RAT MODEL OF ARTERIAL THROMBOSIS INDUCED BY FERRIC-CHLORIDE

被引:374
作者
KURZ, KD [1 ]
MAIN, BW [1 ]
SANDUSKY, GE [1 ]
机构
[1] ELI LILLY INT CORP,LILLY RES LAB,DEPT MORPHOL PATHOL,INDIANAPOLIS,IN 46285
关键词
arterial thrombosis; ferric chloride; rat;
D O I
10.1016/0049-3848(90)90106-M
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The purposes of these studies were to produce a small animal model of arterial thrombosis for study of novel antithrombotic agents, to validate a simple temperature index of occlusive thrombosis, and to describe the composition of the thrombus. Small thermocouple transducers were fabricated from readily available materials. A thermocouple was inserted under a carotid artery of the anesthetized rat and vessel temperature was recorded continuously. Arterial injury was induced by FeC13 solution applied topically to the artery above the thermocouple. To validate the relationship between thrombotic occlusion and vessel temperature, blood flow velocity, proximal to the injury, and temperature were recorded simultaneously. Temperature decreased rapidly when velocity averaged 24 ± 12 percent of control and velocity did not differ from zero within 20 sec. In normal vessels, average flow velocity did not decrease significantly from control until a fixed stenosis decreased diameter by 78 percent. Average time to occlusion (TTO), signaled by the abrupt temperature inflection, ranged from 56 ± 4 min to 14 ± 1 min after 10 and 65 percent FeC13 application respectively. Vessel segments were fixed at various times after FeC13 exposure and examined by scanning electron microscopy. Endothelial damage was observed and was associated with thrombus composed of activated platelets, fibrin strands and entrapped erythrocytes. The results demonstrate that FeC13 dose-dependently induced formation of an occlusive mixed thrombus that was indexed by monitoring the time between FeC13 application and a rapid temperature decrease in the carotid artery of the rat. © 1990.
引用
收藏
页码:269 / 280
页数:12
相关论文
共 50 条
  • [1] An optimized murine model of ferric chloride-induced arterial thrombosis for thrombosis research
    Wang, XK
    Xu, L
    THROMBOSIS RESEARCH, 2005, 115 (1-2) : 95 - 100
  • [2] Hydrogen sulfide attenuates ferric chloride-induced arterial thrombosis in rats
    Qin, Yi-Ren
    You, Shou-Jiang
    Zhang, Yan
    Li, Qian
    Wang, Xian-Hui
    Wang, Fen
    Hu, Li-Fang
    Liu, Chun-Feng
    FREE RADICAL RESEARCH, 2016, 50 (06) : 654 - 665
  • [3] How useful are ferric chloride models of arterial thrombosis?
    Grover, Steven P.
    Mackman, Nigel
    PLATELETS, 2020, 31 (04) : 432 - 438
  • [4] Troubleshooting the rabbit ferric chloride-induced arterial model of thrombosis to assess in vivo efficacy of antithrombotic drugs
    Couture, L.
    Richer, L. P.
    Mercier, M.
    Helie, C.
    Lehoux, D.
    Hossain, S. M.
    JOURNAL OF PHARMACOLOGICAL AND TOXICOLOGICAL METHODS, 2013, 67 (02) : 91 - 97
  • [5] Effects of Modified Je-Ho-Tang on Ferric Chloride-induced Thrombosis in a Rat Model and of Peripheral Circulatory Disturbance in a Mouse Model
    Kim, Seul-Ki
    Jeon, Won Kyung
    JOURNAL OF THE KOREAN SOCIETY FOR APPLIED BIOLOGICAL CHEMISTRY, 2010, 53 (06): : 842 - 846
  • [6] CHEMICAL OXIDATIVE POLYMERIZATION OF ANILINE WITH FERRIC-CHLORIDE
    YASUDA, A
    SHIMIDZU, T
    POLYMER JOURNAL, 1993, 25 (04) : 329 - 338
  • [7] DYNAMICS OF COAGULATION OF KAOLIN PARTICLES WITH FERRIC-CHLORIDE
    CHING, HW
    TANAKA, TS
    ELIMELECH, M
    WATER RESEARCH, 1994, 28 (03) : 559 - 569
  • [8] Demonstration of flow and platelet dependency in a ferric chloride-induced model of thrombosis
    Lockyer, S
    Kambayashi, J
    JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1999, 33 (05) : 718 - 725
  • [9] Ferric Chloride-induced Murine Thrombosis Models
    Li, Wei
    Nieman, Marvin
    Sen Gupta, Anirban
    JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2016, (115):
  • [10] Optimizing outcome measurement with murine ferric chloride-induced thrombosis
    Kastetter, Bryn
    Matrai, Amanda B.
    Cooley, Brian C.
    BLOOD COAGULATION & FIBRINOLYSIS, 2018, 29 (07) : 636 - 643