Martins A N, Doyle T F, Wright S J, Bass B G
Stroke. 1980 Sep-Oct;11(5):469-76. doi: 10.1161/01.str.11.5.469.
To study the effect of histamine (HA) on brain blood flow and capillary permeability, bilateral parietal craniectomies were made in cats anesthetized with nitrous oxide and ketamine. The dura was removed and solutions of HA in mock cerebrospinal fluid (CSF) in varying concentrations ranging from 10(-5) M to 10(-1) M were irrigated continuously onto the exposed brain while local cerebral blood flow was determined polarographically by hydrogen clearance. Capillary permeability was assessed by determining HA's effect on the 125I-albumin space of the brain. Electrical activity was monitored by electrocorticography. HA consistently dilated pial blood vessels and produced within 15 min a dose-related local hyperemia that subsided 30--60 min after HA was removed. Hyperemia was blocked by cimetidine. HA had no appreciable effect on either the blood-brain barrier to albumin or the electrical activity of the cortex. HA is pharmacologically capable of participating directly in the acute hyperemic response of the brain's microcirculation to physiologic and pathologic stimuli but has little effect on cerebrovascular permeability to protein.
为研究组胺(HA)对脑血流和毛细血管通透性的影响,在使用氧化亚氮和氯胺酮麻醉的猫身上进行双侧顶骨开颅术。去除硬脑膜,将浓度范围从10^(-5) M至10^(-1) M的HA溶于模拟脑脊液(CSF)中的溶液持续灌流到暴露的脑表面,同时通过氢清除法用极谱法测定局部脑血流。通过测定HA对脑125I - 白蛋白空间的影响来评估毛细血管通透性。通过皮层脑电图监测电活动。HA持续扩张软脑膜血管,并在15分钟内产生与剂量相关的局部充血,在去除HA后30 - 60分钟充血消退。充血被西咪替丁阻断。HA对白蛋白的血脑屏障或皮层的电活动均无明显影响。HA在药理学上能够直接参与脑微循环对生理和病理刺激的急性充血反应,但对脑血管对蛋白质的通透性影响很小。