Porkert M, Sher S, Reddy U, Cheema F, Niessner C, Kolm P, Jones D P, Hooper C, Taylor W R, Harrison D, Quyyumi A A
Division of Cardiology, Emory University, Atlanta, GA, USA.
J Hum Hypertens. 2008 Jun;22(6):401-7. doi: 10.1038/sj.jhh.1002329. Epub 2008 Mar 6.
Tetrahydrobiopterin (BH(4)) is a cofactor for the nitric oxide (NO) synthase enzymes, such that its insufficiency results in uncoupling of the enzyme, leading to release of superoxide rather than NO in disease states, including hypertension. We hypothesized that oral BH(4) will reduce arterial blood pressure (BP) and improve endothelial function in hypertensive subjects. Oral BH(4) was given to subjects with poorly controlled hypertension (BP >135/85 mm Hg) and weekly measurements of BP and endothelial function made. In Study 1, 5 or 10 mg kg(-1) day(-1) of BH(4) (n=8) was administered orally for 8 weeks, and in Study 2, 200 and 400 mg of BH(4) (n=16) was given in divided doses for 4 weeks. Study 1: significant reductions in systolic (P=0.005) and mean BP (P=0.01) were observed with both doses of BH(4). Systolic BP was 15+/-15 mm Hg (P=0.04) lower after 5 weeks and persisted for the 8-week study period. Study 2: subjects given 400 mg BH(4) had decreased systolic (P=0.03) and mean BP (P=0.04), with a peak decline of 16+/-19 mm Hg (P=0.04) at 3 weeks. BP returned to baseline 4 weeks after discontinuation. Significant improvement in endothelial function was observed in Study 1 subjects and those receiving 400 mg BH(4). There was no significant change in subjects given the 200 mg dose. This pilot investigation indicates that oral BH(4) at a daily dose of 400 mg or higher has a significant and sustained antihypertensive effect in subjects with poorly controlled hypertension, an effect that is associated with improved endothelial NO bioavailability.
四氢生物蝶呤(BH(4))是一氧化氮(NO)合酶的一种辅助因子,因此其不足会导致该酶解偶联,在包括高血压在内的疾病状态下导致超氧化物而非NO的释放。我们假设口服BH(4)会降低高血压受试者的动脉血压(BP)并改善内皮功能。将口服BH(4)给予血压控制不佳(BP>135/85 mmHg)的受试者,并每周测量血压和内皮功能。在研究1中,口服5或10 mg kg(-1) 天(-1) 的BH(4)(n = 8),持续8周;在研究2中,分剂量给予200和400 mg的BH(4)(n = 16),持续4周。研究1:两种剂量的BH(4)均观察到收缩压(P = 0.005)和平均血压(P = 0.01)显著降低。5周后收缩压降低15±15 mmHg(P = 0.04),并在为期8周的研究期间持续存在。研究2:给予400 mg BH(4)的受试者收缩压(P = 0.03)和平均血压(P = 0.04)降低,在3周时峰值下降16±19 mmHg(P = 0.04)。停药4周后血压恢复到基线水平。在研究1的受试者和接受400 mg BH(4)的受试者中观察到内皮功能有显著改善。给予200 mg剂量的受试者没有显著变化。这项初步研究表明,每日剂量400 mg或更高的口服BH(4)对血压控制不佳的受试者具有显著且持续的降压作用,该作用与内皮NO生物利用度的改善有关。