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首页> 外文期刊>BMC Microbiology >Chronic dexamethasone exposure retards growth without altering the digestive tract microbiota composition in goats
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Chronic dexamethasone exposure retards growth without altering the digestive tract microbiota composition in goats

机译:慢性地塞米松暴露可延迟生长,而不会改变山羊消化道微生物群的组成

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Dexamethasone (Dex), an artificially synthetic cortisol substitute, is commonly used as an anti-inflammatory drug, and is also employed to mimic the stress state experimentally. It is well known that chronic stress disturbs the gut microbiota community and digestive functions. However, no relevant studies have been conducted in ruminants. In this study, a low dosage of Dex (0.2 mg/kg body weight, Dex group, n = 5) was consecutively injected intramuscularly for 21 days to simulate chronic stress in growing goats. Goats were injected with saline (0.2 mg/kg body weight) as the control group (Con, n = 5). Dex-treated goats showed a higher number of white blood cells and blood glucose levels (p  0.01), but lower dry matter intake (DMI) and body weight (p  0.01) than those of saline-injected goats. Plasma cortisol concentration decreased significantly in response to the Dex injection compared to the control (p  0.05). The Dex treatment did not change most ruminal volatile fatty acid (VFAs) concentrations before the morning feeding after 1–21 days of treatment (p  0.05); however, ruminal VFA concentrations decreased dramatically 2, 4, 6, and 8 h after the morning feeding on day 21 of the Dex injections. In this study, chronic Dex exposure did not alter the community structure of microbes or methanogenes in the rumen, caecum, or colonic digesta. Only Prevotella increased on days 7 and 14 of Dex treatment, but decreased on day 21, and Methanosphaera was the only genus of methanogene that decreased. Our results suggest that chronic Dex exposure retards growth by decreasing DMI, which may be mediated by higher levels of blood glucose and lower ruminal VFA production. Microbiota in the digestive tract was highly resistant to chronic Dex exposure.
机译:地塞米松(Dex)是一种人工合成的皮质醇替代品,通常用作抗炎药,并且还可以用来模拟实验中的应激状态。众所周知,慢性压力会扰乱肠道菌群和消化功能。但是,反刍动物尚未进行相关研究。在这项研究中,连续21天肌内注射低剂量的Dex(0.2 mg / kg体重,Dex组,n = 5)以模拟正在生长的山羊的慢性应激。山羊注射生理盐水(0.2 mg / kg体重)作为对照组(Con,n = 5)。经Dex处理的山羊的白细胞和血糖水平较高(p 0.05);但是,在Dex注射第21天早上进食后,瘤胃VFA浓度显着下降了2、4、6和8小时。在这项研究中,长期暴露于Dex并没有改变瘤胃,盲肠或结肠消化物中微生物或产甲烷菌的群落结构。在Dex治疗的第7天和第14天,仅普雷沃氏菌增加,但在第21天下降,而甲烷菌是唯一减少的甲烷菌属。我们的结果表明,长期暴露于Dex会通过降低DMI来延缓生长,DMI可能是由较高的血糖水平和较低的瘤胃VFA产生介导的。消化道中的微生物群对慢性Dex暴露具有高度抵抗力。

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