TY - JOUR
T1 - Vitamin C is not essential for carnitine biosynthesis in vivo
T2 - Verification in vitamin C-depleted senescence marker protein-30/gluconolactonase knockout mice
AU - Furusawa, Hajime
AU - Sato, Yasunori
AU - Tanaka, Yasukazu
AU - Inai, Yoko
AU - Amano, Akiko
AU - Iwama, Mizuki
AU - Kondo, Yoshitaka
AU - Handa, Setsuko
AU - Murata, Akira
AU - Nishikimi, Morimitsu
AU - Goto, Sataro
AU - Maruyama, Naoki
AU - Takahashi, Ryoya
AU - Ishigami, Akihito
PY - 2008/9
Y1 - 2008/9
N2 - Carnitine is an essential cofactor in the transport of long-chain fatty acids into the mitochondrial matrix and plays an important role in energy production via β-oxidation. Vitamin C (VC) has long been considered a requirement for the activities of two enzymes in the carnitine biosynthetic pathway, i.e., 6-N-trimethyllysine dioxygenase and γ-butyrobetaine dioxygenase. Our present study using senescence marker protein-30 (SMP30)/gluconolactonase (GNL) knockout (KO) mice, which cannot synthesize VC in vivo, led to the conclusion that this notion is not true. After weaning at 40 d of age, SMP30/GNL KO mice were fed a diet lacking VC and carnitine, then given water containing 1.5 g/l VC (VC(+) mice) or no VC (VC(-) mice) for 75 d. Subsequently, total VC and carnitine levels were measured in the cerebrum, cerebellum, liver, kidney, soleus muscle, extensor digitorum longus muscle, heart, plasma and serum. The total VC levels in all tissues and plasma from VC(-) SMP30/GNL KO mice were negligible, i.e., <2% of the levels in SMP30/GNL KO VC(+) mice; however, the total carnitine levels of both groups were similar in all tissues and serum. In addition, carnitine was produced by incubated liver homogenates from the VC-depleted SMP30/GNL KO mice irrespective of the presence or absence of 1mM VC. Collectively, these results indicate that VC is not essential for carnitine biosynthesis in vivo.
AB - Carnitine is an essential cofactor in the transport of long-chain fatty acids into the mitochondrial matrix and plays an important role in energy production via β-oxidation. Vitamin C (VC) has long been considered a requirement for the activities of two enzymes in the carnitine biosynthetic pathway, i.e., 6-N-trimethyllysine dioxygenase and γ-butyrobetaine dioxygenase. Our present study using senescence marker protein-30 (SMP30)/gluconolactonase (GNL) knockout (KO) mice, which cannot synthesize VC in vivo, led to the conclusion that this notion is not true. After weaning at 40 d of age, SMP30/GNL KO mice were fed a diet lacking VC and carnitine, then given water containing 1.5 g/l VC (VC(+) mice) or no VC (VC(-) mice) for 75 d. Subsequently, total VC and carnitine levels were measured in the cerebrum, cerebellum, liver, kidney, soleus muscle, extensor digitorum longus muscle, heart, plasma and serum. The total VC levels in all tissues and plasma from VC(-) SMP30/GNL KO mice were negligible, i.e., <2% of the levels in SMP30/GNL KO VC(+) mice; however, the total carnitine levels of both groups were similar in all tissues and serum. In addition, carnitine was produced by incubated liver homogenates from the VC-depleted SMP30/GNL KO mice irrespective of the presence or absence of 1mM VC. Collectively, these results indicate that VC is not essential for carnitine biosynthesis in vivo.
KW - Ascorbic acid
KW - Butyrobetaine
KW - Dioxygenase
KW - Gluconolactonase
KW - Senescence marker protein-30
KW - Vitamin C
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UR - http://www.scopus.com/inward/citedby.url?scp=50849130623&partnerID=8YFLogxK
U2 - 10.1248/bpb.31.1673
DO - 10.1248/bpb.31.1673
M3 - Article
C2 - 18758058
AN - SCOPUS:50849130623
SN - 0918-6158
VL - 31
SP - 1673
EP - 1679
JO - Biological and Pharmaceutical Bulletin
JF - Biological and Pharmaceutical Bulletin
IS - 9
ER -