TY - JOUR

T1 - Vitamin C deficiency in weanling guinea pigs

T2 - differential expression of oxidative stress and DNA repair in liver and brain

AU - Lykkesfeldt, Jens

AU - Trueba, Gilberto Perez

AU - Poulsen, Henrik E.

AU - Christen, Stephan

PY - 2007

Y1 - 2007

N2 - Neonates are particularly susceptible to malnutrition due to their limited reserves of micronutrients and their rapid growth. In the present study, we examined the effect of vitamin C deficiency on markers of oxidative stress in plasma, liver and brain of weanling guinea pigs. Vitamin C deficiency caused rapid and significant depletion of ascorbate (P,0001), tocopherols (P,0001) and glutathione (P,0001), and a decrease in superoxide dismutase activity (P¼0005) in the liver, while protein oxidation was significantly increased (P¼0011). No changes in lipid oxidation or oxidatively damaged DNA were observed in this tissue. In the brain, the pattern was markedly different. Of the measured antioxidants, only ascorbate was significantly depleted (P,0001), but in contrast to the liver, ascorbate oxidation (P¼0034), lipid oxidation (P,0001), DNA oxidation (P¼013) and DNA incision repair (P¼0014) were all increased, while protein oxidation decreased (P¼0003). The results show that the selective preservation of brain ascorbate and induction of DNA repair in vitamin C-deficient weanling guinea pigs is not sufficient to prevent oxidative damage. Vitamin C deficiency may therefore be particularly adverse during the neonatal period.

AB - Neonates are particularly susceptible to malnutrition due to their limited reserves of micronutrients and their rapid growth. In the present study, we examined the effect of vitamin C deficiency on markers of oxidative stress in plasma, liver and brain of weanling guinea pigs. Vitamin C deficiency caused rapid and significant depletion of ascorbate (P,0001), tocopherols (P,0001) and glutathione (P,0001), and a decrease in superoxide dismutase activity (P¼0005) in the liver, while protein oxidation was significantly increased (P¼0011). No changes in lipid oxidation or oxidatively damaged DNA were observed in this tissue. In the brain, the pattern was markedly different. Of the measured antioxidants, only ascorbate was significantly depleted (P,0001), but in contrast to the liver, ascorbate oxidation (P¼0034), lipid oxidation (P,0001), DNA oxidation (P¼013) and DNA incision repair (P¼0014) were all increased, while protein oxidation decreased (P¼0003). The results show that the selective preservation of brain ascorbate and induction of DNA repair in vitamin C-deficient weanling guinea pigs is not sufficient to prevent oxidative damage. Vitamin C deficiency may therefore be particularly adverse during the neonatal period.

U2 - 10.1017/S0007114507787457

DO - 10.1017/S0007114507787457

M3 - Journal article

VL - 98

SP - 1116

EP - 1119

JO - British Journal of Nutrition

JF - British Journal of Nutrition

SN - 0007-1145

IS - 6

ER -