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1.
Viruses ; 14(2)2022 02 09.
Artículo en Inglés | MEDLINE | ID: mdl-35215947

RESUMEN

Diphyllin is a natural arylnaphtalide lignan extracted from tropical plants of particular importance in traditional Chinese medicine. This compound has been described as a potent inhibitor of vacuolar (H+)ATPases and hence of the endosomal acidification process that is required by numerous enveloped viruses to trigger their respective viral infection cascades after entering host cells by receptor-mediated endocytosis. Accordingly, we report here a revised, updated, and improved synthesis of diphyllin, and demonstrate its antiviral activities against a panel of enveloped viruses from Flaviviridae, Phenuiviridae, Rhabdoviridae, and Herpesviridae families. Diphyllin is not cytotoxic for Vero and BHK-21 cells up to 100 µM and exerts a sub-micromolar or low-micromolar antiviral activity against tick-borne encephalitis virus, West Nile virus, Zika virus, Rift Valley fever virus, rabies virus, and herpes-simplex virus type 1. Our study shows that diphyllin is a broad-spectrum host cell-targeting antiviral agent that blocks the replication of multiple phylogenetically unrelated enveloped RNA and DNA viruses. In support of this, we also demonstrate that diphyllin is more than just a vacuolar (H+)ATPase inhibitor but may employ other antiviral mechanisms of action to inhibit the replication cycles of those viruses that do not enter host cells by endocytosis followed by low pH-dependent membrane fusion.


Asunto(s)
Antivirales/farmacología , Lignanos/farmacología , Virus/efectos de los fármacos , Animales , Antígenos Virales/metabolismo , Antivirales/síntesis química , Línea Celular , Supervivencia Celular/efectos de los fármacos , Glucósidos/farmacología , Lignanos/síntesis química , ATPasas de Translocación de Protón Vacuolares/antagonistas & inhibidores , Replicación Viral/efectos de los fármacos , Virus/clasificación , Virus/metabolismo
2.
Biomed Res Int ; 2021: 7872406, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-34926691

RESUMEN

Viruses are responsible for a variety of human pathogenesis. Owing to the enhancement of the world population, global travel, and rapid urbanization, and infectious outbreaks, a critical threat has been generated to public health, as preventive vaccines and antiviral therapy are not available. Herbal medicines and refined natural products have resources for the development of novel antiviral drugs. These natural agents have shed light on preventive vaccine development and antiviral therapies. This review intends to discuss the antiviral activities of plant extracts and some isolated plant natural products based on mainly preclinical (in vitro and in vivo) studies. Twenty medicinal herbs were selected for the discussion, and those are commonly recognized antiviral medicinal plants in Ayurveda (Zingiber officinale, Caesalpinia bonducella, Allium sativum, Glycyrrhiza glabra, Ferula assafoetida, Gymnema sylvestre, Gossypium herbaceum, Phyllanthus niruri, Trachyspermum ammi, Withania somnifera, Andrographis paniculata, Centella asiatica, Curcuma longa, Woodfordia fruticose, Phyllanthus emblica, Terminalia chebula, Tamarindus indica, Terminalia arjuna, Azadirachta indica, and Ficus religiosa). However, many viruses remain without successful immunization and only a few antiviral drugs have been approved for clinical use. Hence, the development of novel antiviral drugs is much significant and natural products are excellent sources for such drug developments. In this review, we summarize the antiviral actions of selected plant extracts and some isolated natural products of the medicinal herbs.


Asunto(s)
Antivirales/farmacología , Productos Biológicos/farmacología , Plantas Medicinales/química , Virosis/tratamiento farmacológico , Virus/efectos de los fármacos , Animales , Humanos
3.
J Am Chem Soc ; 143(43): 17891-17909, 2021 11 03.
Artículo en Inglés | MEDLINE | ID: mdl-34677069

RESUMEN

The emergence of multi-drug-resistant pathogens threatens the healthcare systems world-wide. Recent advances in phototherapy (PT) approaches mediated by photo-antimicrobials (PAMs) provide new opportunities for the current serious antibiotic resistance. During the PT treatment, reactive oxygen species or heat produced by PAMs would react with the cell membrane, consequently leaking cytoplasm components and effectively eradicating different pathogens like bacteria, fungi, viruses, and even parasites. This Perspective will concentrate on the development of different organic photo-antimicrobials (OPAMs) and their application as practical therapeutic agents into therapy for local infections, wound dressings, and removal of biofilms from medical devices. We also discuss how to design highly efficient OPAMs by modifying the chemical structure or conjugating with a targeting component. Moreover, this Perspective provides a discussion of the general challenges and direction for OPAMs and what further needs to be done. It is hoped that through this overview, OPAMs can prosper and will be more widely used for microbial infections in the future, especially at a time when the global COVID-19 epidemic is getting more serious.


Asunto(s)
Antiinfecciosos/química , Diseño de Fármacos , Fototerapia/métodos , Animales , Antiinfecciosos/farmacología , Antiinfecciosos/uso terapéutico , Bacterias/efectos de los fármacos , Biopelículas/efectos de los fármacos , Biopelículas/efectos de la radiación , Colorantes/química , Colorantes/farmacología , Equipos y Suministros/microbiología , Equipos y Suministros/virología , Escherichia coli/efectos de los fármacos , Escherichia coli/fisiología , Oftalmopatías/tratamiento farmacológico , Oftalmopatías/patología , Hongos/efectos de los fármacos , Grafito/química , Luz , Nanopartículas/química , Nanopartículas/toxicidad , Fármacos Fotosensibilizantes/química , Fármacos Fotosensibilizantes/farmacología , Fármacos Fotosensibilizantes/uso terapéutico , Teoría Cuántica , Especies Reactivas de Oxígeno/metabolismo , Virus/efectos de los fármacos
4.
Nutrients ; 13(7)2021 Jul 14.
Artículo en Inglés | MEDLINE | ID: mdl-34371920

RESUMEN

Nutraceuticals, including vitamin D, vitamin A, zinc, lactoferrin, polyphenols coenzyme Q, magnesium, and selenium, are implicated in the modulation of the complex molecular pathways involved in the immune response against viral pathogens. A common element of the activity of nutraceuticals is their ability to enhance the innate immune response against pathogens by acting on the major cellular subsets and inducing the release of pro-inflammatory cytokines and antimicrobial peptides. In some cases, this action is accompanied by a direct antimicrobial effect, as evidenced in the specific case of lactoferrin. Furthermore, nutraceuticals act through complex molecular mechanisms to minimize the damage caused by the activation of the immune system against pathogens, reducing the oxidative damage, influencing the antigen presentation, enhancing the differentiation and proliferation of regulatory T cells, driving the differentiation of lymphocyte subsets, and modulating the production of pro-inflammatory cytokines. In this paper, we review the main molecular mechanisms responsible for the immunomodulatory function of nutraceuticals, focusing on the most relevant aspects for the prevention and treatment of viral infections.


Asunto(s)
Antivirales/uso terapéutico , Suplementos Dietéticos , Sistema Inmunológico/efectos de los fármacos , Factores Inmunológicos/uso terapéutico , Virosis/tratamiento farmacológico , Virus/efectos de los fármacos , Animales , Antivirales/efectos adversos , Suplementos Dietéticos/efectos adversos , Interacciones Huésped-Patógeno , Humanos , Sistema Inmunológico/inmunología , Sistema Inmunológico/metabolismo , Sistema Inmunológico/virología , Factores Inmunológicos/efectos adversos , Resultado del Tratamiento , Virosis/inmunología , Virosis/metabolismo , Virosis/virología , Virus/inmunología , Virus/patogenicidad
5.
Molecules ; 26(13)2021 Jun 29.
Artículo en Inglés | MEDLINE | ID: mdl-34209485

RESUMEN

(-)-Epigallocatechin-3-O-gallate (EGCG), the most abundant component of catechins in tea (Camellia sinensis (L.) O. Kuntze), plays a role against viruses through inhibiting virus invasiveness, restraining gene expression and replication. In this paper, the antiviral effects of EGCG on various viruses, including DNA virus, RNA virus, coronavirus, enterovirus and arbovirus, were reviewed. Meanwhile, the antiviral effects of the EGCG epi-isomer counterpart (+)-gallocatechin-3-O-gallate (GCG) were also discussed.


Asunto(s)
Antivirales/farmacología , Tratamiento Farmacológico de COVID-19 , Catequina/análogos & derivados , Té/química , Animales , Antivirales/uso terapéutico , Catequina/farmacología , Catequina/uso terapéutico , Humanos , Internalización del Virus/efectos de los fármacos , Virus/efectos de los fármacos
6.
Drug Des Devel Ther ; 15: 1385-1408, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-33833499

RESUMEN

Viral infectious diseases are serious threats to human health in both developing and developed countries. Although there is the continued development of new drugs from synthetic sources as antiviral agents, medicinal plants continue to provide the basic raw materials for some of the most important antiviral drugs. Alkaloids are a class of pharmacologically active plant compounds that are usually alkaline in nature. In this review, we tried to summarize recent progress in herb-based antiviral research, the advantages of using active plant compounds as antiviral agents, and the inflammatory responses initiated by alkaloids, based on the literature from 2009 to 2019, for the treatment of conditions, including influenza, human immunodeficiency virus, herpes simplex virus, hepatitis, and coxsackievirus infections. Articles are retrieved from PubMed, Google Scholar, and Web of Science using relevant keywords. In particular, the alkaloids from medicinal plants responsible for the molecular mechanisms of anti-inflammatory actions are identified and discussed. This review can provide a theoretical basis and approaches for using various alkaloids as antiviral treatments. More research is needed to develop alkaloidal compounds as antiviral therapeutic agents and potential regulators of the anti-inflammatory response.


Asunto(s)
Alcaloides/farmacología , Antiinflamatorios no Esteroideos/farmacología , Antivirales/farmacología , Extractos Vegetales/farmacología , Plantas Medicinales/química , Alcaloides/química , Animales , Antiinflamatorios no Esteroideos/química , Antivirales/química , Humanos , Inflamación/tratamiento farmacológico , Extractos Vegetales/química , Virosis/tratamiento farmacológico , Virus/efectos de los fármacos
7.
Viruses ; 13(2)2021 02 23.
Artículo en Inglés | MEDLINE | ID: mdl-33672228

RESUMEN

Mushrooms are used in their natural form as a food supplement and food additive. In addition, several bioactive compounds beneficial for human health have been derived from mushrooms. Among them, polysaccharides, carbohydrate-binding protein, peptides, proteins, enzymes, polyphenols, triterpenes, triterpenoids, and several other compounds exert antiviral activity against DNA and RNA viruses. Their antiviral targets were mostly virus entry, viral genome replication, viral proteins, and cellular proteins and influenced immune modulation, which was evaluated through pre-, simultaneous-, co-, and post-treatment in vitro and in vivo studies. In particular, they treated and relieved the viral diseases caused by herpes simplex virus, influenza virus, and human immunodeficiency virus (HIV). Some mushroom compounds that act against HIV, influenza A virus, and hepatitis C virus showed antiviral effects comparable to those of antiviral drugs. Therefore, bioactive compounds from mushrooms could be candidates for treating viral infections.


Asunto(s)
Agaricales/química , Antivirales/farmacología , Extractos Vegetales/farmacología , Animales , Antivirales/química , Humanos , Extractos Vegetales/química , Virosis/tratamiento farmacológico , Virosis/virología , Replicación Viral/efectos de los fármacos , Virus/efectos de los fármacos
8.
Molecules ; 26(3)2021 Jan 26.
Artículo en Inglés | MEDLINE | ID: mdl-33530290

RESUMEN

The emergence of antimicrobial resistance (AMR) has urged researchers to explore therapeutic alternatives, one of which includes the use of natural plant products such as essential oils (EO). In fact, EO obtained from clove, oregano, thymus, cinnamon bark, rosemary, eucalyptus, and lavender have been shown to present significant inhibitory effects on bacteria, fungi, and viruses; many studies have been done to measure EO efficacy against microorganisms. The strategy of combinatory effects via conventional and non-conventional methods revealed that the combined effects of EO-EO or EO-antibiotic exhibit enhanced efficacy. This paper aims to review the antimicrobial effects of EO, modes of EO action (membrane disruption, efflux inhibition, increase membrane permeability, and decrease in intracellular ATP), and their compounds' potential as effective agents against bacteria, fungi, and viruses. It is hoped that the integration of EO applications in this work can be used to consider EO for future clinical applications.


Asunto(s)
Antibacterianos/uso terapéutico , Enfermedades Transmisibles/tratamiento farmacológico , Aceites Volátiles/uso terapéutico , Plantas/química , Antibacterianos/farmacología , Bacterias/efectos de los fármacos , Enfermedades Transmisibles/microbiología , Sinergismo Farmacológico , Hongos/efectos de los fármacos , Humanos , Aceites Volátiles/farmacología , Aceites de Plantas/farmacología , Aceites de Plantas/uso terapéutico , Virus/efectos de los fármacos
9.
J Ethnopharmacol ; 271: 113878, 2021 May 10.
Artículo en Inglés | MEDLINE | ID: mdl-33515683

RESUMEN

ETHNOPHARMACOLOGICAL RELEVANCE: Ricinus communis L., commonly known as castor oil plant, is a precious traditional medicine with a history of thousands of years in the world. Castor oil plant has high traditional and medicinal values for treating liver infections, stomach ache, flatulence, constipation, inflammation, warts, colic, enteritis, fever, headache, and as a counter irritant. Its diverse phytochemicals have a wide range of valuable medicinal activities including hepatoprotective, anti-nociceptive, antioxidant, antiulcer, anticancer, anti-inflammatory, central analgesic, antidiabetic, antimicrobial, antiviral, and wound healing activity. AIM OF THE WORK: To provide a complete characterization of the composition of Ricinus communis leaves using ultra-performance liquid chromatography coupled with hybrid triple time-of-flight mass spectrometry (UPLC-Triple TOF-MS/MS) and different chromatographic techniques and to evaluate its antiviral potential using three mechanisms against three common viruses. MATERIALS AND METHODS: R. communis leaves were extracted with 70% methanol and further partitioned with solvents of increasing polarities: petroleum ether, dichloromethane (CH2Cl2), ethyl acetate, and n-butanol. The CH2Cl2 and n-butanol fractions were subjected to repeated chromatographic separation to isolate the phytochemicals, and their structures were elucidated using nuclear magnetic resonance spectroscopy. UPLC-Triple TOF-MS/MS was performed to determine the different phytochemicals in the ethyl acetate fraction. The antiviral activity of the extracts was investigated using the maximum nontoxic concentration of each against the challenge dose of the virus (CDV) and 1/10 and 1/100 dilutions of the CDV for Coxsackie B virus type 4 (COXB4), herpes simplex virus type 1 (HSV1), and hepatitis A virus (HAV) using Vero cell cultures that were treated according to three protocols to test for anti-replicative, protective, and anti-infective antiviral activity. Cell viability was evaluated using the MTT colorimetric assay and each experiment is repeated three times independently of each other. RESULTS: R. communis leaves possessed antiviral activity. Evaluation of the anti-replicative activity showed that all extracts possessed high anti-replicative activity against HAV especially methanol and methylene chloride fractions and moderate activity against COXB4; butanol > methylene chloride and ethyl acetate > methanol. All extracts showed protective activity against HAV, especially butanol extract, while methanol extracts showed higher non-significant antiviral protective activity against HSV1 vs Acyclovir. Almost no anti-infective effects were recorded for any extract against the studied viruses. CONCLUSION: The discriminatory effect against each virus by different mechanisms suggests the presence of different chemical compounds. The alkaloid and phenolic derivatives of the extracts of R. communis leaves may help develop a drug to prevent or treat common viral infections. Further investigations are recommended to define the bioactive antiviral properties of R. communis leaves.


Asunto(s)
Antivirales/farmacología , Extractos Vegetales/farmacología , Ricinus/química , Aciclovir/farmacología , Aciclovir/toxicidad , Animales , Antivirales/aislamiento & purificación , Antivirales/toxicidad , Supervivencia Celular/efectos de los fármacos , Chlorocebus aethiops , Cromatografía Líquida de Alta Presión , Medicina Tradicional , Metanol/química , Extractos Vegetales/aislamiento & purificación , Extractos Vegetales/toxicidad , Hojas de la Planta/química , Solventes/química , Espectrometría de Masas en Tándem , Células Vero , Virus/efectos de los fármacos
10.
Molecules ; 26(3)2021 Jan 25.
Artículo en Inglés | MEDLINE | ID: mdl-33503834

RESUMEN

Plants have had historical significance in medicine since the beginning of civilization. The oldest medical pharmacopeias of the African, Arabian, and Asian countries solely utilize plants and herbs to treat pain, oral diseases, skin diseases, microbial infections, multiple types of cancers, reproductive disorders among a myriad of other ailments. The World Health Organization (WHO) estimates that over 65% of the world population solely utilize botanical preparations as medicine. Due to the abundance of plants, plant-derived medicines are more readily accessible, affordable, convenient, and have safer side-effect profiles than synthetic drugs. Plant-based decoctions have been a significant part of Jamaican traditional folklore medicine. Jamaica is of particular interest because it has approximately 52% of the established medicinal plants that exist on earth. This makes the island particularly welcoming for rigorous scientific research on the medicinal value of plants and the development of phytomedicine thereof. Viral infections caused by the human immunodeficiency virus types 1 and 2 (HIV-1 and HIV-2), hepatitis virus B and C, influenza A virus, and the severe acute respiratory syndrome coronavirus 2 (SARS CoV-2) present a significant global burden. This is a review of some important Jamaican medicinal plants, with particular reference to their antiviral activity.


Asunto(s)
Antivirales/farmacología , Plantas Medicinales/química , Virus/efectos de los fármacos , Antivirales/efectos adversos , Antivirales/química , Jamaica , Pruebas de Sensibilidad Microbiana , Virus/clasificación
11.
Molecules ; 25(24)2020 Dec 08.
Artículo en Inglés | MEDLINE | ID: mdl-33302377

RESUMEN

Due to the emergence of multidrug-resistant pathogens, it is necessary to develop options to fight infections caused by these agents. Lactoferrin (Lf) is a cationic nonheme multifunctional glycoprotein of the innate immune system of mammals that provides numerous benefits. Lf is bacteriostatic and/or bactericidal, can stimulate cell proliferation and differentiation, facilitate iron absorption, improve neural development and cognition, promote bone growth, prevent cancer and exert anti-inflammatory and immunoregulatory effects. Lactoferrin is present in colostrum and milk and is also produced by the secondary granules of polymorphonuclear leukocytes, which store this glycoprotein and release it at sites of infection. Lf is also present in many fluids and exocrine secretions, on the surfaces of the digestive, respiratory and reproductive systems that are commonly exposed to pathogens. Apo-Lf (an iron-free molecule) can be microbiostatic due to its ability to capture ferric iron, blocking the availability of host iron to pathogens. However, apo-Lf is mostly microbicidal via its interaction with the microbial surface, causing membrane damage and altering its permeability function. Lf can inhibit viral entry by binding to cell receptors or viral particles. Lf is also able to counter different important mechanisms evolved by microbial pathogens to infect and invade the host, such as adherence, colonization, invasion, production of biofilms and production of virulence factors such as proteases and toxins. Lf can also cause mitochondrial and caspase-dependent regulated cell death and apoptosis-like in pathogenic yeasts. All of these mechanisms are important targets for treatment with Lf. Holo-Lf (the iron-saturated molecule) can contain up to two ferric ions and can also be microbicidal against some pathogens. On the other hand, lactoferricins (Lfcins) are peptides derived from the N-terminus of Lf that are produced by proteolysis with pepsin under acidic conditions, and they cause similar effects on pathogens to those caused by the parental Lf. Synthetic analog peptides comprising the N-terminus Lf region similarly exhibit potent antimicrobial properties. Importantly, there are no reported pathogens that are resistant to Lf and Lfcins; in addition, Lf and Lfcins have shown a synergistic effect with antimicrobial and antiviral drugs. Due to the Lf properties being microbiostatic, microbicidal, anti-inflammatory and an immune modulator, it represents an excellent natural alternative either alone or as adjuvant in the combat to antibiotic multidrug-resistant bacteria and other pathogens. This review aimed to evaluate the data that appeared in the literature about the effects of Lf and its derived peptides on pathogenic bacteria, protozoa, fungi and viruses and how Lf and Lfcins inhibit the mechanisms developed by these pathogens to cause disease.


Asunto(s)
Antiinfecciosos/química , Antiinfecciosos/farmacología , Lactoferrina/química , Lactoferrina/farmacología , Péptidos/química , Péptidos/farmacología , Animales , Antiinfecciosos/síntesis química , Antiparasitarios/síntesis química , Antiparasitarios/química , Antiparasitarios/farmacología , Bacterias/efectos de los fármacos , Adhesión Bacteriana/efectos de los fármacos , Pared Celular/efectos de los fármacos , Técnicas de Química Sintética , Hongos/efectos de los fármacos , Interacciones Huésped-Patógeno , Humanos , Péptidos/síntesis química , Proteolisis/efectos de los fármacos , Relación Estructura-Actividad , Virulencia/efectos de los fármacos , Factores de Virulencia , Virus/efectos de los fármacos
12.
J Infect Dev Ctries ; 14(9): 1054-1064, 2020 09 30.
Artículo en Inglés | MEDLINE | ID: mdl-33031096

RESUMEN

INTRODUCTION: The present study aimed to determine the chemical compositions and bioactivities of the essential oil of Atalantia sessiflora Guillaumin (A. sessiflora), including antibacterial, antimycotic, antitrichomonas, anti-inflammatory and antiviral effects. METHODOLOGY: The essential oil from leaves of A. sessiflora was extracted by hydrodistillation using a Clevenger apparatus. Chemical compositions of oil were identified by GC/MS. Antimicrobial and antitrichomonas activity were determined by the microdilution method; anti-inflammatory and antiviral were determined by the MTT method. RESULTS: The average yield of oil was 0.46 ± 0.01% (v/w, dry leaves). A number of 45 constituents were identified by GC/MS. The essential oil comprised four main components. The oil showed antimicrobial activities against Gram-positive strains as Staphylococcus; Gram-negative bacteria such as Klebsiella pneumoniae and Escherichia coli; and finally four Candida species. Enterococcus faecalis and Pseudomonas aeruginosa were least susceptible to the oil of A. sessiflora, as seen in their MIC and MLC values over 16% (v/v). Activity against Trichomonas vaginalis was also undertaken, showing IC50, IC90 and MLC values of 0.016, 0.03 and 0.06% (v/v) respectively, after 48 hours of incubation. The oil of A. sessiflora displayed activity against the nitric oxide generation with the IC50 of 95.94 ± 6.18 µg/mL. The oil was completely ineffective against tested viruses, ssRNA+, ssRNA-, dsRNA, and dsDNA viruses. CONCLUSIONS: This is the first yet comprehensive scientific report about the chemical compositions and pharmacological properties of the essential oil of A. sessiflora. Further studies should be done to evaluate the safety and toxicity of A. sessiflora oil.


Asunto(s)
Antiinfecciosos/farmacología , Antiinflamatorios/farmacología , Antitricomonas/farmacología , Bacterias/efectos de los fármacos , Aceites Volátiles/farmacología , Trichomonas vaginalis/efectos de los fármacos , Animales , Antiinfecciosos/aislamiento & purificación , Antiinflamatorios/aislamiento & purificación , Antitricomonas/aislamiento & purificación , Antivirales/farmacología , Línea Celular , Cromatografía de Gases y Espectrometría de Masas , Humanos , Ratones , Pruebas de Sensibilidad Microbiana , Óxido Nítrico/análisis , Extractos Vegetales/farmacología , Hojas de la Planta/química , Células RAW 264.7 , Rutaceae/química , Vietnam , Virus/efectos de los fármacos
13.
Arch Microbiol ; 202(9): 2569-2578, 2020 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-32671418

RESUMEN

This study screened mastic gum (Pistacia lentiscus L.) for antiviral activity against herpes simplex virus type 2 (HSV-2), coxsackievirus type B3, and adenovirus type 5. The organs of this plant (leaves, stem, and seed) were macerated sequentially using solvents of increasing polarity (hexane, dichloromethane, ethyl acetate, and methanol). Only the methanol extract of stem exhibited significant activity against HSV-2. This extract showed anti-HSV-2 activity with a selectivity index of 51 (50% cytotoxic concentration = 186 µg/mL; 50% inhibitory concentration = 3.63 µg/mL), and demonstrated direct inhibition against this virus with a virucidal selectivity index of 620 (50% virucidal concentration = 0.30 µg/mL). A bio-guided assay involving thin-layer chromatography led to the isolation of two active compounds, which have been identified as dammaradienone and dammaradienol using high-performance liquid chromatography-diode array detection coupled with electrospray ionization mass spectrometry. P. lentiscus has been widely studied for other biological activities. However, to our knowledge, this is the first report of P. lentiscus L. exhibiting antiviral activity.


Asunto(s)
Pistacia/química , Extractos Vegetales/farmacología , Virus/efectos de los fármacos , Adenoviridae/efectos de los fármacos , Antivirales/química , Antivirales/farmacología , Cromatografía Líquida de Alta Presión , Enterovirus/efectos de los fármacos , Herpesvirus Humano 2/efectos de los fármacos , Hojas de la Planta/química , Semillas/química , Solventes/química
14.
Molecules ; 25(11)2020 Jun 05.
Artículo en Inglés | MEDLINE | ID: mdl-32516954

RESUMEN

The presence of resistance to available antivirals calls for the development of novel therapeutic agents. Plant-derived essential oils may serve as alternative sources of virus-induced disease therapy. Previous studies have demonstrated essential oils to be excellent candidates to treat antiviral-resistant infection associated with their chemical complexity which confers broad-spectrum mechanisms of action and non-specific antiviral properties. However, almost no comprehensive reviews are updated to generalize knowledge in this regard and disclose the interplay between the components and their antiviral activities. This review provides an up-to-date overview of the antiviral efficacy of essential oils from a wide range of plant species and their characteristic components, as well as their overall mechanisms of action, focusing on the last decade. The roles of individual components relative to the overall antiviral efficacy of essential oils, together with the antiviral activity of essential oils in comparison with commercial drugs are also discussed. Lastly, the inadequacies in current research and future research are put forward. This review will provide references in the design of new drug prototypes and improve our understanding of the proper applications of essential oils in the future.


Asunto(s)
Antivirales/uso terapéutico , Enfermedades Transmisibles/tratamiento farmacológico , Aceites Volátiles/uso terapéutico , Plantas/química , Virus/efectos de los fármacos , Enfermedades Transmisibles/virología , Humanos
15.
Arch Virol ; 165(9): 1935-1945, 2020 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-32594322

RESUMEN

Plants are a rich source of new antiviral, pharmacologically active agents. The naturally occurring plant alkaloid berberine (BBR) is one of the phytochemicals with a broad range of biological activity, including anticancer, anti-inflammatory and antiviral activity. BBR targets different steps in the viral life cycle and is thus a good candidate for use in novel antiviral drugs and therapies. It has been shown that BBR reduces virus replication and targets specific interactions between the virus and its host. BBR intercalates into DNA and inhibits DNA synthesis and reverse transcriptase activity. It inhibits replication of herpes simplex virus (HSV), human cytomegalovirus (HCMV), human papillomavirus (HPV), and human immunodeficiency virus (HIV). This isoquinoline alkaloid has the ability to regulate the MEK-ERK, AMPK/mTOR, and NF-κB signaling pathways, which are necessary for viral replication. Furthermore, it has been reported that BBR supports the host immune response, thus leading to viral clearance. In this short review, we focus on the most recent studies on the antiviral properties of berberine and its derivatives, which might be promising agents to be considered in future studies in the fight against the current pandemic SARS-CoV-2, the virus that causes COVID-19.


Asunto(s)
Antivirales/farmacología , Berberina/farmacología , Virus/efectos de los fármacos , Animales , Antivirales/química , Berberina/química , Humanos , Extractos Vegetales/química , Extractos Vegetales/farmacología , Virosis/virología , Replicación Viral/efectos de los fármacos , Virus/genética , Virus/crecimiento & desarrollo
16.
Viruses ; 12(5)2020 05 15.
Artículo en Inglés | MEDLINE | ID: mdl-32429324

RESUMEN

Chikungunya and yellow fever virus cause vector-borne viral diseases in humans. There is currently no specific antiviral drug for either of these diseases. Banana plants are used in traditional medicine for treating viral diseases such as measles and chickenpox. Therefore, we tested selected banana cultivars for their antiviral but also cytotoxic properties. Different parts such as leaf, pseudostem and corm, collected separately and extracted with four different solvents (hexane, acetone, ethanol, and water), were tested for in vitro antiviral activity against Chikungunya virus (CHIKV), enterovirus 71 (EV71), and yellow fever virus (YFV). Extracts prepared with acetone and ethanol from leaf parts of several cultivars exhibited strong (EC50 around 10 µg/mL) anti-CHIKV activity. Interestingly, none of the banana plant extracts (concentration 1-100 µg/mL) were active against EV71. Activity against YFV was restricted to two cultivars: Namwa Khom-Pseudostem-Ethanol (5.9 ± 5.4), Namwa Khom-Corm-Ethanol (0.79 ± 0.1) and Fougamou-Corm-Acetone (2.5 ± 1.5). In most cases, the cytotoxic activity of the extracts was generally 5- to 10-fold lower than the antiviral activity, suggesting a reasonable therapeutic window.


Asunto(s)
Antivirales/farmacología , Musa/química , Extractos Vegetales/farmacología , Animales , Antivirales/química , Línea Celular , Supervivencia Celular/efectos de los fármacos , Chlorocebus aethiops , Humanos , Musa/clasificación , Fenol/análisis , Fenol/farmacología , Extractos Vegetales/química , Estructuras de las Plantas/química , Células Vero , Virus/clasificación , Virus/efectos de los fármacos
17.
Chem Biodivers ; 17(6): e2000062, 2020 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-32207224

RESUMEN

This review explores the body of scientific information available on the antimicrobial properties of essential oils against pathogens responsible for respiratory infections and critically compares this to what is recommended in the Layman's aroma-therapeutic literature. Essential oils are predominantly indicated for the treatment of respiratory infections caused by bacteria or viruses (total 79.0 %), the efficacy of which has not been confirmed through clinical trials. When used in combination, they are often blended for presumed holistic synergistic effects. Of the essential oils recommended, all show some degree of antioxidant activity, 50.0 % demonstrate anti-inflammatory effects and 83.3 % of the essential oils showed antihistaminic activity. Of the essential oils reviewed, 43.8 % are considered non-toxic while the remaining essential oils are considered slightly to moderately toxic (43.7 %) or the toxicity is unknown (12.5 %). Recommendations are made for further research into essential oil combinations.


Asunto(s)
Bacterias/efectos de los fármacos , Hongos/efectos de los fármacos , Aceites Volátiles/farmacología , Infecciones del Sistema Respiratorio/patología , Virus/efectos de los fármacos , Antiinfecciosos/química , Antiinfecciosos/farmacología , Antiinfecciosos/uso terapéutico , Antiinflamatorios/química , Antiinflamatorios/uso terapéutico , Antivirales/química , Antivirales/farmacología , Antivirales/uso terapéutico , Humanos , Aceites Volátiles/química , Aceites Volátiles/uso terapéutico , Plantas Medicinales/química , Plantas Medicinales/metabolismo , Infecciones del Sistema Respiratorio/tratamiento farmacológico , Infecciones del Sistema Respiratorio/microbiología
18.
Curr Drug Discov Technol ; 17(4): 469-483, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-31309894

RESUMEN

BACKGROUND AND OBJECTIVE: Infectious diseases are amongst the leading causes of death in the world and central nervous system infections produced by viruses may either be fatal or generate a wide range of symptoms that affect global human health. Most antiviral plants contain active phytoconstituents such as alkaloids, flavonoids, and polyphenols, some of which play an important antiviral role. Herein, we present a background to viral central nervous system (CNS) infections, followed by a review of medicinal plants and bioactive compounds that are effective against viral pathogens in CNS infections. METHODS: A comprehensive literature search was conducted on scientific databases including: PubMed, Scopus, Google Scholar, and Web of Science. The relevant keywords used as search terms were: "myelitis", "encephalitis", "meningitis", "meningoencephalitis", "encephalomyelitis", "central nervous system", "brain", "spinal cord", "infection", "virus", "medicinal plants", and "biological compounds". RESULTS: The most significant viruses involved in central nervous system infections are: Herpes Simplex Virus (HSV), Varicella Zoster Virus (VZV), West Nile Virus (WNV), Enterovirus 71 (EV71), Japanese Encephalitis Virus (JEV), and Dengue Virus (DENV). The inhibitory activity of medicinal plants against CNS viruses is mostly active through prevention of viral binding to cell membranes, blocking viral genome replication, prevention of viral protein expression, scavenging reactive Oxygen Species (ROS), and reduction of plaque formation. CONCLUSION: Due to the increased resistance of microorganisms (bacteria, viruses, and parasites) to antimicrobial therapies, alternative treatments, especially using plant sources and their bioactive constituents, appear to be more fruitful.


Asunto(s)
Antivirales/farmacología , Enfermedades Virales del Sistema Nervioso Central/tratamiento farmacológico , Fitoquímicos/farmacología , Fitoterapia/métodos , Plantas Medicinales/química , Antivirales/uso terapéutico , Enfermedades Virales del Sistema Nervioso Central/virología , Farmacorresistencia Viral/efectos de los fármacos , Humanos , Fitoquímicos/uso terapéutico , Virus/efectos de los fármacos , Virus/patogenicidad
19.
Biomolecules ; 9(10)2019 10 16.
Artículo en Inglés | MEDLINE | ID: mdl-31623122

RESUMEN

Throughout history, medicinal purposes of plants have been studied, documented, and acknowledged as an integral part of human healthcare systems. The development of modern medicine still relies largely on this historical knowledge of the use and preparation of plants and their extracts. Further research into the human microbiome highlights the interaction between immunomodulatory responses and plant-derived, prebiotic compounds. One such group of compounds includes the inulin-type fructans (ITFs), which may also act as signaling molecules and antioxidants. These multifunctional compounds occur in a small proportion of plants, many of which have recognized medicinal properties. Echinacea is a well-known medicinal plant and products derived from it are sold globally for its cold- and flu-preventative and general health-promoting properties. Despite the well-documented phytochemical profile of Echinacea plants and products, little research has looked into the possible role of ITFs in these products. This review aims to highlight the occurrence of ITFs in Echinacea derived formulations and the potential role they play in immunomodulation.


Asunto(s)
Antioxidantes/farmacología , Antivirales/farmacología , Echinacea/química , Fructanos/farmacología , Inmunomodulación , Virus/efectos de los fármacos , Antioxidantes/química , Antioxidantes/aislamiento & purificación , Antivirales/química , Antivirales/aislamiento & purificación , Fructanos/química , Fructanos/aislamiento & purificación , Sistema Inmunológico/efectos de los fármacos , Sistema Inmunológico/inmunología , Extractos Vegetales/química , Extractos Vegetales/aislamiento & purificación , Extractos Vegetales/farmacología , Virus/inmunología
20.
Photochem Photobiol Sci ; 18(11): 2565-2612, 2019 Nov 01.
Artículo en Inglés | MEDLINE | ID: mdl-31397467

RESUMEN

Photodynamic therapy (PDT) is a well-established treatment option in the treatment of certain cancerous and pre-cancerous lesions. Though best-known for its application in tumor therapy, historically the photodynamic effect was first demonstrated against bacteria at the beginning of the 20th century. Today, in light of spreading antibiotic resistance and the rise of new infections, this photodynamic inactivation (PDI) of microbes, such as bacteria, fungi, and viruses, is gaining considerable attention. This review focuses on the PDI of viruses as an alternative treatment in antiviral therapy, but also as a means of viral decontamination, covering mainly the literature of the last decade. The PDI of viruses shares the general action mechanism of photodynamic applications: the irradiation of a dye with light and the subsequent generation of reactive oxygen species (ROS) which are the effective phototoxic agents damaging virus targets by reacting with viral nucleic acids, lipids and proteins. Interestingly, a light-independent antiviral activity has also been found for some of these dyes. This review covers the compound classes employed in the PDI of viruses and their various areas of use. In the medical area, currently two fields stand out in which the PDI of viruses has found broader application: the purification of blood products and the treatment of human papilloma virus manifestations. However, the PDI of viruses has also found interest in such diverse areas as water and surface decontamination, and biosafety.


Asunto(s)
Luz , Fotoquimioterapia/tendencias , Virosis/terapia , Virus/efectos de la radiación , Humanos , Papillomaviridae/efectos de los fármacos , Papillomaviridae/efectos de la radiación , Fármacos Fotosensibilizantes/química , Fármacos Fotosensibilizantes/farmacología , Fármacos Fotosensibilizantes/uso terapéutico , Especies Reactivas de Oxígeno/metabolismo , Virosis/tratamiento farmacológico , Virosis/metabolismo , Virus/efectos de los fármacos , Virus/metabolismo
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