Brand M P, Briddon A, Land J M, Clark J B, Heales S J
Department of Neurochemistry, Institute of Neurology, London, UK.
Brain Res. 1996 Sep 30;735(1):169-72. doi: 10.1016/0006-8993(96)00892-x.
In this study, the effect of tetrahydrobiopterin deficiency on the nitric oxide/cGMP pathway has been investigated in cerebellar slices derived from the hph-1 mouse. This animal displays a partial deficiency of tetrahydrobiopterin. Basal levels of cGMP were significantly reduced (-29.5%) in the hph-1 mouse cerebellum compared to controls. Following kainate stimulation (500 microM) cGMP levels increased in both control and hph-1 preparations but were again significantly lower (-29.1%) in the hph-1 mouse. Exposure of slices to the nitric oxide donors, S-nitroso-N-acetylpenicillamine and S-nitroso-glutathione, revealed no difference in cGMP accumulation between the two groups. These findings suggest that the cerebellar nitric oxide/cGMP pathway may be impaired in partial tetrahydrobiopterin deficiency states due to diminished nitric oxide formation.
在本研究中,已在源自hph - 1小鼠的小脑切片中研究了四氢生物蝶呤缺乏对一氧化氮/cGMP途径的影响。这种动物表现出四氢生物蝶呤部分缺乏。与对照组相比,hph - 1小鼠小脑中cGMP的基础水平显著降低(-29.5%)。在给予红藻氨酸刺激(500微摩尔)后,对照组和hph - 1组制剂中的cGMP水平均升高,但hph - 1小鼠中的cGMP水平再次显著降低(-29.1%)。将切片暴露于一氧化氮供体S - 亚硝基 - N - 乙酰青霉胺和S - 亚硝基谷胱甘肽后,两组之间cGMP积累没有差异。这些发现表明,在部分四氢生物蝶呤缺乏状态下,由于一氧化氮生成减少,小脑一氧化氮/cGMP途径可能受损。