长期COVID -胆碱能神经传递的关键中断?

Marco Leitzke, Donald Troy Roach, Swen Hesse, Peter Schönknecht, Georg-Alexander Becker, Michael Rullmann, Bernhardt Sattler, Osama Sabri
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引用次数: 0

摘要

背景:新冠肺炎大流行后,出现了许多不同症状、不同严重程度的慢性长冠肺炎(LC)患者。直到最近,LC的病理通路仍不清楚,这使得识别通路机制和探索治疗方案成为一个紧迫的挑战。LC症状与胆碱能神经传递受损有明显关系。方法:本文综述了目前关于阻断尼古丁乙酰胆碱受体(nAChRs)对主要受影响器官和细胞系统的影响的文献,并将其与生物碱尼古丁的解阻断作用进行了比较。此外,还提出了可以解释以前无法解释的疫苗接种后综合征(PVS)现象的机制。在假设许多其他病毒后疾病和自身免疫性疾病(ADs)也可能由于胆碱能传递受损的情况下,讨论了不仅SARS-CoV-2而且许多其他病毒可以结合nachr的事实。我们还提供了一份病例报告,通过使用(-)-[18F]氟巴汀全身正电子发射断层扫描(PET)成像显示LC患者胆碱能功能障碍的α4β2 nachr的可用性,并在低剂量经皮尼古丁(LDTN)给药前后显着改善神经系统。最后,对一项涉及231名LDTN用户的调查结果进行了描述性分析和评价。结果:大量的研究已经出现,为LC现象提供了令人信服的解释,表明它可以合理地解释为人体nAChR功能受损。经皮给药10天后,患者未见持久的神经病理表现。这一观察结果伴随着nachr的自由配体结合位点(LBS)数量的显著增加,这是通过(-)-[18F]氟巴汀PET成像确定的。调查分析显示,大多数患者(73.5%)报告LDTN治疗后LC/MEF/CFS疾病的症状有显著改善。结论:总之,根据目前的知识,LDTN似乎是一种有希望和安全的缓解LC症状的方法,没有预期的长期危害。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long COVID - a critical disruption of cholinergic neurotransmission?

Background: Following the COVID-19 pandemic, there are many chronically ill Long COVID (LC) patients with different symptoms of varying degrees of severity. The pathological pathways of LC remain unclear until recently and make identification of path mechanisms and exploration of therapeutic options an urgent challenge. There is an apparent relationship between LC symptoms and impaired cholinergic neurotransmission.

Methods: This paper reviews the current literature on the effects of blocked nicotinic acetylcholine receptors (nAChRs) on the main affected organ and cell systems and contrasts this with the unblocking effects of the alkaloid nicotine. In addition, mechanisms are presented that could explain the previously unexplained phenomenon of post-vaccination syndrome (PVS). The fact that not only SARS-CoV-2 but numerous other viruses can bind to nAChRs is discussed under the assumption that numerous other post-viral diseases and autoimmune diseases (ADs) may also be due to impaired cholinergic transmission. We also present a case report that demonstrates changes in cholinergic transmission, specifically, the availability of α4β2 nAChRs by using (-)-[18F]Flubatine whole-body positron emission tomography (PET) imaging of cholinergic dysfunction in a LC patient along with a significant neurological improvement before and after low-dose transcutaneous nicotine (LDTN) administration. Lastly, a descriptive analysis and evaluation were conducted on the results of a survey involving 231 users of LDTN.

Results: A substantial body of research has emerged that offers a compelling explanation for the phenomenon of LC, suggesting that it can be plausibly explained because of impaired nAChR function in the human body. Following a ten-day course of transcutaneous nicotine administration, no enduring neuropathological manifestations were observed in the patient. This observation was accompanied by a significant increase in the number of free ligand binding sites (LBS) of nAChRs, as determined by (-)-[18F]Flubatine PET imaging. The analysis of the survey shows that the majority of patients (73.5%) report a significant improvement in the symptoms of their LC/MEF/CFS disease as a result of LDTN.

Conclusions: In conclusion, based on current knowledge, LDTN appears to be a promising and safe procedure to relieve LC symptoms with no expected long-term harm.

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CiteScore
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