新冠肺炎中的双嘧达莫和腺苷能通路:果汁或圣杯。

Hayder M Al-Kuraishy, Ali I Al-Gareeb, Engy Elekhnawy, Gaber El-Saber Batiha
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引用次数: 0

摘要

背景:2019冠状病毒病(新冠肺炎)是一种由严重急性呼吸道冠状病毒2型(SARS-CoV-2)引发的全球性传染病。这种流行病可导致促炎激活,并伴有急性肺损伤和急性呼吸窘迫综合征。摘要主体:严重急性呼吸系统综合征冠状病毒2型感染与腺苷的抑制和磷酸二酯酶的激活有关。双嘧达莫(DIP)是一种核苷转运和磷酸二酯酶抑制剂,因此可能影响严重急性呼吸系统综合征冠状病毒2型感染及其伴随的炎症。因此,这项小型回顾研究的主要目的是阐明DIP对新冠肺炎腺信号通路的潜在有益影响。使用具有相关关键词的在线数据库进行了系统搜索。本研究结果表明,DIP通过增加腺苷和抑制磷酸二酯酶,直接或间接缓解新冠肺炎结果。结论:我们的研究得出结论,DIP在新冠肺炎的管理和治疗中具有潜在的治疗效果。这可以通过抗严重急性呼吸系统综合征冠状病毒2型、抗炎和抗血小板特性直接实现,也可以通过增强具有抗炎和免疫调节作用的细胞外腺苷间接实现。然而,需要在该领域进行广泛的随机临床试验以及临床和前瞻性研究,以证明DIP和腺苷调节剂治疗新冠肺炎的安全性和疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dipyridamole and adenosinergic pathway in Covid-19: a juice or holy grail.

Dipyridamole and adenosinergic pathway in Covid-19: a juice or holy grail.

Dipyridamole and adenosinergic pathway in Covid-19: a juice or holy grail.

Background: Coronavirus disease 2019 (Covid-19) is an infectious worldwide pandemic triggered by severe acute respiratory coronavirus 2 (SARS-CoV-2). This pandemic disease can lead to pro-inflammatory activation with associated acute lung injury and acute respiratory distress syndrome.

Main body of the abstract: SARS-CoV-2 infection is linked with inhibition of adenosine and activation of phosphodiesterase. Dipyridamole (DIP) is a nucleoside transport and phosphodiesterase inhibitor so that it may potentially affect SARS-CoV-2 infection and its accompanying inflammations. Therefore, the primary objective of this mini-review study was to elucidate the potential beneficial impacts of DIP on the adenosinergic pathway in Covid-19. A systemic search was done using online databases with relevant keywords. The findings of the present study illustrated that DIP directly or indirectly, through augmentation of adenosine and inhibition of phosphodiesterase, mitigates Covid-19 outcomes.

Conclusion: Our study concluded that DIP has a potential therapeutic effect in the management and treatment of Covid-19. This could be attained either directly, through anti-SARS-CoV-2, anti-inflammatory, and anti-platelets properties, or indirectly, through augmentation of extracellular adenosine, which has anti-inflammatory and immune-regulatory effects. However, extensive randomized clinical trials, and clinical and prospective research in this area are required to demonstrate the safety and therapeutic efficacy of DIP and adenosine modulators in the treatment of Covid-19.

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