Dorheim M A, Tracey W R, Pollock J S, Grammas P
Department of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City 73104.
Biochem Biophys Res Commun. 1994 Nov 30;205(1):659-65. doi: 10.1006/bbrc.1994.2716.
The cerebral microcirculation undergoes specific biochemical changes in Alzheimer's disease. In this study, we have compared the nitric oxide synthase (NOS) activity of brain microvessels isolated from Alzheimer and control brains. L-[3H]-citrulline, the stable co-product generated with nitric oxide (NO) from L-[3H]-arginine, was measured as an indicator of NOS activity. The results indicated a significant increase in NOS activity in microvessels isolated from Alzheimer brains. In addition, using antibodies to both the endothelial and inducible NOS isoforms, we demonstrated a significant increase in enzyme level in Alzheimer-derived vessels. Elevated vascular production of NO, a potentially neurotoxic mediator in the CNS, may contribute to the susceptibility of neurons to injury and cell death in Alzheimer's disease.
在阿尔茨海默病中,脑微循环会发生特定的生化变化。在本研究中,我们比较了从阿尔茨海默病患者大脑和对照大脑中分离出的脑微血管的一氧化氮合酶(NOS)活性。L-[3H]-瓜氨酸是由L-[3H]-精氨酸与一氧化氮(NO)生成的稳定副产物,其含量被用作NOS活性的指标。结果表明,从阿尔茨海默病患者大脑中分离出的微血管中,NOS活性显著增加。此外,使用针对内皮型和诱导型NOS同工型的抗体,我们证明了阿尔茨海默病来源血管中的酶水平显著增加。NO是中枢神经系统中一种潜在的神经毒性介质,其血管生成增加可能导致阿尔茨海默病中神经元易受损伤和细胞死亡。