GTP-cyclohydrolase deficiency induced peripheral and deep microcirculation dysfunction with age

The present study assessed the impact of impaired tetrahydrobiopterin (BH4) production on vasoreactivity from conduit and small arteries along the vascular tree as seen during aging. For this purpose, the mutant hyperphenylalaninemic mouse (hph-1) was used. This model is reported to be deficient in GTP cyclohydrolase I, a rate limiting enzyme in BH4 biosynthesis. BH4 is a key regulator of vascular homeostasis by regulating the nitric oxide synthase 3 (NOS3) activity. In GTP-CH deficient mice, the aortic BH4 levels were decreased, by −77% in 12 week-middle-aged mice (young) and by −83% in 35–45 week-middle-aged mice (middle-aged). In young hph-1, the mesenteric artery ability to respond to flow was slightly reduced by 9%. Aging induced huge modification in many vascular functions. In middle-aged hph-1, we observed a decrease in aortic cGMP levels, biomarker of NO availability (−46%), in flow-mediated vasodilation of mesenteric artery (−31%), in coronary hyperemia response measured in isolated heart following transient ischemia (−27%) and in cutaneous microcirculation dilation in response to acetylcholine assessed in vivo by laser-doppler technic (−69%). In parallel, the endothelium-dependent relaxation in response to acetylcholine in conduit blood vessel, measured on isolated aorta rings, was unchanged in hph-1 mice whatever the age. Our findings demonstrate that in middle-aged GTP-CH depleted mice, the reduction of BH4 was characterized by an alteration of microcirculation dilatory properties observed in various parts of the vascular tree. Large conduit blood vessels vasoreactivity, ie aorta, was unaltered even in middle-aged mice emphasizing the main BH4-deletion impact on the microcirculation. •Reduced tetrahydrobiopterin (BH (BH4) synthesis consequences on conduit and small arteries vasoreactivity during aging.•In middle-aged mice GTP-CH deficient mice, the aortic BH4 level was decreased leading to a reduced NO bioavailability.•In middle-aged, the deficiency in BH4 altered microcirculation dilation of mesenteric, coronary and cutaneous blood vessels.•Large conduit blood vessels vasoreactivity, ie aorta, was unaltered even in middle-aged mice.•Aging emphasizing the main BH4-deletion impact on the microcirculation.