[JAL-TA9对阿尔茨海默病模型小鼠认知障碍的影响]

Suo Zou
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引用次数: 0

摘要

为了找到治疗阿尔茨海默病(AD)的有效药物,已经进行了许多研究。然而,目前尚未开发出适用于临床的有效药物。最近,美国食品和药物管理局(FDA)批准了一种可抑制淀粉样蛋白-β(Aβ)聚集的抗体药物--Lecanemab,用于治疗阿尔茨海默病。然而,目前仍没有治疗多发性硬化症的根本药物。在这项研究中,我们提出了一种通过使用催化剂之一 JAL-TA9 (YKGSGFRMI) 的裂解反应清除 Aβ 的 AD 治疗策略。在海马CA1区和脑室内注射单剂量JAL-TA9可改善APP基因敲入小鼠的短期记忆缺陷。通过Y-迷宫和客观识别测试评估,它还能改善Aβ25-35诱导的模型小鼠的记忆力。这些数据有力地表明,JAL-TA9可有效治疗AD。然而,这些给药方法因其高侵入性而难以应用于临床。因此,我们测试了通过鼻腔给药 JAL-TA9 对痴呆症的改善效果。非常有趣和令人兴奋的是,每三天一次,四次给药后,Aβ25-35诱导的AD模型小鼠的痴呆症得到了改善。这些结果有力地表明,JAL-TA9 是治疗老年痴呆症的最佳候选药物,因为它即使在老年痴呆症的晚期也有效。
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[Effects of JAL-TA9 on cognitive deficits in Alzheimer's disease model mouse].

Many studies have been conducted to find an effective drug for Alzheimer's disease (AD) treatment. However, no effective drug applicable for clinical use has been developed. Recently, the FDA approved Lecanemab, an antibody drug that acts as an aggregation inhibitor against Amyloid-beta (Aβ), for AD treatment. However, there are still no fundamental drugs for AD. In this study, we present a strategy for AD treatment that removes Aβ by cleavage reaction using one of the Catalytides, JAL-TA9 (YKGSGFRMI). A single dose of JAL-TA9 administered into the CA1 region of the hippocampus and the intraventricular space improved the deficits in short-term memory of APP-knock-in mice. It also improved the memory of Aβ25-35-induced model mice, as evaluated by the Y-maze and objective recognition tests. These data strongly suggest that JAL-TA9 could be effective in treating AD. However, these administration methods are difficult to apply clinically due to their high invasiveness. Thus, we tested the improvement effects of dementia by administering JAL-TA9 nasally. It is very interesting and exciting that the dementia of Aβ25-35 induced AD model mice was improved by four applications once every three days. These results strongly suggest that JAL-TA9 is the best candidate for AD treatment because it is effective even in the late stage of AD.

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来源期刊
Folia Pharmacologica Japonica
Folia Pharmacologica Japonica Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
0.40
自引率
0.00%
发文量
132
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