Dl-3-n-butylphthalide promotes angiogenesis in ischemic stroke mice through upregulating autocrine and paracrine sonic hedgehog  

作　　者：Mei-jie Dai Xing-xing Gui Shu-miao Jia Shu-ting Lv Hao Dou Wei Cui 

机构地区：[1]Department of Pharmacology,Shenyang Pharmaceutical University,Shenyang,110016,China

出　　处：《Acta Pharmacologica Sinica》2023年第12期2404-2417,共14页中国药理学报（英文版）

基　　金：the key program of the Educational Department of Liao Ning Province(Nos.LJKZZ20220100).

摘　　要：Dl-3-n-butylphthalide(NBP)is a small-molecule drug used in the treatment of ischemic stroke in China,which is proven to ameliorate the symptoms of ischemic stroke and improve the prognosis of patients.Previous studies have shown that NBP accelerates recovery after stroke by promoting angiogenesis.In this study,we investigated the mechanisms underlying the angiogenesis-promoting effects of NBP in ischemic stroke models in vitro and in vivo.OGD/R model was established in human umbilical vein endothelial cells(HUVECs)and human brain microvascular endothelial cells(HBMECs),while the tMCAO model was established in mice.The cells were pretreated with NBP(10,50,100µM);the mice were administered NBP(4,8 mg/kg,i.v.)twice after tMCAO.We showed that NBP treatment significantly stimulated angiogenesis by inducing massive production of angiogenic growth factors VEGFA and CD31 in both in vitro and in vivo models of ischemic stroke.NBP also increased the tubule formation rate and migration capability of HUVECs in vitro.By conducting the weighted gene co-expression network analysis,we found that these effects were achieved by upregulating the expression of a hedgehog signaling pathway.We demonstrated that NBP treatment not only changed the levels of regulators of the hedgehog signaling pathway but also activated the transcription factor Gli1.The pro-angiogenesis effect of NBP was abolished when the hedgehog signaling pathway was inhibited by GDC-0449 in HUVECs,by Sonic Hedgehog(Shh)knockdown in HUVECs,or by intracerebroventricular injection of AAV-shRNA(shh)-CMV in tMCAO mice.Furthermore,we found that HUVECs produced a pro-angiogenic response not only to autocrine Shh,but also to paracrine Shh secreted by astrocytes.Together,we demonstrate that NBP promotes angiogenesis via upregulating the hedgehog signaling pathway.Our results provide an experimental basis for the clinical use of NBP.

关 键 词：ischemic stroke ANGIOGENESIS Dl-3-n-butylphthalide brain ischemia/reperfusion tMCAO model hedgehog signaling pathway 

分 类 号：R363[医药卫生—病理学]