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内毒素休克期间C3H/HeJ(无反应型)小鼠的碳水化合物代谢

Carbohydrate metabolism in C3H/HeJ (nonresponder) mice during endotoxic shock.

作者信息

McCallum R E, Pontious M L

出版信息

Adv Shock Res. 1979;2:113-27.

PMID:400573
Abstract

This study was undertaken to evaluate the hypoglycemic effects of endotoxin in C3H/HeJ (nonresponder) mice. Endotoxin from Salmonella enteritidis ser Typhimurium strain SR-11 was used and the median lethal dosed (LD50) for random-outbred Swiss-Webster mice and C3H/HeJ mice were 450 microgram and 3,000 microgram, respectively. At intervals after intraperitoneal injection of endotoxin (1 LD50) animals were killed, and blood glucose, liver glucose, and liver glycogen levels were killed, and blood glucose, liver glucose, and liver glycogen levels were measured. The time course of carbohydrate depletion in both strains of mice was almost identical. Little change from controls was noted, however, in nonresponder mice given the LD50 dose for normal responder mice. Passive transfer of plasma from C3H/HeJ mice appeared to protect conventional responder mice from the carbohydrate-depleting effects of endotoxin; whereas, passive transfer of peritoneal cells from C3HeB/FeJ responder mice to nonresponders appeared to sensitize C3H/HeJ mice to this effect. In order to evaluate clearance and detoxification of endotoxin in non-responder mice, 14 C-labeled lipopolysaccharide was prepared from bacteria grown in broth containing D-glucose-14 C(U). Mice were injected intravenously with labeled endotoxin, and blood, liver, spleen, kidney, heart, lung, and brain were counted for radioactivity at intervals after injection. Results from these tracer studies indicate that the clearance of lipopolysaccharide in nonresponder mice is slower than that seen in conventional animals. The results of this study further support the suggestion that endotoxin exerts its effects on carbohydrate metabolism via mediators resulting from endotoxin-cell surface interactions.

摘要

本研究旨在评估内毒素对C3H/HeJ(无反应)小鼠的降血糖作用。使用了肠炎沙门氏菌鼠伤寒血清型SR-11的内毒素,随机远交瑞士韦伯斯特小鼠和C3H/HeJ小鼠的半数致死剂量(LD50)分别为450微克和3000微克。在腹腔注射内毒素(1个LD50)后的不同时间点处死动物,测量血糖、肝糖和肝糖原水平。两种品系小鼠碳水化合物消耗的时间进程几乎相同。然而,给予正常反应小鼠LD50剂量的无反应小鼠与对照组相比变化不大。C3H/HeJ小鼠血浆的被动转移似乎能保护传统反应小鼠免受内毒素的碳水化合物消耗作用;而将C3HeB/FeJ反应小鼠的腹腔细胞被动转移到无反应小鼠似乎会使C3H/HeJ小鼠对这种作用敏感。为了评估无反应小鼠对内毒素的清除和解毒情况,从在含有D-葡萄糖-14C(U)的肉汤中生长的细菌制备了14C标记的脂多糖。给小鼠静脉注射标记的内毒素,在注射后的不同时间点对血液、肝脏、脾脏、肾脏、心脏、肺和大脑进行放射性计数。这些示踪研究的结果表明,无反应小鼠中脂多糖的清除比传统动物慢。本研究结果进一步支持了内毒素通过内毒素-细胞表面相互作用产生的介质对碳水化合物代谢发挥作用的观点。

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