乙醇喂养大鼠呼吸中氢和甲烷的变化。

Naoyuki Kawagoe, Sho Kijma, Hideki Tanaka, Ikutaka Takemoto, Kenji Suzuki, Takahiro Saito, Fumiya Komatsu, Atsushi Yamada, Eri Kumade, Yosuke Sasaki, Tadashi Maeda, Hidenori Kido, Takamasa Ishii, Toshiyasu Watanabe, Taito Miyazaki, Nazuo Hike, Hiroaki Zai, Yoshihisa Urita, Hitoshi Nakajima, Kazuho Arai, Tsunehiko Imai
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引用次数: 0

摘要

长期饮酒可引起生态失调,但很难确定酒精对胃肠道微生物群结构和活性的影响。因此,我们设计了一种无创氢呼吸试验(HBT)来研究乙醇喂养大鼠肠道微生物群化学特征的变化。13只F344/DuCri大鼠从4周龄开始饲喂含16%乙醇溶液的商业糊化食品。6只8周龄乙醇喂养大鼠和7只24周龄乙醇喂养大鼠进行了HBTs。作为对照,对16只8周龄雄性大鼠、6只24周龄雄性大鼠和5只48周龄雄性大鼠进行HBTs。6只24周龄雄性大鼠每隔1周检查2次。禁食24小时后进行HBTs。大鼠口服4 mL/kg 65%乳果糖溶液,饲养于动物笼中。呼气采样袋中每隔10分钟收集一次过期空气,持续180分钟。呼气分析仪测量呼气样本中的氢(H2)和甲烷(CH4)水平并进行表达。以百万分之一(ppm)表示。H2和CH4水平升高在雄性大鼠中更为常见。H2和CH4的最大值以8周龄大鼠最高,其次是48周龄和24周龄大鼠。与对照组不同,在口服乳果糖后180分钟内,没有喂食乙醇的大鼠呼出超过2ppm的H2或CH4。这种变化比衰老和性别分化更为明显。我们得出结论,慢性乙醇消耗与H2和CH4的产生密切相关。无症状的重度饮酒者可能有生态失调,包括肠道微生物群发酵性能较低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alteration of Breath Hydrogen and Methane in Ethanol-Fed Rats.

Chronic alcohol consumption can cause dysbiosis, but it is difficult to determine the effect of alcohol on the structure and activity of gastrointestinal tract microbiota. We therefore designed a noninvasive hydrogen breath test (HBT) to investigate the alteration in the chemical profile of gut microbiota in ethanol-fed rats. Thirteen F344/DuCri rats were fed on a commercial mash food with 16% ethanol solution drinking fluid from 4 weeks of age. HBTs were carried out on six 8-week-old and seven 24-week-old ethanol-fed rats. As controls, HBTs were carried out on sixteen 8-week-old, six 24-week-old, and five 48-week-old male rats. Six 24-week- old male rats were examined twice at 1-week intervals. HBTs were performed after fasting for 24 hr. Rats were orally administrated 4 mL/kg of 65% lactulose solution and housed in an animal chamber. The expired air was collected in a breath-sampling bag at 10-min intervals for 180 min. The hydrogen (H2) and methane (CH4) levels in the breath sample were measured using a breath analyzer and were expressed.as parts- per million (ppm). Elevated H2 and CH4 levels were more frequent in male rats. Maximal values of H2 and CH4 were highest in 8-week- old rats, followed by 48-week-old and 24-week-old rats. No ethanol-fed rat exhaled more than 2 ppm of H2 or CH4 until 180 min after the oral administration of lactulose, unlike the controls. This alteration was more obvious than that of aging or gender differentiation. We conclude that there is a close association between chronic ethanol consumption and H2 and CH4 production. An asymptomatic heavy drinker might have dysbiosis that involves gut microbiota with lower fermentation performance.

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