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1.
Biochem Pharmacol ; 177: 113937, 2020 07.
Artículo en Inglés | MEDLINE | ID: mdl-32224142

RESUMEN

Latent HIV reservoirs are the main obstacle to eradicate HIV infection. One strategy proposes to eliminate these viral reservoirs by pharmacologically reactivating the latently infected T cells. We show here that a 4-deoxyphorbol ester derivative isolated from Euphorbia amygdaloides ssp. semiperfoliata, 4ß-dPE A, reactivates HIV-1 from latency and could potentially contribute to decrease the viral reservoir. 4ß-dPE A shows two effects in the HIV replication cycle, infection inhibition and HIV transactivation, similarly to other phorboids PKC agonists such PMA and prostratin and to other diterpene esters such SJ23B. Our data suggest 4ß-dPE A is non-tumorigenic, unlike the related compound PMA. As the compounds are highly similar, the lack of tumorigenicity by 4ß-dPE A could be due to the lack of a long side lipophilic chain that is present in PMA. 4ß-dPE activates HIV transcription at nanomolar concentrations, lower than the concentration needed by other latency reversing agents (LRAs) such as prostratin and similar to bryostatin. PKCθ/MEK activation is required for the transcriptional activity, and thus, anti-latency activity of 4ß-dPE A. However, CD4, CXCR4 and CCR5 receptors down-regulation effect seems to be independent of PCK/MEK, suggesting the existence of at least two different targets for 4ß-dPE A. Furthermore, NF-κb transcription factor is involved in 4ß-dPE HIV reactivation, as previously shown for other PKCs agonists. We also studied the effects of 4ß-dPE A in combination with other LRAs. When 4ß-dPE A was combined with another PKC agonists such as prostratin an antagonic effect was achieved, while, when combined with an HDAC inhibitor such as vorinostat, a strong synergistic effect was obtained. Interestingly, the latency reversing effect of the combination was synergistically diminishing the EC50 value but also increasing the efficacy showed by the drugs alone. In addition, combinations of 4ß-dPE A with antiretroviral drugs as CCR5 antagonist, NRTIs, NNRTIs and PIs, showed a consistent synergistic effect, suggesting that the combination would not interefer with antiretroviral therapy (ART). Finally, 4ß-dPE A induced latent HIV reactivation in CD4 + T cells of infected patients under ART at similar levels than the tumorigenic phorbol derivative PMA, showing a clear reactivation effect. In summary, we describe here the mechanism of action of a new potent deoxyphorbol derivative as a latency reversing agent candidate to decrease the size of HIV reservoirs.


Asunto(s)
Fármacos Anti-VIH/farmacología , Infecciones por VIH/metabolismo , VIH-1/fisiología , Quinasas de Proteína Quinasa Activadas por Mitógenos/metabolismo , Ésteres del Forbol/farmacología , Proteína Quinasa C/metabolismo , Activación Viral/efectos de los fármacos , Vorinostat/farmacología , Brioestatinas/farmacología , Linfocitos T CD4-Positivos/efectos de los fármacos , Linfocitos T CD4-Positivos/virología , Supervivencia Celular/efectos de los fármacos , Sinergismo Farmacológico , Infecciones por VIH/patología , Infecciones por VIH/virología , VIH-1/efectos de los fármacos , Humanos , Células Jurkat , Transducción de Señal/efectos de los fármacos , Latencia del Virus/efectos de los fármacos
2.
Braz. j. microbiol ; Braz. j. microbiol;45(1): 135-142, 2014. ilus, tab
Artículo en Inglés | LILACS | ID: lil-709467

RESUMEN

In Colombia, knowledge of the yeast and yeast-like fungi community is limited because most studies have focused on species with clinical importance. Sediments and water represent important habitats for the study of yeast diversity, especially for yeast species with industrial, biotechnological, and bioremediation potential. The main purpose of this study was to identify and compare the diversity of yeast species associated with sediment and water samples from two artificial lakes in Universidad del Valle (Cali-Colombia). Yeast samplings were performed from fifteen sediment samples and ten water samples. Grouping of similar isolates was initially based on colony and cell morphology, which was then complemented by micro/mini satellite primed PCR banding pattern analysis by using GTG5 as single primer. A representative isolate for each group established was chosen for D1/D2 domain sequencing and identification. In general, the following yeast species were identified: Candida albicans, Candida diversa, Candida glabrata, Candida pseudolambica, Cryptococcus podzolicus, Cryptococcus rajasthanensis, Cryptococcus laurentii, Williopsis saturnus, Hanseniaspora thailandica, Hanseniaspora uvarum, Rhodotorula mucilaginosa, Saccharomyces cerevisiae, Torulaspora delbrueckii, Torulaspora pretoriensis, Tricosporon jirovecii, Trichosporon laibachii and Yarrowia lypolitica. Two possible new species were also found, belonging to the Issatchenkia sp. and Bullera sp. genera. In conclusion, the lakes at the Universidad del Valle campus have significant differences in yeast diversity and species composition between them.


Asunto(s)
Biodiversidad , Lagos/microbiología , Levaduras/clasificación , Levaduras/aislamiento & purificación , Colombia , ADN de Hongos/química , ADN de Hongos/genética , ADN Ribosómico/química , ADN Ribosómico/genética , Sedimentos Geológicos/microbiología , Datos de Secuencia Molecular , Reacción en Cadena de la Polimerasa , ARN Ribosómico/genética , Análisis de Secuencia de ADN , Microbiología del Agua , Levaduras/genética
3.
Phytomedicine ; 17(1): 69-74, 2010 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-19748255

RESUMEN

Screening of plants from the Iberian Peninsula for anti-human immunodeficiency virus (-HIV) activity revealed that aqueous extract of Tuberaria lignosa gave positive results. Following an activity-guided procedure, the crude extract was counterextracted, and the subsequent fractions obtained tested for their anti-HIV activity in vitro. The bioassay-guided fractionation of the extract afforded an ellagitannin enriched fraction (EEF) isolated for the first time from this species. This EEF exhibited antiviral activity against HIV in MT-2 infected cells, with an IC(50) value of 2.33mug/ml (selectivity index greater than 21). Inhibition of HIV infection by EEF appears to be mediated by CD4 down-regulation, the main receptor for HIV entry. CXCR4 and CCR5 receptors were not affected by EEF, explaining why EEF is able to inhibit R5 and X4 infections.


Asunto(s)
Fármacos Anti-VIH/uso terapéutico , Cistaceae/química , Infecciones por VIH/prevención & control , VIH/efectos de los fármacos , Taninos Hidrolizables/uso terapéutico , Extractos Vegetales/uso terapéutico , Integración Viral/efectos de los fármacos , Fármacos Anti-VIH/aislamiento & purificación , Fármacos Anti-VIH/farmacología , Linfocitos T CD4-Positivos/metabolismo , Regulación hacia Abajo , Humanos , Taninos Hidrolizables/aislamiento & purificación , Taninos Hidrolizables/farmacología , Concentración 50 Inhibidora , Células Jurkat , Extractos Vegetales/química , Extractos Vegetales/farmacología , Receptores CCR5 , Receptores CXCR4
4.
Phytother Res ; 16(6): 550-4, 2002 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-12237813

RESUMEN

As part of our screening of anti-AIDS agents from natural sources, extracts of 15 medicinal plants widely used in the folk medicines of North America and Europe were evaluated in vitro. Most of the extracts tested were relatively nontoxic to human lymphocytic MT-2 cells, but only the extracts of Hysopp officinalis and Dittrichia viscosa exhibited anti-HIV activity in an in vitro MTT assay. The 50% hydroalcohol extract of Hysopp officinalis and the aqueous extract of Dittrichia viscosa showed inhibitory effects against HIV-1 induced infections in MT-2 cells at concentrations ranging from 50 to 100 microg/mL and 25 to 400 microg/mL, respectively. Both extracts showed no appreciable cytotoxicity at these concentrations.


Asunto(s)
Fármacos Anti-VIH/farmacología , Evaluación Preclínica de Medicamentos/métodos , VIH/efectos de los fármacos , Extractos Vegetales/farmacología , Asteraceae , Europa (Continente) , Formazáns , Humanos , Lamiaceae , América del Norte , Extractos Vegetales/toxicidad , Sales de Tetrazolio , Células Tumorales Cultivadas
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