{"title":"Influence of prednisolone on β-secretase enzyme activity in vitro","authors":"Ko Ishikawa, Y. Imai, T. Tokuda, S. Ikeda","doi":"10.1002/NRC.10062","DOIUrl":null,"url":null,"abstract":"Epidemiological studies have shown that anti-inflammatory medications decrease the incidence of Alzheimer's disease (AD). Our previous studies showed that a regimen of prednisolone decreased the amyloid β-protein (Aβ) concentration in the cerebrospinal fluid of AD patients. However, the detailed mechanism by which prednisolone decreased the Aβ concentration is unknown. In the present study we tested whether prednisolone has a direct inhibitory activity against β-secretase by using an in vitro enzyme assay system. β-Secretase, a fluorogenic substrate of β-secretase, and either prednisolone or β-secretase inhibitor were coincubated, and then the increase in fluorescence intensity was monitored. Prednisolone (1×10−3M–1×10−9) had no effect on the β-secretase activity, whereas β-secretase inhibitor inhibited it. This result shows it to be unlikely that prednisolone has an effect on the intracerebral Aβ metabolism via the modulation of β-secretase activity.","PeriodicalId":19198,"journal":{"name":"Neuroscience Research Communications","volume":"33 1","pages":"83-87"},"PeriodicalIF":0.0000,"publicationDate":"2003-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuroscience Research Communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/NRC.10062","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Epidemiological studies have shown that anti-inflammatory medications decrease the incidence of Alzheimer's disease (AD). Our previous studies showed that a regimen of prednisolone decreased the amyloid β-protein (Aβ) concentration in the cerebrospinal fluid of AD patients. However, the detailed mechanism by which prednisolone decreased the Aβ concentration is unknown. In the present study we tested whether prednisolone has a direct inhibitory activity against β-secretase by using an in vitro enzyme assay system. β-Secretase, a fluorogenic substrate of β-secretase, and either prednisolone or β-secretase inhibitor were coincubated, and then the increase in fluorescence intensity was monitored. Prednisolone (1×10−3M–1×10−9) had no effect on the β-secretase activity, whereas β-secretase inhibitor inhibited it. This result shows it to be unlikely that prednisolone has an effect on the intracerebral Aβ metabolism via the modulation of β-secretase activity.
流行病学研究表明,抗炎药物可降低阿尔茨海默病(AD)的发病率。我们之前的研究表明,泼尼松龙治疗方案降低了AD患者脑脊液中淀粉样蛋白β (a β)的浓度。然而,泼尼松龙降低Aβ浓度的具体机制尚不清楚。在本研究中,我们用体外酶测定系统测试了强的松龙是否对β-分泌酶有直接抑制活性。将β-分泌酶的荧光底物β-Secretase与强的松龙或β-分泌酶抑制剂共孵育,然后监测荧光强度的增加。强的松龙(1×10−3M-1×10−9)对β-分泌酶活性无影响,而β-分泌酶抑制剂对其有抑制作用。这一结果表明,强的松龙不太可能通过调节β分泌酶活性来影响脑内Aβ代谢。