1. Academic Validation
  2. Ac-YVAD-cmk improves neurological function by inhibiting caspase-1-mediated inflammatory response in the intracerebral hemorrhage of rats

Ac-YVAD-cmk improves neurological function by inhibiting caspase-1-mediated inflammatory response in the intracerebral hemorrhage of rats

  • Int Immunopharmacol. 2019 Oct;75:105771. doi: 10.1016/j.intimp.2019.105771.
Hongsheng Liang 1 Yong Sun 2 Aili Gao 3 Nannan Zhang 4 Ying Jia 5 Shanshan Yang 6 Meng Na 1 Huailei Liu 1 Xingbo Cheng 1 Xiaofeng Fang 1 Wei Ma 1 Xiangtong Zhang 7 Fan Wang 8
Affiliations

Affiliations

  • 1 Department of Neurosurgery, First Affiliated Hospital of Harbin Medical University, Harbin, P.R. China.
  • 2 Department of Neurosurgery, First Affiliated Hospital of Harbin Medical University, Harbin, P.R. China; Department of Neurosurgery, Xinyang Central Hospital, Xinyang, P.R. China.
  • 3 School of Life Science, Northeast Agricultural University, Harbin, P.R. China.
  • 4 Department of Epidemiology, School of Public Health, Harbin Medical University, Harbin, Heilongjiang Province, P.R. China.
  • 5 Department of Pathology, First Affiliated Hospital of Harbin Medical University, Harbin, P.R. China.
  • 6 Department of Neurology, First Affiliated Hospital of Harbin Medical University, Harbin, P.R. China.
  • 7 Department of Neurosurgery, First Affiliated Hospital of Harbin Medical University, Harbin, P.R. China. Electronic address: zgxgtg@sina.com.
  • 8 Department of Epidemiology, School of Public Health, Harbin Medical University, Harbin, Heilongjiang Province, P.R. China. Electronic address: yifan.701@163.com.
Abstract

Objective: Intracerebral hemorrhage (ICH) is acknowledged as a serious clinical problem lacking effective treatments. And caspase-1-mediated inflammatory response happened during the progression of ICH. Therefore, we aimed to investigate the effects of Caspase-1 inhibitor Ac-YVAD-cmk on ICH.

Materials and methods: Microglia cells were isolated and activated by Thrombin for 24 h. Then the transcript and protein expressions of NLRP3 and inflammatory factors were assessed by RT-PCR and western blotting. Moreover, Ac-YVAD-cmk was injected into the ICH model. The mNSS and brain water content were tested at 24 h post-ICH. Finally, the pathological changes of microglia activation following ICH were discovered by the immunohistochemical and HE staining ways.

Results: Ac-YVAD-cmk inhibited the activation of pro-caspase-1 and decreased brain edema, in association with decreasing activated microglia and the expression of inflammation-related factors at 24 h post-ICH. Consequently, Ac-YVAD-cmk reduced the release of mature IL-1β/IL-18 in perihematoma, improved the behavioral performance, and alleviated microglia in perihematoma region in ICH rats.

Conclusions: These results indicate that Caspase-1 could amplify the plural inflammatory responses in the ICH. Administration of Ac-YVAD-cmk has the potential to be a novel therapeutic strategy for ICH.

Keywords

Ac-YVAD-cmk; Caspase-1; Intracerebral hemorrhage; Microglia.

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