Premium
Endothelium‐derived hydrogen sulfide acts as a hyperpolarizing factor and exerts neuroprotective effects via activation of large‐conductance Ca 2+ ‐activated K + channels
Author(s) -
Wen JiYue,
Zhang Jie,
Chen Shuo,
Chen Ye,
Zhang Yang,
Ma ZiYao,
Zhang Fang,
Xie WeiMing,
Fan YiFei,
Duan JingSi,
Chen ZhiWu
Publication year - 2021
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/bph.15607
Subject(s) - iberiotoxin , hyperpolarization (physics) , neuroprotection , chemistry , apamin , endothelium derived hyperpolarizing factor , pharmacology , neuroscience , potassium channel , biophysics , membrane potential , biochemistry , medicine , biology , resting potential , stereochemistry , nuclear magnetic resonance spectroscopy
Background and Purpose Endothelium‐derived hyperpolarizing factor (EDHF) has been suggested as a therapeutic target for vascular protection against ischaemic brain injury. However, the molecular entity of EDHF and its action on neurons remains unclear. This study was undertaken to demonstrate whether the hydrogen sulfide (H 2 S) acts as EDHF and exerts neuroprotective effect via large‐conductance Ca 2+ ‐activated K + (BK Ca /K Ca 1.1) channels. Experimental Approach The whole‐cell patch‐clamp technology was used to record the changes of BK Ca currents in rat neurons induced by EDHF. The cerebral ischaemia/reperfusion model of mice and oxygen–glucose deprivation/reoxygenation (OGD/R) model of neurons were used to explore the neuroprotection of EDHF by activating BK Ca channels in these neurons. Key Results Increases of BK Ca currents and membrane hyperpolarization in hippocampal neurons induced by EDHF could be markedly inhibited by BK Ca channel inhibitor iberiotoxin or endothelial H 2 S synthase inhibitor propargylglycine. The H 2 S donor, NaHS‐induced BK Ca current and membrane hyperpolarization in neurons were also inhibited by iberiotoxin, suggesting that H 2 S acts as EDHF and activates the neuronal BK Ca channels. Besides, we found that the protective effect of endothelium‐derived H 2 S against mice cerebral ischaemia/reperfusion injury was disrupted by iberiotoxin. Importantly, the inhibitory effect of NaHS or BK Ca channel opener on OGD/R‐induced neuron injury and the increment of intracellular Ca 2+ level could be inhibited by iberiotoxin but enhanced by co‐application with L‐type but not T‐type calcium channel inhibitor. Conclusion and Implications Endothelium‐derived H 2 S acts as EDHF and exerts neuroprotective effects via activating the BK Ca channels and then inhibiting the T‐type calcium channels in hippocampal neurons.