Jones S B, Kotsonis P, Majewski H
Department of Pharmacology, University of Melbourne, Parkville, Victoria, Australia.
Shock. 1994 Nov;2(5):370-5. doi: 10.1097/00024382-199411000-00012.
The study was designed to investigate the effects of endotoxin administration on norepinephrine release in vivo in the rat. The norepinephrine release rate was calculated from the steady-state concentration of endogenous norepinephrine and [3H]norepinephrine in the central venous pool after infusion of [3H]norepinephrine intra-arterially. This method corrects for both metabolism and disposition as the infused tracer closely follows the normal pathway of neuronally released norepinephrine. Measurements were made in anesthetized intact rats as well as in pithed rats with electrically stimulated sympathetic outflow (3 Hz). Comparisons were made before and for 60 min following administration of bacterial endotoxin (10 mg/kg intravenously) or an equal volume of saline (vehicle). Plasma levels of norepinephrine and epinephrine increased significantly in both anesthetized and pithed preparations after endotoxin, whereas plasma norepinephrine clearance decreased only in anesthetized rats. Norepinephrine release rates were significantly increased in anesthetized as well as in pithed rat preparations after endotoxin. Plasma epinephrine was elevated more in pithed than anesthetized rats. The blood pressure fall was more rapid in pithed compared to anesthetized rats following endotoxin, which probably indicates that the central nervous system is able to compensate to some extent for the blood pressure fall in the anesthetized rat. Heart rate was unchanged in both preparations following endotoxin. Significant increases in norepinephrine release rates induced by bacterial endotoxin in pithed rats with constant frequency sympathetic nerve stimulation suggests that some factor in endotoxicosis enhances the release of norepinephrine by an action at peripheral nerve terminals.
本研究旨在探讨内毒素给药对大鼠体内去甲肾上腺素释放的影响。去甲肾上腺素释放率是根据动脉内注入[³H]去甲肾上腺素后,中心静脉池中内源性去甲肾上腺素和[³H]去甲肾上腺素的稳态浓度计算得出的。由于注入的示踪剂紧密遵循神经元释放的去甲肾上腺素的正常途径,该方法校正了代谢和处置过程。在麻醉的完整大鼠以及交感神经传出经电刺激(3Hz)的脊髓毁损大鼠中进行测量。在静脉注射细菌内毒素(10mg/kg)或等体积生理盐水(赋形剂)之前及之后60分钟进行比较。内毒素给药后,麻醉和脊髓毁损的大鼠制剂中去甲肾上腺素和肾上腺素的血浆水平均显著升高,而仅在麻醉大鼠中血浆去甲肾上腺素清除率降低。内毒素给药后,麻醉和脊髓毁损的大鼠制剂中去甲肾上腺素释放率均显著增加。脊髓毁损大鼠的血浆肾上腺素升高幅度大于麻醉大鼠。与麻醉大鼠相比,脊髓毁损大鼠在内毒素给药后血压下降更快,这可能表明中枢神经系统能够在一定程度上补偿麻醉大鼠的血压下降。内毒素给药后,两种制剂中的心率均无变化。在交感神经持续频率刺激的脊髓毁损大鼠中,细菌内毒素诱导的去甲肾上腺素释放率显著增加,这表明内毒素血症中的某些因素通过作用于外周神经末梢来增强去甲肾上腺素的释放。