Kitani K, Sato Y, Kanai S, Ohta M, Nokubo M, Masuda Y
First Laboratory of Clinical Physiology, Tokyo Metropolitan Institute of Gerontology, Japan.
Arch Gerontol Geriatr. 1988 Dec;7(4):261-71. doi: 10.1016/0167-4943(88)90009-x.
The effects of age on the neurotoxicity of phenobarbital and its anticonvulsant effect were examined in female BDF1 mice of different ages by means of a rotorod test and the pentylenetetrazole (PTZ)-induced maximal seizure, respectively. The minimal neurotoxic concentrations (MTCs) of phenobarbital in both plasma and brain evaluated by a rotorod test were 50% lower (p less than 0.05) in old (24-months-old) mice compared with the respective values in young (6-months-old) mice, while 12-months values were the highest of the three groups. Mice given some dosages of phenobarbital, particularly old (24-months-old) mice, died within the 15-min observation period after an i.p. injection of PTZ (150 mg/kg) without demonstrating a hindlimb extensor component (HLE) of maximal seizure. When these animals were classified as responders with regard to the anticonvulsant effect of phenobarbital, the minimal effective concentrations (MECs) in plasma and brain required for abolishing the PTZ-induced maximal seizure in old mice were only 10-20% those of young mice. Present results coupled with our past studies using electroshock seizure suggest that both the neurotoxicity and the efficacy of phenobarbital increase with age in mice.
分别通过转棒试验和戊四氮(PTZ)诱导的最大惊厥发作,研究了年龄对不同年龄段雌性BDF1小鼠苯巴比妥神经毒性及其抗惊厥作用的影响。通过转棒试验评估,老年(24月龄)小鼠血浆和脑中苯巴比妥的最小神经毒性浓度(MTCs)比幼年(6月龄)小鼠的相应值低50%(p<0.05),而12月龄小鼠的值在三组中最高。腹腔注射PTZ(150mg/kg)后,给予一定剂量苯巴比妥的小鼠,特别是老年(24月龄)小鼠,在15分钟观察期内死亡,未表现出最大惊厥发作的后肢伸展成分(HLE)。当根据苯巴比妥的抗惊厥作用将这些动物分类为反应者时,老年小鼠消除PTZ诱导的最大惊厥发作所需的血浆和脑中最小有效浓度(MECs)仅为幼年小鼠的10%-20%。目前的结果与我们过去使用电休克惊厥的研究表明,苯巴比妥的神经毒性和疗效在小鼠中均随年龄增长而增加。