Higenamine protects neuronal cells from oxygen‐glucose deprivation/reoxygenation‐induced injury. Issue 3 (30th September 2018)
- Record Type:
- Journal Article
- Title:
- Higenamine protects neuronal cells from oxygen‐glucose deprivation/reoxygenation‐induced injury. Issue 3 (30th September 2018)
- Main Title:
- Higenamine protects neuronal cells from oxygen‐glucose deprivation/reoxygenation‐induced injury
- Authors:
- Zhang, Yi
Zhang, Jingjing
Wu, Chuntao
Guo, Sheng
Su, Jing
Zhao, Wendong
Xing, Hongxia - Abstract:
- Abstract: Higenamine, a plant‐based alkaloid, exhibits various properties, such as antiapoptotic and antioxidative effects. Previous studies proved that higenamine possesses potential therapeutic effects for ischemia/reperfusion (I/R) injuries. However, the role of higenamine in cerebral I/R injury has not been fully evaluated. Therefore, we aimed to investigate the effect of higenamine on cerebral I/R injury and the potential mechanism. Our data showed that higenamine ameliorated oxygen‐glucose deprivation/reperfusion (OGD/R)‐induced neuronal cells injury. Induction of reactive oxygen species and malonaldehyde production, and the inhibition of superoxide dismutase and glutathione peroxidase activity caused by OGD/R were attenuated by higenamine. In addition, higenamine inhibited the increases in caspase‐3 activity and Bax expression, and inhibited the decrease in Bcl‐2 expression. Furthermore, higenamine elevated the expression levels of p‐Akt, heme oxygenase‐1 (HO‐1) and nuclear factor erythroid 2‐related factor 2 (Nrf2). The inhibitor of PI3K/Akt (LY294002) abolished the protective effects of higenamine on OGD/R‐induced neuronal cells. These findings indicated that higenamine protects neuronal cells against OGD/R‐induced injury by regulating the Akt and Nrf2/HO‐1‐signaling pathways. Collectively, higenamine might be considered as new strategy for the prevention and treatment of cerebral I/R injury. Abstract : Higenamine protects neuronal cells against oxygen‐glucoseAbstract: Higenamine, a plant‐based alkaloid, exhibits various properties, such as antiapoptotic and antioxidative effects. Previous studies proved that higenamine possesses potential therapeutic effects for ischemia/reperfusion (I/R) injuries. However, the role of higenamine in cerebral I/R injury has not been fully evaluated. Therefore, we aimed to investigate the effect of higenamine on cerebral I/R injury and the potential mechanism. Our data showed that higenamine ameliorated oxygen‐glucose deprivation/reperfusion (OGD/R)‐induced neuronal cells injury. Induction of reactive oxygen species and malonaldehyde production, and the inhibition of superoxide dismutase and glutathione peroxidase activity caused by OGD/R were attenuated by higenamine. In addition, higenamine inhibited the increases in caspase‐3 activity and Bax expression, and inhibited the decrease in Bcl‐2 expression. Furthermore, higenamine elevated the expression levels of p‐Akt, heme oxygenase‐1 (HO‐1) and nuclear factor erythroid 2‐related factor 2 (Nrf2). The inhibitor of PI3K/Akt (LY294002) abolished the protective effects of higenamine on OGD/R‐induced neuronal cells. These findings indicated that higenamine protects neuronal cells against OGD/R‐induced injury by regulating the Akt and Nrf2/HO‐1‐signaling pathways. Collectively, higenamine might be considered as new strategy for the prevention and treatment of cerebral I/R injury. Abstract : Higenamine protects neuronal cells against oxygen‐glucose deprivation/reoxygenation‐induced injury by regulating the Akt and Nrf2/HO‐1‐signaling pathways. Collectively, higenamine might be considered as new strategy for the prevention and treatment of cerebral ischemia/reperfusion injury. … (more)
- Is Part Of:
- Journal of cellular biochemistry. Volume 120:Issue 3(2019)
- Journal:
- Journal of cellular biochemistry
- Issue:
- Volume 120:Issue 3(2019)
- Issue Display:
- Volume 120, Issue 3 (2019)
- Year:
- 2019
- Volume:
- 120
- Issue:
- 3
- Issue Sort Value:
- 2019-0120-0003-0000
- Page Start:
- 3757
- Page End:
- 3764
- Publication Date:
- 2018-09-30
- Subjects:
- cell apoptosis -- cerebral ischemia/reperfusion injury -- higenamine -- oxidative stress
Cytochemistry -- Periodicals
572 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-4644 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jcb.27656 ↗
- Languages:
- English
- ISSNs:
- 0730-2312
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4955.010000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23459.xml