Baranczyk-Kuzma A, Audus K L, Guillot F L, Borchardt R T
Department of Biochemistry, Warsaw Medical School, Poland.
Neurochem Res. 1992 Feb;17(2):209-14. doi: 10.1007/BF00966802.
The specific activity of adenylate cyclase was assayed in homogenates of gray matter, freshly isolated and primary cultured microvessel endothelial cells from bovine cerebral cortex. Specific activities for the tissues were 14.6 +/- 2.1, 15.6 +/- 2.7, and 8.4 +/- 1.5 pmol cAMP/mg protein/min +/- SD for gray matter, cultured microvessels, and freshly isolated microvessels, respectively. Adenylate cyclase associated with gray matter and cultured microvessels was sensitive to histamine and selected catecholamines. Perhaps due to metabolic deficiencies, adenylate cyclase of freshly isolated microvessels exhibited little or no response to either the catecholamines or histamine. Angiotensin II stimulated adenylate cyclase of both freshly isolated and cultured microvessels but had no effect on gray matter. Bradykinin did not stimulate cAMP generation in any of the tissues. Overall results support the role of cAMP in regulating brain microvessel functions and suggest that primary cultures of brain microvessels may be useful in examining cAMP-mediated biochemical pathways at the blood-brain barrier.
在新鲜分离的和原代培养的牛大脑皮质微血管内皮细胞以及灰质匀浆中测定了腺苷酸环化酶的比活性。这些组织的比活性分别为:灰质14.6±2.1、培养的微血管15.6±2.7、新鲜分离的微血管8.4±1.5 pmol cAMP/毫克蛋白/分钟±标准差。与灰质和培养的微血管相关的腺苷酸环化酶对组胺和选定的儿茶酚胺敏感。可能由于代谢缺陷,新鲜分离的微血管的腺苷酸环化酶对儿茶酚胺或组胺几乎没有反应。血管紧张素II刺激新鲜分离的和培养的微血管的腺苷酸环化酶,但对灰质没有影响。缓激肽在任何组织中都不刺激cAMP的生成。总体结果支持cAMP在调节脑微血管功能中的作用,并表明脑微血管的原代培养可能有助于研究血脑屏障处cAMP介导的生化途径。