首页> 外文期刊>Mediators of inflammation >Protective Effect of Adrenomedullin on Rat Leydig Cells from Lipopolysaccharide-Induced Inflammation and Apoptosis via the PI3K/Akt Signaling Pathway ADM on Rat Leydig Cells from Inflammation and Apoptosis
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Protective Effect of Adrenomedullin on Rat Leydig Cells from Lipopolysaccharide-Induced Inflammation and Apoptosis via the PI3K/Akt Signaling Pathway ADM on Rat Leydig Cells from Inflammation and Apoptosis

机译:肾上腺素对大鼠Leydig细胞的保护作用通过PI3K / AKT信号通路免受PI3K / AKT信号通路的炎症和细胞凋亡免受炎症和细胞凋亡的大鼠Leydig细胞

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摘要

This study was carried out to investigate whether ADM can modulate LPS-induced inflammation and apoptosis in rat Leydig cells. Leydig cells were treated with ADM before LPS-induced cytotoxicity. We determined the concentrations of ROS, MDA, GSH, LDH, and testosterone and the MMP. The mRNA levels of IL-1, IL-6, iNOS, and COX-2 were obtained, and the concentrations of IL-1, IL-6, NO, and PGE2 were determined. Apoptosis was assessed by TUNEL and detection of DNA fragmentation. The levels of mRNA and protein were determined for Bcl-2, Bax, caspase-3, and PARP. The protein contents for total and p-Akt were measured. ADM pretreatment significantly elevated the MMP and testosterone concentration and reduced the levels of ROS, MDA, GSH, and LDH. ADM pretreatment significantly decreased the mRNA levels of IL-1, IL-6, iNOS, and COX-2 and the concentrations of IL-1, IL-6, NO, and PGE2. LPS-induced TUNEL-positive Leydig cells were significantly decreased by ADM pretreatment, a result further confirmed by decreased DNA fragmentation. ADM pretreatment decreased apoptosis by significantly promoting Bcl-2 and inhibiting Bax, caspase-3, and PARP expressions. The LPS activity that reduced p-Akt level was significantly inhibited by ADM pretreatment. ADM protected rat Leydig cells from LPS-induced inflammation and apoptosis, which might be associated with PI3K/Akt mitochondrial signaling pathway.
机译:进行该研究以研究ADM是否可以调节LPS诱导的大鼠Leydig细胞中的炎症和细胞凋亡。在LPS诱导的细胞毒性之前用ADM治疗LEYDIG细胞。我们确定了ROS,MDA,GSH,LDH和睾酮和MMP的浓度。获得IL-1,IL-6,InOS和COX-2的mRNA水平,测定IL-1,IL-6,NO和PGE2的浓度。调节细胞凋亡并通过TUNEL和DNA碎片检测进行评估。测定mRNA和蛋白质的水平,用于Bcl-2,Bax,Caspase-3和PARP。测量总和P-AKT的蛋白质含量。 ADM预处理明显升高了MMP和睾酮浓度,降低了ROS,MDA,GSH和LDH的水平。 ADM预处理显着降低IL-1,IL-6,InOS和COX-2的mRNA水平以及IL-1,IL-6,NO和PGE2的浓度。通过ADM预处理显着降低了LPS诱导的TUNEL阳性LEYDIG细胞,通过降低的DNA碎裂进一步证实了结果。 ADM预处理通过显着促进Bcl-2和抑制Bax,Caspase-3和PARP表达来降低细胞凋亡。通过ADM预处理显着抑制了降低P-AKT水平的LPS活性。 ADM保护大鼠LEYDIG细胞来自LPS诱导的炎症和凋亡,这可能与PI3K / AKT线粒体信号通路相关。

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  • 来源
    《Mediators of inflammation》 |2016年第3期|共16页
  • 作者单位

    Wuhan Univ Renmin Hosp Dept Orthoped 238 Liberat Rd Wuhan 430060 Hubei Peoples R China;

    Wuhan Univ Renmin Hosp Dept Urol 238 Liberat Rd Wuhan 430060 Hubei Peoples R China;

    Wuhan Univ Renmin Hosp Dept Urol 238 Liberat Rd Wuhan 430060 Hubei Peoples R China;

    Wuhan Univ Renmin Hosp Dept Urol 238 Liberat Rd Wuhan 430060 Hubei Peoples R China;

    Wuhan Univ Renmin Hosp Dept Urol 238 Liberat Rd Wuhan 430060 Hubei Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 病理学;
  • 关键词

  • 入库时间 2022-08-20 03:50:58

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