Literature DB >> 35501362

Novel Caspase-1 inhibitor CZL80 improves neurological function in mice after progressive ischemic stroke within a long therapeutic time-window.

Ling Pan1, Wei-Dong Tang1, Ke Wang1, Qi-Feng Fang1, Meng-Ru Liu1, Zhan-Xun Wu1, Yi Wang1,2, Sun-Liang Cui3, Gang Hu4, Ting-Jun Hou3, Wei-Wei Hu1, Zhong Chen5,6, Xiang-Nan Zhang7.   

Abstract

Progressive ischemic stroke (PIS) is featured by progressive neurological dysfunction after ischemia. Ischemia-evoked neuroinflammation is implicated in the progressive brain injury after cerebral ischemia, while Caspase-1, an active component of inflammasome, exaggerates ischemic brain injury. Current Caspase-1 inhibitors are inadequate in safety and druggability. Here, we investigated the efficacy of CZL80, a novel Caspase-1 inhibitor, in mice with PIS. Mice and Caspase-1-/- mice were subjected to photothrombotic (PT)-induced cerebral ischemia. CZL80 (10, 30 mg·kg-1·d-1, i.p.) was administered for one week after PT onset. The transient and the progressive neurological dysfunction (as foot faults in the grid-walking task and forelimb symmetry in the cylinder task) was assessed on Day1 and Day4-7, respectively, after PT onset. Treatment with CZL80 (30 mg/kg) during Day1-7 significantly reduced the progressive, but not the transient neurological dysfunction. Furthermore, we showed that CZL80 administered on Day4-7, when the progressive neurological dysfunction occurred, produced significant beneficial effects against PIS, suggesting an extended therapeutic time-window. CZL80 administration could improve the neurological function even as late as Day43 after PT. In Caspase-1-/- mice with PIS, the beneficial effects of CZL80 were abolished. We found that Caspase-1 was upregulated during Day4-7 after PT and predominantly located in activated microglia, which was coincided with the progressive neurological deficits, and attenuated by CZL80. We showed that CZL80 administration did not reduce the infarct volume, but significantly suppressed microglia activation in the peri-infarct cortex, suggesting the involvement of microglial inflammasome in the pathology of PIS. Taken together, this study demonstrates that Caspase-1 is required for the progressive neurological dysfunction in PIS. CZL80 is a promising drug to promote the neurological recovery in PIS by inhibiting Caspase-1 within a long therapeutic time-window.
© 2022. The Author(s), under exclusive licence to Shanghai Institute of Materia Medica, Chinese Academy of Sciences and Chinese Pharmacological Society.

Entities:  

Keywords:  Caspase-1 inhibitor; microglia; neuroinflammation; neurological dysfunction; progressive ischemic stroke; therapeutic time-window

Year:  2022        PMID: 35501362     DOI: 10.1038/s41401-022-00913-7

Source DB:  PubMed          Journal:  Acta Pharmacol Sin        ISSN: 1671-4083            Impact factor:   6.150


  52 in total

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Journal:  Stroke       Date:  2002-06       Impact factor: 7.914

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Review 3.  Inflammation and Stroke: An Overview.

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4.  Opening a New Time Window for Treatment of Stroke by Targeting HDAC2.

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Journal:  J Neurosci       Date:  2017-06-07       Impact factor: 6.167

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Authors:  Rongrong Wang; Hongjian Pu; Qing Ye; Ming Jiang; Jie Chen; Jingyan Zhao; Sicheng Li; Yaan Liu; Xiaoming Hu; Marcelo Rocha; Ashutosh P Jadhav; Jun Chen; Yejie Shi
Journal:  Stroke       Date:  2020-02-12       Impact factor: 10.170

6.  A proposal for the classification of etiologies of neurologic deterioration after acute ischemic stroke.

Authors:  James E Siegler; Amelia K Boehme; Karen C Albright; Alexander J George; Dominique J Monlezun; T Mark Beasley; Sheryl Martin-Schild
Journal:  J Stroke Cerebrovasc Dis       Date:  2013-07-16       Impact factor: 2.136

Review 7.  Neuroprotection in acute stroke: targeting excitotoxicity, oxidative and nitrosative stress, and inflammation.

Authors:  Ángel Chamorro; Ulrich Dirnagl; Xabier Urra; Anna M Planas
Journal:  Lancet Neurol       Date:  2016-05-11       Impact factor: 44.182

8.  Progressing stroke: towards an internationally agreed definition.

Authors:  Philip Birschel; John Ellul; David Barer
Journal:  Cerebrovasc Dis       Date:  2004-01-13       Impact factor: 2.762

9.  Organizational update: the world health organization global status report on noncommunicable diseases 2014; one more landmark step in the combat against stroke and vascular disease.

Authors:  Shanthi Mendis; Stephen Davis; Bo Norrving
Journal:  Stroke       Date:  2015-04-14       Impact factor: 7.914

Review 10.  Post-stroke inflammation-target or tool for therapy?

Authors:  Kate Lykke Lambertsen; Bente Finsen; Bettina Hjelm Clausen
Journal:  Acta Neuropathol       Date:  2018-11-27       Impact factor: 17.088

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