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  1. Article ; Online: Diagnosis and treatment of latent tuberculosis infection in patients undergoing treatment with immunobiologic agents: a four-year experience in an endemic area.

    Lopes, Diana Maria de Almeida / Pinheiro, Valéria Goes Ferreira / Monteiro, Helena Serra Azul

    Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia

    2019  Volume 45, Issue 6, Page(s) e20180225

    Abstract: Objective: To describe the incidence of active tuberculosis and the occurrence of adverse events after isoniazid treatment in patients with latent tuberculosis infection (LTBI) who also had chronic inflammatory diseases and were treated with ... ...

    Abstract Objective: To describe the incidence of active tuberculosis and the occurrence of adverse events after isoniazid treatment in patients with latent tuberculosis infection (LTBI) who also had chronic inflammatory diseases and were treated with immunobiologic agents in an endemic area in Brazil.
    Methods: The diagnosis of LTBI was based on anamnesis, clinical examination, chest X-ray, and a tuberculin skin test (TST). Patients received prophylactic treatment (isoniazid for six months) in accordance with the Brazilian guidelines.
    Results: A total of 101 patients were evaluated between July of 2011 and July of 2015. Of those, 55 (54.46%) were women (mean age, 53.16 ± 1.76 years) and 46 (45.54%) were men (mean age, 45.39 ± 2.13 years). A total of 79 patients (78.22%) were being treated with immunobiologic agents and 22 (21.78%) were being treated with immunomodulatory or immunosuppressive agents. In the screening for LTBI, 53 patients (52.48%) had a TST induration ≥ 10 mm. Chest X-ray findings consistent with LTBI were observed in 36 patients (35.64%). Isoniazid preventive therapy was effective in 96 (95.05%) of the 101 patients evaluated. It is of note that 84 (83.17%) of the patients experienced no adverse effects from the use of isoniazid and that 83 (98.81%) of those patients completed the prophylactic treatment (p = 0.002). Active tuberculosis was diagnosed in 5 (6.33%) of the 79 patients treated with immunobiologic agents and in 1 (4.55%) of the 22 patients treated with other immunomodulators/immunosuppressants.
    Conclusions: A six-month course of isoniazid proved to be safe and effective in the treatment of LTBI, which is essential to reducing the risk of developing active tuberculosis.
    MeSH term(s) Adult ; Aged ; Antibiotic Prophylaxis/methods ; Antitubercular Agents/therapeutic use ; Brazil/epidemiology ; Endemic Diseases ; Female ; Humans ; Immunologic Factors/therapeutic use ; Immunosuppressive Agents/therapeutic use ; Isoniazid/therapeutic use ; Latent Tuberculosis/diagnosis ; Latent Tuberculosis/drug therapy ; Latent Tuberculosis/epidemiology ; Male ; Middle Aged ; Multivariate Analysis ; Prospective Studies ; Radiography, Thoracic ; Risk Factors ; Time Factors ; Treatment Outcome ; Tuberculin Test/methods ; Young Adult
    Chemical Substances Antitubercular Agents ; Immunologic Factors ; Immunosuppressive Agents ; Isoniazid (V83O1VOZ8L)
    Language Portuguese
    Publishing date 2019-10-14
    Publishing country Brazil
    Document type Journal Article
    ZDB-ID 2223157-2
    ISSN 1806-3756 ; 1806-3713
    ISSN (online) 1806-3756
    ISSN 1806-3713
    DOI 10.1590/1806-3713/e20180225
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  2. Article ; Online: New nitrosyl ruthenium complexes with combined activities for multiple cardiovascular disorders.

    Gouveia Júnior, Florêncio Sousa / Silveira, João Alison de Moraes / Holanda, Thais Muratori / Marinho, Aline Diogo / Ridnour, Lisa A / Wink, David A / de Siqueira, Rodrigo José Bezerra / Monteiro, Helena Serra Azul / Sousa, Eduardo Henrique Silva de / Lopes, Luiz Gonzaga de França

    Dalton transactions (Cambridge, England : 2003)

    2023  Volume 52, Issue 16, Page(s) 5176–5191

    Abstract: Nitrosyl ruthenium complexes are promising platforms for nitric oxide (NO) and nitroxyl (HNO) release, which exert their therapeutic application. In this context, we developed two polypyridinic compounds with the general ... ...

    Abstract Nitrosyl ruthenium complexes are promising platforms for nitric oxide (NO) and nitroxyl (HNO) release, which exert their therapeutic application. In this context, we developed two polypyridinic compounds with the general formula
    MeSH term(s) Animals ; Rats ; Coordination Complexes ; Nitric Oxide/chemistry ; Nitrogen Oxides/chemistry ; Ruthenium/chemistry ; Sulfhydryl Compounds/chemistry ; Cardiovascular Diseases
    Chemical Substances Coordination Complexes ; Nitric Oxide (31C4KY9ESH) ; Nitrogen Oxides ; nitroxyl (GFQ4MMS07W) ; Ruthenium (7UI0TKC3U5) ; Sulfhydryl Compounds
    Language English
    Publishing date 2023-04-25
    Publishing country England
    Document type Journal Article
    ZDB-ID 1472887-4
    ISSN 1477-9234 ; 1364-5447 ; 0300-9246 ; 1477-9226
    ISSN (online) 1477-9234 ; 1364-5447
    ISSN 0300-9246 ; 1477-9226
    DOI 10.1039/d3dt00059a
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  3. Article ; Online: Phosphodiesterase-5 inhibitor sildenafil attenuates kidney injury induced by Bothrops alternatus snake venom.

    Jorge, Antônio Rafael Coelho / Marinho, Aline Diogo / Silveira, João Alison de Moraes / Nogueira Junior, Francisco Assis / de Aquino, Pedro Everson Alexandre / Alves, Ana Paula Negreiros Nunes / Jorge, Roberta Jeane Bezerra / Ferreira Junior, Rui Seabra / Monteiro, Helena Serra Azul

    Toxicon : official journal of the International Society on Toxinology

    2021  Volume 202, Page(s) 46–52

    Abstract: Acute kidney injury pathogenesis in envenoming by snakes is multifactorial and involves immunologic reactions, hemodynamic disturbances, and direct nephrotoxicity. Sildenafil (SFC), a phosphodiesterase 5 inhibitor, has been reported to protect against ... ...

    Abstract Acute kidney injury pathogenesis in envenoming by snakes is multifactorial and involves immunologic reactions, hemodynamic disturbances, and direct nephrotoxicity. Sildenafil (SFC), a phosphodiesterase 5 inhibitor, has been reported to protect against pathological kidney changes.
    Objective: This study aimed to investigate the protective effect of sildenafil against Bothrops alternatus snake venom (BaV)-induced nephrotoxicity.
    Methods: Kidneys from Wistar rats (n = 6, weighing 260-300 g) were isolated and divided into four groups: (1) perfused with a modified Krebs-Henseleit solution (MKHS) containing 6 g% of bovine serum albumin; (2) administered 3 μg/mL SFC; (3) perfused with 3 μg/mL BaV; and (4) administered SFC + BaV, both at 3 μg/mL. Subsequently, the perfusion pressure (PP), renal vascular resistance (RVR), urinary flow (UF), glomerular filtration rate (GFR), and percentage of electrolyte tubular sodium and chloride transport (%TNa
    Results: All renal parameters evaluated were reduced with BaV. In the SFC + BaV group, SFC restored PP to normal values and promoted a significant increase in %TNa
    Conclusion: Our data suggest the involvement of phosphodiesterase-5 and cGMP in BaV-induced nephrotoxicity since its effects were attenuated by the administration of SFC.
    MeSH term(s) Animals ; Bothrops ; Cyclic Nucleotide Phosphodiesterases, Type 5 ; Kidney ; Phosphodiesterase 5 Inhibitors/therapeutic use ; Rats ; Rats, Wistar ; Sildenafil Citrate/therapeutic use ; Snake Venoms/toxicity
    Chemical Substances Phosphodiesterase 5 Inhibitors ; Snake Venoms ; Sildenafil Citrate (BW9B0ZE037) ; Cyclic Nucleotide Phosphodiesterases, Type 5 (EC 3.1.4.35)
    Language English
    Publishing date 2021-09-10
    Publishing country England
    Document type Journal Article
    ZDB-ID 204479-1
    ISSN 1879-3150 ; 0041-0101
    ISSN (online) 1879-3150
    ISSN 0041-0101
    DOI 10.1016/j.toxicon.2021.08.024
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  4. Article ; Online: The nitric oxide pathway is involved in the anti-inflammatory effect of the rutheniumcomplex [Ru(bpy)2(2-MIM)(NO)](PF6)3.

    Carvalho, Isadora Oliveira / Queiroz, Cléo Vanessa Gomes / Marques, Gabriela Fernandes Oliveira / Craveiro, Raquel Magalhães Castelo Branco / Xavier Júnior, Francisco Antônio Félix / Gouveia Júnior, Florêncio Sousa / Lopes, Luiz Gonzaga de França / Chaves, Edna Maria Camelo / Monteiro, Helena Serra Azul / Assreuy, Ana Maria Sampaio / Evangelista, Janaina Serra Azul Monteiro

    European journal of pharmacology

    2022  Volume 921, Page(s) 174869

    Abstract: Metal coordination complexes are chemotherapeutic and anti-inflammatory agents. The ruthenium complex FOR811A ([Ru(bpy) ...

    Abstract Metal coordination complexes are chemotherapeutic and anti-inflammatory agents. The ruthenium complex FOR811A ([Ru(bpy)
    MeSH term(s) 2,2'-Dipyridyl/analogs & derivatives ; Animals ; Anti-Inflammatory Agents/adverse effects ; Carrageenan/adverse effects ; Edema/chemically induced ; Edema/drug therapy ; Edema/metabolism ; Inflammation/chemically induced ; Inflammation/drug therapy ; Inflammation/metabolism ; Mice ; Nitric Oxide/metabolism ; Organometallic Compounds/pharmacology ; Organometallic Compounds/therapeutic use
    Chemical Substances Anti-Inflammatory Agents ; Organometallic Compounds ; bis(bipyridyl)ruthenium(II) ; Nitric Oxide (31C4KY9ESH) ; 2,2'-Dipyridyl (551W113ZEP) ; Carrageenan (9000-07-1)
    Language English
    Publishing date 2022-03-03
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 80121-5
    ISSN 1879-0712 ; 0014-2999
    ISSN (online) 1879-0712
    ISSN 0014-2999
    DOI 10.1016/j.ejphar.2022.174869
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  5. Article ; Online: High Salt Intake Promotes Different Responses to Urodilatin and Uroguanylin in the Isolated Rat Kidney.

    Jorge, Antonio Rafael Coelho / Costa, Pedro Henrique Sá / Monteiro, Helena Serra Azul / Fonteles, Manassés Claudino

    Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme

    2017  Volume 50, Issue 2, Page(s) 152–159

    Abstract: Urodilatin (UD) and uroguanylin (UGN) have been implicated in the regulation of salt and water homeostasis, particularly in the balance handling of salt intake. In this sense, the aim of the present work was to study the main effects of these peptides in ...

    Abstract Urodilatin (UD) and uroguanylin (UGN) have been implicated in the regulation of salt and water homeostasis, particularly in the balance handling of salt intake. In this sense, the aim of the present work was to study the main effects of these peptides in kidneys from animals subjected to high NaCl (2%) intake, during 10 days in metabolic cages. The control group received only normal water, whereas the treated group drank 2% solution of NaCl (NaCl 2%). In addition, we studied effect of subthreshold UD (0.14 nM) and UGN (0.06 μM) doses in NaCl 2% after a 30-min control period. Kidney perfusion was performed with Krebs-Henseleit containing 6 g% bovine albumin previously dialyzed. The effects of UD (0.14 nM) promoted reduction of PP, RVR, and UF in the NaCl 2% group. We also observed an increase in %TNa
    MeSH term(s) Animals ; Atrial Natriuretic Factor/pharmacology ; Glomerular Filtration Rate/drug effects ; Kidney/drug effects ; Natriuretic Peptides/pharmacology ; Peptide Fragments/pharmacology ; Perfusion ; Pressure ; Rats, Inbred WKY ; Sodium Chloride, Dietary/administration & dosage ; Urination/drug effects ; Vascular Resistance/drug effects
    Chemical Substances Natriuretic Peptides ; Peptide Fragments ; Sodium Chloride, Dietary ; uroguanylin (152175-68-3) ; Ularitide (740Y5J48Z8) ; Atrial Natriuretic Factor (85637-73-6)
    Language English
    Publishing date 2017-12-12
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 80125-2
    ISSN 1439-4286 ; 0018-5043
    ISSN (online) 1439-4286
    ISSN 0018-5043
    DOI 10.1055/s-0043-120669
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  6. Article ; Online: Plants and Phytocompounds Active Against Bothrops Venoms.

    Jorge, Roberta Jeane Bezerra / Martins, René Duarte / Araújo, Renata Mendonça / da Silva, Meykson Alexandre / Monteiro, Helena Serra Azul / Ximenes, Rafael Matos

    Current topics in medicinal chemistry

    2019  Volume 19, Issue 22, Page(s) 2003–2031

    Abstract: Snakebite envenomation is an important health problem in tropical countries, with severe human and social consequences. In Latin America, the Bothrops species constitute the main threat to humans, and the envenomation caused by these species quickly ... ...

    Abstract Snakebite envenomation is an important health problem in tropical countries, with severe human and social consequences. In Latin America, the Bothrops species constitute the main threat to humans, and the envenomation caused by these species quickly develops into severe local tissue damage, including swelling, hemorrhaging, myonecrosis, skin ulceration, and pain. The systemic effects of envenomation are usually neutralized by antivenom serum therapy, despite its intrinsic risks. However, neutralization of local tissue damage remains a challenge. To improve actual therapy, two major alternatives are proposed: the rational design of new specific antibodies for most of the tissue damaging/ poor immunogenic toxins, or the search for new synthetic or natural compounds which are able to inhibit these toxins and complement the serum therapy. Natural compounds isolated from plants, mainly from those used in folk medicine to treat snakebite, are a good choice for finding new lead compounds to improve snakebite treatment and minimize its consequences for the victims. In this article, we reviewed the most promising plants and phytocompounds active against bothropic venoms.
    MeSH term(s) Animals ; Antivenins/chemistry ; Antivenins/isolation & purification ; Antivenins/pharmacology ; Biological Products/chemistry ; Biological Products/isolation & purification ; Biological Products/pharmacology ; Bothrops ; Humans ; Molecular Structure ; Phytochemicals/chemistry ; Phytochemicals/isolation & purification ; Phytochemicals/pharmacology ; Plant Extracts/chemistry ; Plant Extracts/isolation & purification ; Plant Extracts/pharmacology ; Snake Venoms/antagonists & inhibitors
    Chemical Substances Antivenins ; Biological Products ; Phytochemicals ; Plant Extracts ; Snake Venoms
    Language English
    Publishing date 2019-07-23
    Publishing country United Arab Emirates
    Document type Journal Article ; Review
    ZDB-ID 2064823-6
    ISSN 1873-4294 ; 1568-0266
    ISSN (online) 1873-4294
    ISSN 1568-0266
    DOI 10.2174/1568026619666190723153925
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  7. Article: Harpalyce brasiliana Benth: A prolific source of bioactive flavonoids with antiophidic potential

    Pontes, Marcela de Castro Nogueira Diniz / Torres-Rêgo, Manoela / de Aquino, Ana Karoline Silva / de Aquino, Nayara Coriolano / Teles, Yanna Carolina Ferreira / Ximenes, Rafael Matos / Monteiro, Helena Serra Azul / Silveira, Edilberto Rocha / Araújo, Renata Mendonça

    Phytochemistry letters. 2021 Feb., v. 41

    2021  

    Abstract: Harpalyce brasiliana Benth (Leguminoseae) has been previously described as a prolific source of flavonoids, such as flavonols, isoflavonoids and mainly pterocarpans. This plant has been used in folk medicine and its isolated compounds have been reported ... ...

    Abstract Harpalyce brasiliana Benth (Leguminoseae) has been previously described as a prolific source of flavonoids, such as flavonols, isoflavonoids and mainly pterocarpans. This plant has been used in folk medicine and its isolated compounds have been reported for their anti-inflammatory, antitumor and antiophidic properties. This study reports a phytochemical investigation of the leaves, heartwood, and roots of H. brasiliana and evaluates its effect against the Bothrops jararacussu (Bj) envenomation. The isolation of all substances was performed using different chromatographic methods and the structures were elucidated by 1D and 2D NMR, IR and MS analysis. The new isoflavonoids harpalycin II-A (4) and harpalycin I-A (9) were isolated from the leaves and heartwood, respectively. Thirteen known flavonoids were isolated from leaves, heartwood, and roots. The treatment of rats with cabenegrin A-II (14) reversed the biochemical (glucose, aspartate aminotransferase, alanine transaminase, urea, creatinine, uric acid, and creatine kinase) and hematological (erythrocytes, hemoglobin, hematocrit, hemoglobin and platelets) alterations induced by Bj venom. In addition, cabenegrin A-II demonstrated significant inhibition of the hypotensive effect of Bj venom. These data demonstrated the isolation of two new isoflavonoids of species, as well as the promising antiophidic effect of bioactive flavonoids from H. brasiliana.
    Keywords Bothrops ; Harpalyce ; alanine transaminase ; antihypertensive effect ; aspartate transaminase ; blood platelets ; chromatography ; creatine kinase ; creatinine ; erythrocytes ; flavonols ; glucose ; heartwood ; hematocrit ; hemoglobin ; isoflavonoids ; leaves ; rats ; roots ; traditional medicine ; urea ; uric acid ; venoms
    Language English
    Dates of publication 2021-02
    Size p. 158-167.
    Publishing place Elsevier Ltd
    Document type Article
    Note NAL-light
    ISSN 1874-3900
    DOI 10.1016/j.phytol.2020.09.025
    Database NAL-Catalogue (AGRICOLA)

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  8. Article: Phosphodiesterase-5 inhibitor sildenafil attenuates kidney injury induced by Bothrops alternatus snake venom

    Jorge, Antônio Rafael Coelho / Marinho, Aline Diogo / Silveira, João Alison de Moraes / Nogueira Junior, Francisco Assis / de Aquino, Pedro Everson Alexandre / Alves, Ana Paula Negreiros Nunes / Jorge, Roberta Jeane Bezerra / Ferreira Junior, Rui Seabra / Monteiro, Helena Serra Azul

    Toxicon. 2021 Oct. 30, v. 202

    2021  

    Abstract: Acute kidney injury pathogenesis in envenoming by snakes is multifactorial and involves immunologic reactions, hemodynamic disturbances, and direct nephrotoxicity. Sildenafil (SFC), a phosphodiesterase 5 inhibitor, has been reported to protect against ... ...

    Abstract Acute kidney injury pathogenesis in envenoming by snakes is multifactorial and involves immunologic reactions, hemodynamic disturbances, and direct nephrotoxicity. Sildenafil (SFC), a phosphodiesterase 5 inhibitor, has been reported to protect against pathological kidney changes.This study aimed to investigate the protective effect of sildenafil against Bothrops alternatus snake venom (BaV)-induced nephrotoxicity.Kidneys from Wistar rats (n = 6, weighing 260–300 g) were isolated and divided into four groups: (1) perfused with a modified Krebs-Henseleit solution (MKHS) containing 6 g% of bovine serum albumin; (2) administered 3 μg/mL SFC; (3) perfused with 3 μg/mL BaV; and (4) administered SFC + BaV, both at 3 μg/mL. Subsequently, the perfusion pressure (PP), renal vascular resistance (RVR), urinary flow (UF), glomerular filtration rate (GFR), and percentage of electrolyte tubular sodium and chloride transport (%TNa⁺, %TCl⁻, respectively) were evaluated. The cyclic guanosine monophosphate (cGMP) levels were analyzed in the perfusate, and the kidneys were removed to perform oxidative stress and histopathological analyses.All renal parameters evaluated were reduced with BaV. In the SFC + BaV group, SFC restored PP to normal values and promoted a significant increase in %TNa⁺ and %TCl⁻. cGMP levels were increased in the SFC + BaV group. The oxidative stress biomarkers, malondialdehyde (MDA) and glutathione (GSH), were reduced by BaV. In the SFC + BaV group, a decrease in MDA without an increase in GSH was observed. These findings were confirmed by histological analysis, which showed improvement mainly in tubulis.Our data suggest the involvement of phosphodiesterase-5 and cGMP in BaV-induced nephrotoxicity since its effects were attenuated by the administration of SFC.
    Keywords Bothrops ; acute kidney injury ; biomarkers ; bovine serum albumin ; chlorides ; cyclic GMP ; electrolytes ; glomerular filtration rate ; glutathione ; hemodynamics ; histology ; histopathology ; kidneys ; malondialdehyde ; nephrotoxicity ; oxidative stress ; pathogenesis ; protective effect ; snake venoms ; sodium ; urea cycle
    Language English
    Dates of publication 2021-1030
    Size p. 46-52.
    Publishing place Elsevier Ltd
    Document type Article
    ZDB-ID 204479-1
    ISSN 1879-3150 ; 0041-0101
    ISSN (online) 1879-3150
    ISSN 0041-0101
    DOI 10.1016/j.toxicon.2021.08.024
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  9. Article ; Online: In silico study of azithromycin, chloroquine and hydroxychloroquine and their potential mechanisms of action against SARS-CoV-2 infection.

    Braz, Helyson Lucas Bezerra / Silveira, João Alison de Moraes / Marinho, Aline Diogo / de Moraes, Maria Elisabete Amaral / Moraes Filho, Manoel Odorico de / Monteiro, Helena Serra Azul / Jorge, Roberta Jeane Bezerra

    International journal of antimicrobial agents

    2020  Volume 56, Issue 3, Page(s) 106119

    Abstract: Coronavirus disease 2019 (COVID-19) is a highly transmissible viral infection caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Clinical trials have reported improved outcomes resulting from an effective reduction or absence of ... ...

    Abstract Coronavirus disease 2019 (COVID-19) is a highly transmissible viral infection caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Clinical trials have reported improved outcomes resulting from an effective reduction or absence of viral load when patients were treated with chloroquine (CQ) or hydroxychloroquine (HCQ). In addition, the effects of these drugs were improved by simultaneous administration of azithromycin (AZM). The receptor-binding domain (RBD) of the SARS-CoV-2 spike (S) protein binds to the cell surface angiotensin-converting enzyme 2 (ACE2) receptor, allowing virus entry and replication in host cells. The viral main protease (M
    MeSH term(s) Amino Acid Motifs ; Angiotensin-Converting Enzyme 2 ; Antiviral Agents/chemistry ; Antiviral Agents/pharmacology ; Azithromycin/chemistry ; Azithromycin/pharmacology ; Betacoronavirus/chemistry ; Betacoronavirus/metabolism ; Binding Sites ; COVID-19 ; Cathepsin L/antagonists & inhibitors ; Cathepsin L/chemistry ; Cathepsin L/metabolism ; Chloroquine/chemistry ; Chloroquine/pharmacology ; Coronavirus 3C Proteases ; Coronavirus Infections/drug therapy ; Coronavirus Infections/virology ; Cysteine Endopeptidases/chemistry ; Cysteine Endopeptidases/metabolism ; Host-Pathogen Interactions/drug effects ; Host-Pathogen Interactions/genetics ; Humans ; Hydroxychloroquine/chemistry ; Hydroxychloroquine/pharmacology ; Molecular Docking Simulation ; Pandemics ; Peptidyl-Dipeptidase A/chemistry ; Peptidyl-Dipeptidase A/genetics ; Peptidyl-Dipeptidase A/metabolism ; Pneumonia, Viral/drug therapy ; Pneumonia, Viral/virology ; Protein Binding ; Protein Interaction Domains and Motifs ; Protein Structure, Secondary ; SARS-CoV-2 ; Spike Glycoprotein, Coronavirus/antagonists & inhibitors ; Spike Glycoprotein, Coronavirus/chemistry ; Spike Glycoprotein, Coronavirus/genetics ; Spike Glycoprotein, Coronavirus/metabolism ; Thermodynamics ; Viral Nonstructural Proteins/antagonists & inhibitors ; Viral Nonstructural Proteins/chemistry ; Viral Nonstructural Proteins/metabolism ; Virus Attachment/drug effects
    Chemical Substances Antiviral Agents ; Spike Glycoprotein, Coronavirus ; Viral Nonstructural Proteins ; spike protein, SARS-CoV-2 ; Hydroxychloroquine (4QWG6N8QKH) ; Azithromycin (83905-01-5) ; Chloroquine (886U3H6UFF) ; Peptidyl-Dipeptidase A (EC 3.4.15.1) ; ACE2 protein, human (EC 3.4.17.23) ; Angiotensin-Converting Enzyme 2 (EC 3.4.17.23) ; Cysteine Endopeptidases (EC 3.4.22.-) ; CTSL protein, human (EC 3.4.22.15) ; Cathepsin L (EC 3.4.22.15) ; Coronavirus 3C Proteases (EC 3.4.22.28)
    Keywords covid19
    Language English
    Publishing date 2020-07-30
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 1093977-5
    ISSN 1872-7913 ; 0924-8579
    ISSN (online) 1872-7913
    ISSN 0924-8579
    DOI 10.1016/j.ijantimicag.2020.106119
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  10. Article ; Online: 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.

    Costa, Paula Priscila Correia / Waller, Stefanie Bressan / Dos Santos, Gilvan Ribeiro / Gondim, Fladimir de Lima / Serra, Daniel Silveira / Cavalcante, Francisco Sales Ávila / Gouveia Júnior, Florêncio Sousa / de Paula Júnior, Valdir Ferreira / Sousa, Eduardo Henrique Silva / Lopes, Luiz Gonzaga de França / Ribeiro, Wesley Lyeverton Correia / Monteiro, Helena Serra Azul

    PloS one

    2021  Volume 16, Issue 3, Page(s) e0248394

    Abstract: 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 ... ...

    Abstract 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, p<0.05), indicating that FOR811A corrected the lung parenchyma and relaxed the smooth muscles of the bronchi. Similar to control groups (Ctl+Sal; Ctl+FOR), FOR811A increased the inspiratory capacity and static compliance in asthmatic animals (Ast+Sal, p<0.05), showing that this metallodrug improved the capacity of inspiration during asthma. The morphometric parameters showed that FOR811A decreased the alveolar collapse and kept the bronchoconstriction during asthma. Beyond that, the molecular docking using FOR811A showed a strong interaction in the distal portion of the heme group of the soluble guanylate cyclase, particularly with cysteine residue (Cys141). In summary, FOR811A relaxed bronchial smooth muscles and improved respiratory mechanics during asthma, providing a protective effect and promising use for the development of an anti-asthmatic drug.
    MeSH term(s) Animals ; Anti-Asthmatic Agents/chemistry ; Anti-Asthmatic Agents/pharmacology ; Asthma/drug therapy ; Asthma/physiopathology ; Female ; Mice ; Nitric Oxide Donors/chemistry ; Nitric Oxide Donors/pharmacology ; Organometallic Compounds/chemistry ; Organometallic Compounds/pharmacology ; Respiratory Mechanics/drug effects ; Ruthenium/chemistry ; Ruthenium/pharmacology
    Chemical Substances Anti-Asthmatic Agents ; Nitric Oxide Donors ; Organometallic Compounds ; Ruthenium (7UI0TKC3U5)
    Language English
    Publishing date 2021-03-12
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1932-6203
    ISSN (online) 1932-6203
    DOI 10.1371/journal.pone.0248394
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