长期给予神经激肽SP可改善老年褐家鼠的迷宫表现

Rüdiger U. Hasenöhrl, Christian Frisch, Susanne Nikolaus, Joseph P. Huston
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引用次数: 34

摘要

与衰老相关的功能缺陷可能至少部分是基于中枢神经系统营养因子可用性的降低。神经激肽浓度的降低,包括非肽物质P (SP),也伴随着衰老。因此,考虑到SP代谢的变化以及已知的记忆源性和神经营养/神经保护作用,外源性SP治疗可能会影响与年龄相关的联想过程缺陷。在本研究中,30个月大的Wistar大鼠在莫里斯水迷宫任务和运动协调测试前一周开始每天注射SP(50或250 μg/kg,腹腔注射)。对照组为车辆注射的老年大鼠和成年大鼠(3月龄)。在迷宫测试期间,连续15天每天测试后5小时施用这些物质,最后一次给药后,再继续进行4天的迷宫测试。本研究的主要发现是长期给药SP(50和250 μg/kg)均能改善老年大鼠的迷宫表现。在迷宫测试过程中,SP的这种促进作用在药物治疗结束后也很明显。此外,长期应用50-250 μg/kg剂量范围的SP可减少与年龄相关的运动能力缺陷。
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Chronic administration of neurokinin SP improves maze performance in aged Rattus norvegicus

Deficits in associative functions seen with senescence may be based, at least in part, on a decreased availability of trophic factors in the CNS. A reduced concentration of neurokinins, including undecapeptide substance P (SP), also accompanies aging. Thus, given the change in SP metabolism and the known mnemogenic as well as neurotrophic/neuroprotective effects of the peptide, it seems possible that age-related deficits in associative processes could be influenced by treatment with exogenous SP. In the present study, 30-month-old Wistar rats were injected daily with SP (50 or 250 μg/kg, intraperitoneally) starting 1 week before they were tested on the Morris water maze task and on motor coordination tests. Control groups included vehicle-injected old and adult (3-month-old) rats. Over the days of maze testing, application of the substances was performed 5 h after testing daily for 15 days and after the last drug delivery, maze testing was continued for 4 more days. The main finding of this study is that chronic administration of both dosages of SP (50 and 250 μg/kg) improved the maze performance of the old rats. This facilitatory effect of SP on performance was also evident after the drug treatment had been terminated in the course of maze testing. Furthermore, chronic application of SP in a dose range of 50–250 μg/kg was found to reduce age-related deficits in motor capacities.

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