Wright David W, Ritchie James C, Mullins Richard E, Kellermann Arthur L, Denson Donald D
Department of Emergency Medicine, Emory University School of Medicine, Emergency Medicine Research Center, 49 Jessie Hill Jr Drive, Atlanta, GA 30303, USA.
J Clin Pharmacol. 2005 Jun;45(6):640-8. doi: 10.1177/0091270005276201.
Progesterone (PG) has been shown to provide substantial neuroprotection after traumatic brain injury (TBI) in multiple animal models. As a first step in assessing applicability to humans, the authors examined the effects of acute TBI and extracranial trauma on the pharmacokinetics of PG given by intravenous infusion. Multiple blood samples were obtained from 11 female and 21 male trauma patients receiving PG and 1 female and 3 male patients receiving placebo infusions for 72 hours. Values for C(SS), CL, t(1/2), and Vd were obtained using AUC((0-72)) and postinfusion blood samples. C(SS) values were 337 +/- 135 ng/mL, which were significantly lower than the target concentration of 450 +/- 100 ng/mL. The lower C(SS) is attributed to the CL, which was higher than anticipated. In addition, t(1/2) was longer and V(d) was higher than anticipated. These results demonstrate that stable PG concentrations can be rapidly achieved following TBI.
在多个动物模型中,已证实孕酮(PG)在创伤性脑损伤(TBI)后可提供显著的神经保护作用。作为评估其对人类适用性的第一步,作者研究了急性TBI和颅外创伤对静脉输注PG的药代动力学的影响。从11名接受PG输注的女性和21名接受PG输注的男性创伤患者以及1名接受安慰剂输注的女性和3名接受安慰剂输注的男性患者中采集了多个血样,持续72小时。使用AUC((0 - 72))和输注后血样获得C(SS)、CL、t(1/2)和Vd值。C(SS)值为337±135 ng/mL,显著低于450±100 ng/mL的目标浓度。较低的C(SS)归因于CL,其高于预期。此外,t(1/2)较长,V(d)高于预期。这些结果表明,TBI后可迅速达到稳定的PG浓度。