Myers A K, Bader T J
Department of Physiology and Biophysics, Georgetown University Medical Center, Washington, D.C. 20007.
Circ Shock. 1987;23(2):143-50.
Previous studies have shown that platelet activating factor (PAF) is a potentially important mediator of the acute hypotensive response to endotoxin. Direct administration of PAF to rodents induces profound hypotension and hemoconcentration; normal blood pressure recovery requires an intact sympatho-adrenal medullary system. Because adrenal steroids are also important in the physiological response to shock, the present studies were conducted to determine whether treatment of rodents with cortisone or surgical adrenalectomy would alter cardiovascular parameters during recovery from PAF challenge. When rats were pretreated daily for four days with cortisone (25 mg/kg, sc), the hypotensive response to PAF injection (2 micrograms/kg, iv) was significantly blunted (P less than 0.05). In adrenalectomized rats, recovery of blood pressure was significantly delayed (P less than 0.01). Heart rate was not significantly changed in the anesthetized rat preparation used. Pretreatment of mice with cortisone (25 mg/kg/day, sc, 4 days) completely blocked the increased vascular permeability, as measured by a rise in hematocrit induced by PAF (2 micrograms/kg, iv) (P less than 0.001). Adrenalectomized mice had a rise in hematocrit similar to that in sham-operated animals. Lung wet:dry weight ratio after PAF challenge was unaffected by cortisone or adrenalectomy. These results suggest that adrenal cortical glucocorticoids, in addition to adrenal medullary catecholamines, participate in the recovery from the cardiovascular alterations following PAF administration. Further, the efficacy of steroid pretreatment in shock models might involve, in part, the inhibition or reversal of PAF-induced cardiovascular alterations.
先前的研究表明,血小板活化因子(PAF)是对内毒素急性降压反应的一种潜在重要介质。直接给啮齿动物注射PAF会导致严重的低血压和血液浓缩;血压的正常恢复需要完整的交感 - 肾上腺髓质系统。由于肾上腺类固醇在休克的生理反应中也很重要,因此进行了本研究以确定用可的松治疗啮齿动物或手术切除肾上腺是否会改变PAF激发后恢复过程中的心血管参数。当大鼠每天用可的松(25mg/kg,皮下注射)预处理四天时,对PAF注射(2μg/kg,静脉注射)的降压反应明显减弱(P<0.05)。在肾上腺切除的大鼠中,血压恢复明显延迟(P<0.01)。在所使用的麻醉大鼠制剂中,心率没有明显变化。用可的松(25mg/kg/天,皮下注射,4天)预处理小鼠完全阻断了PAF(2μg/kg,静脉注射)诱导的血管通透性增加,这通过血细胞比容升高来衡量(P<0.001)。肾上腺切除的小鼠血细胞比容升高与假手术动物相似。PAF激发后的肺湿重与干重之比不受可的松或肾上腺切除术的影响。这些结果表明,除了肾上腺髓质儿茶酚胺外,肾上腺皮质糖皮质激素也参与了PAF给药后心血管改变的恢复。此外,类固醇预处理在休克模型中的疗效可能部分涉及抑制或逆转PAF诱导的心血管改变。