TY - JOUR
T1 - Development of Delta Opioid Receptor Antagonists Which Prevent Alzheimer’s Disease-Like Pathology in the 5X-Familial Alzheimer’s Disease [5XFAD] Mouse Model
AU - Tanguturi, Parthasaradhireddy
AU - Mitchell, Stefanie
AU - Moukha-Chafiq, Omar
AU - Zhang, Sixue
AU - Tillotson, John
AU - Ananthan, Subramaniam
AU - Augelli-Szafran, Corinne E.
AU - Streicher, John M.
N1 - Publisher Copyright:
© 2025 The Authors. Published by American Chemical Society
PY - 2025/9/12
Y1 - 2025/9/12
N2 - 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.
AB - 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.
KW - Alzheimer’s Disease
KW - Antagonist
KW - Aβ1−42
KW - Delta Opioid Receptor
KW - β-Secretase
UR - https://www.scopus.com/pages/publications/105015811413
UR - https://www.scopus.com/pages/publications/105015811413#tab=citedBy
U2 - 10.1021/acsptsci.5c00509
DO - 10.1021/acsptsci.5c00509
M3 - Article
AN - SCOPUS:105015811413
SN - 2575-9108
VL - 8
SP - 3346
EP - 3370
JO - ACS Pharmacology and Translational Science
JF - ACS Pharmacology and Translational Science
IS - 9
ER -