Development of Delta Opioid Receptor Antagonists Which Prevent Alzheimer’s Disease-Like Pathology in the 5X-Familial Alzheimer’s Disease [5XFAD] Mouse Model

IF 3.7 Q1 CHEMISTRY, MEDICINAL
Parthasaradhireddy Tanguturi, Stefanie Mitchell, Omar Moukha-Chafiq, Sixue Zhang, John Tillotson, Subramaniam Ananthan, Corinne E. Augelli-Szafran and John M. Streicher*, 
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引用次数: 0

Abstract

Alzheimer’s Disease is a growing health concern, with no available disease-modifying treatments. A previous report suggested that a Delta Opioid Receptor (DOR) antagonist could prevent Alzheimer’s-like pathology; however, no DOR antagonists are clinically approved. We thus expanded on our previous structure–activity relationship work on morphinan scaffold DOR antagonists to generate and evaluate new DOR antagonist ligands. We identified a lead compound 12 (SRI-22136) with sub-nM DOR potency, high selectivity, and high inhibition of β-secretase activity. We further evaluated 12 in CD-1 mice, finding full antagonist efficacy at 1 mg/kg by the intraperitoneal route. We then tested the ability of 12 to prevent Alzheimer’s-like pathology in a 5XFAD transgenic mouse model, with daily treatment from 2 to 5 months of age. This treatment completely prevented Alzheimer’s-like pathology, including memory deficits, β-secretase activity, Aβ1–42 accumulation, and brain inflammatory markers. Together these results suggest 12 as a potential new lead compound to prevent Alzheimer’s Disease.

Abstract Image

阿片受体拮抗剂在5x -家族性阿尔茨海默病[5XFAD]小鼠模型中预防阿尔茨海默病样病理的研究
阿尔茨海默病是一个日益严重的健康问题,目前还没有有效的治疗方法。先前的一份报告表明,Delta阿片受体(DOR)拮抗剂可以预防阿尔茨海默病样病理;然而,尚无临床批准的DOR拮抗剂。因此,我们扩展了之前关于吗啡肽支架DOR拮抗剂的结构-活性关系研究,以生成和评估新的DOR拮抗剂配体。我们鉴定出一种先导化合物12 (SRI-22136),具有亚纳米级DOR效价、高选择性和高抑制β分泌酶活性。我们进一步在CD-1小鼠中评估了12种,通过腹腔注射方式发现1 mg/kg的完全拮抗剂效果。然后,我们在5XFAD转基因小鼠模型中测试了12预防阿尔茨海默病样病理的能力,从2个月大到5个月大,每天给药。这种治疗完全预防了阿尔茨海默病样病理,包括记忆缺陷、β分泌酶活性、a - β1 - 42积累和脑炎症标志物。总之,这些结果表明12是一种潜在的新的先导化合物,可以预防阿尔茨海默病。
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来源期刊
ACS Pharmacology and Translational Science
ACS Pharmacology and Translational Science Medicine-Pharmacology (medical)
CiteScore
10.00
自引率
3.30%
发文量
133
期刊介绍: ACS Pharmacology & Translational Science publishes high quality, innovative, and impactful research across the broad spectrum of biological sciences, covering basic and molecular sciences through to translational preclinical studies. Clinical studies that address novel mechanisms of action, and methodological papers that provide innovation, and advance translation, will also be considered. We give priority to studies that fully integrate basic pharmacological and/or biochemical findings into physiological processes that have translational potential in a broad range of biomedical disciplines. Therefore, studies that employ a complementary blend of in vitro and in vivo systems are of particular interest to the journal. Nonetheless, all innovative and impactful research that has an articulated translational relevance will be considered. ACS Pharmacology & Translational Science does not publish research on biological extracts that have unknown concentration or unknown chemical composition. Authors are encouraged to use the pre-submission inquiry mechanism to ensure relevance and appropriateness of research.
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