Your browser doesn't support javascript.
loading
Xingnaojing Injection Protects against Cerebral Ischemia Reperfusion Injury via PI3K/Akt-Mediated eNOS Phosphorylation.
Zhang, Yue-Ming; Qu, Xiao-Yu; Zhai, Jing-Hui; Tao, Li-Na; Gao, Huan; Song, Yan-Qing; Zhang, Si-Xi.
Affiliation
  • Zhang YM; Department of Pharmacy, The First Hospital of Jilin University, Changchun, Jilin 130021, China.
  • Qu XY; Department of Pharmacy, The First Hospital of Jilin University, Changchun, Jilin 130021, China.
  • Zhai JH; Department of Pharmacy, The First Hospital of Jilin University, Changchun, Jilin 130021, China.
  • Tao LN; Department of Pharmacy, The First Hospital of Jilin University, Changchun, Jilin 130021, China.
  • Gao H; Department of Pharmacy, The First Hospital of Jilin University, Changchun, Jilin 130021, China.
  • Song YQ; Department of Pharmacy, The First Hospital of Jilin University, Changchun, Jilin 130021, China.
  • Zhang SX; Department of Pharmacy, The First Hospital of Jilin University, Changchun, Jilin 130021, China.
Article in En | MEDLINE | ID: mdl-30158991
ABSTRACT
Xingnaojing (XNJ) injection, derived from traditional Chinese medicine formulation, has a protective effect against stroke, but the underlying mechanism is unclear, which severely limited its clinical application. This research aims to elucidate the role and mechanism of XNJ in reducing cerebral ischemic reperfusion (I/R) injury. Rats received 2 h cerebral ischemia followed by reperfusion of 24 h and were intraperitoneally given 5, 10, or 15 ml/kg XNJ 24 h before ischemia and at the onset of reperfusion, respectively. TTC staining, HE staining, and neurological score were implied to evaluate the effectiveness of XNJ. The protein expressions of PI3K/Akt and eNOS signaling were measured. Experiments were further performed in human brain microvascular endothelial cells (HBMECs) to investigate the protective mechanisms of XNJ. HBMECs were subjected to 3 h oxygen and glucose deprivation following 24 h of reoxygenation (OGD) to mimic cerebral I/R in vitro. PI3K inhibitor LY294002 was added with or without the preconditioning of XNJ. Multiple methods including western blot, immunofluorescence, DAPI staining, JC-1, and flow cytometry were carried out to evaluate the effect of XNJ on HBMECs. XNJ could improve rat cerebral ischemic injury and OGD induced HBMECs apoptosis. In vivo and in vitro researches indicated that the mechanism might be relevant to the activation of PI3K/Akt/eNOS signaling.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Evid Based Complement Alternat Med Year: 2018 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Evid Based Complement Alternat Med Year: 2018 Document type: Article Affiliation country: China