Brady Sally, York Malcolm, Scudamore Cheryl, Williams Thomas, Griffiths William, Turton John
Centre for Toxicology, Department of Pharmacology, School of Pharmacy, University of London.
Toxicol Pathol. 2010 Feb;38(2):287-91. doi: 10.1177/0192623309357948. Epub 2010 Jan 25.
The current studies demonstrate the effect of low-dose intraperitoneal (IP) administration of isoprotenerol (ISO) and subcutaneous (SC) versus IP routes of administration of ISO on serum cardiac troponin I (cTnI) levels in female Hanover Wistar rats, providing additional evidence to support acceptance of cTnI as a cardiac biomarker. At 2 hr postdosing with 0-500 microg/kg ISO, mean serum cTnI levels were increased in a dose-related fashion at > or =10 microg/kg with no evidence of cardiac pathology. At 24 h, cTnI concentrations were generally at control levels, but histologic cardiomyocyte injury was evident in a proportion of the animals given > or =10 microg/kg. In a second experiment, rats given SC ISO at 5,000 microg/kg and necropsied at 0, 1, 2, and 4 hr postdosing had higher levels of serum cTnI than animals given the same dose IP.
目前的研究表明,低剂量腹腔注射异丙肾上腺素(ISO)以及皮下注射(SC)与腹腔注射ISO相比,对雌性汉诺威Wistar大鼠血清心肌肌钙蛋白I(cTnI)水平的影响,为支持将cTnI作为心脏生物标志物提供了额外证据。在给予0 - 500微克/千克ISO给药后2小时,当剂量≥10微克/千克时,平均血清cTnI水平呈剂量相关增加,且无心脏病理学证据。在24小时时,cTnI浓度通常处于对照水平,但在给予剂量≥10微克/千克的部分动物中,组织学上心肌细胞损伤明显。在第二个实验中,给予5000微克/千克皮下注射ISO并在给药后0、1、2和4小时进行尸检的大鼠,其血清cTnI水平高于给予相同剂量腹腔注射的动物。