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1.
Microbiol Spectr ; : e0438522, 2023 Mar 28.
Artigo em Inglês | MEDLINE | ID: mdl-36975835

RESUMO

Candida auris is a multidrug-resistant fungus known to be a global public health problem. The skin-based transmission, together with the marked resistance to drugs, resulted in its rapid spread to all continents. The aim of this study was to identify an essential oil (EO) active in the fight against C. auris. A total of 15 EOs were tested against 10 clinical strains of C. auris. Cinnamomum zeylanicum EO (CZ-EO) was the most effective (MIC90 and MFC90 equal to 0.06% vol/vol). Three fractions obtained from CZ-EO, and the cinnamaldehyde (CIN), the major chemical compound, were tested to identify the principal compound effectives against C. auris. All CIN-containing samples showed anti-fungal activity. To study the synergy with fluconazole, CZ-EO, its active fraction (FR2), and CIN were tested in checkerboard tests. Results show that CZ-EO and FR2, but not CIN, synergize with fluconazole. Furthermore, only the copresence of CZ-EO or FR2 synergize with fluconazole at therapeutic concentrations of the drug (0.45 ± 0.32 µg/mL and 0.64 ± 0.67 µg/mL, respectively), while CIN only shows additive activity. In vivo studies conducted on Galleria mellonella larvae show the absence of toxicity of CZ-EO up to concentrations of 16% vol/vol, and the ability of CZ-EO to reactivate the efficacy of fluconazole when formulated at synergic concentrations. Finally, biochemical tests were made to study the mechanism of action of CZ-EO. These studies show that in the presence of both fluconazole and CZ-EO, the activity of fungal ATPases decreases and, at the same time, the amount of intracellular drug increases. IMPORTANCE This study highlights how small doses of CZ-EO are able to inhibit the secretion of fluconazole and promote its accumulation in the fungal cell. In this manner, the drug is able to exert its pharmacological effects bypassing the resistance of the yeast. If further studies will confirm this synergy, it will be possible to develop new therapeutic formulations active in the fight against C. auris resistances.

2.
Nat Prod Res ; 32(16): 1926-1950, 2018 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-28748726

RESUMO

Natural products (NPs) are secondary metabolites produced and used by organisms for defending or adapting purposes. These molecules were naturally selected during thousands of years to improve the specificity and cover a very wide range of functions, depending on the origin, the habitat and the specific activity carried out in the organism of origin. Due to these intrinsic features, NPs have been used as healing agents since thousands of years and still today continue to be the most important source of new potential therapeutic preparations.The purpose of this review is to provide information about the historical evolution of the NPs investigation methods, focusing attention on the relative benefit/problems emerged after the improvement of the scientific investigations about them, especially over the last two centuries. Taken together, the reported information lead to the central role of NPs in the future of drug development for human needs.


Assuntos
Produtos Biológicos/uso terapêutico , Descoberta de Drogas/métodos , Descoberta de Drogas/história , Descoberta de Drogas/tendências , História do Século XX , História do Século XXI , Humanos , Compostos Fitoquímicos
3.
Fish Shellfish Immunol ; 34(5): 1335-44, 2013 May.
Artigo em Inglês | MEDLINE | ID: mdl-23470814

RESUMO

The pharmacological potential of Aloe arborescens Miller leaf components was investigated, with special attention deserved to immune modulatory effects on the Sparus aurata fibroblast cell line SAF-1. The cells were treated with Aloe extract at different concentrations (1.2-4.8 mg ml(-1)) for various times (24-72 h). The lowest concentration did not provoke any cellular damage observable by SEM and did not affect ATP amounts after 24 and 48 h, while even induced a significant increase over controls after 72 h. We next examined the transcription kinetics of different immune-related genes (IL-1ß, TGF-ß, TNF-α, COX-2, IFN-I, Mx and MHCI-α) in SAF-1 cells stimulated with LPS or poly I:C. The Aloe extract (1.2 mg ml(-1)) acted as a powerful immune stimulant in LPS- or poly I:C-activated SAF-1 cells, inducing a synergic effect on interconnected genes that are expected to be involved in different aspects of the immune responses. These reports provide a new perspective for the use of A. arborescens to prevent or oppose bacterial and viral fish diseases and to face, as an alternative strategy based on natural plant extracts, the growing unwillingness to rely upon standard solutions involving antibiotics or antimicrobial chemicals.


Assuntos
Aloe/química , Regulação da Expressão Gênica , Extratos Vegetais/farmacologia , Dourada/genética , Dourada/imunologia , Animais , Linhagem Celular , Lipopolissacarídeos/farmacologia , Folhas de Planta/química , Poli I-C/farmacologia
4.
Plant Biol (Stuttg) ; 11(2): 179-93, 2009 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-19228325

RESUMO

Trivalent chromium has previously been found to effectively inhibit kiwifruit pollen tube emergence and elongation in vitro. In the present study, a photometric measure of increases in tube wall production during germination showed that 25 and 50 mum CrCl(3) treatment induced a substantial reduction in levels of polysaccharides in walls over those in controls. Moreover, chromium-treated kiwifruit pollen tubes had irregular and indented cell walls. Callose, the major tube wall polysaccharide, was deposited in an anomalous punctuate pattern. Arabinogalactan proteins (AGPs), which are integral in maintaining correct tube growth and shape in kiwifruit pollen, were found to be strongly altered in their distribution after CrCl(3) treatment compared to control tube walls. Transmission electron microscopy-immunogold analysis using four monoclonal antibodies (JIM8, JIM13, JIM14 and MAC207) revealed discontinuous AGP distribution within the treated tube walls. Such clearly discernable alterations in the molecular and morphological architecture of pollen tube walls may be detrimental in vivo for the male gametophyte to accomplish its vital role in the fertilisation process.


Assuntos
Actinidia/metabolismo , Parede Celular/química , Cromo/toxicidade , Glucanos/metabolismo , Mucoproteínas/metabolismo , Tubo Polínico/metabolismo , Actinidia/citologia , Anticorpos Monoclonais , Parede Celular/fisiologia , Celulose/metabolismo , Flores , Proteínas de Plantas/metabolismo , Tubo Polínico/citologia , Tubo Polínico/ultraestrutura , Polissacarídeos/metabolismo , Reprodução , Poluentes do Solo/toxicidade , Estresse Fisiológico
5.
Plant Biol (Stuttg) ; 9(6): 800-6, 2007 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-17564946

RESUMO

In vitro toxicity of the antimicrobial peptides (AMPs) magainin 1 and 2 to a higher plant organism, i.e., the bicellular male gametophyte of Actinidia Deliciosa (kiwifruit), is investigated. Heavy damage to the plasma membrane, the primary cellular target of the peptides, was rapidly induced: in as few as 15 min, from 70 to nearly 100 % of pollen grains were rendered unviable by 20 microM magainin 1 or 2, respectively. Therefore, kiwifruit pollen sensitivity to natural magainins seemed to be higher if compared to the sensitivity of other pollen species towards magainin 2 amide or synthetic magainin analogues. Strong dose-dependent inhibitory effects on kiwifruit pollen performance were registered: as for magainin 1, the EC (50) at 120 min varied from 14.0 (germination) to 15.8 microM (tube elongation). The inhibitory effect was much greater when administering magainin 1 to elongating tubes rather than to ungerminated pollen grains. The two peptides differentially affected kiwifruit pollen, in line with the previously documented greater activity of magainin 2 in other cell systems. Furthermore, 20 microM magainin 1-treated pollen grains took on a shrivelled shape within 30 min of incubation, an increasingly widespread effect with higher peptide concentration. At the ultrastructural level, both protoplast shrinkage and striking organelle alterations were evident, including chromatin condensation, swelling and loss of mitochondrial cristae, dilation of rough endoplasmic reticulum cisternae, and vacuolization of cytoplasm. To our knowledge, similar alterations in animal or plant cells treated with AMPs have not been described yet.


Assuntos
Actinidia/efeitos dos fármacos , Peptídeos Catiônicos Antimicrobianos/farmacologia , Citotoxinas/farmacologia , Pólen/efeitos dos fármacos , Proteínas de Xenopus/farmacologia , Actinidia/crescimento & desenvolvimento , Actinidia/ultraestrutura , Germinação/efeitos dos fármacos , Magaininas , Plantas Geneticamente Modificadas/efeitos dos fármacos , Plantas Geneticamente Modificadas/metabolismo , Pólen/crescimento & desenvolvimento , Pólen/ultraestrutura
6.
Toxicol In Vitro ; 15(2): 143-51, 2001 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-11287173

RESUMO

Herbicides are chemical compounds widely used in agriculture. As their intensive application is becoming a cause of environmental pollution, detailed and more sophisticated investigations are needed to understand better their consequences at the biological level. After herbicides are dispersed in the fields, they establish chemical interactions with both target and non-target plants. In both cases, herbicides can interact with the plant reproductive apparatus; consequently they could play a role during the fertilisation process in higher plants. Using an antibody to the alpha-tubulin subunit in immunofluorescence and immunoelectron microscopy techniques, we investigated the distribution of microtubules in Nicotiana tabacum pollen tubes grown under in vitro conditions in the presence of five different herbicides selected among those used frequently in central Italy. Herbicides have a specific effect on the microtubular apparatus of both pollen tube and generative cell. In addition to other tests and assays, these results suggest that the microtubule cytoskeleton of pollen tubes can be used as a bioindicator for studying the toxicity effects induced by herbicides.


Assuntos
Dicamba/efeitos adversos , Dicamba/toxicidade , Glicina/efeitos adversos , Herbicidas/efeitos adversos , Herbicidas/toxicidade , Microtúbulos/efeitos dos fármacos , Oxidiazóis/efeitos adversos , Oxidiazóis/toxicidade , Éteres Fenílicos/efeitos adversos , Pólen/efeitos dos fármacos , Testes de Toxicidade , Trifluralina/efeitos adversos , Imunofluorescência , Glicina/análogos & derivados , Éteres Difenil Halogenados , Imuno-Histoquímica , Técnicas In Vitro , Microscopia Confocal , Microscopia Imunoeletrônica , Microtúbulos/patologia , Plantas Tóxicas , Nicotiana , Glifosato
7.
Plant Cell ; 12(9): 1719-36, 2000 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-11006343

RESUMO

Pollen tube growth depends on the differential distribution of organelles and vesicles along the tube. The role of microtubules in organelle movement is uncertain, mainly because information at the molecular level is limited. In an effort to understand the molecular basis of microtubule-based movement, we isolated from tobacco pollen tubes polypeptides that cosediment with microtubules in an ATP-dependent manner. Major polypeptides released from microtubules by ATP (ATP-MAPs) had molecular masses of 90, 80, and 41 kD. Several findings indicate that the 90-kD ATP-MAP is a kinesin-related motor: binding of the polypeptide to microtubules was enhanced by the nonhydrolyzable ATP analog AMP-PNP; the 90-kD polypeptide reacted specifically with a peptide antibody directed against a highly conserved region in the motor domain of the kinesin superfamily; purified 90-kD ATP-MAP induced microtubules to glide in motility assays in vitro; and the 90-kD ATP-MAP cofractionated with microtubule-activated ATPase activity. Immunolocalization studies indicated that the 90-kD ATP-MAP binds to organelles associated with microtubules in the cortical region of the pollen tube. These findings suggest that the 90-kD ATP-MAP is a kinesin-related microtubule motor that moves organelles in the cortex of growing pollen tubes.


Assuntos
Microtúbulos/fisiologia , Nicotiana/fisiologia , Organelas/metabolismo , Plantas Tóxicas , Pólen/crescimento & desenvolvimento , Adenosina Trifosfatases/metabolismo , Trifosfato de Adenosina/farmacologia , Transporte Biológico/efeitos dos fármacos , Fracionamento Químico , Immunoblotting , Cinesinas/análise , Microscopia de Fluorescência , Peptídeos/metabolismo , Proteínas de Plantas/metabolismo , Pólen/ultraestrutura , Ligação Proteica , Nicotiana/citologia
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