Department of Neural Development and Disease, Korea Brain Research Institute (KBRI), 61, Cheomdan-ro, Daegu, 41068, Republic of Korea.
Department of Brain and Cognitive Sciences, Daegu Gyeongbuk Institute of Science and Technology, Daegu, 42988, Republic of Korea.
Mol Brain. 2023 Aug 14;16(1):63. doi: 10.1186/s13041-023-01051-9.
Alzheimer's disease (AD) is a neurodegenerative disease characterized by Aβ deposition, tauopathy, neuroinflammation, and impaired cognition. The recent identification of associations between protein kinases and AD pathology has spurred interest in tyrosine kinase inhibitors (TKIs) as potential strategic therapeutic agents for AD. In the present study, we investigated whether the TKIs ibrutinib, PD180970, and cabozantinib, which have different on-targets, selectively regulate AD pathology in 3.5- to 4-month-old 5xFAD mice (a model of the early phase of AD). Ibrutinib (10 mg/kg, i.p.) effectively reduced amyloid-β (Aβ) plaque number, tau hyperphosphorylation and neuroinflammation in 5xFAD mice. Surprisingly, PD180970 (10 mg/kg, i.p.) did not alter Aβ plaque number or neuroinflammatory responses and exacerbated tau hyperphosphorylation in 5xFAD mice. Cabozantinib (10 mg/kg, i.p.) had no effect on amyloidopathy but partially relieved tau hyperphosphorylation and astrogliosis. Taken together, our results suggest that not all TKIs have therapeutic effects on AD pathology in a mouse model of AD. Consequently, optimization of drug dosage, injection periods and administration routes should be considered when repurposing TKIs as novel AD therapeutics.
阿尔茨海默病(AD)是一种神经退行性疾病,其特征是 Aβ 沉积、tau 病、神经炎症和认知障碍。最近发现蛋白激酶与 AD 病理学之间存在关联,这激发了人们对酪氨酸激酶抑制剂(TKIs)作为 AD 潜在治疗策略的兴趣。在本研究中,我们研究了三种不同作用靶点的 TKI(伊布替尼、PD180970 和卡博替尼)是否选择性地调节 3.5-4 月龄 5xFAD 小鼠(AD 早期阶段的模型)中的 AD 病理学。伊布替尼(10mg/kg,腹腔注射)可有效减少 5xFAD 小鼠的淀粉样蛋白-β(Aβ)斑块数量、tau 过度磷酸化和神经炎症。令人惊讶的是,PD180970(10mg/kg,腹腔注射)并未改变 Aβ 斑块数量或神经炎症反应,反而加剧了 5xFAD 小鼠的 tau 过度磷酸化。卡博替尼(10mg/kg,腹腔注射)对淀粉样蛋白病变没有影响,但部分缓解了 tau 过度磷酸化和星形胶质细胞增生。综上所述,我们的结果表明,并非所有 TKI 在 AD 小鼠模型中都对 AD 病理学具有治疗作用。因此,当将 TKIs 重新用作新型 AD 治疗药物时,应考虑优化药物剂量、注射周期和给药途径。