首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Inhibition of tumour necrosis factor and reversal of endotoxin-induced shock by U-83836E a second generation lazaroid in rats
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Inhibition of tumour necrosis factor and reversal of endotoxin-induced shock by U-83836E a second generation lazaroid in rats

机译:U-83836E(一种第二代的lazaroid)在大鼠中抑制肿瘤坏死因子并逆转内毒素诱发的休克

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摘要

class="enumerated" style="list-style-type:decimal">Antioxidants can exert protective effects in endotoxic shock by either a reduction of the oxidant damage or attenuation of Tumour Necrosis Factor (TNF-α) production.Lazaroids are a family of compounds that inhibit lipid peroxidation. Besides, they can also reduce TNF-α. U-83836E is a new lazaroid lacking the glucocorticoid ring.Aim of our study was to investigate the effect of U-83836E on TNF-α production either in vivo or in vitro. Endotoxic shock was produced in male rats by a single intravenous (i.v.) injection of 20 mg kg−1 of S. enteritidis lipopolysaccharide (LPS). LPS administration reduced survival rate (0% survival, 72 h after endotoxin administration), decreased mean arterial blood pressure, increased serum and macrophage TNF-α and enhanced plasma malonylaldehyde (MAL) levels. Furthermore aortic rings from shocked rats showed a marked hyporeactivity to phenylephrine (PE 1 nM–10 μM).Treatment with U-83836E (7.5, 15 and 30 mg kg−1, i.v.) 5 min after endotoxin challenge significantly protected against LPS induced lethality (90% survival rate and 80% survival rate 24 h and 72 h after LPS injection respectively, following the highest dose of the drug), reduced hypotension, blunted plasma MAL, decreased serum and macrophage TNF-α and restored the hyporeactivity of aortic rings to control values. In vitro LPS stimulation (50 μg ml−1 for 4 h) significantly increased cytokine production in macrophages (MΦ) harvested from untreated normal rats. Pretreatment with pertussis toxin (PT; 0.1, 1 and 10 ng ml−1 4 h before LPS) significantly increased TNF-α production. PT effects on these LPS responses were correlated with a PT mediated ADP ribosylation of a 41 kDa protein. U-83836E (50 μM) reduced, in a dose dependent manner, LPS induced TNF-α production and inhibited the PT effects on cytokine production and on ADP ribosylation of the protein.Our data suggest that lazaroids may affect the early events associated with LPS receptor mediated activation of a G protein in LPS induced TNF-α production. These molecular events may explain, at least in part, the in vivo inhibition of cytokine production and reversal of endotoxic shock.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 抗氧化剂可以通过减少氧化剂的损害或减轻肿瘤坏死因子(TNF-α)的产生而对内毒素性休克发挥保护作用。 类胡萝卜素是抑制脂质过氧化的一类化合物。此外,它们还可以降低TNF-α。 U-83836E是一种新的缺乏糖皮质激素环的类风疹。 我们的研究目的是研究U-83836E对体内或体外TNF-α产生的影响。雄性大鼠通过一次静脉内(i.v.)注射20μmgkg -1 肠炎沙门氏菌脂多糖(LPS)产生内毒素性休克。 LPS的给药降低了生存率(内毒素给药72h后存活率为0%),平均动脉血压降低,血清和巨噬细胞TNF-α升高,血浆丙二醛(MAL)水平升高。此外,休克大鼠的主动脉环对苯肾上腺素(PE 1 nM–10 M)表现出明显的低反应性。 用U-83836E(7.5、15和30 mg kg -1 )治疗,iv)内毒素攻击后5分钟显着保护LPS诱导的致死性(最高剂量的LPS注射后24小时和72小时,分别为90%的存活率和80%的存活率),低血压降低,血浆MAL降低,降低血清和巨噬细胞TNF-α并恢复主动脉环对控制值的反应不足。体外LPS刺激(50μg/ ml −1 4 h)显着增加了未经治疗的正常大鼠收获的巨噬细胞(MΦ)中细胞因子的产生。百日咳毒素(LP; LPS前4µh分别以0.1、1和10μngml -1 -1 预处理)可显着增加TNF-α的产生。 PT对这些LPS反应的影响与PT介导的41 kDa蛋白的ADP核糖基化有关。 U-83836E(50μm)以剂量依赖性方式降低LPS诱导的TNF-α产生,并抑制PT对细胞因子产生和蛋白的ADP核糖基化的作用。 我们的数据表明,拟南芥可能影响LPS诱导的TNF-α产生中与LPS受体介导的G蛋白活化相关的早期事件。这些分子事件至少可以部分解释体内抑制细胞因子的产生和内毒素休克的逆转。

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