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1.
Int J Biol Macromol ; 149: 432-442, 2020 Apr 15.
Article in English | MEDLINE | ID: mdl-32004601

ABSTRACT

Dermatophytes belonging to Trichophyton ssp. are important anthropophilic and zoophilic pathogens, which developed resistance to griseofulvin, the common antifungal drug used to treat dermatophytosis. In this context, Moringa oleifera seed proteins have been described as antifungal agents with potential applications. Thus, this work aimed to evaluate the antidermatophytic in vitro, focusing on mechanisms, and in vivo potential of Mo-CBP4, purified from M. oleifera seeds. Mo-CBP4was purified after protein extraction with 50 mM Tris-HCl buffer, pH 8.0, and chromatography on chitin and CM Sepharose™ columns and antidermatophytic potential of Mo-CBP4 evaluated in vitro and in vivo. In vitro, Mo-CBP4 reduced in 50% the germination of microconidia of Trichophyton mentagrophytes at 45 µM; but did not show inhibition of mycelial growth. Mo-CBP4 (45 µM) presents the inhibitory activity even when incubated with N-acetyl-d-glucosamine (NAG). Analysis of the mechanisms of Mo-CBP4 revealed an increase in membrane permeability, ROS overproduction and damage to cell wall leading to microconidia death. Furthermore, using in vivo models, Mo-CBP4 (5, 10 and 20 mg g-1) reduced the severity and time of dermatophytosis. Altogether, these findings indicate that Mo-CBP4 has great potential for the development of novel antifungal drugs for the clinical treatment of dermatophytosis.


Subject(s)
Hydrogels/pharmacology , Moringa oleifera/chemistry , Mycoses/drug therapy , Plant Proteins/chemistry , Allergens/adverse effects , Allergens/chemistry , Antifungal Agents/chemistry , Antifungal Agents/pharmacology , Chitin/chemistry , Humans , Hydrogels/chemistry , Mycoses/microbiology , Mycoses/pathology , Plant Proteins/pharmacology , Seeds/chemistry , Skin/drug effects , Skin/pathology , Spores, Fungal/drug effects , Spores, Fungal/pathogenicity , Tinea/drug therapy , Tinea/microbiology , Tinea/pathology
2.
Int J Biol Macromol ; 143: 814-824, 2020 Jan 15.
Article in English | MEDLINE | ID: mdl-31734363

ABSTRACT

Plant proteins are emerging as an alternative to conventional treatments against candidiasis. The aim of this study was to better understand the mechanism of action of Mo-CBP2 against Candida spp, evaluating redox system activity, lipid peroxidation, DNA degradation, cytochrome c release, medium acidification, and membrane interaction. Anti-candida activity of Mo-CBP2 decreased in the presence of ergosterol, which was not observed with antioxidant agents. C. albicans treated with Mo-CBP2 also had catalase and peroxidase activities inhibited, while superoxide dismutase was increased. Mo-CBP2 increased the lipid peroxidation, but it did not alter the ergosterol profile in live cells. External medium acidification was strongly inhibited, and cytochrome c release and DNA degradation were detected. Mo-CBP2 interacts with cell membrane constituents, changes redox system enzymes in C. albicans and causes lipid peroxidation by ROS overproduction. DNA degradation and cytochrome c release suggest apoptotic or DNAse activity. Lipid peroxidation and H+-ATPases inhibition may induce the process of apoptosis. Finally, Mo-CBP2 did not have a cytotoxic effect in mammalian Vero cells. This study highlights the biotechnological potential of Mo-CBP2 as a promising molecule with low toxicity and potent activity. Further studies should be performed to better understand its mode of action and toxicity.


Subject(s)
Candida/drug effects , Cell Membrane/metabolism , Moringa oleifera/chemistry , Plant Proteins/pharmacology , Seeds/chemistry , Sterols/metabolism , Animals , Antifungal Agents/pharmacology , Antioxidants/pharmacology , Cell Survival/drug effects , Chlorocebus aethiops , Cytochromes c/metabolism , DNA Fragmentation/drug effects , Ergosterol/metabolism , Glucose/pharmacology , Itraconazole/pharmacology , Lipid Peroxidation/drug effects , Nystatin/pharmacology , Oxidation-Reduction , Reactive Oxygen Species/metabolism , Vero Cells
3.
Biomed Res Int ; 2013: 578781, 2013.
Article in English | MEDLINE | ID: mdl-23691507

ABSTRACT

Among the Bauhinia species, B. cheilantha stands out for its seed protein content. However, there is no record of its nutritional value, being used in a nonsustainable way in the folk medicine and for large-scale extraction of timber. The aim of this study was to investigate the food potential of B. cheilantha seeds with emphasis on its protein quality to provide support for flora conservation and use as raw material or as prototype for the development of bioproducts with high added socioeconomic value. B. cheilantha seeds show high protein content (35.9%), reasonable essential amino acids profile, low levels of antinutritional compounds, and nutritional parameters comparable to those of legumes widely used such as soybean and cowpea. The heat treatment of the seeds as well as the protein extraction process (to obtain the protein concentrate) increased the acceptance of diets by about 100% when compared to that of raw Bc diet. These wild legume seeds can be promising alternative source of food to overcome the malnutrition problem faced by low income people adding socioeconomic value to the species.


Subject(s)
Bauhinia/chemistry , Desert Climate , Medicine, Traditional , Nutritive Value , Seeds/chemistry , Toxicity Tests , Amino Acids/analysis , Animals , Lectins/metabolism , Male , Mice , Rats , Rats, Wistar , Seeds/enzymology , Trypsin/metabolism , Urease/metabolism
4.
Molecules ; 17(7): 7854-63, 2012 Jun 28.
Article in English | MEDLINE | ID: mdl-22743589

ABSTRACT

The objective of this study was to evaluate the reactivity of an in-house antigen, extracted from a strain of C. posadasii isolated in northeastern Brazil, by radial immunodiffusion and Western blotting, as well as to establish its biochemical characterization. The protein antigen was initially extracted with the use of solid ammonium sulfate and characterized by 1-D electrophoresis. Subsequently, it was tested by means of double radial immunodiffusion and Western blotting. A positive reaction was observed against the antigen by both immunodiagnostic techniques tested on sera from patients suffering from coccidioidomycosis. Besides this, two immunoreactive protein bands were observed and were revealed to be a ß-glucosidase and a glutamine synthetase after sequencing of the respective N-terminal regions. Our in-house Coccidioides antigen can be promising as a quick and low-cost diagnostic tool without the risk of direct manipulation of the microorganism.


Subject(s)
Antigens, Fungal/immunology , Coccidioides/immunology , Coccidioidomycosis/diagnosis , Coccidioidomycosis/immunology , Immunologic Tests/methods , Amino Acid Sequence , Antigens, Fungal/chemistry , Electrophoresis, Polyacrylamide Gel , Humans , Molecular Sequence Data , Molecular Weight
5.
Protein Pept Lett ; 18(11): 1078-85, 2011 Nov.
Article in English | MEDLINE | ID: mdl-21675945

ABSTRACT

Moringa oleifera Lam. is a perennial multipurpose tree that has been successfully used in folk medicine to cure several inflammatory processes. The aim of this study was to purify and characterize a chitin-binding protein from Moringa oleifera seeds, named Mo-CBP4, and evaluate its antinociceptive and anti-inflammatory effects in vivo. The protein was purified by affinity chromatography on chitin followed by ion exchange chromatography. Acetic acid-induced abdominal constrictions assay was used for the antinociceptive and anti-inflammatory activity assessments. Mo-CBP4 is a glycoprotein (2.9% neutral carbohydrate) composed of two protein subunits with apparent molecular masses of 28 and 18 kDa (9 kDa in the presence of reducing agent). The intraperitoneal injection of Mo-CBP4 (3.5 and 10 mg/kg) into mice 30 min before acetic acid administration potently and significantly reduced the occurrence of abdominal writhing in a dose dependent manner by 44.7% and 100%, respectively. In addition, the oral administration of the protein (10 mg/kg) resulted in 18% and 52.8% reductions in abdominal writhing when given 30 and 60 min prior to acetic acid administration, respectively. Mo-CBP4, when administered by intraperitoneal route, also caused a significant and dose-dependent inhibition of peritoneal capillary permeability induced by acid acetic and significantly inhibited leukocyte accumulation in the peritoneal cavity. In conclusion, this pioneering study describes that the chitin-binding protein Mo-CBP4, from M. oleifera seeds, exhibits anti-inflammatory and antinociceptive properties and scientifically supports the use of this multipurpose tree in folk medicine.


Subject(s)
Chitin/metabolism , Moringa oleifera/chemistry , Pain/drug therapy , Plant Proteins/isolation & purification , Plant Proteins/pharmacology , Seeds/chemistry , Acetates/pharmacology , Analgesics/isolation & purification , Analgesics/metabolism , Analgesics/pharmacology , Analgesics/therapeutic use , Animals , Anti-Inflammatory Agents/isolation & purification , Anti-Inflammatory Agents/metabolism , Anti-Inflammatory Agents/pharmacology , Anti-Inflammatory Agents/therapeutic use , Behavior, Animal/drug effects , Endopeptidases/metabolism , Inflammation/chemically induced , Inflammation/drug therapy , Male , Mice , Pain/chemically induced , Plant Proteins/metabolism , Plant Proteins/therapeutic use , Proteolysis
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