutrophils that culminates in diffuse alveolar data and tissue hypoxia. In this context, no specific drug has yet been applied to treat the syndrome. Therefore, finding new therapeutic targets that can treat the syndrome has become a research study. In view of this, methyl-eugenol (ME) has become the target of this study. The aim of this work was to carry out an in silico pharmacological and toxicological analysis with ADMET, as well as to determine, by means of molecular docking, the interaction affinity of the 5-LOX and COX-2 enzymes with ME and then the in vivo tests; in which male rats were distributed into five groups with five rats each, in which some groups were subjected to the process of ischemia and reperfusion (I/R). Groups G4 and G5 were treated by inhalation with ME (10 %). After completing these procedures, statistical analysis and lung histology were carried out. In the ADMET prediction, ME showed high intestinal absorption and a medium-permeability blood-brain barrier. ME had no violations of Lipinski's rule, demonstrating high potential as a drug candidate. Molecular docking showed that ME had the highest binding affinity with the 5-LOX enzyme. Finally, the statistical and histological analyses of the in vivo test showed acute and accentuated lung damage in the G1 group, while in the G4 and G5 groups, ME showed pharmacological efficacy, reducing the number of inflammatory cells, free macrophages and free radicals. The results indicate that ME oil is a favorable therapeutic approach in the treatment of ARDS. (c) 2024 SAAB. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:341 / 349
页数:9
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