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1.
Curr Protein Pept Sci ; 21(3): 324-330, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-31951168

RESUMEN

The fungal genus Metarhizium has been used as an entomopathogen worldwide for approximately 140 years, and its mechanism of infection and its virulence factors have been studied. The present review is a compilation of virulence factors described in the literature to date and their participation in specific stages of the infection process.


Asunto(s)
Proteínas Fúngicas/genética , Metarhizium/genética , Micosis/genética , Factores de Virulencia/genética , Metarhizium/patogenicidad , Micosis/microbiología
2.
Biol Res ; 47: 74, 2014 Dec 22.
Artículo en Inglés | MEDLINE | ID: mdl-25723052

RESUMEN

BACKGROUND: Nitrosative and oxidative stress play a key role in obesity and diabetes-related mitochondrial dysfunction. The objective was to investigate the effect of curcumin treatment on state 3 and 4 oxygen consumption, nitric oxide (NO) synthesis, ATPase activity and lipid oxidation in mitochondria isolated from liver and kidneys of diabetic db/db mice. RESULTS: Hyperglycaemia increased oxygen consumption and decreased NO synthesis in liver mitochondria isolated from diabetic mice relative to the control mice. In kidney mitochondria, hyperglycaemia increased state 3 oxygen consumption and thiobarbituric acid-reactive substances (TBARS) levels in diabetic mice relative to control mice. Interestingly, treating db/db mice with curcumin improved or restored these parameters to normal levels; also curcumin increased liver mitochondrial ATPase activity in db/db mice relative to untreated db/db mice. CONCLUSIONS: These findings suggest that hyperglycaemia modifies oxygen consumption rate, NO synthesis and increases TBARS levels in mitochondria from the liver and kidneys of diabetic mice, whereas curcumin may have a protective role against these alterations.


Asunto(s)
Curcumina/farmacología , Diabetes Mellitus Tipo 2/dietoterapia , Riñón/efectos de los fármacos , Peroxidación de Lípido/efectos de los fármacos , Hígado/efectos de los fármacos , Mitocondrias/efectos de los fármacos , Adenosina Trifosfatasas/efectos de los fármacos , Animales , Peso Corporal/efectos de los fármacos , Respiración de la Célula/efectos de los fármacos , Diabetes Mellitus Tipo 2/complicaciones , Diabetes Mellitus Tipo 2/fisiopatología , Suplementos Dietéticos , Modelos Animales de Enfermedad , Genotipo , Hiperglucemia/dietoterapia , Hiperglucemia/etiología , Masculino , Ratones , Mitocondrias/enzimología , Mitocondrias Hepáticas/efectos de los fármacos , Mitocondrias Hepáticas/enzimología , Óxido Nítrico/análisis , Óxido Nítrico/metabolismo , Estrés Oxidativo/efectos de los fármacos , Consumo de Oxígeno/efectos de los fármacos , Selección Artificial
3.
Biol. Res ; 47: 1-8, 2014. graf
Artículo en Inglés | LILACS | ID: biblio-950770

RESUMEN

BACKGROUND: Nitrosative and oxidative stress play a key role in obesity and diabetes-related mitochondrial dysfunction. The objective was to investigate the effect of curcumin treatment on state 3 and 4 oxygen consumption, nitric oxide (NO) synthesis, ATPase activity and lipid oxidation in mitochondria isolated from liver and kidneys of diabetic db/db mice. RESULTS: Hyperglycaemia increased oxygen consumption and decreased NO synthesis in liver mitochondria isolated from diabetic mice relative to the control mice. In kidney mitochondria, hyperglycaemia increased state 3 oxygen consumption and thiobarbituric acid-reactive substances (TBARS) levels in diabetic mice relative to control mice. Interestingly, treating db/db mice with curcumin improved or restored these parameters to normal levels; also curcumin increased liver mitochondrial ATPase activity in db/db mice relative to untreated db/db mice. CONCLUSIONS: These findings suggest that hyperglycaemia modifies oxygen consumption rate, NO synthesis and increases TBARS levels in mitochondria from the liver and kidneys of diabetic mice, whereas curcumin may have a protective role against these alterations.


Asunto(s)
Animales , Masculino , Ratones , Peroxidación de Lípido/efectos de los fármacos , Curcumina/farmacología , Diabetes Mellitus Tipo 2/dietoterapia , Riñón/efectos de los fármacos , Hígado/efectos de los fármacos , Mitocondrias/efectos de los fármacos , Consumo de Oxígeno/efectos de los fármacos , Peso Corporal/efectos de los fármacos , Mitocondrias Hepáticas/efectos de los fármacos , Mitocondrias Hepáticas/enzimología , Adenosina Trifosfatasas/efectos de los fármacos , Estrés Oxidativo/efectos de los fármacos , Respiración de la Célula/efectos de los fármacos , Suplementos Dietéticos , Diabetes Mellitus Tipo 2/complicaciones , Diabetes Mellitus Tipo 2/fisiopatología , Modelos Animales de Enfermedad , Selección Artificial , Genotipo , Hiperglucemia/dietoterapia , Hiperglucemia/etiología , Mitocondrias/enzimología , Óxido Nítrico/análisis , Óxido Nítrico/metabolismo
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