The fibrin-derived peptide Bβ15-42 is cardioprotective in a pig model of myocardial ischemia-reperfusion injury

被引:51
作者
Roesner, Jan P.
Petzelbauer, Peter [1 ]
Koch, Alexander
Mersmann, Jan
Zacharowski, Paula A.
Boehm, Olaf
Reingruber, Sonja
Pasteiner, Waltraud
Mascher, Daniel
Wolzt, Michael
Barthuber, Carmen
Noedge-Schomburg, Gabi E. F.
Scheeren, Thomas W. L.
Zacharowski, Kai
机构
[1] Univ Hosp Rostock, Dept Anaesthesia, Rostock, Germany
[2] Med Univ Vienna, Dept Gen Dermatol, Vienna, Austria
[3] Univ Hosp Bristol, Bristol Royal Infirm, Dept Anaesthesia, Mol Cardioprotect & Inflammat Grp, Bristol, Avon, England
[4] Univ Hosp Dusseldorf, Mol Cardioprotect & Inflammat Grp, Dept Anaesthesia, Dusseldorf, Germany
[5] Fibrex Med Inc, Vienna, Austria
[6] Med Univ Vienna, Dept Clin Pharmacol, Vienna, Austria
[7] Univ Hosp Dusseldorf, Dept Clin Chem, Dusseldorf, Germany
关键词
fibrin fragments; ischemia; reperfusion; pig; human;
D O I
10.1097/01.CCM.0000269035.30231.76
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective: The fibrin-derived peptide B beta(15-42) has been shown to reduce infarct size in rodent models of ischemia-reperfusion injury. To increase its potential for translation into the clinic, we studied the effects of B beta(15-42) in pigs, whose coronary anatomy is similar to that of humans. In addition, we evaluated the pharmacokinetics and safety of B beta(15-42) in several species, including humans. Design: Animal study and phase I trial. Setting: University hospital and contract research laboratories. Subjects: Pigs/healthy volunteers. Interventions: Male farm-bred Landrace pigs were subjected to 1 hr of left anterior descending coronary artery occlusion followed by 3 hrs of reperfusion. At the time of reperfusion, B beta(15-42) (2.4 mg/kg, n = 6) or random peptide (control; 2.4 mg/kg, n = 6) was administered as an intravenous bolus. As a positive control, pigs were subjected to ischemic preconditioning (n = 6). Cardiac damage and hemodynamics were recorded. Biodistribution and pharmacokinetics of B beta(15-42) were determined in rats and dogs. In a phase I trial involving 30 male healthy volunteers, pharmacokinetics and safety were tested in a randomized, double-blinded, placebo-controlled, parallel-group, single ascending dose study. Measurements and Main Results: B beta(15-42) and ischemic preconditioning significantly reduced myocardial infarct size and troponin I levels. B beta(15-42) also reduces interleukin-6 levels, underlining its anti-inflammatory properties. Furthermore, in humans, the pharmacokinetics of the peptide B beta(15-42) were comparable to those of animals, and no serious adverse effects were observed. Conclusions: B beta(15-42) elicits cardioprotection in pigs and is clinically safe in phase I testing of humans. This study confirms the new concept of a pathogenic role of fibrin derivatives in myocardial reperfusion injury, which can be inhibited by peptide B beta(15-42).
引用
收藏
页码:1730 / 1735
页数:6
相关论文
共 23 条
[1]   Endothelial cell VE-cadherin functions as a receptor for the β15-42 sequence of fibrin [J].
Bach, TL ;
Barsigian, C ;
Yaen, CH ;
Martinez, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (46) :30719-30728
[2]   Prognostic value of plasma interleukin-6 concentrations and the -174 G>C and -572 G>C promoter polymorphisms of the interleukin-6 gene in patients with acute myocardial infarction treated with thrombolysis [J].
Bennermo, M ;
Held, C ;
Green, F ;
Strandberg, LE ;
Ericsson, CG ;
Hansson, LO ;
Watkins, H ;
Hamsten, A ;
Tornvall, P .
ATHEROSCLEROSIS, 2004, 174 (01) :157-163
[3]   Myocardial protection at a crossroads - The need for translation into clinical therapy [J].
Bolli, R ;
Becker, L ;
Gross, G ;
Mentzer, R ;
Balshaw, D ;
Lathrop, DA .
CIRCULATION RESEARCH, 2004, 95 (02) :125-134
[4]   Mechanisms, management and future directions for reperfusion injury after acute myocardial infarction [J].
Cannon, RO .
NATURE CLINICAL PRACTICE CARDIOVASCULAR MEDICINE, 2005, 2 (02) :88-94
[5]   Changes in myocardial electrical impedance induced by coronary artery occlusion in pigs with and without preconditioning - Correlation with local ST-segment potential and ventricular arrhythmias [J].
Cinca, J ;
Warren, M ;
Carreno, A ;
Tresanchez, M ;
Armadans, L ;
Gomez, P ;
SolerSoler, J .
CIRCULATION, 1997, 96 (09) :3079-3086
[6]   Early time course of myocardial electrical impedance during acute coronary artery occlusion in pigs, dogs, and humans [J].
del Rio, CL ;
McConnell, PI ;
Clymer, BD ;
Dzwonczyk, R ;
Michler, RE ;
Billman, GE ;
Howie, MB .
JOURNAL OF APPLIED PHYSIOLOGY, 2005, 99 (04) :1576-1581
[7]   The inflammatory response in myocardial infarction [J].
Frangogiannis, NG ;
Smith, CW ;
Entman, ML .
CARDIOVASCULAR RESEARCH, 2002, 53 (01) :31-47
[8]   Interaction of fibrin(ogen) with the endothelial cell receptor VE-Cadherin:: Mapping of the receptor-binding site in the NH2-terminal portions of the fibrin β chains [J].
Gorlatov, S ;
Medved, L .
BIOCHEMISTRY, 2002, 41 (12) :4107-4116
[9]   Application of cl-esterase inhibitor during reperfusion of ischemic myocardium -: Dose-related beneficial versus detrimental effects [J].
Horstick, G ;
Berg, O ;
Heimann, A ;
Götze, O ;
Loos, M ;
Hafner, G ;
Bierbach, B ;
Petersen, S ;
Bhakdi, S ;
Darius, H ;
Horstick, M ;
Meyer, J ;
Kempski, O .
CIRCULATION, 2001, 104 (25) :3125-3131
[10]   Myocardial ischemia induces interleukin-6 and tissue factor production in patients with coronary artery disease - A dobutamine stress echocardiography study [J].
Ikonomidis, I ;
Athanassopoulos, G ;
Lekakis, J ;
Venetsanou, K ;
Marinou, M ;
Stamatelopoulos, K ;
Cokkinos, DV ;
Nihoyannopoulos, P .
CIRCULATION, 2005, 112 (21) :3272-3279