School of Basic Pharmaceutical and Toxicological Sciences, College of Pharmacy, University of Louisiana at Monroe, 1800 Bienville Drive, Monroe, LA 71201, USA.
Department of Pathology and Translational Pathobiology, LSU Health Shreveport, 1501 Kings Highway, Shreveport, LA 71103, USA.
Nutrients. 2021 May 18;13(5):1702. doi: 10.3390/nu13051702.
Alzheimer's disease (AD) is a complex progressive neurodegenerative disorder affecting humans mainly through the deposition of Aβ-amyloid (Aβ) fibrils and accumulation of neurofibrillary tangles in the brain. Currently available AD treatments only exhibit symptomatic relief but do not generally intervene with the amyloid and tau pathologies. The extra-virgin olive oil (EVOO) monophenolic secoiridoid -(-)-oleocanthal (OC) showed anti-inflammatory activity through COX system inhibition with potency comparable to the standard non-steroidal anti-inflammatory drug (NSAID) like ibuprofen. OC also showed positive in vitro, in vivo, and clinical therapeutic effects against cardiovascular diseases, many malignancies, and AD. Due to its pungent, astringent, and irritant taste, OC should be formulated in acceptable dosage form before its oral use as a potential nutraceutical. The objective of this study is to develop new OC oral formulations, assess whether they maintained OC activity on the attenuation of β-amyloid pathology in a 5xFAD mouse model upon 4-month oral dosing use. Exploration of potential OC formulations underlying molecular mechanism is also within this study scope. OC powder formulation (OC-PF) and OC-solid dispersion formulation with erythritol (OC-SD) were prepared and characterized using FT-IR spectroscopy, powder X-ray diffraction, and scanning electron microscopy (ScEM) analyses. Both formulations showed an improved OC dissolution profile. OC-PF and OC-SD improved memory deficits of 5xFAD mice in behavioral studies. OC-PF and OC-SD exhibited significant attenuation of the accumulation of Aβ plaques and tau phosphorylation in the brain of 5xFAD female mice. Both formulations markedly suppressed C3AR1 (complement component 3a receptor 1) activity by targeting the downstream marker STAT3. Collectively, these results demonstrate the potential for the application of OC-PF as a prospective nutraceutical or dietary supplement to control the progression of amyloid pathogenesis associated with AD.
阿尔茨海默病(AD)是一种复杂的进行性神经退行性疾病,主要通过大脑中 Aβ-淀粉样蛋白(Aβ)纤维的沉积和神经原纤维缠结的积累对人类产生影响。目前可用的 AD 治疗方法仅表现出症状缓解,但通常不会干预淀粉样蛋白和 tau 病理学。特级初榨橄榄油(EVOO)单酚类次萜 -(-)-橄榄苦苷(OC)通过抑制 COX 系统显示出抗炎活性,其效力与布洛芬等标准非甾体抗炎药(NSAID)相当。OC 还在体外、体内和临床试验中显示出对心血管疾病、许多恶性肿瘤和 AD 的积极治疗效果。由于其辛辣、收敛和刺激性味道,OC 在口服用作潜在的营养保健品之前,应在可接受的剂量形式中进行配方。本研究的目的是开发新的 OC 口服制剂,评估它们在经过 4 个月口服给药后是否能保持对 5xFAD 小鼠模型中β-淀粉样蛋白病理的衰减作用。本研究还探索了潜在 OC 制剂的分子机制。OC 粉末制剂(OC-PF)和与赤藓糖醇的 OC 固体分散体制剂(OC-SD)通过傅里叶变换红外光谱(FT-IR)、粉末 X 射线衍射(PXRD)和扫描电子显微镜(ScEM)分析进行了制备和表征。两种制剂都显示出改善的 OC 溶解曲线。OC-PF 和 OC-SD 在行为研究中改善了 5xFAD 小鼠的记忆缺陷。OC-PF 和 OC-SD 在 5xFAD 雌性小鼠的大脑中表现出 Aβ 斑块积累和 tau 磷酸化的显著衰减。两种制剂都通过靶向下游标志物 STAT3 显著抑制了 C3AR1(补体成分 3a 受体 1)的活性。总之,这些结果表明,OC-PF 作为一种有前途的营养保健品或膳食补充剂,具有控制与 AD 相关的淀粉样蛋白发病机制进展的应用潜力。