Gard Paul Richard, Fidalgo Sara, Lotter Isabelle, Richardson Cassandra, Farina Nicolas, Rusted Jennifer, Tabet Naji
School of Pharmacy and Biomolecular Sciences, University of Brighton, Brighton, UK.
School of Pharmacy and Biomolecular Sciences, University of Brighton, Brighton, UK.
Exp Gerontol. 2017 Mar;89:1-7. doi: 10.1016/j.exger.2017.01.006. Epub 2017 Jan 7.
Activities of aminopeptidases A, B, and N (ApA, ApB & ApN) and insulin-regulated aminopeptidase (IRAP) have been seen to be decreased amongst patients with Alzheimer's disease (AD). All of these enzymes are involved with the brain renin-angiotensin system which is believed to be involved with learning and memory. This study aimed to explore the time course and the mechanisms underlying these changes. Serum samples were collected from 45 AD patients at the start of the study, and again 13months later (n=37). The control group was 22 healthy, older, adults. Enzyme activity was determined at two substrate concentrations to allow Michaelis-Menten analysis of the enzyme activity. The results indicated that there was decreased activity of ApA, ApB and ApN amongst AD patients but no difference in serum IRAP activity. There were no associations between enzyme activity and age, gender nor scores on psychomotor tests. Consideration of the data for the two time points for AD patients showed that the changes in ApB occurred at an early stage of the disease and persisted, whilst those of ApA and ApN only became apparent at later stages of the disease. Although differences in Michaelis-Menten parameters were not statistically significant, consideration of the values suggested that the decrease in ApB activity may be a result of changes in enzyme protein conformation, whilst that of ApN may be a consequence of decreased enzyme expression. Importantly, the different time courses of the effects and the differential changes in enzyme affinity and expression indicated that the observed changes with progression of AD were not a 'class effect' for serum aminopeptidases but were idiosyncratic for the individual enzymes.
在阿尔茨海默病(AD)患者中,已发现氨肽酶A、B和N(ApA、ApB和ApN)以及胰岛素调节氨肽酶(IRAP)的活性降低。所有这些酶都与大脑肾素 - 血管紧张素系统有关,该系统被认为与学习和记忆有关。本研究旨在探讨这些变化的时间进程及其潜在机制。在研究开始时从45名AD患者中采集血清样本,13个月后再次采集(n = 37)。对照组为22名健康的老年人。在两种底物浓度下测定酶活性,以便对酶活性进行米氏分析。结果表明,AD患者中ApA、ApB和ApN的活性降低,但血清IRAP活性无差异。酶活性与年龄、性别以及精神运动测试得分之间无关联。对AD患者两个时间点的数据进行分析表明,ApB的变化发生在疾病早期并持续存在,而ApA和ApN的变化仅在疾病后期才明显。尽管米氏参数的差异无统计学意义,但对这些值的分析表明,ApB活性的降低可能是酶蛋白构象变化的结果,而ApN活性的降低可能是酶表达减少的结果。重要的是,效应的不同时间进程以及酶亲和力和表达的差异变化表明,随着AD进展观察到的变化并非血清氨肽酶的“类效应”,而是个别酶的特异效应。