Department of Physiology and Pharmacology "V. Erspamer", SAPIENZA University of Rome-P.le A. Moro, 5, 00185 Rome, Italy.
Epitech Group SpA - 35030 Saccolongo (PD), Italy.
Int J Mol Sci. 2020 May 27;21(11):3802. doi: 10.3390/ijms21113802.
At the earliest stage of Alzheimer's disease (AD), although patients are still asymptomatic, cerebral alterations have already been triggered. In addition to beta amyloid (Aβ) accumulation, both glial alterations and neuroinflammation have been documented at this stage. Starting treatment at this prodromal AD stage could be a valuable therapeutic strategy. AD requires long-term care; therefore, only compounds with a high safety profile can be used, such as the new formulation containing palmitoylethanolamide and luteolin (co-ultra PEALut) already approved for human use. Therefore, we investigated it in an in vivo pharmacological study that focused on the prodromal stage of AD.
We tested the anti-inflammatory and neuroprotective effects of co-ultra PEALut (5 mg/Kg) administered for 14 days in rats that received once, 5 µg Aβ into the hippocampus.
Glial activation and elevated levels of proinflammatory mediators were observed in Aβ-infused rats. Early administration of co-ultra PEALut prevented the Aβ-induced astrogliosis and microgliosis, the upregulation in gene expression of pro-inflammatory cytokines and enzymes, as well as the reduction of mRNA levels BDNF and GDNF. Our findings also highlight an important neuroprotective effect of co-ultra PEALut treatment, which promoted neuronal survival.
Our results reveal the presence of cellular and molecular modifications in the prodromal stage of AD. Moreover, the data presented here demonstrate the ability of co-ultra PEALut to normalize such Aβ-induced alterations, suggesting it as a valuable therapeutic strategy.
在阿尔茨海默病(AD)的最早阶段,尽管患者仍无症状,但已经引发了大脑改变。除了β淀粉样蛋白(Aβ)积累外,在这个阶段还记录到了神经胶质改变和神经炎症。在这个前驱 AD 阶段开始治疗可能是一种有价值的治疗策略。AD 需要长期护理;因此,只有具有高安全性的化合物才能使用,例如已经批准用于人类的含有棕榈酸乙醇酰胺和叶黄素的新制剂(联合超 PEALut)。因此,我们在一项专注于 AD 前驱期的体内药理学研究中对此进行了研究。
我们测试了联合超 PEALut(5mg/Kg)在接受单次 5µg Aβ注入海马体的大鼠中连续 14 天给药的抗炎和神经保护作用。
在 Aβ 输注大鼠中观察到神经胶质激活和促炎介质水平升高。联合超 PEALut 的早期给药可预防 Aβ 诱导的星形胶质细胞增生和小胶质细胞增生、促炎细胞因子和酶的基因表达上调,以及 BDNF 和 GDNF 的 mRNA 水平降低。我们的研究结果还突出了联合超 PEALut 治疗的重要神经保护作用,它促进了神经元的存活。
我们的结果揭示了 AD 前驱期存在细胞和分子改变。此外,这里呈现的数据表明联合超 PEALut 能够使这种 Aβ 诱导的改变正常化,这表明它是一种有价值的治疗策略。