Saija A, Princi P, Pisani A, Santoro G, De Pasquale R, Massi M, Costa G
Dept. Farmaco-Biologico (School of Pharmacy), University of Messina, Italy.
Life Sci. 1992;51(7):467-77. doi: 10.1016/0024-3205(92)90023-i.
Changes in blood-brain barrier (BBB) permeability and cerebral metabolic activity following intravenous injection of kainic acid (KA; 6, 12 mg/Kg) in rats were assessed by calculating respectively a blood-to-brain transfer constant (Ki) for [14C]alpha-aminoisobutyric acid and local cerebral glucose utilization (LCGU) values, at different times (1 h, or acute seizures phase, and 48 h, or chronic pathology phase) after the induction of seizures. A significant increase in the local permeability of the BBB was observed 1 h after the injection of KA 6 mg/Kg (eliciting no significant changes in cerebral metabolic activity, except within the frontal cortex and the hippocampus) and 12 mg/Kg (which induced a marked and widespread enhancement of LCGU). On the contrary, during the pathology phase, persistent regional increases in Ki values were evidenced in rats treated with the lowest dose of the convulsant, but not in rats injected with KA 12 mg/Kg (a dose able to cause extensive neuronal damage). Thus one can speculate that: 1) KA-induced regional changes in the permeability of the BBB are not correlated with changes in neuronal activity; 2) opening of the BBB is not reliably associated with neuronal injury.
通过分别计算癫痫发作诱导后不同时间点(1小时,即急性癫痫发作期;48小时,即慢性病理期)[¹⁴C]α-氨基异丁酸的血脑转移常数(Ki)和局部脑葡萄糖利用率(LCGU)值,评估大鼠静脉注射海藻酸(KA;6、12毫克/千克)后血脑屏障(BBB)通透性和脑代谢活性的变化。注射6毫克/千克KA(除额叶皮质和海马体外,未引起脑代谢活性显著变化)和12毫克/千克KA(引起LCGU显著广泛增强)后1小时,观察到BBB局部通透性显著增加。相反,在病理期,用最低剂量惊厥剂处理的大鼠中Ki值持续区域升高,但注射12毫克/千克KA(能引起广泛神经元损伤的剂量)的大鼠中未出现。因此可以推测:1)KA诱导的BBB通透性区域变化与神经元活动变化无关;2)BBB开放与神经元损伤无可靠关联。