Kelly S J, Bernard K, Muñoz C, Lawrence R C, Thacker J, Grillo C A, Piroli G G, Reagan L P
Department of Psychology, University of South Carolina, Columbia, SC 29208, USA.
Psychopharmacology (Berl). 2009 Jan;202(1-3):225-35. doi: 10.1007/s00213-008-1301-x. Epub 2008 Sep 2.
Development of cognitive-enhancing drugs that delay or halt mild cognitive impairment progression to Alzheimer's disease would be of great benefit.
The aim of this study was to examine the ability of (S)-2,3-dihydro-[3,4]-cyclopentano-1,2,4-benzothiadiazine-1,1-dioxide (S 18986), a positive allosteric modulator of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors, to improve behavioral performance and alleviate age-related deficits in oxidative stress status in the prelimbic cortex and hippocampus.
Daily administration of S 18986 (0.1, 0.3, and 1.0 mg/kg) or vehicle was given to separate groups of male rats starting at 12 months of age. Additionally, daily vehicle administration was given to a group of rats starting at 3 months of age. Four months after initiation of drug administration, rats were trained and tested in an operant-delayed alternation task and a reinforcer devaluation task. Upon completion of testing, oxidative stress status was assessed in the prelimbic cortex and hippocampus.
S 18986 dose-dependently altered responses in the reinforcer devaluation task such that aged rats came to resemble young rats. There were no age or drug effects in the operant-delayed alternation task. Levels of the lipid peroxidation product 4-hydroxy-nonenal (HNE) were increased, and Cu/Zn-superoxide dismutase (SOD) levels were decreased in prelimbic cortex in aged rats, changes that were reversed by S 18986. Similarly, age-related increases in hippocampal HNE levels were prevented by S 18986.
Positive modulation of AMPA receptor activity may be a therapeutic approach to halt or slow progression of mild cognitive impairment via improvement in oxidative stress status in the hippocampus and prelimbic cortex.
开发能够延缓或阻止轻度认知障碍发展为阿尔茨海默病的认知增强药物将带来巨大益处。
本研究的目的是检验α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体的正向变构调节剂(S)-2,3-二氢-[3,4]-环戊烷并-1,2,4-苯并噻二嗪-1,1-二氧化物(S 18986)改善行为表现以及减轻前边缘皮层和海马体中与年龄相关的氧化应激状态缺陷的能力。
从12月龄开始,将雄性大鼠分成不同组,分别每日给予S 18986(0.1、0.3和1.0mg/kg)或赋形剂。此外,从3月龄开始,对一组大鼠每日给予赋形剂。给药开始四个月后,对大鼠进行操作延迟交替任务和强化物贬值任务的训练和测试。测试完成后,评估前边缘皮层和海马体中的氧化应激状态。
S 18986在强化物贬值任务中剂量依赖性地改变反应,使老年大鼠的表现类似于年轻大鼠。在操作延迟交替任务中没有年龄或药物效应。老年大鼠前边缘皮层中脂质过氧化产物4-羟基壬烯醛(HNE)水平升高,铜/锌超氧化物歧化酶(SOD)水平降低,这些变化被S 18986逆转。同样,S 18986可预防海马体中与年龄相关的HNE水平升高。
AMPA受体活性的正向调节可能是一种通过改善海马体和前边缘皮层的氧化应激状态来阻止或减缓轻度认知障碍进展的治疗方法。