Altered tetrahydrobiopterin metabolism in atherosclerosis: implications for use of oxidized tetrahydrobiopterin analogues and thiol antioxidants
J Vásquez-Vivar, D Duquaine, J Whitsett… - … , and vascular biology, 2002 - Am Heart Assoc
J Vásquez-Vivar, D Duquaine, J Whitsett, B Kalyanaraman, S Rajagopalan
Arteriosclerosis, thrombosis, and vascular biology, 2002•Am Heart AssocObjective—Tetrahydrobiopterin (BH4) is of fundamental importance for the normal function
of endothelial NO synthase. The purpose of this study was to investigate the effects of
hyperlipidemia on vascular BH4 levels and the effect of supplementation with sepiapterin in
the presence and absence of N-acetylcysteine (NAC). Methods and Results—New Zealand
White rabbits were fed normal chow (normocholesterolemic [NC] group) or hyperlipidemic
chow (hyperlipidemic [HL] group) for 8 to 10 weeks. Mean cholesterol levels were 1465±333 …
of endothelial NO synthase. The purpose of this study was to investigate the effects of
hyperlipidemia on vascular BH4 levels and the effect of supplementation with sepiapterin in
the presence and absence of N-acetylcysteine (NAC). Methods and Results—New Zealand
White rabbits were fed normal chow (normocholesterolemic [NC] group) or hyperlipidemic
chow (hyperlipidemic [HL] group) for 8 to 10 weeks. Mean cholesterol levels were 1465±333 …
Objective— Tetrahydrobiopterin (BH4) is of fundamental importance for the normal function of endothelial NO synthase. The purpose of this study was to investigate the effects of hyperlipidemia on vascular BH4 levels and the effect of supplementation with sepiapterin in the presence and absence of N-acetylcysteine (NAC).
Methods and Results— New Zealand White rabbits were fed normal chow (normocholesterolemic [NC] group) or hyperlipidemic chow (hyperlipidemic [HL] group) for 8 to 10 weeks. Mean cholesterol levels were 1465±333 and 53±17 mg/dL in the HL and NC group, respectively. Markedly diminished BH4 levels were found in the HL group compared with the NC group, but these levels could be restored after 6 hours of incubation with sepiapterin. Peak relaxations to acetylcholine and A23187 were impaired in the HL group. Supplementation with sepiapterin resulted in a further diminution of relaxation in the HL but not NC group. Incubation with NAC for 6 hours failed to raise BH4 levels, whereas NAC in conjunction with sepiapterin raised BH4 levels ≈221-fold. However, this increase did not improve relaxations to A23187 and acetylcholine.
Conclusions— Prolonged exposure to sepiapterin impairs vasorelaxation in hyperlipidemia despite repletion of endogenous BH4. Antioxidant thiols do not correct this impairment. These studies have implications for the use of sepiapterin in the correction of vasomotor tone in atherosclerosis.
Am Heart Assoc