Hshieh Tammy T, Fong Tamara G, Marcantonio Edward R, Inouye Sharon K
Warren Alpert Medical School of Brown University, Providence, RI, USA.
J Gerontol A Biol Sci Med Sci. 2008 Jul;63(7):764-72. doi: 10.1093/gerona/63.7.764.
Deficits in cholinergic function have been postulated to cause delirium and cognitive decline. This review examines current understanding of the cholinergic deficiency hypothesis in delirium by synthesizing evidence on potential pathophysiological pathways. Acetylcholine synthesis involves various precursors, enzymes, and receptors, and dysfunction in these components can lead to delirium. Insults to the brain, like ischemia and immunological stressors, can precipitously alter acetylcholine levels. Imbalances between cholinergic and other neurotransmitter pathways may result in delirium. Furthermore, genetic, enzymatic, and immunological overlaps exist between delirium and dementia related to the cholinergic pathway. Important areas for future research include identifying biomarkers, determining genetic contributions, and evaluating response to cholinergic drugs in delirium. Understanding how the cholinergic pathway relates to delirium may yield innovative approaches in the diagnosis, prevention, and treatment of this common, costly, and morbid condition.
胆碱能功能缺陷被认为会导致谵妄和认知衰退。本综述通过综合潜在病理生理途径的证据,审视了当前对谵妄中胆碱能缺乏假说的理解。乙酰胆碱的合成涉及多种前体、酶和受体,这些成分的功能障碍会导致谵妄。脑损伤,如缺血和免疫应激源,可急剧改变乙酰胆碱水平。胆碱能和其他神经递质途径之间的失衡可能导致谵妄。此外,谵妄和与胆碱能途径相关的痴呆之间存在遗传、酶和免疫重叠。未来研究的重要领域包括识别生物标志物、确定遗传因素以及评估谵妄患者对胆碱能药物的反应。了解胆碱能途径与谵妄的关系可能会为这种常见、代价高昂且病态的疾病的诊断、预防和治疗带来创新方法。