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首页> 外文期刊>Journal of Ethnopharmacology: An Interdisciplinary Journal Devoted to Bioscientific Research on Indigenous Drugs >Ligusticum chuanxiong as a potential neuroprotectant for preventing serum deprivation-induced apoptosis in rat pheochromocytoma cells: functional roles of mitogen-activated protein kinases.
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Ligusticum chuanxiong as a potential neuroprotectant for preventing serum deprivation-induced apoptosis in rat pheochromocytoma cells: functional roles of mitogen-activated protein kinases.

机译:川xi作为一种潜在的神经保护剂,可预防血清嗜铬细胞瘤细胞中血清剥夺诱导的细胞凋亡:促分裂原活化蛋白激酶的功能性作用。

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ETHNOPHARMACOLOGICAL RELEVANCE: Ligusticum chuanxiong (LC) as a common component in many traditional Chinese medicinal formulas and decoctions has been used to treat different central nervous diseases, suggesting a neuroprotective function. AIM OF THE STUDY: To investigate the functional roles of mitogen-activated protein kinases (MAPKs) in mediating the neuroprotection of LC. MATERIALS AND METHODS: Different extractions of LC were applied with or without MAPK inhibitor to test their protection against serum deprivation-induced apoptosis in rat neuronal-like pheochromocytoma (PC12) cells as revealed by an MTT assay or Hoechst staining. Western blot was used to identify the activations of MAPKs. RESULTS: The most effective butanol extraction (LC-BuOH) was used in the following experiments. LC-BuOH reversed serum deprivation-induced decreased phosphorylation of extracellular signal-regulated kinase (ERK) and increased phosphorylation of c-Jun NH(2)-terminal kinase (JNK) and p38, the family of MAPKs. A PKA inhibitor, blocked the protection of LC-BuOH and partially blocked LC-BuOH-induced alterations in MAPKs, suggesting that the LC-BuOH regulates MAPKs through both PKA-dependent and -independent pathways. Although PD 98059, an inhibitor of MEK which activates ERK, blocked LC-BuOH-induced ERK phosphorylation, it did not block the protection of LC-BuOH. CONCLUSIONS: LC-BuOH mediates protection by suppressing JNK/p38 instead of activating ERK activity.
机译:人种药理学相关性:川Li(LC)是许多传统中药配方和汤剂中的常见成分,已被用于治疗不同的中枢神经疾病,提示其具有神经保护功能。研究目的:研究促分裂原活化蛋白激酶(MAPK)在介导LC的神经保护中的功能。材料与方法:MTT分析或Hoechst染色显示,在有或没有MAPK抑制剂的情况下,均采用不同的LC提取物来测试其对大鼠神经元样嗜铬细胞瘤(PC12)细胞的血清剥夺诱导的细胞凋亡的保护作用。免疫印迹用于鉴定MAPKs的激活。结果:在以下实验中使用了最有效的丁醇萃取(LC-BuOH)。 LC-BuOH逆转血清剥夺诱导的细胞外信号调节激酶(ERK)磷酸化减少和c-Jun NH(2)-末端激酶(JNK)和p38(MAPK家族)的磷酸化增加。 PKA抑制剂可阻断LC-BuOH的保护并部分阻断LC-BuOH诱导的MAPK改变,这表明LC-BuOH可通过PKA依赖性和非依赖性途径调节MAPK。尽管PD 98059(一种激活ERK的MEK抑制剂)阻止了LC-BuOH诱导的ERK磷酸化,但它并未阻止LC-BuOH的保护。结论:LC-BuOH通过抑制JNK / p38而不是激活ERK活性来介导保护作用。

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