Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 12 de 12
Filtrar
Mais filtros











Base de dados
Intervalo de ano de publicação
1.
Oxid Med Cell Longev ; 2020: 1903056, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32566076

RESUMO

Polysaccharides from the pulps (CAP) and seeds (CAS) of Crataegus azarolus L. var. aronia were extracted by hot water method. Both polysaccharides were characterized by scanning electron microscopy (SEM), Congo red test, FT-IR spectroscopy, and their antioxidant, α-amylase, antiacetylcholinesterase, and antibacterial activities were evaluated. CAP showed the highest total carbohydrate (82.35%) and uronic acid (29.39%) contents. The Congo red test revealed the lack of triple-helical conformation for both polysaccharides. The comparison of both infrared spectra indicated similar patterns with the presence of typical bands of polysaccharides. However, the microstructure of both samples indicated differences when analyzed by SEM. CAP displayed higher antioxidant, α-amylase, and acetylcholinesterase inhibitory activities. Besides, CAP showed the strongest antimicrobial effects against seven microorganisms and, notably, the Gram-positive bacteria. Overall, the results suggest that polysaccharides from C. azarolus L. var. aronia may be considered as novel sources of antioxidants and recommended as enzyme inhibitory agents in food and pharmaceutical industries.


Assuntos
Acetilcolinesterase/metabolismo , Antibacterianos/farmacologia , Antioxidantes/farmacologia , Inibidores da Colinesterase/farmacologia , Crataegus/química , Polissacarídeos/isolamento & purificação , Polissacarídeos/farmacologia , alfa-Amilases/antagonistas & inibidores , Sequestradores de Radicais Livres/farmacologia , Peróxido de Hidrogênio/metabolismo , Concentração Inibidora 50 , Quelantes de Ferro/farmacologia , Testes de Sensibilidade Microbiana , Conformação Molecular , Polissacarídeos/ultraestrutura , Espectroscopia de Infravermelho com Transformada de Fourier
2.
Inflammopharmacology ; 28(2): 563-574, 2020 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-31792766

RESUMO

Brachychiton populneus is one of the unexploited Tunisian plants, traditionally eaten as food and used for medicinal purposes. The present study aimed to investigate the phytochemical components of the seeds, leaves and flowers from B. populneus using three different solvents and to explore their antioxidant, anti-inflammatory and neuroprotective effects. Further, this study was focused on the identification of phenolic compounds from the most active extract. In vitro, all extracts showed strong antioxidant property by DPPH, ferrous ion chelating and lipid peroxidation-inhibiting assays, noticeable anti-inflammatory activity by protein denaturation and membrane stabilization methods and important neuroprotective effects by acetylcholinesterase inhibitory test. In vivo, B. populneus (50, 100 and 200 mg/kg, i.p.) showed significant dose-response anti-inflammatory effects against carrageenan-induced paw edema. With respect to the phenolic profile, the leaf methanol extract presented eight phenolic acids, one flavone and four flavonoids, with salvianolic acid B (820.3 mg/kg), caffeic acid (224.03 mg/kg), syringic acid (100.2 mg/kg) and trans-ferulic acid (60.02 mg/kg) as the major compounds. The results of the current study suggested that B. populneus could be a precious source of health-benefitting biomolecules and may be developed as new antioxidant, anti-inflammatory and AChE inhibitors.


Assuntos
Anti-Inflamatórios/farmacologia , Antioxidantes/farmacologia , Malvaceae/química , Extratos Vegetais/farmacologia , Acetilcolinesterase/administração & dosagem , Acetilcolinesterase/efeitos dos fármacos , Acetilcolinesterase/isolamento & purificação , Acetilcolinesterase/farmacologia , Animais , Anti-Inflamatórios/administração & dosagem , Anti-Inflamatórios/isolamento & purificação , Antioxidantes/administração & dosagem , Antioxidantes/isolamento & purificação , Carragenina , Inibidores da Colinesterase , Relação Dose-Resposta a Droga , Peroxidação de Lipídeos/efeitos dos fármacos , Masculino , Camundongos , Fármacos Neuroprotetores/administração & dosagem , Fármacos Neuroprotetores/isolamento & purificação , Fármacos Neuroprotetores/farmacologia , Extratos Vegetais/administração & dosagem , Solventes/química , Espectrometria de Massas por Ionização por Electrospray
3.
Inflammopharmacology ; 28(4): 939-948, 2020 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-31646410

RESUMO

Nicotine mediates some of the injurious effects caused by consuming tobacco products. The aim of this work is to investigate the protective effects of Mentha spicata extract (ME) supplementation on the testis and brain of nicotine-induced oxidative damage rats. ME extract showed interesting hydrogen peroxide-scavenging activity. HPLC-DAD analysis of ME revealed the presence of nine compounds among them gallic acid was the major one (165.44 µg/g ME). Thirty-two rats were randomly divided into four groups: control, a nicotine-treated group (1 mg/kg i.p.), a group receiving ME (100 mg/kg), and a group receiving both ME (100 mg/kg) and nicotine (1 mg/kg). After 2 months of treatment, the in vivo results showed that nicotine exhibited an increase in the body, brain, testis and accessory sex organ weights, sperm count and sperm motility. In addition, exposure to nicotine significantly (p < 0.01) increased acetylcholinesterase level (AChE) in brain, lipid peroxidation level in brain and testis as compared to control group. The antioxidant enzymes results showed that nicotine treatment induced a significant decrease (p < 0.01) in brain and testis antioxidant enzymes such as catalase, superoxide dismutase and glutathione peroxidase as compared to control group. Interestingly, pretreatment with ME significantly (p < 0.01) restored the majority of these biological parameters to normal levels, as well as a histological improvement. Obtained results suggest that ME contains promising substances that counteract the nicotine-intoxication and can be efficient in the prevention of brain and testis toxicity complications.


Assuntos
Acetilcolinesterase/metabolismo , Encefalopatias/tratamento farmacológico , Mentha spicata/química , Nicotina/efeitos adversos , Estresse Oxidativo/efeitos dos fármacos , Extratos Vegetais/farmacologia , Testículo/efeitos dos fármacos , Animais , Antioxidantes/farmacologia , Encéfalo/efeitos dos fármacos , Encéfalo/metabolismo , Encefalopatias/induzido quimicamente , Encefalopatias/metabolismo , Catalase/metabolismo , Inibidores da Colinesterase/efeitos adversos , Glutationa/metabolismo , Glutationa Peroxidase/metabolismo , Peroxidação de Lipídeos/efeitos dos fármacos , Masculino , Ratos , Ratos Wistar , Motilidade dos Espermatozoides/efeitos dos fármacos , Espermatozoides/efeitos dos fármacos , Superóxido Dismutase/metabolismo , Testículo/metabolismo
4.
Appl Physiol Nutr Metab ; 44(11): 1134-1140, 2019 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-30802143

RESUMO

Nicotine is a potential inducer of oxidative stress, through which it can damage numerous biological molecules. Natural antioxidants that prevent or slow the progression and severity of nicotine toxicity may have a significant health impact. The purpose of this study, conducted on Wistar rats, was to evaluate the beneficial effects of green tea (Camellia sinensis) extract on nicotine treatment-induced damage on kidney. Our results showed that nicotine significantly (p < 0.01) increased serum and kidney malondialdehyde, the serum contents of urea, creatinine, and uric acid. In addition, nicotine intoxication significantly (p < 0.01) decreased the levels of vitamins E and C in serum and kidney tissue as well as the activities of superoxide dismutase, catalase, and glutathione peroxidase. Interestingly, animals that were pretreated with green tea, prior to nicotine administration, showed a significant nephroprotection, revealed by a significant reduction-induced oxidative damage for all tested markers. The nephroprotective activity of green tea is mediated, at least in part, by the antioxidant effect of its constituents.


Assuntos
Antioxidantes/farmacologia , Camellia sinensis/química , Rim/efeitos dos fármacos , Nicotina/toxicidade , Chá/química , Animais , Ácido Ascórbico/análise , Catalase/metabolismo , Glutationa Peroxidase/metabolismo , Masculino , Malondialdeído/análise , Estresse Oxidativo , Substâncias Protetoras/farmacologia , Ratos Wistar , Superóxido Dismutase/metabolismo , Vitamina E/análise
5.
Inflammopharmacology ; 27(5): 975-984, 2019 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-29679184

RESUMO

Amaranthus spinosus has been consumed traditionally to prevent various diseases including abdominal pain. In this study, the phytochemical composition, antioxidant and analgesic activities of an ethyl acetate extract of A. spinosus leaves (ASEA) were evaluated. The ASEA had the highest concentrations of total phenols (462.2 mg GAE/g DW), condensed tannin (5.01 mg CE/g DW) and total flavonoid contents (30.07 mg CE/g DW) compared to the chloroform, n-hexane, n-butanol and water extracts. Similarly, ASEA showed the most effective total antioxidant activity (45.45 µg/mL), DPPH scavenging activity (27.32 µg/mL) and hydrogen peroxide scavenging activity (30.60 µg/mL). ASEA with the doses of 200-600 mg/kg (p.o.) clearly demonstrated antinociceptive effects by reducing acetic acid-induced abdominal contortions with a maximal inhibition of 79.57% at 600 mg/kg and increasing latencies of the hot-plate paw-licking response. The tested doses also significantly (p < 0.001) decreased the reaction time in the formalin test at the neurogenic and inflammatory phases. ASEA contained ten polyphenols with caffeic acid being the predominant polyphenol. Overall, this study gave evidence that A. spinosus is a new antioxidant and analgesic agent, and justified its traditional use for the treatment of pain.


Assuntos
Acetatos/química , Amaranthus/química , Analgésicos/farmacologia , Antioxidantes/farmacologia , Extratos Vegetais/farmacologia , Folhas de Planta/química , Polifenóis/farmacologia , Analgésicos/química , Animais , Antioxidantes/química , Cromatografia Líquida de Alta Pressão/métodos , Flavonoides/química , Flavonoides/farmacologia , Camundongos , Dor/tratamento farmacológico , Fenóis/química , Extratos Vegetais/química , Polifenóis/química
6.
Pain Res Manag ; 2018: 4838413, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-30073041

RESUMO

Plants provide an alternative source to manage different human disorders due to various metabolites. The aim of this study is to investigate the phytochemical constituents of the methanolic extracts of Euphorbia retusa and to evaluate their antioxidant, anti-inflammatory, and analgesic activities. The phytochemical results obtained by HPLC and by chemical assay reactions have revealed the richness of the methanolic extract of E. retusa in active compounds, in particular polyphenols, flavonoids, and tannins. The methanolic extract shows significant antioxidant activities in vitro, in the DPPH and the FRAP assays. The antinociceptive activity was evaluated using acetic acid and hot-plate models of pain in mice. The anti-inflammatory activity was evaluated by carrageenan-induced paw edema. Oral pretreatment with the methanolic extract of E. retusa (200 mg/kg) exhibited a significant inhibition of pain induced either by acetic acid or by the heating plate and in a manner comparable to the standard drug paracetamol. E. retusa significantly reduced paw edema starting from the 3rd hour after carrageenan administration by increasing the activity of antioxidant enzymes (SOD, CAT, and GPx) in liver and paw tissues and decreasing the levels of MDA. These results may confirm the interesting potential of this plant as a treatment of various inflammatory and pain diseases.


Assuntos
Euphorbia/química , Inflamação/tratamento farmacológico , Extratos Vegetais/química , Extratos Vegetais/farmacologia , Ácido Acético/toxicidade , Analgésicos/química , Analgésicos/farmacologia , Analgésicos/uso terapêutico , Animais , Anti-Inflamatórios/farmacologia , Anti-Inflamatórios/uso terapêutico , Antioxidantes/química , Antioxidantes/farmacologia , Antioxidantes/uso terapêutico , Carragenina/toxicidade , Catalase/metabolismo , Modelos Animais de Doenças , Relação Dose-Resposta a Droga , Edema/tratamento farmacológico , Inflamação/induzido quimicamente , Peroxidação de Lipídeos/efeitos dos fármacos , Camundongos , Nitroazul de Tetrazólio/metabolismo , Medição da Dor , Superóxido Dismutase/metabolismo , Tiazolidinedionas/metabolismo
7.
J Ethnopharmacol ; 225: 116-127, 2018 Oct 28.
Artigo em Inglês | MEDLINE | ID: mdl-29958959

RESUMO

ETHNOPHARMACOLOGICAL RELEVANCE: Lycium europaeum Linn. is widely used to treat the burning of the skin and well-known as a medicinal plant having various biological activities. AIMS OF THE STUDY: The purpose of the present study is to characterize the polysaccharide from L. europaeum L. leaves (LEP) and to explore its antioxidant, anti-inflammatory and hepato-nephroprotective properties. MATERIALS AND METHODS: The structural and functional characteristics of LEP were investigated using X-ray diffraction techniques (XRD), Scanning Electron Microscopy (SEM), and FT-IR Spectroscopy. The antioxidant activity was evaluated using 2,2-diphenyl-1-picrylhydrazyl and hydrogen peroxide scavenging assays. Hepato-renal effects were studied using CCl4 and cisplatin-induced liver and kidney injuries in mice, respectively. Anti-inflammatory activity was assessed on carrageenan-induced paw edema. RESULTS: The LEP showed an interesting water-holding capacity and effective foaming and emulsifying properties. XRD analysis suggested that LEP form a semi-crystalline polymer with an amorphous structure. FT-IR profile showed the presence of pyranose ring in LEP. SEM and helix-coil transition analyses indicated that LEP had a lamellar structure with angular edges and didn't present a triple helical conformation in solution. In vitro, LEP indicated significant concentration-dependent antioxidant activity. In vivo, LEP treatment significantly reduced the effects of CCl4 intoxication on serum liver biomarkers (AST, ALT, LDH, and GGT) and the effect of cisplatin on serum renal biomarkers (urea, blood urea nitrogen, creatinine, and uric acid). Meanwhile, LEP diminishes significantly the effect of CCl4 and cisplatin on the level of lipid peroxidation in liver and kidney tissues, respectively. Additionally, the normal histological structure of liver and kidney was restored after treatment with the polysaccharide. LEP possessed a significant anti-inflammatory activity on acute inflammation induced by carrageenan in mice. CONCLUSION: Overall, the findings of this study support the traditional use of L. europaeum L. This plant may also be used as a good agent for protection against inflammatory diseases and hepato-renal injuries in patients with cancer.


Assuntos
Anti-Inflamatórios/uso terapêutico , Antioxidantes/uso terapêutico , Doença Hepática Induzida por Substâncias e Drogas/tratamento farmacológico , Nefropatias/tratamento farmacológico , Lycium , Polissacarídeos/uso terapêutico , Animais , Anti-Inflamatórios/química , Antioxidantes/química , Compostos de Bifenilo/química , Tetracloreto de Carbono , Carragenina , Doença Hepática Induzida por Substâncias e Drogas/sangue , Doença Hepática Induzida por Substâncias e Drogas/metabolismo , Cisplatino , Edema/tratamento farmacológico , Peróxido de Hidrogênio/química , Rim/efeitos dos fármacos , Rim/patologia , Nefropatias/sangue , Fígado/efeitos dos fármacos , Fígado/patologia , Camundongos , Picratos/química , Folhas de Planta , Polissacarídeos/química
8.
Appl Physiol Nutr Metab ; 43(1): 77-83, 2018 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-28892646

RESUMO

The aim of this study was to investigate the protective effect of Mentha spicata supplementation against nicotine-induced oxidative damage in the liver and erythrocytes of Wistar rats. Bioactive substances were determined by liquid chromatography - electrospray ionization - tandem mass spectrometry analysis. Animals were divided into 4 groups of 6 rats each: a normal control group, a nicotine-treated group (1 mg/kg), a group receiving M. spicata extract (100 mg/kg), and a group receiving both M. spicata extract (100 mg/kg) and nicotine (1 mg/kg). Many phenolic acids were identified in the M. spicata aqueous extract. After 2 months of treatment, nicotine induced an increase in the level of white blood cells and a marked decrease in erythrocytes, hemoglobin, and haematocrit. Aspartate transaminase, alanine transaminase, alkaline phosphatase, and lactate dehydrogenase activities were also found to be higher in nicotine-treated group than those of the control group. Furthermore, nicotine-treated rats exhibited oxidative stress, as evidenced by a decrease in antioxidant enzymes activities and an increase in lipid peroxidation level in liver and erythrocytes. Interestingly, the oral administration of M. spicata extract by nicotine-treated rats alleviated such disturbances. M. spicata contained bioactive compounds that possess important antioxidant potential and protected liver and erythrocytes against nicotine-induced damage.


Assuntos
Antioxidantes/farmacologia , Doença Hepática Induzida por Substâncias e Drogas/prevenção & controle , Eritrócitos/efeitos dos fármacos , Fígado/efeitos dos fármacos , Mentha spicata , Nicotina , Estresse Oxidativo/efeitos dos fármacos , Extratos Vegetais/farmacologia , Animais , Antioxidantes/química , Antioxidantes/isolamento & purificação , Biomarcadores/sangue , Doença Hepática Induzida por Substâncias e Drogas/sangue , Doença Hepática Induzida por Substâncias e Drogas/etiologia , Doença Hepática Induzida por Substâncias e Drogas/patologia , Cromatografia Líquida , Citoproteção , Modelos Animais de Doenças , Eritrócitos/metabolismo , Peroxidação de Lipídeos/efeitos dos fármacos , Fígado/metabolismo , Fígado/patologia , Masculino , Mentha spicata/química , Fitoterapia , Extratos Vegetais/química , Extratos Vegetais/isolamento & purificação , Plantas Medicinais , Ratos Wistar , Espectrometria de Massas por Ionização por Electrospray , Espectrometria de Massas em Tandem , Fatores de Tempo
9.
Biomed Pharmacother ; 95: 1441-1450, 2017 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-28946192

RESUMO

In this study, the antioxidant, antinociceptive, hepatoprotective, nephroprotective properties and the bioactive composition of Lycium europaeum were investigated. Polyphenols and total tannin contents were measured by colorimetric methods The antioxidant activity in vitro was evaluated using the reducing power, 2,2-diphenyl-1-picrylhydrazyl radical and phosphomolybdenum assays. The hepatotoxicity and nephrotoxicity effects were studied using carbon tetrachloride (CCl4)-induced liver and renal injuries in mice. The analgesic activity was explored using the hot-plate and acetic acid tests in mice. Results showed that the methanol fraction of L. europaeum (LEM) had the highest level of total phenolic, total tannin, and flavonoid. HPLC-DAD analysis revealed the presence of twelve compounds among them caffeic acid was the major compound (140.18µg/g of extract). This fraction also showed the best antioxidant activity in vitro in the three used assays. In vivo, in the mice studies, CCl4 administration induced hepatotoxicity and nephrotoxicity by a significant rise in the levels of serum liver biomarkers (gamma glutamyl transferase, lactate dehydrogenase, and aminotransferases) and serum renal biomarkers (urea, creatinine, and uric acid). Similarly, levels of lipid peroxidation (MDA) in both tissues were found increased by CCl4 intoxication. Pretreatment with LEM and quercetin significantly restored the majority of these biological parameters to normal levels, as well as an improvement of histopathological changes. In addition, LEM showed an interesting analgesic activity. LEM decreased significantly the number of writhing induced by acetic acid and prolonged the reaction time in response to thermal stimulus in mice. Therefore, it was speculated that the obtained results highlighted the potential use of L. europaeum as a source of bioactive compounds with pharmacological advantages.


Assuntos
Analgésicos/farmacologia , Antioxidantes/farmacologia , Rim/patologia , Fígado/patologia , Lycium/química , Compostos Fitoquímicos/farmacologia , Substâncias Protetoras/farmacologia , Animais , Tetracloreto de Carbono , Flavonoides/análise , Rim/efeitos dos fármacos , Fígado/efeitos dos fármacos , Masculino , Malondialdeído/metabolismo , Metanol , Camundongos , Fenóis/análise , Extratos Vegetais/farmacologia , Quercetina/farmacologia , Ratos Wistar , Taninos/análise , Testes de Toxicidade Aguda
10.
Biomed Pharmacother ; 83: 1327-1334, 2016 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-27571876

RESUMO

Citrus limon is a member of the large Rutaceae family characterized by its therapeutic proprieties and has been widely used in traditional medicine to treat various diseases. This study investigates the protective effect of Citrus limon essential oil against a high dose of aspirin-induced acute liver and kidney damage in female Wistar albino rats. Twenty-eight adult female Wistar rats were divided into 4 groups of 7 each: (1) a control group; (2) a group of rats which was kept untreated for 56days then treated with aspirin (A) (600mg/kg) for 4 days; (3) a group fed with essential oil of Citrus limon for 56days then (A) for 4 days; and (4) a group of rats receiving essential oil of Citrus limon for 56 days, then given NaCl for 4 days. Estimations of biochemical parameters in blood were determined. Lipid peroxidation levels (TBARS), superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidas (GPx) activities in liver and kidney was determined. A histopathological study was done. Under our experimental conditions, aspirin induced an increase of serum biochemical parameters and it resulted in an oxidative stress in both liver and kidney. This was evidenced by significant increase in TBARS in liver and kidney by 108% and 55%, respectively, compared to control. On the other hand, a decrease in the activities of SOD by 78% and 53%, CAT by 53% and 78%, and GPx by 78% and 51% in liver and kidney, respectively. Administration of EOC to rats attenuated the induced an effect of the high dose of aspirin induced in the afore mentioned serum biochemical parameters. In conclusion, our data suggest that treatment with essential oil of Citrus limon prevented the liver and kidney damage induced by aspirin.


Assuntos
Aspirina/toxicidade , Citrus , Rim/efeitos dos fármacos , Fígado/efeitos dos fármacos , Óleos Voláteis/farmacologia , Animais , Anti-Inflamatórios não Esteroides/toxicidade , Feminino , Rim/metabolismo , Rim/patologia , Fígado/metabolismo , Fígado/patologia , Óleos Voláteis/isolamento & purificação , Estresse Oxidativo/efeitos dos fármacos , Estresse Oxidativo/fisiologia , Componentes Aéreos da Planta , Folhas de Planta , Substâncias Protetoras/isolamento & purificação , Substâncias Protetoras/farmacologia , Ratos , Ratos Wistar
11.
J Oleo Sci ; 65(8): 701-12, 2016 Aug 01.
Artigo em Inglês | MEDLINE | ID: mdl-27430382

RESUMO

Aromatic and medicinal plants are sources of natural antioxidants thanks to their secondary metabolites. Administration of Pinus halepensis L. (Pinaceae family) in previous studies was found to alleviate deleterious effects of aspirin-induced damage on liver and kidney. The present study, carried out on female rats, evaluates the effects of P. halepensis L. essential oil (EOP) on aspirin (A)-induced damage to liver and kidney. The animals used in this study were rats (n=28) divided into 4 groups of 7 each: (1) a control group (C); (2) a group given NaCl for 56 days then treated with (A) (600 mg/kg) for 4 days (A); (3) a group fed with (EOP) for 56 days then (A) for 4 days; and a group fed with only (EOP) for 56 days and given NaCl for 4 days. Estimations of biochemical parameters in blood were determined using kit methods (Spinreact). Lipid peroxidation levels (TBARS), superoxide dismutase (SOD) and catalase (CAT), glutathione peroxidase (GPx) activities were determined. Histopathological study was done by immersing pieces of both organs in a fixative solution followed by paraffin embeddeding and hematoxylin-eosin staining. Under our experimental conditions, Aspirin at dose 600 mg/kg body weight induced an increase of serum biochemical parameters as well as an oxidative stress in both organs. An increase occurred in TBARS by 108% and 55%, a decrease in SOD by 78% and 53%, CAT by 53% and 78%, and GPx by 78% and 51% in liver and kidney, respectively, compared to control. Administration of EOP given to rats enabled correction in these parameters. It could be concluded that the treatment with P. halepensis L. essential oil inhibited aspirin-induced liver and kidney damage.


Assuntos
Aspirina/efeitos adversos , Doença Hepática Induzida por Substâncias e Drogas/prevenção & controle , Nefropatias/prevenção & controle , Rim/efeitos dos fármacos , Fígado/efeitos dos fármacos , Óleos Voláteis/farmacologia , Pinus/química , Substâncias Protetoras/farmacologia , Doença Aguda , Albinismo , Animais , Doença Hepática Induzida por Substâncias e Drogas/patologia , Feminino , Rim/metabolismo , Rim/patologia , Nefropatias/induzido quimicamente , Nefropatias/patologia , Fígado/metabolismo , Fígado/patologia , Óleos Voláteis/administração & dosagem , Óleos Voláteis/isolamento & purificação , Estresse Oxidativo/efeitos dos fármacos , Substâncias Protetoras/administração & dosagem , Substâncias Protetoras/isolamento & purificação , Ratos , Ratos Wistar
12.
Peptides ; 32(4): 656-63, 2011 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-21262299

RESUMO

AaCtx is the first chlorotoxin-like peptide isolated from Androctonus australis scorpion venom. Its amino acid sequence shares 70% similarity with chlorotoxin from Leiurus quinquestriatus scorpion venom, from which it differs by twelve amino acids. Due to its very low concentration in venom (0.05%), AaCtx was chemically synthesized. Both native and synthetic AaCtx were active on invasion and migration of human glioma cells. However, their activity was found to be lower than that of chlorotoxin. The molecular model of AaCtx shows that most of amino acids differing between AaCtx and chlorotoxin are localized on the N-terminal loop and the α-helix. Based on known compounds that block chloride channels, we suggest that the absence of negative charged amino acids on AaCtx structure may be responsible for its weak activity on glioma cells migration and invasion. This finding serves as a starting point for structure-function relationship studies leading to design high specific anti-glioma drugs.


Assuntos
Peptídeos/química , Peptídeos/isolamento & purificação , Venenos de Escorpião/química , Sequência de Aminoácidos , Animais , Adesão Celular , Linhagem Celular Tumoral , Cromatografia em Gel , Cromatografia Líquida de Alta Pressão , Humanos , Masculino , Camundongos , Modelos Moleculares , Dados de Sequência Molecular , Peptídeos/síntese química , Peptídeos/toxicidade , Homologia de Sequência de Aminoácidos , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA