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1.
J Nat Med ; 76(1): 102-109, 2022 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-34417964

RESUMO

One new compound, crocusatin M (1), and three new glycosidic compounds, crocusatins N-P (2-4), along with nine known compounds were isolated from the dried stigmas of Crocus sativus. The structures of new compounds were elucidated on the basis of spectroscopic analysis, and the absolute configurations of 1, 2, and 3 were unambiguously assigned by the comparison of experimental and calculated ECD data. This is the first report of the isolation of 4 with the HMG moiety from the genus Crocus. Compounds 1 and 4 exhibited weak anti-inflammatory activities on inhibiting lipopolysaccharide (LPS)-induced NO production.


Assuntos
Anti-Inflamatórios/farmacologia , Crocus , Monoterpenos/farmacologia , Anti-Inflamatórios/isolamento & purificação , Crocus/química , Flores/química , Monoterpenos/isolamento & purificação , Compostos Fitoquímicos/isolamento & purificação , Compostos Fitoquímicos/farmacologia
2.
AIDS ; 35(12): 2054-2057, 2021 10 01.
Artigo em Inglês | MEDLINE | ID: mdl-34074818

RESUMO

Dietary supplements and medications containing polyvalent cations can interact with integrase strand transfer inhibitors (INSTIs) and decrease exposure to INSTIs. In this cross-sectional study of 513 people with HIV (PWH) who were on stable antiretroviral therapy, 57.5% and 6.6% reported concurrent use of dietary supplements and antacids, respectively. In the multivariable analysis, the use of antacids, but not dietary supplements containing polyvalent cations, was associated with HIV viremia in PWH who received INSTI-based ART.


Assuntos
Infecções por HIV , Inibidores de Integrase de HIV , Integrase de HIV , HIV-1 , Antiácidos/uso terapêutico , Cátions/uso terapêutico , Estudos Transversais , Suplementos Nutricionais , Farmacorresistência Viral , Infecções por HIV/tratamento farmacológico , Inibidores de Integrase de HIV/uso terapêutico , Humanos
3.
Zhongguo Zhong Yao Za Zhi ; 45(24): 5929-5943, 2020 Dec.
Artigo em Chinês | MEDLINE | ID: mdl-33496132

RESUMO

Ganjiang Lingzhu Decoction is one of the first 100 classical prescriptions published by China in 2018. According to the published literature, it was found that there is no review on the history, evolution and research progress of this prescription. In order to reflect the history, modifications, quality control and clinical applications, this paper focuses on the origination, evolution, current development and modern studies of Ganjiang Lingzhu Decoction, in the hope of providing a reference for the heritage and innovation of other classical prescriptions.


Assuntos
Medicamentos de Ervas Chinesas , Medicina Tradicional Chinesa , China , Prescrições , Controle de Qualidade
4.
J Int AIDS Soc ; 17: 18993, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25174641

RESUMO

INTRODUCTION: The Jarisch-Herxheimer reaction, a febrile inflammatory reaction that often occurs after the first dose of chemotherapy in spirochetal diseases, may result in deleterious effects to patients with neurosyphilis and to pregnant women. A single 2-g oral dose of azithromycin is an alternative treatment to benzathine penicillin G for early syphilis in areas with low macrolide resistance. With its potential anti-inflammatory activity, the impact of azithromycin on the incidence of the Jarisch-Herxheimer reaction in HIV-positive patients with early syphilis has rarely been investigated. METHODS: In HIV-positive patients with early syphilis, the Jarisch-Herxheimer reaction was prospectively investigated using the same data collection form in 119 patients who received benzathine penicillin G between 2007 and 2009 and 198 who received azithromycin between 2012 and 2013, when shortage of benzathine penicillin G occurred in Taiwan. Between 2012 and 2013, polymerase chain reaction (PCR) assay was performed to detect Treponema pallidum DNA in clinical specimens, and PCR restriction fragment length polymorphism of the 23S ribosomal RNA was performed to detect point mutations (2058G or A2059G) that are associated with macrolide resistance. RESULTS: The overall incidence of the Jarisch-Herxheimer reaction was significantly lower in patients receiving azithromycin than those receiving benzathine penicillin G (14.1% vs. 56.3%, p<0.001). The risk increased with higher rapid plasma reagin (RPR) titres (adjusted odds ratio [AOR] per 1-log2 increase, 1.21; confidence interval [CI], 1.04-1.41), but decreased with prior penicillin therapy for syphilis (AOR, 0.37; 95% CI, 0.19-0.71) and azithromycin treatment (AOR, 0.15; 95% CI, 0.08-0.29). During the study period, 310 specimens were obtained from 198 patients with syphilis for PCR assays, from whom T. pallidum was identified in 76 patients, one of whom (1.3%) was found to be infected with T. pallidum harbouring the macrolide resistance mutation (A2058G). In subgroup analyses confined to the 75 patients infected with T. pallidum lacking resistance mutation, a statistically significantly lower risk for the Jarisch-Herxheimer reaction following azithromycin treatment was noted. CONCLUSIONS: Treatment with azithromycin was associated with a lower risk for the Jarisch-Herxheimer reaction than that with benzathine penicillin G in HIV-positive patients with early syphilis. Previous benzathine penicillin G therapy for syphilis decreased the risk, whereas higher RPR titres increased the risk, for the reaction.


Assuntos
Antibacterianos/uso terapêutico , Azitromicina/uso terapêutico , Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos/epidemiologia , Febre/epidemiologia , Penicilina G Benzatina/uso terapêutico , Sífilis/tratamento farmacológico , Treponema pallidum/efeitos dos fármacos , Adulto , Antibacterianos/efeitos adversos , Antibacterianos/farmacologia , Azitromicina/efeitos adversos , Azitromicina/farmacologia , Estudos de Coortes , DNA Bacteriano/química , DNA Bacteriano/genética , DNA Ribossômico/química , DNA Ribossômico/genética , Feminino , Febre/induzido quimicamente , Infecções por HIV/complicações , Humanos , Incidência , Masculino , Testes de Sensibilidade Microbiana , Penicilina G Benzatina/efeitos adversos , Penicilina G Benzatina/farmacologia , Reação em Cadeia da Polimerase , Polimorfismo de Fragmento de Restrição , Estudos Prospectivos , RNA Ribossômico 23S/genética , Sífilis/diagnóstico , Taiwan , Treponema pallidum/classificação , Treponema pallidum/genética
5.
Biochim Biophys Acta ; 1803(9): 1072-82, 2010 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-20488213

RESUMO

The inhibition of the complex III of the mitochondrial respiratory chain under hypoxia-ischemia has been observed. However, the downstream events of this inhibition remain to be studied. In this paper, we used the Q(i) site inhibitor antimycin A and the Q(o) site inhibitor myxothiazol to inhibit the Q(i) site and the Q(o) site of the complex III and studied the effect and mechanism of the inhibition of these sites on voltage-gated Ca(2+) currents (I(Ca)) in rat prefrontal neurons with whole cell patch-clamp method in slices. The results showed that antimycin A inhibited I(Ca), but myxothiazol increased it. Further mechanism study showed that antimycin A inhibited I(Ca) via the H(2)O(2)-hydroxyl radicals/cPKC (mainly PKCbetaI) pathway, whereas myxothiazol increased I(Ca) via the superoxide anion/nPKC (mainly the PKCdelta) pathway.


Assuntos
Sinalização do Cálcio , Córtex Cerebral/metabolismo , Complexo III da Cadeia de Transporte de Elétrons/antagonistas & inibidores , Neurônios/fisiologia , Oxidantes/farmacologia , Proteína Quinase C/fisiologia , Animais , Antimicina A/farmacologia , Canais de Cálcio/metabolismo , Canais de Cálcio/fisiologia , Sinalização do Cálcio/efeitos dos fármacos , Domínio Catalítico/efeitos dos fármacos , Córtex Cerebral/efeitos dos fármacos , Complexo III da Cadeia de Transporte de Elétrons/química , Complexo III da Cadeia de Transporte de Elétrons/metabolismo , Isoenzimas/metabolismo , Isoenzimas/fisiologia , Metacrilatos/farmacologia , Mitocôndrias/efeitos dos fármacos , Mitocôndrias/metabolismo , Mitocôndrias/fisiologia , Modelos Biológicos , Neurônios/efeitos dos fármacos , Neurônios/metabolismo , Técnicas de Patch-Clamp , Proteína Quinase C/metabolismo , Ratos , Ratos Sprague-Dawley , Potenciais Sinápticos/efeitos dos fármacos , Tiazóis/farmacologia
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