Anti-asthmatic effect of nitric oxide metallo-donor FOR811A [cis-[Ru(bpy)2(2-MIM)(NO)](PF6)3] in the respiratory mechanics of Swiss mice

Autor: Paula Priscila Correia Costa, Eduardo H.S. Sousa, Daniel Silveira Serra, Valdir Ferreira de Paula Junior, Fladimir de Lima Gondim, Gilvan Ribeiro dos Santos, Florêncio Sousa Gouveia Júnior, Helena Serra Azul Monteiro, Luiz Gonzaga de França Lopes, Stefanie Bressan Waller, Francisco Sales Ávila Cavalcante, Wesley Lyeverton Correia Ribeiro
Rok vydání: 2020
Předmět:
0301 basic medicine
Pulmonology
Physiology
Pharmacology
Pulmonary compliance
Biochemistry
chemistry.chemical_compound
Mice
Database and Informatics Methods
0302 clinical medicine
Airway resistance
Medical Conditions
Medicine and Health Sciences
Drug Interactions
Anti-Asthmatic Agents
Post-Translational Modification
Musculoskeletal System
Smooth Muscles
Multidisciplinary
Chemistry
Muscles
Neurochemistry
Animal Models
medicine.anatomical_structure
Experimental Organism Systems
Medicine
Bronchoconstriction
Female
medicine.symptom
Neurochemicals
Anatomy
Research Article
Science
Health Informatics
Mouse Models
Heme
Nitric Oxide
Research and Analysis Methods
Ruthenium
Nitric oxide
03 medical and health sciences
Respiratory Disorders
Model Organisms
Parenchyma
medicine
Organometallic Compounds
Animals
Nitric Oxide Donors
Respiratory Physiology
Asthma
Lung
Biology and Life Sciences
Proteins
medicine.disease
CTL
030104 developmental biology
030228 respiratory system
Respiratory Mechanics
Animal Studies
Neuroscience
Zdroj: PLoS ONE
PLoS ONE, Vol 16, Iss 3, p e0248394 (2021)
ISSN: 1932-6203
Popis: We aimed at evaluating the anti-asthmatic effect of cis-[Ru(bpy)2(2-MIM)(NO)](PF6)3 (FOR811A), a nitrosyl-ruthenium compound, in a murine model of allergic asthma. The anti-asthmatic effects were analyzed by measuring the mechanical lung and morphometrical parameters in female Swiss mice allocated in the following groups: untreated control (Ctl+Sal) and control treated with FOR811A (Ctl+FOR), along asthmatic groups untreated (Ast+Sal) and treated with FOR811A (Ast+FOR). The drug-protein interaction was evaluated by in-silico assay using molecular docking. The results showed that the use of FOR811A in experimental asthma (Ast+FOR) decreased the pressure-volume curve, hysteresis, tissue elastance, tissue resistance, and airway resistance, similar to the control groups (Ctl+Sal; Ctl+FOR). However, it differed from the untreated asthmatic group (Ast+Sal, pp
Databáze: OpenAIRE