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1.
Appl Biochem Biotechnol ; 175(3): 1507-18, 2015 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-25410800

RESUMO

A proteinaceous glycopeptide was isolated from the posterior salivary gland (PSG) of Sepia pharaonis by gel (Sephadex G-100) filtration chromatography and purified by reversed-phase high-performance liquid chromatography (RP-HPLC). Among the collected fractions, fraction 12 showed a retention time (RT) of 31 min. The total protein and neutral sugar contents of the purified glycopeptide were recorded as 68.14 and 2.95 mg, respectively. The molecular weight of the purified glycopeptide was found to be ~50 kDa. The infrared (IR) and circular dichroism (CD) spectroscopy confirmed the presence of peptide and secondary structure in the purified glycopeptide. The antibacterial activity of the purified glycopeptide against avian bacterial strains was also determined. Gas chromatography-mass spectrometry (GC-MS) of the purified glycopeptide revealed the likely compounds for the antibacterial activity such as 22, 23-dibromostigmasterol acetate, 3-methyl 2-(2-oxypropyl) furan, and 2,4,4-trimethyl-3-hydroxymethyl-5A-(3-methyl-but-2-enyl)-cyclohexene. These three compounds found in the purified glycopeptide could be responsible for the antibacterial activity against the avian pathogens. The results of this study suggest that the purified glycopeptide from the PSG of S. pharaonis could be an antibacterial agent against avian bacterial pathogens.


Assuntos
Antibacterianos/isolamento & purificação , Antibacterianos/farmacologia , Glicopeptídeos/isolamento & purificação , Glicopeptídeos/farmacologia , Glândulas Salivares/química , Sepia/química , Animais , Antibacterianos/química , Fracionamento Químico , Galinhas , Cromatografia em Gel , Cromatografia Líquida de Alta Pressão , Cromatografia de Fase Reversa , Dicroísmo Circular , Eletroforese em Gel de Poliacrilamida , Glicopeptídeos/química , Testes de Sensibilidade Microbiana , Peso Molecular , Espectrofotometria Infravermelho , Fatores de Tempo
2.
Am J Physiol Regul Integr Comp Physiol ; 293(1): R162-8, 2007 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-17409260

RESUMO

In adult animals and humans, activation of kappa-opioid receptors results in a diuresis. The aim of the present study was to investigate whether kappa-opioids are also diuretic early in life and whether this is altered during postnatal maturation. Therefore, the renal effects of the kappa-opioid-receptor agonist U-50488H were measured in two separate age groups of conscious lambs at two stages of postnatal maturation (approximately 1 wk and approximately 6 wk) under physiological conditions. To evaluate whether the renal responses to U-50488H resulted from receptor-dependent effects, responses to U-50488H were also tested in the presence of the specific kappa-opioid-receptor antagonist 5'-guanidinonaltrindole (GNTI). Urinary flow rate, free water clearance, and electrolyte excretions and clearances were measured for 30 min before and for 90 min after intravenous injection of U-50488H or vehicle. An increase in urinary flow rate accompanied by an increase in free water clearance occurred in response to administration of U-50488H but not vehicle. There were no effects of U-50488H on electrolyte excretions or clearances at either 1 or 6 wk of postnatal life. Although there were no effects of GNTI on any of the measured or calculated variables, the aforementioned diuretic response to U-50488H was abolished by pretreatment with GNTI in both age groups. We conclude that kappa-opioid receptors are diuretic early in life and that this response does not appear to be altered as postnatal maturation proceeds. Therefore, these data provide evidence that activation of kappa-opioid receptors early in life may lead to alterations in fluid balance.


Assuntos
(trans)-Isômero de 3,4-dicloro-N-metil-N-(2-(1-pirrolidinil)-ciclo-hexil)-benzenoacetamida/farmacologia , Analgésicos não Narcóticos/farmacologia , Rim/efeitos dos fármacos , Receptores Opioides kappa/agonistas , Envelhecimento/fisiologia , Animais , Animais Recém-Nascidos , Diurese/efeitos dos fármacos , Relação Dose-Resposta a Droga , Eletrólitos/urina , Guanidinas/farmacologia , Rim/crescimento & desenvolvimento , Naltrexona/análogos & derivados , Naltrexona/farmacologia , Receptores Opioides kappa/antagonistas & inibidores , Ovinos , Urodinâmica/fisiologia
3.
Life Sci ; 76(5): 585-97, 2004 Dec 17.
Artigo em Inglês | MEDLINE | ID: mdl-15556170

RESUMO

Increased oxidative stress and antioxidant deficit have been suggested to play a major role in adriamycin induced cardiomyopathy and congestive heart failure due to multiple treatments with adriamycin. In this study the cardio protective effect of Centella asiatica on myocardial marker enzymes and antioxidant enzymes in adriamycin induced cardiomyopathy was investigated in rats. The rats administered with adriamycin (2.5 mg/kg body wt, i.p) caused myocardial damage that was manifested by the elevation of serum marker (LDH, CPK, GOT and GPT) enzymes and showed significant changes in the antioxidant enzymes (SOD, CAT, GPx, GST). Pre-co-treatment with Centella asiatica(200 mg/kg of body wt/oral) extract significantly prevented these alterations and restored the enzyme activities to near normal levels. These findings demonstrate the cardio protective effect of Centella asiatica on antioxidant tissue defense system during adriamycin induced cardiac damage in rats.


Assuntos
Antioxidantes/metabolismo , Cardiomiopatias/prevenção & controle , Centella/química , Doxorrubicina/toxicidade , Miocárdio/enzimologia , Administração Oral , Animais , Cardiomiopatias/enzimologia , Cardiomiopatias/metabolismo , Injeções Intraperitoneais , Peróxidos Lipídicos/metabolismo , Masculino , Miocárdio/metabolismo , Extratos Vegetais/administração & dosagem , Extratos Vegetais/isolamento & purificação , Extratos Vegetais/uso terapêutico , Ratos , Ratos Wistar
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