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磷酸二酯酶10A抑制可减轻脓毒症和神经损伤中的NLRP3激活及细胞焦亡

PDE10A Inhibition Reduces NLRP3 Activation and Pyroptosis in Sepsis and Nerve Injury.

作者信息

Berk Bradford C, Chávez Camila Lage, George Hsu Chia

机构信息

Department of Physical Medicine and Rehabilitation, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA.

Department of Medicine, University of Rochester School of Medicine and Dentistry, Rochester, NY 14624, USA.

出版信息

Int J Mol Sci. 2025 May 8;26(10):4498. doi: 10.3390/ijms26104498.

Abstract

Cell death and inflammation are key innate immune responses, but excessive activation can cause tissue damage. The NLRP3 inflammasome is a promising target for reducing inflammation and promoting recovery. Immunometabolism regulates NLRP3 responses in neurological and inflammatory diseases through cyclic nucleotide signaling. Targeting phosphodiesterases (PDEs), which hydrolyze cAMP and cGMP, offer a novel approach to mitigate inflammation. While 14 PDE inhibitors are FDA-approved, PDE10A's role in NLRP3 inflammasome activation remains unclear. This study investigates the effects of PDE10A inhibition on inflammasome-driven inflammation using two PDE10A inhibitors, MP-10 and TP-10, in macrophage and animal models of sepsis and traumatic nerve injury. Our results show that PDE10A inhibition reduces inflammasome activation by preventing ASC speck formation and by lowering levels of cleaved caspase-1, gasdermin D, and IL-1β, which are key mediators of pyroptosis. In the sepsis model, MP-10 significantly reduced inflammation, decreased plasma IL-1β, alleviated thrombocytopenia, and improved organ damage markers. In the nerve injury model, PDE10A inhibition enhanced motor function recovery and reduced muscle atrophy-related gene expression. These findings suggest that PDE10A inhibition could be a promising therapeutic approach for inflammatory and neuromuscular injuries. Given MP-10's established safety in human trials, Phase 2 clinical studies for sepsis and nerve injury are highly promising.

摘要

细胞死亡和炎症是关键的先天性免疫反应,但过度激活会导致组织损伤。NLRP3炎性小体是减轻炎症和促进恢复的一个有前景的靶点。免疫代谢通过环核苷酸信号传导调节神经和炎症性疾病中的NLRP3反应。靶向水解cAMP和cGMP的磷酸二酯酶(PDEs)提供了一种减轻炎症的新方法。虽然有14种PDE抑制剂已获美国食品药品监督管理局(FDA)批准,但PDE10A在NLRP3炎性小体激活中的作用仍不清楚。本研究使用两种PDE10A抑制剂MP-10和TP-10,在脓毒症和创伤性神经损伤的巨噬细胞和动物模型中研究PDE10A抑制对炎性小体驱动的炎症的影响。我们的结果表明,PDE10A抑制通过阻止ASC斑点形成以及降低裂解的半胱天冬酶-1、gasdermin D和IL-1β的水平来减少炎性小体激活,这些都是细胞焦亡的关键介质。在脓毒症模型中,MP-10显著减轻炎症,降低血浆IL-1β水平,缓解血小板减少,并改善器官损伤标志物。在神经损伤模型中,PDE10A抑制增强运动功能恢复并降低肌肉萎缩相关基因的表达。这些发现表明,PDE10A抑制可能是治疗炎症性和神经肌肉损伤的一种有前景的治疗方法。鉴于MP-10在人体试验中已确立的安全性,针对脓毒症和神经损伤的2期临床研究前景广阔。

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