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16,16-二甲基前列腺素E2在未受照射和受照射小鼠以及未受照射的非人类灵长类动物中的药代动力学和生物分布

Pharmacokinetics and Biodistribution of 16,16 dimethyl Prostaglandin E2 in Non-Irradiated and Irradiated Mice and Non-Irradiated Non-Human Primates.

作者信息

Langevin Brooke, Singh Pratibha, Plett P Artur, Sampson Carol H, Masters Andi, Gibbs Allison, Faria Eduardo De, Triesler Sarah, Zodda Andrew, Jackson Isabel L, Orschell Christie M, Gopalakrishnan Mathangi, Pelus Louis M

机构信息

Center for Translational Medicine, University of Maryland School of Pharmacy, Baltimore, Maryland 21201.

Department of Medicine, Division of Hematology/Oncology, Indiana University School of Medicine, Indianapolis, Indiana 46202.

出版信息

Radiat Res. 2024 Jan 1;201(1):7-18. doi: 10.1667/RADE-23-00040.1.

Abstract

Exposure to high-dose ionizing radiation can lead to life-threatening injuries and mortality. Bone marrow is the most sensitive organ to radiation damage, resulting in the hematopoietic acute radiation syndrome (H-ARS) with the potential sequelae of infection, hemorrhage, anemia, and death if untreated. The development of medical countermeasures (MCMs) to protect or mitigate radiation injury is a medical necessity. In our well-established murine model of H-ARS we have demonstrated that the prostaglandin E2 (PGE2) analog 16,16 dimethyl-PGE2 (dmPGE2) has survival efficacy as both a radioprotectant and radiomitigator. The purpose of this study was to investigate the pharmacokinetics (PK) and biodistribution of dmPGE2 when used as a radioprotector in irradiated and non-irradiated inbred C57BL/6J mice, PK in irradiated and non-irradiated Jackson Diversity Outbred (JDO) mice, and the PK profile of dmPGE2 in non-irradiated non-human primates (NHPs). The C57BL/6J and JDO mice each received a single subcutaneous (SC) dose of 35 ug of dmPGE2 and were randomized to either receive radiation 30 min later or remain non-irradiated. Plasma and tissue PK profiles were established. The NHP were dosed with 0.1 mg/kg by SC administration and the PK profile in plasma was established. The concentration time profiles were analyzed by standard non-compartmental analysis and the metrics of AUC0-Inf, AUC60-480 (AUC from 60-480 min), Cmax, and t1/2 were evaluated. AUC60-480 represents the postirradiation time frame and was used to assess radiation effect. Overall, AUC0-Inf, Cmax, and t1/2 were numerically similar between strains (C57BL/6J and JDO) when combined, regardless of exposure status (AUC0-Inf: 112.50 ng·h/ml and 114.48 ng·h/ml, Cmax: 44.53 ng/ml and 63.96 ng/ml; t1/2: 1.8 h and 1.1 h, respectively). PK metrics were numerically lower in irradiated C57BL/6J mice than in non-irradiated mice [irradiation ratio: irradiated values/non-irradiated values = 0.71 for AUC60-480 (i.e., 29% lower), and 0.6 for t1/2]. In JDO mice, the radiation ratio was 0.53 for AUC60-480 (i.e., 47% lower), and 1.7 h for t1/2. The AUC0-Inf, Cmax, and t1/2 of the NHPs were 29.20 ng·h/ml, 7.68 ng/ml, and 3.26 h, respectively. Despite the numerical differences seen between irradiated and non-irradiated groups in PK parameters, the effect of radiation on PK can be considered minimal based on current data. The biodistribution in C57BL/6J mice showed that dmPGE2 per gram of tissue was highest in the lungs, regardless of exposure status. The radiation ratio for the different tissue AUC60-480 in C57BL/6J mice ranged between 0.5-1.1 (50% lower to 10% higher). Spleen, liver and bone marrow showed close to twice lower exposures after irradiation, whereas heart had a 10% higher exposure. Based on the clearance values from mice and NHP, the estimated allometric scaling coefficient was 0.81 (95% CI: 0.75, 0.86). While slightly higher than the current literature estimates of 0.75, this scaling coefficient can be considered a reasonable estimate and can be used to scale dmPGE2 dosing from animals to humans for future trials.

摘要

暴露于高剂量电离辐射可导致危及生命的损伤和死亡。骨髓是对辐射损伤最敏感的器官,会引发造血急性放射综合征(H-ARS),若不治疗,可能会出现感染、出血、贫血等后遗症并导致死亡。研发用于保护或减轻辐射损伤的医学对策(MCMs)是医学上的必要需求。在我们成熟的H-ARS小鼠模型中,我们已证明前列腺素E2(PGE2)类似物16,16-二甲基-PGE2(dmPGE2)作为辐射防护剂和辐射缓解剂均具有生存疗效。本研究的目的是调查dmPGE2在受辐照和未受辐照的近交系C57BL/6J小鼠中用作辐射防护剂时的药代动力学(PK)和生物分布,在受辐照和未受辐照的杰克逊多样性远交(JDO)小鼠中的PK,以及dmPGE2在未受辐照的非人灵长类动物(NHP)中的PK概况。C57BL/6J和JDO小鼠均接受35μg dmPGE2的单次皮下(SC)给药,并随机分为两组,一组在30分钟后接受辐射,另一组保持未受辐照状态。建立了血浆和组织PK概况。NHP通过SC给药,剂量为0.1mg/kg,并建立了血浆中的PK概况。通过标准的非房室分析对浓度-时间曲线进行分析,并评估AUC0-Inf、AUC60-480(60至480分钟的AUC)、Cmax和t1/2等指标。AUC60-480代表辐照后的时间范围,用于评估辐射效应。总体而言,合并时,各品系(C57BL/6J和JDO)之间的AUC0-Inf、Cmax和t1/2在数值上相似,无论暴露状态如何(AUC0-Inf:分别为112.50ng·h/ml和114.至480分钟的AUC)、Cmax和t1/2在数值上相似,无论暴露状态如何(AUC0-Inf:分别为112.50ng·h/ml和114.48ng·h/ml,Cmax:分别为44.53ng/ml和63.96ng/ml;t1/2:分别为1.8小时和1.1小时)。受辐照的C57BL/6J小鼠的PK指标在数值上低于未受辐照的小鼠[辐照比:辐照值/未辐照值 = AUC60-480为0.71(即低29%),t1/2为0.6]。在JDO小鼠中,AUC60-480的辐照比为0.53(即低47%),t1/2为1.7小时。NHP的AUC0-Inf、Cmax和t1/2分别为29.20ng·h/ml、7.68ng/ml和3.26小时。尽管在PK参数方面,辐照组和未辐照组之间存在数值差异,但根据目前的数据,辐射对PK的影响可被视为最小。C57BL/6J小鼠的生物分布表明,无论暴露状态如何,每克组织中dmPGE2含量在肺中最高。C57BL/6J小鼠不同组织AUC60-480的辐照比在0.5至1.1之间(低50%至高10%)。脾脏、肝脏和骨髓在辐照后的暴露量接近低两倍,而心脏的暴露量高10%。根据小鼠和NHP的清除值,估计的异速生长比例系数为0.81(95%CI:0.75,0.86)。虽然略高于当前文献估计的0.75,但该比例系数可被视为合理估计,可用于将dmPGE2的给药剂量从动物换算到人类,用于未来的试验。

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