Your browser doesn't support javascript.
loading
Senkyunolide H protects PC12 cells from OGD/R-induced injury via cAMP-PI3K/AKT signaling pathway.
Jiang, Yunyao; Luo, Yanyan; Chen, Xinyi; Liu, Nan; Hou, Jincai; Piao, Jingpei; Song, Chao; Si, Chuanling; Hu, Weicheng; Li, Xueqin.
Afiliação
  • Jiang Y; Institute for Chinese Materia Medica, School of Pharmaceutical Sciences, Tsinghua University, Beijing, 100084, China. Electronic address: yunyao86@126.com.
  • Luo Y; Tianjin Key Laboratory of Pulp & Paper, Tianjin University of Science & Technology, Tianjin, 300457, China. Electronic address: lyy122525@163.com.
  • Chen X; Institute for Chinese Materia Medica, School of Pharmaceutical Sciences, Tsinghua University, Beijing, 100084, China. Electronic address: rosettaxinyi@163.com.
  • Liu N; Beijing Increasepharm Safety and Efficacy Co., Ltd, Beijing, 102206, China. Electronic address: nanliu0304@163.com.
  • Hou J; Jing-Jin-Ji Joint Innovation Pharmaceutical (Beijing) Co., Ltd., Beijing, 100083, China. Electronic address: jincaihou@126.com.
  • Piao J; College of Life Sciences, Jilin Normal University, Siping, 136000, China. Electronic address: parkfreedom@163.com.
  • Song C; School of Life Sciences, Huaiyin Normal University, Huaian, 223300, China. Electronic address: hytcsongchao@163.com.
  • Si C; Tianjin Key Laboratory of Pulp & Paper, Tianjin University of Science & Technology, Tianjin, 300457, China. Electronic address: sichli@tust.edu.cn.
  • Hu W; School of Life Sciences, Huaiyin Normal University, Huaian, 223300, China. Electronic address: hu_weicheng@163.com.
  • Li X; Department of General Practice, The Affiliated Huaian NO.1 People's Hospital of Nanjing Medical University, Huai'an, 223300, China. Electronic address: doctorlixq@sina.com.
J Ethnopharmacol ; 282: 114659, 2022 Jan 10.
Article em En | MEDLINE | ID: mdl-34543683
ETHNOPHARMACOLOGICAL RELEVANCE: Senkyunolide H (SNH) is a bioactive phthalide isolated from Ligusticum chuanxiong Hort rhizome and was reported to have multiple pharmacological effects. AIM OF THE STUDY: The study was performed to verify the potency of SNH protecting PC12 cells from oxygen glucose deprivation/reperfusion (OGD/R)-induced injury and to elucidate the underlying mechanisms. MATERIALS AND METHODS: OGD/R model was established in PC12 cells and the cell viability was measured by MTT assay. The cell morphology was observed using scanning electron microscope (SEM). The potential targets of SNH and related targets of OGD/R were screened, and a merged protein-protein interaction (PPI) network of SNH and OGD/R was constructed based on the network pharmacology analysis. Kyoto Encyclopedia of Genes and Genomes (KEGG) database was used for pathway analysis. Intracellular cAMP level and the protein expression levels were measured to elucidate the underlying mechanisms. RESULTS: SNH pretreatment protected PC12 cells against OGD/R-induced cell death. SNH also significantly protected the cell protrusion. A merged PPI network was constructed and the shared candidate targets significantly enriched in cAMP signaling pathway. The level of intracellular cAMP and the protein level of p-CREB, p-AKT, p-PDK1 and PKA protein were up-regulated after the treatment of SNH compared with OGD/R modeling. CONCLUSIONS: The present study indicated that SNH protected PC12 cells from OGD/R-induced injury via cAMP-PI3K/AKT signaling pathway.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxigênio / Benzofuranos / Traumatismo por Reperfusão / AMP Cíclico / Fosfatidilinositol 3-Quinases / Glucose Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxigênio / Benzofuranos / Traumatismo por Reperfusão / AMP Cíclico / Fosfatidilinositol 3-Quinases / Glucose Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article