Experimental Medicine and Toxicology, Imperial College London, Hammersmith Hospital, Ducane Road, London, W12 ONN, UK.
Eur Respir J. 2010 Aug;36(2):323-30. doi: 10.1183/09031936.00188809. Epub 2010 Mar 11.
Tetrahydrobiopterin (BH(4)) is an essential cofactor for nitric oxide synthases (NOS). This study investigated the effect of increasing BH(4) levels on hypoxia-induced pulmonary vasoconstriction (HPV). Sprague Dawley rats and hph-1 (BH(4) deficient) mice were given BH(4) before and during HPV in an isolated perfused lung preparation. BH(4) inhibited HPV in a concentration-dependent manner and increased NO metabolites in the perfusate. Bradykinin-induced reductions in HPV were blunted in hph-1 mice and pre-administration of BH(4) restored the response. The effect of BH(4) was attenuated by l-NAME (NOS inhibitor), PTIO (NO scavenger), and catalase (H(2)O(2) catalyser) administered prior to HPV but enhanced by MnTMPyP (superoxide dismutase mimetic). The effect of BH(4) on HPV was partially recapitulated by NH(4), a stereoisomer that shares antioxidant properties with BH(4) but is not a NOS cofactor. The bioavailability of BH(4) is an important determinant of the pulmonary vascular response to hypoxia. Its effects are mediated via nitric oxide, hydrogen peroxide and its antioxidant properties, and are attenuated by oxidant stress. Pharmacological administration of BH(4) may have therapeutic potential in pulmonary hypertension.
四氢生物蝶呤(BH4)是一氧化氮合酶(NOS)的必需辅助因子。本研究探讨了增加 BH4 水平对缺氧性肺血管收缩(HPV)的影响。在离体灌流肺制备中,给予 Sprague Dawley 大鼠和 hph-1(BH4 缺乏)小鼠 BH4 以在 HPV 之前和期间增加 BH4 水平。BH4 以浓度依赖性方式抑制 HPV,并增加灌流液中的 NO 代谢物。在 hph-1 小鼠中,缓激肽诱导的 HPV 减少减弱,而 BH4 的预先给予恢复了反应。BH4 的作用在 HPV 之前给予 l-NAME(NOS 抑制剂)、PTIO(NO 清除剂)和 catalase(H2O2 催化剂)时被减弱,但在 MnTMPyP(超氧化物歧化酶模拟物)时增强。BH4 对 HPV 的作用部分由 NH4 重现,NH4 是与 BH4 具有抗氧化特性但不是 NOS 辅助因子的立体异构体。BH4 的生物利用度是肺血管对缺氧反应的重要决定因素。其作用通过一氧化氮、过氧化氢及其抗氧化特性介导,并被氧化应激减弱。BH4 的药理给药可能在肺动脉高压中具有治疗潜力。