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抗坏血酸的膳食摄入减轻脂多糖诱导的ODS大鼠败血症和脓毒症炎症反应。

Dietary Intake of Ascorbic Acid Attenuates Lipopolysaccharide-Induced Sepsis and Septic Inflammation in ODS Rats.

作者信息

Kawade Noe, Tokuda Yuki, Tsujino Shogo, Aoyama Hiroaki, Kobayashi Misato, Murai Atsushi, Horio Fumihiko

机构信息

Department of Animal Sciences, Graduate School of Bioagricultural Sciences, Nagoya University.

Toxicology Division, Institute of Environmental Toxicology.

出版信息

J Nutr Sci Vitaminol (Tokyo). 2018;64(6):404-411. doi: 10.3177/jnsv.64.404.

Abstract

The aim of this study was to verify the protective effects of ascorbic acid (AsA) against lipopolysaccharide (LPS)-induced sepsis. The study was conducted using osteogenic disorder Shionogi (ODS) rats, which are unable to synthesize AsA. Male ODS rats (6 wk old) were fed either an AsA-free diet (AsA-deficient group), a diet supplemented with 300 mg/kg AsA (control group), or a diet supplemented with 3,000 mg/kg AsA (high-AsA group) for 8 d. On day 8, all the rats were intraperitoneally injected with LPS (15 mg/kg body weight). Forty-eight hours after the injection, the survival rates of the rats in the control (39%) and the high-AsA (61%) groups were significantly higher than that in the AsA-deficient group (5.5%). Next, we measured several inflammatory parameters during 10 h after administering LPS. At 6 h, elevated serum levels of markers for hepatic and systemic injuries were suppressed in rats fed AsA. Similarly, 10 h after LPS injection, the elevation in the serum levels of markers for renal injury were also suppressed proportionally to the amount of AsA in the diet. The elevated serum concentrations of TNFα and IL-1β by LPS in the AsA-deficient group decreased in groups fed AsA. Hematic TNFα mRNA levels at 6 h after the LPS injection were also lowered by feeding AsA. These results demonstrated that the dietary intake of AsA improved the survival rates and suppressed the inflammatory damage, in a dose-dependent manner, caused during sepsis induced by LPS in ODS rats.

摘要

本研究的目的是验证抗坏血酸(AsA)对脂多糖(LPS)诱导的败血症的保护作用。该研究使用了无法合成AsA的成骨障碍史氏(ODS)大鼠。雄性ODS大鼠(6周龄)分别喂食无AsA饮食(AsA缺乏组)、添加300 mg/kg AsA的饮食(对照组)或添加3000 mg/kg AsA的饮食(高AsA组),持续8天。在第8天,所有大鼠腹腔注射LPS(15 mg/kg体重)。注射后48小时,对照组(39%)和高AsA组(61%)大鼠的存活率显著高于AsA缺乏组(5.5%)。接下来,我们在给予LPS后的10小时内测量了几个炎症参数。在6小时时,喂食AsA的大鼠血清中肝脏和全身损伤标志物水平的升高受到抑制。同样,在LPS注射后10小时,血清中肾损伤标志物水平的升高也与饮食中AsA的量成比例地受到抑制。AsA缺乏组中LPS引起的血清TNFα和IL-1β浓度升高在喂食AsA的组中降低。LPS注射后6小时的血液TNFα mRNA水平也因喂食AsA而降低。这些结果表明,饮食摄入AsA以剂量依赖的方式提高了存活率,并抑制了ODS大鼠LPS诱导的败血症期间引起的炎症损伤。

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