Comparison of edoxaban and enoxaparin in a rat model of AlCl3-induced thrombosis of the superior sagittal sinus

被引:2
作者
Hachenberger, M. [1 ,2 ]
Yeniguen, M. [1 ,2 ,3 ]
Suenner, L. [1 ,2 ]
Hinchliffe, D. [1 ]
Mueller, C. [4 ]
Wietelmann, A. [5 ]
Gerriets, T. [1 ,2 ,6 ]
Tschernatsch, M. [1 ,2 ,6 ]
Juenemann, M. [1 ,2 ]
Gerner, S. T. [1 ,7 ]
Doeppner, T. R. [1 ,7 ,8 ,9 ]
Huttner, H. B. [1 ,7 ,8 ]
Braun, T. [1 ,2 ]
机构
[1] Justus Liebig Univ Giessen, Dept Neurol, Klin Str 33, D-35385 Giessen, Germany
[2] Heart & Brain Res Grp, D-35385 Giessen, Germany
[3] Neuroctr Wetzlar, Sportparkstr 2, D-35578 Wetzlar, Germany
[4] Kerckhoff Klin Bad Nauheim, Dept Radiol, D-61231 Bad Nauheim, Germany
[5] Max Planck Inst Heart & Lung Res, Sci Serv Grp Magnet Resonance Imaging, D-61231 Bad Nauheim, Germany
[6] Die Neurologen, Frankfurter Str 34, D-61231 Bad Nauheim, Germany
[7] Univ Marburg, Ctr Mind Brain & Behav CMBB, D-35032 Marburg, Germany
[8] Justus Liebig Univ Giessen, D-35032 Marburg, Germany
[9] Univ Goettingen, Med Sch, Dept Neurol, D-37075 Gottingen, Germany
关键词
Rat; Sinus thrombosis; Cerebral venous thrombosis; Stroke; Edoxaban; FACTOR XA INHIBITOR; VENOUS THROMBOSIS; IN-VITRO; STROKE;
D O I
10.1007/s00210-023-02546-x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cerebral sinus venous thrombosis (CSVT) is an uncommon disease that is usually treated with anticoagulation (heparin, low-molecular heparin, or vitamin K-antagonists). We compared treatment with edoxaban, an oral factor Xa-antagonist, that has not been approved in patients with CSVT, with enoxaparin, a well-established therapy, in a rat model of CSVT. Fifty male Wistar rats were randomized into 5 groups (10 animals each) and subjected to aluminum chloride (AlCl3)-induced thrombosis of the superior sagittal sinus (SSS) or sham procedure. Animals with thrombosis of the SSS were treated with edoxaban, enoxaparin, or placebo. Diagnostic workup included neurological examination, MRI imaging, MR-flow measurements of the SSS, and immunohistochemical staining. Neurological examination revealed no differences between treatment groups. Seven days after initial thrombosis, flow in the SSS was lower in the active treatment group as compared to sham-operated animals (p < 0.05). Flow in the SSS in the active treatment groups (edoxaban 1 h prior to thrombosis: 0.16 cm/s +/- 0.06 cm/s; edoxaban 6 h after thrombosis: 0.13 cm/s +/- 0.05 cm/s; enoxaparin: 0.13 cm/s +/- 0.04 cm/s; placebo: 0.07 cm/s +/- 0.02 cm/s) was higher as compared to placebo (p < 0.05), but there were no differences between the active treatment groups (p > 0.05). Immunohistochemical staining showed no differences in the actively treated animals. Edoxaban proved to be similar to enoxaparin in a model of experimental AlCl3-induced CSVT.
引用
收藏
页码:3887 / 3892
页数:6
相关论文
共 14 条
[1]   Recanalization after cerebral venous thrombosis. A randomized controlled trial of the safety and efficacy of dabigatran etexilate versus dose-adjusted warfarin in patients with cerebral venous and dural sinus thrombosis [J].
Ferro, Jose M. ;
Bendszus, Martin ;
Jansen, Olav ;
Coutinho, Jonathan M. ;
Dentali, Francesco ;
Kobayashi, Adam ;
Aguiar de Sousa, Diana ;
Neto, Lia L. ;
Miede, Corinna ;
Caria, Jorge ;
Huisman, Holger ;
Diener, Hans-Christoph .
INTERNATIONAL JOURNAL OF STROKE, 2022, 17 (02) :189-197
[2]   Cerebral Venous Thrombosis: an Update [J].
Ferro, Jose M. ;
de Sousa, Diana Aguiar .
CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS, 2019, 19 (10)
[3]   DU-176b, a potent and orally active factor Xa inhibitor:: in vitro and in vivo pharmacological profiles [J].
Furugohri, T. ;
Isobe, K. ;
Honda, Y. ;
Kamisato-Matsumoto, C. ;
Sugiyama, N. ;
Nagahara, T. ;
Morishima, Y. ;
Shibano, T. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2008, 6 (09) :1542-1549
[4]  
Guidetti Gianni F., 2015, Advances in Biological Regulation, V59, P36, DOI 10.1016/j.jbior.2015.06.001
[5]   THE ROTAROD TEST - AN EVALUATION OF ITS EFFECTIVENESS IN ASSESSING MOTOR DEFICITS FOLLOWING TRAUMATIC BRAIN INJURY [J].
HAMM, RJ ;
PIKE, BR ;
ODELL, DM ;
LYETH, BG ;
JENKINS, LW .
JOURNAL OF NEUROTRAUMA, 1994, 11 (02) :187-196
[6]   Edoxaban, a direct factor Xa inhibitor, suppresses tissue-factor induced human platelet aggregation and clot-bound factor Xa in vitro: Comparison with an antithrombin-dependent factor Xa inhibitor, fondaparinux [J].
Honda, Yuko ;
Kamisato, Chikako ;
Morishima, Yoshiyuki .
THROMBOSIS RESEARCH, 2016, 141 :17-21
[7]   Risk impact of edoxaban in the management of stroke and venous thromboembolism [J].
Hurst, Katherine V. ;
O'Callaghan, John Matthew ;
Handa, Ashok .
VASCULAR HEALTH AND RISK MANAGEMENT, 2016, 12 :329-335
[8]   Risk factors for recurrent venous thromboembolism in the European collaborative paediatric database on cerebral venous thrombosis:: a multicentre cohort study [J].
Kenet, Gili ;
Kirkham, Fenella ;
Niederstadt, Thomas ;
Heinecke, Achim ;
Saunders, Dawn ;
Stoll, Monika ;
Brenner, Benjamin ;
Bidlingmaier, Christoph ;
Heller, Christine ;
Knoefler, Ralf ;
Schobess, Rosemarie ;
Zieger, Barbara ;
Sebire, Guillaume ;
Nowak-Goettl, Ulrike .
LANCET NEUROLOGY, 2007, 6 (07) :595-603
[9]   Edoxaban, a direct oral factor Xa inhibitor, ameliorates coagulation, microvascular thrombus formation, and acute liver injury in a lipopolysaccharide-induced coagulopathy model in rats [J].
Morishima, Yoshiyuki ;
Shibutani, Tomoko ;
Noguchi, Kengo ;
Ito, Yusuke ;
Honda, Yuko .
JOURNAL OF THROMBOSIS AND THROMBOLYSIS, 2021, 52 (01) :9-17
[10]   Combined effect of a direct oral anticoagulant edoxaban and an inhibitor of activated thrombin-activatable fibrinolysis inhibitor on clot lysis [J].
Morishima, Yoshiyuki ;
Kamisato, Chikako ;
Honda, Yuko .
JOURNAL OF THROMBOSIS AND THROMBOLYSIS, 2020, 49 (01) :94-99