Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, Jouf University, Sakaka, Saudi Arabia.
Department of Microbiology, Government College University, Faisalabad, Pakistan.
Cell Reprogram. 2021 Apr;23(2):57-72. doi: 10.1089/cell.2020.0087.
Adenosine plays a significant role in neurotransmission process by controlling the blood pressure, while adenosine triphosphate (ATP) acts as a neuromodulator and neurotransmitter and by activation of P2 receptors, regulates the contractility of the heart. Adenosine signaling is essential in the process of regeneration by regulating proliferation, differentiation, and apoptosis of stem cells. In this review, we have selected neurological disorders (Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, multiple sclerosis, and epilepsy) with clinical trials using antagonists and epigenetic tools targeting adenosine receptor as a therapeutic approach in the treatment of these disorders. Promising results have been reported from many clinical trials. It has been found that higher expression levels of A2A and P2X7 receptors in neurological disorders further complicate the disease condition. Therefore, modulations of these receptors by using antagonists of these receptors or SAM (S-adenosylmethionine) therapy as an epigenetic tool could be useful in reversing the complications of these disorders. Finally, we suggest that modulation of adenosine receptors in neurological disorders can increase the regenerative phase by increasing the rate of proliferation and differentiation in the damaged tissues.
腺苷通过控制血压在神经传递过程中发挥重要作用,而三磷酸腺苷 (ATP) 作为神经调质和神经递质,通过激活 P2 受体,调节心脏的收缩性。腺苷信号在通过调节干细胞的增殖、分化和凋亡来进行再生的过程中至关重要。在本综述中,我们选择了使用针对腺苷受体的拮抗剂和表观遗传工具的临床试验的神经紊乱(阿尔茨海默病、帕金森病、肌萎缩侧索硬化症、多发性硬化症和癫痫),作为治疗这些疾病的治疗方法。许多临床试验报告了有希望的结果。已经发现,在神经紊乱中 A2A 和 P2X7 受体的更高表达水平进一步使疾病状况复杂化。因此,通过使用这些受体的拮抗剂或 SAM(S-腺苷甲硫氨酸)治疗作为表观遗传工具来调节这些受体,可能有助于逆转这些疾病的并发症。最后,我们认为调节神经紊乱中的腺苷受体可以通过增加受损组织中的增殖和分化率来增加再生阶段。