Sharma D, Maurya A K, Singh R
School of Life Sciences, Jawaharlal Nehru University, New Delhi, India.
Neurobiol Aging. 1993 Jul-Aug;14(4):319-30. doi: 10.1016/0197-4580(93)90117-t.
Changes in lipid peroxidation, lipofuscin concentration, and multiple unit activity (MUA recorded in conscious animals) in the CA3 region were studied in the hippocampus of male Wistar rats aged 4, 8, 16, and 24 months. The lipid peroxidation and lipofuscin concentration were increased with age. The MUA, however, declined with age. Correlational analyses were performed for the four age groups to determine the relationship between the age-associated decline in MUA with the age-related alterations in lipid peroxidation and lipofuscin concentrations. The age-related increase in lipid peroxidation correlated positively with the age-associated increase in lipofuscin concentration. The age-related increases in lipid peroxidation and lipofuscin concentration correlated negatively with the changes in MUA. Since lipid peroxidation may affect neuronal electrophysiology, our data suggested that age-related increase in lipid peroxidation may contribute to an age-associated decline in neuronal electrical activity. Centrophenoxine effects were studied on the three above-mentioned age-associated changes in the hippocampus. The drug had no effect on all three parameters in 4- and 8-month-old rats. In 16- and 24-month-old rats, however, the drug significantly increased the MUA but concomitantly decreased lipofuscin concentration and lipid peroxidation. Correlational analyses of the data on MUA, lipid peroxidation and lipofuscin concentration from the centrophenoxine-treated animals showed that the drug-induced diminution in both lipofuscin and lipid peroxidation was significantly correlated with the drug-induced increase in MUA. The differential effect of the drug in younger (4-8 months) and older (16-24 months) animals indicated that the stimulation of MUA was clearly associated with concomitant decrease in lipid peroxidation and lipofuscin concentration.
在4、8、16和24月龄的雄性Wistar大鼠海马体中,研究了CA3区脂质过氧化、脂褐素浓度以及清醒动物中记录的多单位活动(MUA)的变化。脂质过氧化和脂褐素浓度随年龄增长而增加。然而,MUA随年龄下降。对四个年龄组进行了相关分析,以确定与年龄相关的MUA下降与脂质过氧化和脂褐素浓度的年龄相关变化之间的关系。与年龄相关的脂质过氧化增加与脂褐素浓度的年龄相关增加呈正相关。脂质过氧化和脂褐素浓度的年龄相关增加与MUA的变化呈负相关。由于脂质过氧化可能影响神经元电生理学,我们的数据表明,与年龄相关的脂质过氧化增加可能导致与年龄相关的神经元电活动下降。研究了甲氯芬酯对海马体上述三种与年龄相关变化的影响。该药物对4月龄和8月龄大鼠的所有三个参数均无影响。然而,在16月龄和24月龄大鼠中,该药物显著增加了MUA,但同时降低了脂褐素浓度和脂质过氧化。对甲氯芬酯处理动物的MUA、脂质过氧化和脂褐素浓度数据进行的相关分析表明,药物诱导的脂褐素和脂质过氧化减少与药物诱导的MUA增加显著相关。该药物在年轻(4 - 8个月)和老年(16 - 24个月)动物中的差异作用表明,MUA的刺激明显与脂质过氧化和脂褐素浓度的同时降低有关。