Unknown

Dataset Information

0

Hederagenin Attenuates Cerebral Ischaemia/Reperfusion Injury by Regulating MLK3 Signalling.


ABSTRACT: Cerebral ischaemia/reperfusion (CI/R) injury is a major challenge due to the lack of effective neuroprotective drugs. Hederagenin (HE) is the aglycone part of saponins extracted from Hedera helix Linné that has exhibited anti-apoptotic and anti-inflammatory effects; however, the role of HE in CI/R has not been elucidated. In this study, mice were intraperitoneally (i.p.) injected with HE (26.5, 53, or 106 ?mol/kg body weight) for 3 days after middle cerebral artery occlusion (MCAO). Neural function and brain infarct volume were evaluated. HE treatment attenuated CI/R-induced apoptosis and inflammatory cytokine expression within the infarcted areas. HE treatment also decreased the activation of the MLK3 signalling pathway, which potentiates CI/R damage via the MAPK and NF?B pathways. Due to HE's safety profile, it has potential to be used for the clinical treatment of ischaemic stroke.

SUBMITTER: Yu H 

PROVIDER: S-EPMC7406912 | biostudies-literature | 2020

REPOSITORIES: biostudies-literature

altmetric image

Publications

Hederagenin Attenuates Cerebral Ischaemia/Reperfusion Injury by Regulating MLK3 Signalling.

Yu Hailong H   Song Lilong L   Cao Xiang X   Li Wei W   Zhao Yuanyuan Y   Chen Jian J   Li Jun J   Chen Yingzhu Y   Yu Wenkui W   Xu Yun Y  

Frontiers in pharmacology 20200730


Cerebral ischaemia/reperfusion (CI/R) injury is a major challenge due to the lack of effective neuroprotective drugs. Hederagenin (HE) is the aglycone part of saponins extracted from <i>Hedera helix Linné</i> that has exhibited anti-apoptotic and anti-inflammatory effects; however, the role of HE in CI/R has not been elucidated. In this study, mice were intraperitoneally (i.p.) injected with HE (26.5, 53, or 106 μmol/kg body weight) for 3 days after middle cerebral artery occlusion (MCAO). Neura  ...[more]

Similar Datasets

| S-EPMC9001073 | biostudies-literature
| S-EPMC8099895 | biostudies-literature
| S-EPMC7483549 | biostudies-literature
| S-EPMC4882992 | biostudies-literature
| S-EPMC6933328 | biostudies-literature
| S-EPMC3822653 | biostudies-literature
| S-EPMC3581775 | biostudies-literature
| S-EPMC4549033 | biostudies-literature
| S-EPMC7810957 | biostudies-literature
| S-EPMC10899177 | biostudies-literature