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Influence of vitamin B12 status and different folic acid dietary levels on the methylation cycle during growth and aging in rats

Published online by Cambridge University Press:  15 August 2011

T. Partearroyo
Affiliation:
Department of Pharmacy and Food Sciences, Facultad de Farmacia, Universidad CEU San Pablo, 28668, Madrid, Spain
N. Úbeda
Affiliation:
Department of Pharmacy and Food Sciences, Facultad de Farmacia, Universidad CEU San Pablo, 28668, Madrid, Spain
G. Varela-Moreiras
Affiliation:
Department of Pharmacy and Food Sciences, Facultad de Farmacia, Universidad CEU San Pablo, 28668, Madrid, Spain
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Abstract

Type
Abstract
Copyright
Copyright © The Authors 2011

Elevated folic acid (FA) intakes create analogous conditions to those of metabolic folate deficiency(Reference Troen, Mitchell and Sorensen1). In a similar way, vitamin B12 status influences the physiological response to different FA doses in the organism(Reference Morris, Jacques and Rosenberg2). In previous studies, we have demonstrated that FA deficiency compromises methionine metabolism, whereas supplementation does not show additional positive effect compared to control diet in growing animals(Reference Partearroyo, Ubeda and Alonso-Aperte3). However, there is no information on the FA supplementation effect on the methionine cycle in vitamin B12 deficiency in two critical physiological states such as growth and aging.

The methionine/methylation metabolism during growth and aging was determined to evaluate the global effect of different levels of dietary FA and vitamin B12.

Male Sprague–Dawley rats (6 weeks, n 50, and 20-month-old, n 35) were assigned into four groups at three levels of folic acid both in the absence of vitamin B12 for 30 d: [CB/CF (50 μg vitamin B12; 2 mg FA), DB/DF (0 μg vitamin B12; 0 mg FA), DB/CF (0 μg vitamin B12; 2 mg FA) and DB/SF (0 μg vitamin B12; 8 mg FA)]. Manipulation of the animals was performed following European Union Normative (2003/65/CE). Student's t test was used to evaluate the differences in the same group between the two populations (*P<0.05, **P<0.01 and P<0.001).

Fig. 1. Serum folate.

Fig. 2. Serum vitamin B12.

Fig. 3. Serum vitamin B6.

Fig. 4. Serum homocysteine.

Fig. 5. DNA methylation in brain.

Fig. 6. DNA methylation in liver.

Serum homocysteine, vitamin B6 and FA concentrations were lower in aging v. weanling rats (Figs. 1, 3 and 4, respectively), but serum vitamin B12 values were higher (Fig. 2). However, aging seemed not to affect the folate liver stores (data not shown). Only during growth, both vitamins deficiency induced a hepatic DNA hypomethylation that was reverted when rats were FA supplemented (Fig. 5).

There were some parameters of methionine cycle in weanling rats and none in aging rats that recovered similar values to controls when rats deficient in vitamin B12 were supplemented with FA. Therefore, FA supplementation should also be accompanied by the same nutritional action for vitamin B12 in order to solve these alterations in this vitamin B12 deficient group.

References

1.Troen, AM, Mitchell, B, Sorensen, B et al. (2006) J Nutr 136, 189–94.CrossRefGoogle Scholar
2.Morris, MS, Jacques, PF, Rosenberg, IH et al. (2007) Am J Clin Nutr 85, 193200.CrossRefGoogle Scholar
3.Partearroyo, T, Ubeda, N, Alonso-Aperte, E et al. (2010) Ann Nutr Metab 56, 143151.CrossRefGoogle Scholar
Figure 0

Fig. 1. Serum folate.

Figure 1

Fig. 2. Serum vitamin B12.

Figure 2

Fig. 3. Serum vitamin B6.

Figure 3

Fig. 4. Serum homocysteine.

Figure 4

Fig. 5. DNA methylation in brain.

Figure 5

Fig. 6. DNA methylation in liver.