Centro de Investigación Biomédica en Red Enfermedades Neurodegenerativas (CiberNed), National Institute of Health Carlos, 28029 Madrid, Spain.
Institut de Neurociències UB, Campus Mundet, 08035 Barcelona, Spain.
Int J Mol Sci. 2024 May 15;25(10):5378. doi: 10.3390/ijms25105378.
Alzheimer's disease (AD) remains a significant health challenge, with an increasing prevalence globally. Recent research has aimed to deepen the understanding of the disease pathophysiology and to find potential therapeutic interventions. In this regard, G protein-coupled receptors (GPCRs) have emerged as novel potential therapeutic targets to palliate the progression of neurodegenerative diseases such as AD. Orexin and cannabinoid receptors are GPCRs capable of forming heteromeric complexes with a relevant role in the development of this disease. On the one hand, the hyperactivation of the orexins system has been associated with sleep-wake cycle disruption and Aβ peptide accumulation. On the other hand, cannabinoid receptor overexpression takes place in a neuroinflammatory environment, favoring neuroprotective effects. Considering the high number of interactions between cannabinoid and orexin systems that have been described, regulation of this interplay emerges as a new focus of research. In fact, in microglial primary cultures of APPSw/Ind mice model of AD there is an important increase in CBR-OXR complex expression, while OXR antagonism potentiates the neuroprotective effects of CBR. Specifically, pretreatment with the OXR antagonist has been shown to strongly potentiate CBR signaling in the cAMP pathway. Furthermore, the blockade of OXR can also abolish the detrimental effects of OXR overactivation in AD. In this sense, CBR-OXR becomes a new potential therapeutic target to combat AD.
阿尔茨海默病(AD)仍然是一个重大的健康挑战,其在全球的患病率呈上升趋势。最近的研究旨在加深对疾病病理生理学的理解,并寻找潜在的治疗干预措施。在这方面,G 蛋白偶联受体(GPCR)已成为治疗神经退行性疾病(如 AD)的新的潜在治疗靶点。食欲素和大麻素受体是 GPCR,能够与异源二聚体复合物形成,在这种疾病的发展中具有重要作用。一方面,食欲素系统的过度激活与睡眠-觉醒周期紊乱和 Aβ肽积累有关。另一方面,大麻素受体在神经炎症环境中过度表达,有利于神经保护作用。鉴于已经描述了大麻素和食欲素系统之间的大量相互作用,这种相互作用的调节成为新的研究焦点。事实上,在 AD 的 APPsw/Ind 小鼠模型的原代小胶质细胞培养物中,CBR-OXR 复合物的表达显著增加,而 CBR 拮抗作用增强了 CBR 的神经保护作用。具体来说,用 OXR 拮抗剂预处理已被证明可强烈增强 CBR 信号在 cAMP 通路中的作用。此外,OXR 的阻断也可以消除 OXR 过度激活在 AD 中的有害作用。在这种意义上,CBR-OXR 成为治疗 AD 的新的潜在治疗靶点。