Chakraborty Abhijit, Yeung Sally, Pyszczynski Nancy A, Jusko William J
Department of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, State University of New York at Buffalo, 565 Hochstetter Hall, Buffalo, New York 14260, USA.
J Pharm Sci. 2005 Mar;94(3):590-603. doi: 10.1002/jps.20257.
The pharmacodynamic interactions between recombinant mouse interleukin-10 (IL-10) and prednisolone were examined in lipopolysaccharide (LPS)-induced experimental endotoxemia in Balb/c mice. Treatment phases consists of single doses of IL-10 (10 microg/kg i.p.), prednisolone (25 (mg/kg i.p.), IL-10 (2.5 microg/kg i.p.) with prednisolone (6.25 mg/kg i.p.), or placebo (saline). Measurements included plasma steroid kinetics and IL-10 concentrations and responses to LPS including proinflammatory cytokines (TNF-alpha, IFN-gamma) and circulatory NO measured as plasma nitrate/nitrite concentrations. The intraperitoneal dosing of LPS produced large and transient elevations of plasma TNF-alpha, IFN-gamma, and NO concentrations. Noncompartmental and model fitting using extended indirect response models based on drug inhibition of multiphase stimulation of biomarkers by LPS were used to describe the in vivo pharmacodynamics and drug interactions. Dosing with prednisolone, IL-10, or their combinations produced strong inhibition of cytokine and NO production. The IC50 values of prednisolone ranged from 54 to 171 ng/mL, and IC50 values for IL-10 ranged from 0.06 to 0.69 ng/mL. The production of NO was described as a cascading consequence of the TNF-alpha and IFN-gamma plasma concentrations. The joint dosing of IL-10 with prednisolone produces moderately synergistic immunosuppressive effects in this system. Both drugs were sufficiently protective in suppressing the inflammatory mediators when administered prior to the LPS trigger, while such effects were modest when administered after the inflammatory stimulus was provoked. The integrated and complex pharmacokinetic/pharmacodynamic models well capture the in vivo processes, drug potencies, and interactions of IL-10 and prednisolone.
在脂多糖(LPS)诱导的Balb/c小鼠实验性内毒素血症中,研究了重组小鼠白细胞介素-10(IL-10)与泼尼松龙之间的药效学相互作用。治疗阶段包括单剂量的IL-10(10微克/千克腹腔注射)、泼尼松龙(25毫克/千克腹腔注射)、IL-10(2.5微克/千克腹腔注射)与泼尼松龙(6.25毫克/千克腹腔注射),或安慰剂(生理盐水)。测量指标包括血浆类固醇动力学、IL-10浓度以及对LPS的反应,包括促炎细胞因子(TNF-α、IFN-γ)和作为血浆硝酸盐/亚硝酸盐浓度测量的循环一氧化氮。腹腔注射LPS导致血浆TNF-α、IFN-γ和NO浓度大幅且短暂升高。使用基于LPS对生物标志物多相刺激的药物抑制作用的扩展间接反应模型进行非房室和模型拟合,以描述体内药效学和药物相互作用。给予泼尼松龙、IL-10或其组合可强烈抑制细胞因子和NO的产生。泼尼松龙的IC50值范围为54至171纳克/毫升,IL-10的IC50值范围为0.06至0.69纳克/毫升。NO的产生被描述为TNF-α和IFN-γ血浆浓度的级联结果。在该系统中,IL-10与泼尼松龙联合给药产生适度的协同免疫抑制作用。在LPS触发之前给药时,两种药物在抑制炎症介质方面都具有足够的保护作用,而在炎症刺激引发后给药时,这种作用则较为适度。整合的复杂药代动力学/药效学模型很好地捕捉了IL-10和泼尼松龙的体内过程、药物效力和相互作用。