Effect of organic phosphates on methemoglobin reduction by ascorbic acid.
نویسندگان
چکیده
The rate of methemoglobin reduction by ascorbic acid was accelerated in the presence of ATP,2,3-diphosphoglycerate (2,3-DPG), and inositol hexaphosphate (IHP). The acceleration was as much as three times, four times, and ten times in the presence of ATP, 2.3-DPG, and IHP at pH 7.0, respectively. The changes of the concentrations of methemoglobin and ascorbic acid during the methemoglobin reduction were determined, and the reaction was found to proceed stoichiometrically in the presence of IHP. The reduction rate of methemoglobin by ascorbic acid was compared at different concentrations of organic phosphates (ATP,2,3-DPG, and IHP) at various pH values (6.3, 7.0, 7.7). From the changes in the reduction rate under different concentrations of organic phosphates, the dissociation constants of ATP, 2,3-DPG, and IHP to methemoglobin could be determined and were estimated to be 3.3 X 10(-4) M, 2 X 10(-3) M, and 8 X 10(-6) M at pH 7.0, respectively. On the basis of these results, the acceleration mechanism of methemoglobin reduction by ascorbic acid due to the presence of organic phosphates was described. The physiological role of 2,3-DPG in human red cells was discussed in relation to the reduction of methemoglobin by ascorbic acid.
منابع مشابه
The basis for EDTA-stimulation of methemoglobin reduction in hemolysates of human erythrocytes.
THE BASIS FOR EDTA-STIMULATION OF METHEMOGLOBIN REDUCTION IN HEMOLYSATES OF HUMAN ERYTHROCYTES Lucy Jean Sannes* and Donald E. Hultquist ** Department of Biological Chemistry The University of Michigan Ann Arbor, Michigan 48109 Received November lo,1979 Summary: We have studied the stimulation by EDTA of methemoglobin reduction in hemolysates of human erythrocytes. The EDTA effect has been show...
متن کاملMechanism of methemoglobin reduction by ascorbic acid under anaerobic conditions.
The time course of methemoglobin reduction by ascorbic acid under anaerobic conditions was analyzed by using isoelectric focusing on Ampholine plate gel in order to compare results obtained by studies of the changes in absorption during the reaction. The intermediate hemoglobin which appeared all through the reaction was single and identified as the alpha3+beta2+ valency hybrid. In the presence...
متن کاملThe Reduction of Methemoglobin by Ascorbic Acid* by Carl S. Vestling
In this laboratory a study of the oxygen capacities of chemically modified hemoglobins has recently been undertaken. In connection with this work the reduction of methemoglobin under carefully controlled conditions offered itself as a problem, since the combination of a ferriheme with globin leads to methemoglobin. In view of this consideration and of the recent reports of Cox and Wendel (l), M...
متن کاملAn in vitro demonstration of Pro-oxidant effect of Ascorbic acid in sheep erythrocyte hemolysate and purified hemoglobin preparations
In vitro studies have demonstrated pro-oxidant effect of ascorbic acid on sheep erythrocyte hemolysate and on purified ruminant hemoglobin preparations. Methemoglobin formation was concentration dependent over ca. 3.4 through 34 μmole ascorbic acid with sheep hemolysate (r=0.97, p<0.01, n= 3 each) and over ca. 5.68 through 22.7 μmole ascorbic acid with purified ruminant Hb preparations (r >0.99...
متن کاملHereditary methemoglobinemia in Alaskan Eskimos and Indians.
acterized by cyanosis, a variable amount of hemoglobin in the oxidized form methemoglobin, a compensatory polycythemia, and no other pathologic changes. According to a recent review by Gibson1 fewer than 50 cases have been reported, although Dines2 suggests that there are more than 100. Available evidence indicates that the condition is inherited as a recessive trait.3 In air, hemoglobin umider...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- The Journal of biological chemistry
دوره 251 23 شماره
صفحات -
تاریخ انتشار 1976