BLOOD TRANSAMINASE ACTIVITIES IN VITAMIN B6 DEFICIENCY: EFFECT OF CONCURRENT THIAMINE AND RIBOFLAVIN DEFICIENCIES

1965 ◽  
Vol 43 (4) ◽  
pp. 591-599 ◽  
Author(s):  
M. C. Cheney ◽  
G. H. Beaton

Factorial design experiments in rats revealed that blood transaminase activity was sensitive to vitamin B6 dosage and was not affected by concurrent variation in riboflavin or thiamine administration.The blood transaminase activity was a better index of vitamin B6 nutritional status than was body weight response or liver transaminase activity. Similarly, erythrocyte transketolase activity was found to reflect thiamine dosage, and plasma riboflavin level to reflect riboflavin dosage, regardless of manipulation of pyridoxine dosage.

1965 ◽  
Vol 43 (4) ◽  
pp. 579-589 ◽  
Author(s):  
M. C. Cheney ◽  
D. M. Curry ◽  
G. H. Beaton

The lowering of blood glutamic–oxaloacetic (GOT) and glutamic–pyruvic (GPT) transaminase activities was found to be specific for vitamin B6 deprivation among several B vitamins tested and in the presence of a simultaneous restriction of eight B vitamins, cortisone administration, or variation of dietary protein level. It was found that changes in blood transaminase activity did not always parallel those seen in liver transaminase activity. In the determination of vitamin B6 nutritional status, blood GPT activity appeared to be more sensitive than GOT activity and would seem to be as sensitive an indicator as xanthurenic acid excretion after a tryptophan load.


1967 ◽  
Vol 45 (2) ◽  
pp. 343-351 ◽  
Author(s):  
M. C. Cheney ◽  
Z. I. Sabry ◽  
G. H. Beaton

To assess the usefulness of the erythrocyte transaminases, glutamic–oxaloacetic and glutamic–pyruvic, in the evaluation of vitamin B6 nutritional status, the response of these enzymes to repletion following 1, 4, and 10 weeks of vitamin B6 depletion was compared with that of the plasma and liver transaminases in the rat. The responses of the erythrocyte enzymes reflected the state of vitamin B6 nutrition most accurately and, unlike the plasma and liver transaminases, were not affected by other factors. Repletion produced a rapid response in the erythrocyte enzymes; however, restoration of control levels appeared to depend on red cell turnover, particularly after prolonged depletion periods. This finding suggests that the apoenzyme, as well as the coenzyme, is depleted during vitamin B6 deficiency.


1963 ◽  
Vol 41 (5) ◽  
pp. 1215-1222 ◽  
Author(s):  
J. G. Heddle ◽  
E. W. McHenry ◽  
G. H. Beaton

DL-Penicillamine administered in the diet at the 0.25% level produced a marked lowering of food intake and body weight. Using blood transaminase activities as criteria, a definite antagonism to vitamin B6 was demonstrated. The response of animals to the drug did not differ between sexes. Transaminase activity changes were apparent within 13 days of treatment. They were not the result of a reduced food intake. Administration of 800 μg of pyridoxine hydrochloride per 10 g of diet to animals receiving penicillamine approximated the maximal prevention of the effects of the drug upon food intake, body weight, and transaminase activity. The effects were not completely prevented by dosages of vitamin B6 as high as 2000 μg per 10 g of diet. Attention is drawn to the possible significance of these studies in the treatment of patients (Wilson's disease) with penicillamine. On the basis of extrapolations from the present studies in rats, 50 mg of pyridoxine hydrochloride might be expected to give near-maximal protection against possible vitamin B6-antagonistic effects of 1.5 g of DL-penicillamine.


1963 ◽  
Vol 41 (1) ◽  
pp. 1215-1222 ◽  
Author(s):  
J. G. Heddle ◽  
E. W. McHenry ◽  
G. H. Beaton

DL-Penicillamine administered in the diet at the 0.25% level produced a marked lowering of food intake and body weight. Using blood transaminase activities as criteria, a definite antagonism to vitamin B6 was demonstrated. The response of animals to the drug did not differ between sexes. Transaminase activity changes were apparent within 13 days of treatment. They were not the result of a reduced food intake. Administration of 800 μg of pyridoxine hydrochloride per 10 g of diet to animals receiving penicillamine approximated the maximal prevention of the effects of the drug upon food intake, body weight, and transaminase activity. The effects were not completely prevented by dosages of vitamin B6 as high as 2000 μg per 10 g of diet. Attention is drawn to the possible significance of these studies in the treatment of patients (Wilson's disease) with penicillamine. On the basis of extrapolations from the present studies in rats, 50 mg of pyridoxine hydrochloride might be expected to give near-maximal protection against possible vitamin B6-antagonistic effects of 1.5 g of DL-penicillamine.


2021 ◽  
pp. 247412642110287
Author(s):  
Diana Driscoll ◽  
David Callanan

Purpose: This work reports retinal findings in an adult patient with vitamin B6 deficiency. Methods: A case review of a single patient is presented. Results: A patient with a Roth-type retinal lesion and a history of nonepileptic seizures was found to have lymphocytic colitis. She was treated with pyridoxine, which resolved her seizures and the white-centered hemorrhage. Conclusions: Vitamin B6 deficiency should be considered in the differential diagnosis of patients presenting with white-centered hemorrhages and a history of nonepileptic seizures.


1983 ◽  
Vol 50 (1) ◽  
pp. 33-42 ◽  
Author(s):  
David A. Bender

1. The effects of the administration of oestradiol and vitamin B6 on tryptophan metabolism in the rat have been assessed by measurement of the release of 14CO2 from [14C]tryptophan, in vivo, in order to determine whether, and to what extent, the abnormalities of tryptophan metabolism that are associated with oestrogen administration can be attributed to drug-induced vitamin B6 deficiency or depletion. Two positional isomers of [14C]tryptophan have been used; [ring-2-14C]tryptophan as an index of the activity of tryptophan oxygenase (L-tryptophan: oxygen oxidoreductase (decyclizing), EC 1.13.11.11) and [methylene-14C]trytophan as an index of the activity of kynureninase (L-kynurenine hydrolase, EC 3.7.1.3).2. The administration of 500 μg oestradiol/kg body-weight led to a reduction in the release of 14CO2 from both positional isomers of tryptophan, suggesting that the activities of both tryptophan oxygenase and kynureninase are reduced following oestrogen treatment. The kinetics of the release of 14CO2 from [methylene-14C]tryptophan after the administration of oestradiol were compatible with competitive inhibition of kynureninase by oestradiol or a metabolite.3. The administration of 10 mg pyridoxine hydrochloride/kg body-weight also reduced the production of 14CO2 from both positional isomers of 14C]tryptophan, suggesting some toxicity of such a high dose of the vitamin.4. In animals which had received the supplementary dose of vitamin B6, the administration of oestradiol led to further reduction in the production of 14CO2 from [ring-2-14C]tryptophan, suggesting a further reduction in the activity of tryptophan oxygenase, and an increase in the production of 14CO2 from [methylen-14C]tryptophan, but with a delay in the peak of production.5. These results confirm that there is no induction of tryptophan oxygenase by oestradiol, but rather reduced activity of the enzyme after the administration of a relatively high dose of the hormone. They also confirm that the inhibition of kynureninase by oestrogen metabolites that has been reported previously in partially-purified enzyme preparations also occurs in vivo.6. It is suggested that the abnormal results of the tryptophan load test that have been reported in women receiving oestrogens, and which have been interpreted as indicating some extent of drug-induced vitamin B6 deficiency, can be accounted for by the inhibition of tryptophan metabolism by oestrogens or their metabolites. Therefore it seems likely that the practice of administering supplements of vitamin B6 to women receiving oestrogens may not be appropriate, and indeed may exacerbate the changes in tryptophan metabolism that result from the administration of oestrogens. The tryptophan load test would appear to be unreliable as an index of vitamin B6 nutritional status in women receiving oestrogens.


2015 ◽  
Vol 4 ◽  
Author(s):  
Marie-Édith Côté-Robitaille ◽  
Christiane L. Girard ◽  
Frédéric Guay ◽  
J. Jacques Matte

AbstractHomocysteine (Hcy) is an intermediary sulphur amino acid recognised for pro-oxidative properties in several species which may weaken immune competence in piglets. In this species, there is an acute 10-fold increase of concentrations of plasma Hcy (pHcy) during the first 2 weeks of life. The present experiment aimed to determine if pHcy in piglets can be regulated by oral supplementations of betaine as a methyl group supplier, creatine for reducing the demand for methyl groups, choline with both previous functions and vitamin B6 as enzymic co-factor for Hcy catabolism. A total of seventeen sows (second parity) were fed gestation and lactation diets supplemented with folic acid (10 mg/kg) and vitamin B12 (150 µg/kg). Eight piglets in each litter received daily one of the eight following oral treatments (mg/kg body weight): (1) control (saline); (2) betaine (50); (3) choline (70); (4) creatine (300); (5) pyridoxine (0·2); (6) treatments 2 and 5; (7) treatments 3 and 4; and (8) treatments 2, 3, 4 and 5. According to age, pHcy increased sharply from 2·48 µm at birth to 17·96 µm at 21 d of age (P < 0·01). Concentrations of pHcy tended to be lower (P = 0·09) in treated than in control piglets but the highest and sole pairwise significant decrease (23 %) was observed between treatments 1 and 8 (P = 0·03). Growth from birth to 21 d of age was not influenced by treatments (P > 0·70). Therefore, it appears possible to reduce pHcy concentrations in suckling piglets but a combination of all chosen nutrients is required.


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