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1.
Biochem Mol Biol Int ; 46(1): 147-56, 1998 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-9784849

RESUMEN

Thiol groups of hemoglobin and blood glutathione are higher in Geochelone carbonaria than in Geochelone denticulata. Exposure of stripped hemolysate of both tortoises to terc-butyl hydroperoxide, resulted in a higher ferroheme oxidation of G. denticulata hemoglobin. In this example glutathione reductase and glutathione peroxidase, were not active due to the absence of GSH and NADPH, suggesting that the thiol groups of G. carbonaria hemoglobin act as antioxidant, similar to GSH. In the total hemolysate, however, where the antioxidant enzymes are active, both species showed similar levels of hemoglobin oxidation, suggesting that the protective effect of thiol groups of hemoglobin are less effective for heme protection. The activity of glutathione reductase and glutathione peroxidase was higher in erythrocytes of G. denticulata and the activity of catalase and superoxide dismutase was higher in erythrocytes of G. carbonaria.


Asunto(s)
Catalasa/sangre , Eritrocitos/enzimología , Glutatión Peroxidasa/sangre , Glutatión Reductasa/sangre , Superóxido Dismutasa/sangre , Tortugas/sangre , Animales , Glutatión/sangre , Hemoglobinas/metabolismo , Peroxidación de Lípido , Oxidación-Reducción , Compuestos de Sulfhidrilo/metabolismo , terc-Butilhidroperóxido/metabolismo
2.
Biochem Mol Biol Int ; 40(2): 355-64, 1996 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-8896757

RESUMEN

The reaction of thiol reagents with G. carbonaria hemoglobin was studied, and the oxygen equilibrium and kinetic of oxidation of derivatives determined. The oxygen affinity and kinetic of oxidation of hemoglobin derivatives were modified to various extents depending on the nature of thiol reagents used. Diamide yielded approximately 80% polymeric hemoglobin, although the oxidation kinetic, and the functional properties, were practically invariant (T1/2 = 10.0 min.; P50 = 5.0 mm Hg at pH 7.4; alkaline Bohr effect = -0.64). Iodoacetamide did not modify the electrophoretic pattern significantly, although all the free SH groups of hemoglobin were alkylated. A P50 of 2.5 mmHg at pH 7.4 and the Bohr effect of -0.15 were obtained; the T1/2 of about 6.4 min. was shorter than that for un-modified Hb. Similar T1/2 were obtained for Hb treated with oxidized glutathione, which produced polymeric Hb and glutathionyl-Hb. The oxygen binding characteristics showed that both of Hb derivatives, glutathionyl-Hb and polymeric Hb, maintain the capacity to transport the gas.


Asunto(s)
Hemo/metabolismo , Hemoglobinas/metabolismo , Oxihemoglobinas/metabolismo , Reactivos de Sulfhidrilo/farmacología , Animales , Diamida/farmacología , Glutatión/análogos & derivados , Glutatión/metabolismo , Glutatión/farmacología , Disulfuro de Glutatión , Hemoglobinas/efectos de los fármacos , Concentración de Iones de Hidrógeno , Yodoacetamida/farmacología , Cinética , Sustancias Macromoleculares , Oxidación-Reducción , Oxihemoglobinas/efectos de los fármacos , Tortugas
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