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CB1和CB2大麻素受体的正变构调节增强了双重CB1R/CB2R正位激动剂的神经保护活性。

Positive Allosteric Modulation of CB1 and CB2 Cannabinoid Receptors Enhances the Neuroprotective Activity of a Dual CB1R/CB2R Orthosteric Agonist.

作者信息

Polini Beatrice, Cervetto Chiara, Carpi Sara, Pelassa Simone, Gado Francesca, Ferrisi Rebecca, Bertini Simone, Nieri Paola, Marcoli Manuela, Manera Clementina

机构信息

Department of Pharmacy, University of Pisa, 56126 Pisa, Italy.

Department of Pharmacy, Section of Pharmacology and Toxicology, University of Genova, 16126 Genova, Italy.

出版信息

Life (Basel). 2020 Dec 8;10(12):333. doi: 10.3390/life10120333.

Abstract

Preclinical studies highlighted that compounds targeting cannabinoid receptors could be useful for developing novel therapies against neurodegenerative disorders. However, the chronic use of orthosteric agonists alone has several disadvantages, limiting their usefulness as clinically relevant drugs. Positive allosteric modulators might represent a promising approach to achieve the potential therapeutic benefits of orthosteric agonists of cannabinoid receptors through increasing their activity and limiting their adverse effects. The aim of the present study was to show the effects of positive allosteric ligands of cannabinoid receptors on the activity of a potent dual orthosteric agonist for neuroinflammation and excitotoxic damage by excessive glutamate release. The results indicate that the combination of an orthosteric agonist with positive allosteric modulators could represent a promising therapeutic approach to the treatment of neurodegenerative disorders.

摘要

临床前研究强调,靶向大麻素受体的化合物可能有助于开发针对神经退行性疾病的新型疗法。然而,单独长期使用正构激动剂存在几个缺点,限制了它们作为临床相关药物的实用性。正变构调节剂可能是一种有前景的方法,通过增加其活性并限制其不良反应,来实现大麻素受体正构激动剂的潜在治疗益处。本研究的目的是展示大麻素受体正变构配体对一种强效双重正构激动剂活性的影响,该正构激动剂可通过过量谷氨酸释放来引发神经炎症和兴奋性毒性损伤。结果表明,正构激动剂与正变构调节剂的联合使用可能是治疗神经退行性疾病的一种有前景的治疗方法。

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