AstraZeneca, Innovative Medicines, Drug Safety Metabolism, Mereside, Alderley Park, Macclesfield, Cheshire SK10 4TG, United Kingdom.
AstraZeneca, Innovative Medicines, Drug Safety Metabolism, Mereside, Alderley Park, Macclesfield, Cheshire SK10 4TG, United Kingdom.
Regul Toxicol Pharmacol. 2014 Apr;68(3):325-31. doi: 10.1016/j.yrtph.2014.01.001. Epub 2014 Jan 14.
Historically, satellite groups are often used for rodent toxicokinetic profiling because of the haematological consequences of blood sampling. If microsampling is shown to be toxicologically benign, its adoption in rat studies would enable comparison of exposure and toxicity in individual animals (as happens in non-rodent studies) as well as obviating need for satellite groups.
Groups of 10 male (200-300g) and female (150-250g) rats aged 10weeks were vehicle dosed and either left unsampled, conventional blood volume sampled (6×200μL) or microsampled (6×32μL) on Days 1 and 14. At termination on Day 15, clinical pathology plus liver and spleen weights and histopathology were obtained.
All clinical pathology parameters were within background range. However, compared to unsampled controls, conventional volume sampled rats showed a statistically significant (p<0.001) decrease in haemaglobin, haematocrit and red blood cell count, an increase in reticulocytes (at least p<0.01), increased AST and GLDH and, in males only, an increase in monocytes and neutrophils. In contrast, microsampled animals showed no changes except for a slight, toxicologically insignificant decrease in haemoglobin concentration (15.0g/dL compared to the unsampled group mean of 14.4g/dL) in females (p<0.05) and a small increase in monocytes (p<0.05) in males.
Microsampling of adult rats is possible without adverse toxicological consequences.
从历史上看,由于血液采样会导致血液学后果,卫星组通常用于啮齿动物毒代动力学分析。如果微采样被证明在毒理学上是良性的,那么在大鼠研究中采用它将能够比较单个动物的暴露和毒性(就像在非啮齿类动物研究中一样),并避免需要卫星组。
10 只雄性(200-300g)和 10 只雌性(150-250g)10 周龄大鼠分为一组,给予载体处理,在第 1 天和第 14 天分别进行未采样、常规血液量采样(6×200μL)或微采样(6×32μL)。在第 15 天处死时,进行临床病理学检查以及肝脏和脾脏重量和组织病理学检查。
所有临床病理学参数均在背景范围内。然而,与未采样对照相比,常规体积采样大鼠的血红蛋白、红细胞压积和红细胞计数显著下降(p<0.001),网织红细胞增加(至少 p<0.01),AST 和 GLDH 增加,仅雄性大鼠单核细胞和中性粒细胞增加。相比之下,微采样动物除了雌性动物血红蛋白浓度略有下降(15.0g/dL 与未采样组平均值 14.4g/dL 相比,p<0.05)和雄性动物单核细胞略有增加(p<0.05)外,无其他变化。
成年大鼠的微采样是可行的,不会产生不良的毒理学后果。