Saija A, Princi P, De Pasquale R, Costa G
Department Farmaco-Biologico, School of Pharmacy, University of Messina, Italy.
Neuropharmacology. 1989 Sep;28(9):997-1002. doi: 10.1016/0028-3908(89)90202-5.
The state of deep surgical anaesthesia, induced by intraperitoneal injection of pentobarbital sodium (54 mg/kg) or ketamine hydrochloride (150 mg/kg) in the rat, was accompanied by a significant reduction in the permeability of the blood-brain barrier evaluated by calculating a unidirectional blood-to-brain constant (Ki) for the circulating tracer [14C]alpha-aminoisobutyric acid. Pentobarbital-induced anaesthesia was also characterized by a widespread and marked depression of local cerebral glucose utilization; on the contrary, when rats were anaesthetized with ketamine, cerebral glucose utilization increased in the striatum and hippocampus and decreased in the cerebellum and brain-stem. It is suggested, as a hypothesis, that two different mechanisms, depending on the kind of the anaesthetic drug used, may be involved in the changes in the permeability of the blood-brain barrier, observed in anaesthetized animals: (a) a neurogenic component; (b) a direct interaction of the anaesthetic with elements of the microvasculature.
通过向大鼠腹腔注射戊巴比妥钠(54毫克/千克)或氯胺酮盐酸盐(150毫克/千克)诱导产生深度外科麻醉状态,在此状态下,通过计算循环示踪剂[¹⁴C]α-氨基异丁酸的单向血脑常数(Ki)来评估,血脑屏障的通透性显著降低。戊巴比妥诱导的麻醉还具有广泛且明显的局部脑葡萄糖利用抑制特征;相反,当用氯胺酮麻醉大鼠时,纹状体和海马体中的脑葡萄糖利用增加,而小脑和脑干中的脑葡萄糖利用减少。作为一种假设,有人提出,根据所使用麻醉药物的种类不同,两种不同的机制可能参与了在麻醉动物中观察到的血脑屏障通透性变化:(a)神经源性成分;(b)麻醉剂与微血管成分的直接相互作用。