4.7 Article

OL-FS13 alleviates experimental cerebral ischemia-reperfusion injury

期刊

EXPERIMENTAL NEUROLOGY
卷 357, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.expneurol.2022.114180

关键词

Neuroprotection; Cerebral ischemia; Bioactive peptide; Oxidative stress; Reperfusion

资金

  1. National Natural Science Foundation of China [32060212, 81760648, 82160159]
  2. Project of Yunnan Applied Basic Research Project-Kunming Medical University Union Foundation [202101AY070001-006, 2018FE001 (-161), 2019FE001 (-020) )]
  3. Yunnan Applied Basic Research Project Foundation [2019FB128]
  4. Endocrine Clinical Medical Center of Yunnan Province [ZX2019-02-02]
  5. Scientific Research Fund Projects from the Department of Education of Yunnan Province [2021 J0205]
  6. Innovative Team of Precise Prevention and Treatment against Metabolic of Yunnan University

向作者/读者索取更多资源

In this study, a novel neuroprotective peptide OL-FS13 was identified from the odorous frog species Odorrana livida, showing significant improvement in cerebral ischemia-reperfusion injury and providing a new drug candidate for clinical treatment.
Cerebral ischemia-reperfusion (I/R) is the main cause of neurological injury after stroke. However, existing treatments for I/R injury are relatively poor, and relevant drugs need to be further explored. Amphibians have received increasing attention as a resource bank of bioactive peptides. However, reports on neuroprotective peptides from amphibians remain extremely rare. Here, we identified a new neuroprotective peptide (OL-FS13, amino acid sequence: FSLLLTWWRRRVC) from the odorous frog species Odorrana livida using a constructed cDNA library. OL-FS13 significantly improving infarct volume, behavioral and histological abnormalities in rats, and also showed neuroprotective activities in PC12 cell (by oxygen glucose deprivation/reoxygenation, OGD/R). Mechanistically, OL-FS13 increased the level of antioxidative enzymes to resist oxidative stress and alleviated endoplasmic reticulum (ER) stress induced by I/R and OGD/R. The use of ML385 (Nrf2 inhibitor) indicated that OL-FS13 relieved nerve damage caused by oxidative and ER stress by increasing the nuclear displacement of Nrf2. Collectively, this research provides a novel drug candidate for the clinical cerebral I/R curation.

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