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丙磺舒,一种对中枢神经系统疾病和神经炎症可能有新用途的老药。

Probenecid, an Old Drug with Potential New Uses for Central Nervous System Disorders and Neuroinflammation.

作者信息

García-Rodríguez Claudia, Mujica Paula, Illanes-González Javiera, López Araceli, Vargas Camilo, Sáez Juan C, González-Jamett Arlek, Ardiles Álvaro O

机构信息

Centro Interdisciplinario de Neurociencia de Valparaíso, Facultad de Ciencias, Universidad de Valparaíso, Valparaíso 2360102, Chile.

Escuela de Química y Farmacia, Facultad de Farmacia, Universidad de Valparaíso, Valparaíso 2360102, Chile.

出版信息

Biomedicines. 2023 May 24;11(6):1516. doi: 10.3390/biomedicines11061516.

Abstract

Probenecid is an old uricosuric agent used in clinics to treat gout and reduce the renal excretion of antibiotics. In recent years, probenecid has gained attention due to its ability to interact with membrane proteins such as TRPV2 channels, organic anion transporters, and pannexin 1 hemichannels, which suggests new potential therapeutic utilities in medicine. Some current functions of probenecid include their use as an adjuvant to increase the bioavailability of several drugs in the Central Nervous System (CNS). Numerous studies also suggest that this drug has important neuroprotective, antiepileptic, and anti-inflammatory properties, as evidenced by their effect against neurological and neurodegenerative diseases. In these studies, the use of probenecid as a Panx1 hemichannel blocker to reduce neuroinflammation is highlighted since neuroinflammation is a major trigger for diverse CNS alterations. Although the clinical use of probenecid has declined over the years, advances in its use in preclinical research indicate that it may be useful to improve conventional therapies in the psychiatric field where the drugs used have a low bioavailability, either because of a deficient passage through the blood-brain barrier or a high efflux from the CNS or also a high urinary clearance. This review summarizes the history, pharmacological properties, and recent research uses of probenecid and discusses its future projections as a potential pharmacological strategy to intervene in neurodegeneration as an outcome of neuroinflammation.

摘要

丙磺舒是一种用于临床治疗痛风和减少抗生素肾脏排泄的老一代促尿酸排泄药。近年来,丙磺舒因其能够与膜蛋白相互作用而受到关注,这些膜蛋白包括瞬时受体电位香草酸亚型2(TRPV2)通道、有机阴离子转运体和泛连接蛋白1半通道,这提示了其在医学上具有新的潜在治疗用途。丙磺舒目前的一些功能包括用作佐剂以提高几种药物在中枢神经系统(CNS)中的生物利用度。大量研究还表明,这种药物具有重要的神经保护、抗癫痫和抗炎特性,这在其对神经和神经退行性疾病的作用中得到了证实。在这些研究中,强调了使用丙磺舒作为泛连接蛋白1半通道阻滞剂来减轻神经炎症,因为神经炎症是多种中枢神经系统改变的主要触发因素。尽管多年来丙磺舒的临床应用有所减少,但临床前研究中其应用的进展表明,在精神科领域,由于药物通过血脑屏障的能力不足、从中枢神经系统的高流出率或高尿清除率,导致所用药物的生物利用度较低,而丙磺舒可能有助于改善传统疗法。本综述总结了丙磺舒的历史、药理特性和近期的研究用途,并讨论了其作为一种潜在的药理学策略干预神经炎症导致的神经退行性变的未来前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d854/10295187/3cb63a49e944/biomedicines-11-01516-g001.jpg

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