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首页> 外文期刊>Frontiers in Medicine >Effect of Endotoxemia Induced by Intraperitoneal Injection of Lipopolysaccharide on the Mg isotopic Composition of Biofluids and Tissues in Mice
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Effect of Endotoxemia Induced by Intraperitoneal Injection of Lipopolysaccharide on the Mg isotopic Composition of Biofluids and Tissues in Mice

机译:腹腔内注射脂多糖诱导的内毒素血症对小鼠生物流体和组织Mg同位素组成的影响

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Endotoxemia induced in vivo in mice by intraperitoneal injection of lipopolysaccharide (LPS) leads to (neuro)inflammation and sepsis. Also the homeostasis of mineral elements can be altered through mechanisms that still are poorly understood. The isotopic composition of Mg and the concentrations of the minor elements Ca, K, Mg, Na, P, and S were determined in biological fluids and tissues of young (14–28 weeks) and aged (40–65 weeks) LPS-injected mice and age-matched controls to reveal potential effects of the LPS-induced infection. Blood plasma of young and aged LPS-injected mice showed a heavy Mg isotopic composition, as well as elevated Mg and P concentrations, compared to matched controls. The plasma Mg isotopic composition was correlated with the P concentration in aged mice. Also the liver Mg isotopic composition was strongly affected in the young and aged LPS-injected mice, while for aged mice, an additional effect on the urine Mg isotopic composition was established. These observations were hypothetically associated with liver inflammation and/or hepatotoxicity, and reduced urinary Mg excretion, respectively. Also a regional endotoxin-induced difference was observed in the brain Mg isotopic composition for the aged mice only, and was attributed to potential disruption of the blood-brain barrier.
机译:通过腹膜内注射脂多糖(LPS)在小鼠体内诱导的内毒血症导致(神经)炎症和败血症。此外,矿物元素的稳态也可以通过仍然明白的机制来改变。 Mg的同位素组合物和次要元素Ca,K,Mg,Na,P和S的浓度在杨(14-28周)和老化(40-65周)的生物流体和组织中测定LPS注射小鼠和年龄匹配的对照,以揭示LPS诱导的感染的潜在影响。与匹配的对照相比,年轻和老年LPS注射小鼠的血液血浆表明重镁同位素组合物,以及升高的Mg和P浓度。等离子体Mg同位素组合物与老年小鼠中的P浓度相关。此外,肝脏Mg同位素组合物在年轻和老年的LPS注射的小鼠中受到强烈影响,而对于老年小鼠,建立了对尿Mg同位素组合物的额外作用。这些观察结果与肝脏炎症和/或肝毒性分别麻痹相关,并分别降低尿mg排泄。此外,在脑MG同位素组合物中仅观察到脑部脑损伤的小鼠的区域内毒素诱导的差异,并且归因于血脑屏障的潜在破坏。

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