Total Flavones of Rhododendron simsii Planch Flower Protect against Cerebral Ischemia-Reperfusion Injury via the Mechanism of Cystathionine- γ-Lyase-Produced H2S

Shuo Chen; Jian-Hua Zhang; You-Yang Hu; Dong-Hua Hu; Shan-Shan Gao; Yi-Fei Fan; Yu-Ling Wang; Yi Jiao; Zhi-Wu Chen

doi:10.1155/2018/8903849

Total Flavones of Rhododendron simsii Planch Flower Protect against Cerebral Ischemia-Reperfusion Injury via the Mechanism of Cystathionine- γ-Lyase-Produced H₂S

Evid Based Complement Alternat Med. 2018 May 31:2018:8903849. doi: 10.1155/2018/8903849. eCollection 2018.

Authors

Shuo Chen¹, Jian-Hua Zhang^{2

3}, You-Yang Hu^{2

4}, Dong-Hua Hu², Shan-Shan Gao², Yi-Fei Fan¹, Yu-Ling Wang², Yi Jiao², Zhi-Wu Chen²

Affiliations

¹ Department of Physiology, Anhui Medical University, Hefei, Anhui 230032, China.
² Department of Pharmacology, Anhui Medical University, Hefei, Anhui 230032, China.
³ Department of Cardiology, First Affiliated Hospital of Jinan University, Guangzhou, Guangdong 510630, China.
⁴ Department of Anesthesiology, Anhui Chest Hospital, Hefei, Anhui 230032, China.

Abstract

Total flavones of Rhododendron simsii Planch flower (TFR) have a significant protective effect against cerebral ischemia-reperfusion injury. However, its mechanism is unclear. This study investigated the protection of TFR against cerebral ischemia-reperfusion injury via cystathionine-γ-lyase- (CSE-) produced H₂S mechanism. CSE^-/- mice and CSE-siRNA-transfected rat were used. Relaxation of cerebral basilar artery (CBA), H₂S, and CSE mRNA were measured. TFR significantly inhibited cerebral ischemia-reperfusion-induced abnormal neurological symptom and cerebral infarct in the normal rats and the CSE^+/+ mice, but not in the CSE^-/- mice, and the inhibition was markedly attenuated in CSE-siRNA-transfected rat; TFR elicited a significant vasorelaxation in rat CBA, and the relaxation was markedly attenuated by removal of endothelium or CSE-siRNA transfection or coapplication of NO synthase inhibitor L-NAME and PGI₂ synthase inhibitor Indo. CSE inhibitor PPG drastically inhibited TFR-evoked vasodilatation resistant to L-NAME and Indo in endothelium-intact rat CBA. TFR significantly increased CSE mRNA expression in rat CBA endothelial cells and H₂S production in rat endothelium-intact CBA. The increase of H₂S production resistant to L-NAME and Indo was abolished by PPG. Our data indicate that TFR has a protective effect against the cerebral ischemia-reperfusion injury via CSE-produced H₂S and endothelial NO and/or PGI₂ to relax the cerebral artery.