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Development and Characterization of a Model for Inducing Fetal Hemoglobin Production in Cynomolgus Macaques (Macaca fasicularis)

机译:诱导胎儿血红蛋白生成的模型的开发与表征在鱼蟹猕猴(Macaca Fasicularis)中诱导胎儿血红蛋白

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Hydroxyurea induces production of fetal hemoglobin (HbF), a tetramer of a and y globin proteins and corresponding heme molecules, normally found in less than 1% of adult RBC. Increases in circulating HbF are correlated with clinical improvement of patients with hemoglobinopathies, and hydroxyurea, as a daily medication, is the standard treatment for sickle cell anemia. Although olive baboons (Papio anubis) are considered a key model species for HbF induction, cynomolgus macaques (Macaca fasicularis) are another species that conserves the ability to produce HbF into maturity. In this study, moderate anemia was experimentally induced in cynomolgus macaques by phlebotomy, to stimulate accelerated erythropoiesis and HbF production. In contrast to previous studies, vascular access ports were implanted for phlebotomy of conscious monkeys, followed by fluid replacement. As total Hgb levels dropped, reticulocyte counts and the percentage of HbF-expressing cells increased. Once total Hgb levels declined to less than 8 g/dL, 2 courses of oral hydroxyurea (once daily for 5 d) were completed, with a 9-d interval between courses. After hydroxyurea dosing, the percentage of HbF-expressing cells and total HbF were increased significantly. In addition, a significant but transient decrease in reticulocyte count and a transient increase in MCV occurred, replicating the characteristic response of patients receiving hydroxyurea. Daily clinical observations revealed no serious health issues or decreases in food consumption or activity levels. Methods were established for assessing the patency of vascular access ports. This study details a new protocol for the safe and routine induction of moderate anemia in cynomolgus macaques and validates its use in the investigation of novel pharmacologic entities to induce the production of HbF.
机译:羟基脲诱导胎儿血红蛋白(HBF)的产生,A和Y珠蛋白的四聚体和相应的血红素分子,通常在不到1%的成年RBC中发现。循环HBF的增加与血吸虫病患者的临床改善相关,羟基脲作为日常药物,是镰状细胞贫血的标准治疗。虽然橄榄狒狒(Papio Anubis)被认为是HBF诱导的关键模型物种,但食蟹猴(Macaca Fasicularis)是另一个物种,从而节省了生产HBF的能力。在这项研究中,通过静脉切开术,在Cynomolgus Macaques实验诱导中度贫血,以刺激加速的促红细胞生成和HBF产生。与先前的研究相比,植入血管进入口植入了意识猴的静脉切开,然后液体更换。作为总HGB水平掉落,网状细胞计数和表达HBF的细胞的百分比增加。一旦总HGB水平下降至少于8克/平方米,完成了2种口腔羟基脲(每日5 d一次),课程之间的9-D间隔。在羟基脲给液后,表达HBF的细胞和总HBF的百分比显着增加。此外,出现了网状细胞计数的显着但瞬态的减少和MCV的瞬态增加,复制接受羟基脲的患者的特征响应。每日临床观察显示粮食消费或活动水平没有严重的健康问题或减少。建立了评估血管进入端口的通畅的方法。本研究详细介绍了一种新的Cynomolgus Macaques中适度贫血的安全和常规诱导的新方案,并验证其在新型药理学实体调查中诱导HBF的生产。

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