Department of Neuropharmacology, School of Pharmaceutical Sciences, Shoolini University of Biotechnology and Management Sciences, Solan, H.P. 173229, India.
School of Medicine, Washington University, St. Louis, USA.
Ageing Res Rev. 2022 Jan;73:101533. doi: 10.1016/j.arr.2021.101533. Epub 2021 Nov 26.
Circadian rhythms are 24-hour natural rhythms regulated by the suprachiasmatic nucleus, also known as the "master clock". The retino-hypothalamic tract entrains suprachiasmatic nucleus with photic information to synchronise endogenous circadian rhythms with the Earth's light-dark cycle. However, despite the robustness of circadian rhythms, an unhealthy lifestyle and chronic photic disturbances cause circadian rhythm disruption in the suprachiasmatic nucleus's TTFL loops via affecting glutamate and γ-aminobutyric acid-mediated neurotransmission in the suprachiasmatic nucleus. Recently, considerable evidence has been shown correlating CRd with the incidence of Alzheimer's disease. The present review aims to identify the existence and signalling of endocannabinoids in CRd induced Alzheimer's disease through retino-hypothalamic tract- suprachiasmatic nucleus-cortex. Immunohistochemistry has confirmed the expression of cannabinoid receptor 1 in the suprachiasmatic nucleus to modulate the circadian phases of the master clock. Literature also suggests that cannabinoids may alter activity of suprachiasmatic nucleus by influencing the activity of their major neurotransmitter γ-aminobutyric acid or by interacting indirectly with the suprachiasmatic nucleus's two other major inputs i.e., the geniculo-hypothalamic tract-mediated release of neuropeptide Y and serotonergic inputs from the dorsal raphe nuclei. Besides, the expression of cannabinoid receptor 2 ameliorates cognitive deficits via reduction of tauopathy and microglial activation. In conclusion, endocannabinoids may be identified as a putative target for correcting CRd and decelerating Alzheimer's disease.
昼夜节律是由视交叉上核(也称为“主钟”)调节的 24 小时自然节律。视网膜-下丘脑束通过光信息使视交叉上核与内源性昼夜节律同步,与地球的光-暗循环同步。然而,尽管昼夜节律具有很强的稳定性,但不健康的生活方式和慢性光干扰会通过影响视交叉上核中的谷氨酸和γ-氨基丁酸介导的神经传递,破坏视交叉上核的 TTFL 循环中的昼夜节律。最近,有大量证据表明 CRd 与阿尔茨海默病的发病率有关。本综述旨在通过视网膜-下丘脑束-视交叉上核-皮质确定 CRd 诱导的阿尔茨海默病中内源性大麻素的存在和信号转导。免疫组织化学已经证实大麻素受体 1 在视交叉上核中的表达可以调节主钟的昼夜节律相位。文献还表明,大麻素可能通过影响其主要神经递质γ-氨基丁酸的活性,或通过与视交叉上核的另外两个主要输入(即,来自背侧中缝核的神经肽 Y 的基因下丘脑血管释放和 5-羟色胺能传入)间接相互作用,来改变视交叉上核的活性。此外,大麻素受体 2 的表达通过减少 tau 病和小胶质细胞激活来改善认知缺陷。总之,内源性大麻素可能被确定为纠正 CRd 和减缓阿尔茨海默病的潜在靶点。