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Melatonin Ameliorates Inflammation and Oxidative Stress by Suppressing the p38MAPK Signaling Pathway in LPS-Induced Sheep Orchitis

机译:褪黑素通过抑制LPS诱导的绵羊睾丸炎中的P38MAPK信号通路来改善炎症和氧化应激

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摘要

Gram-negative bacterial infections of the testis can lead to infectious orchitis, which negatively influences steroid hormone synthesis and spermatogenesis. Lipopolysaccharide (LPS), a major component of the Gram-negative bacterial cell wall, acts via toll like receptors 4 (TLR4) to trigger innate immune responses and activate nuclear factor kappa B signaling. The protective mechanisms of melatonin on LPS-induced infectious orchitis have not been reported. Herein, we developed an LPS-induced sheep infectious orchitis model. In this model, the phagocytic activity of testicular macrophages (TM) was enhanced after melatonin treatment. Moreover, we found that melatonin suppressed secretion of TM pro-inflammatory factors by suppressing the p38MAPK pathway and promoting Leydig cell testosterone secretion. Expressions of GTP cyclohydrolase-I and NADPH oxidase-2 were reduced by melatonin while heme oxygenase-1 expression was up-regulated. Thus, melatonin reduced the severity of LPS-induced orchitis by stimulating antioxidant activity. The results of this study provide a reference for the treatment of acute infectious orchitis.
机译:睾丸的革兰氏阴性细菌感染可以导致传染性睾丸炎,这对类固醇激素合成和精子发生负面影响。脂多糖(LPS)是革兰氏阴性细菌细胞壁的主要成分,通过损伤等受体4(TLR4)起作用以引发先天性免疫应答并激活核因子Kappa B信号。尚未报道褪黑激素对LPS诱导的感染睾丸炎的保护机制。在此,我们开发了一种LPS诱导的绵羊感染睾丸炎。在该模型中,在褪黑激素处理后提高了睾丸巨噬细胞(TM)的吞噬活性。此外,我们发现褪黑素通过抑制P38MAPK途径和促进Leydig细胞睾酮分泌来抑制TM促炎因子的分泌。通过褪黑激素减少了GTP环丙酶-1和NADPH氧化酶-2的表达,同时升调血红素氧合酶-1表达。因此,褪黑激素通过刺激抗氧化活性降低了LPS诱导的睾丸炎的严重程度。该研究的结果为治疗急性传染性睾丸炎提供了参考。

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