Thromb Haemost 1995; 74(06): 1583-1590
DOI: 10.1055/s-0038-1649986
Original Articles
Animal Models
Schattauer GmbH Stuttgart

Inhibition of Thrombus Formation by Endothelin-1 in Canine Models of Arterial Thrombosis

Robert J Leadley Jr
The Cardiovascular Diseases Research, UpJohn Laboratories, Kalamazoo, MI, USA
,
William R Humphrey
The Cardiovascular Diseases Research, UpJohn Laboratories, Kalamazoo, MI, USA
,
Laurence A Erickson
The Cardiovascular Diseases Research, UpJohn Laboratories, Kalamazoo, MI, USA
,
Ronald J Shebuski
The Cardiovascular Diseases Research, UpJohn Laboratories, Kalamazoo, MI, USA
› Author Affiliations
Further Information

Publication History

Received 28 February 1995

Accepted after resubmission 07 September 1995

Publication Date:
10 July 2018 (online)

Summary

The effect of enclothelin-l (ET-1) on thrombus formation in vivo was evaluated in two well-established canine models of coronary artery thrombosis. First, the possible antithrombotic effect of ET-1 was examined using the cyclic flow reduction (CFR) model of coronary artery stenosis, vascular endothelial cell and intimal smooth muscle cell injury, and periodic acute platelet thrombus formation. Using a rating system of 0 (no inhibition) to 3 (complete inhibition), ET-1 administration at 0.1, 0.5, and 1.0 μg/kg, i.v. bolus, produced scores of 1.0 ± 0.2 (n = 10), 1.8 ± 0.4 (n = 8), and 2.1 ± 0.3 (n = 7), respectively. ET-1 injection inhibited ex vivo platelet aggregation induced by ADP and U-46619 by 30-60%. When aspirin was administered at 5 mg/kg prior to ET-1 administration at 0.5 pg/kg, ET-1 produced a CFR rating of 2.7 ± 0.2 (n = 6). However, higher dose aspirin (30 mg/kg, i.v.) significantly inhibited the antithrombotic effect of ET-1 (0.5 ± 0.5, n = 4). The antithrombotic effect of ET-1 was also examined using an electrolytic injury model of arterial thrombosis. The time required to produce an occlusive thrombus during the experiments in which ET-1 was administered at 10 and 20 ng kg-1 min-1 was 77 ± 15 (p <0.08) and 105 ± 16 min (p <0.05), respectively, compared to 44 ± 5 min when vehicle was infused. Cardiovascular changes following occlusion were not significantly different between dogs given ET-1 and those given vehicle, suggesting that elevated plasma levels of ET-1 did not exacerbate the adverse effects of coronary occlusion. In addition, plasma ET-1 levels were elevated significantly after occlusion in the dogs given vehicle (from 7.4 to 12.4 pg/ml). Taken together, these data provide further evidence to support the notion that ET-1 release during ischemia may be involved in a protective mechanism that impedes thrombus formation in the stenosed coronary artery.

 
  • References

  • 1 Yanagasawa M, Kurihara M, Kimura H, Tomobe Y, Kobayashi M, Mitsui Y, Yazaki Y, Goto K, Masaki T. A novel vasoconstrictor peptide produced by vascular endothelial cells. Nature 1988; 332: 411-415
  • 2 Akagi M, Masaki S, Kitazumi K, Mio M, Tasaka K. Comparative study of the adverse effects of various radiographic contrast media, including iover-sol, a new low-osmolarity medium. II. The complement system and endothelial cells Methods Find Exp Clin Pharmacol 1991; 13 (07) 449-454
  • 3 Lerman A, Edwards BS, Hallett JW, Heublein DM, Sandberg SM, Burnett JC. Circulating and tissue endothelin immunoreactivity in advanced atherosclerosis. N Engl J Med 1991; 325: 997-1001
  • 4 Yasuda M, Kohno M, Tahara A, Itagane H, Toda I, Akioka K, Teragaki M, Oku H, Takeuchi K, Takeda T. Circulating immunoreactive endothelin in ischemic heart disease. Am Heart J 1990; 119: 801-806
  • 5 Saito Y, Nakao K, Mukoyama M, Imura H. Increased plasma endothelin level in patients with essential hypertension (Letter). N Engl J Med 1990; 322: 205
  • 6 Shichiri M, Hirata Y, Ando K, Emori T, Ohta K, Kimoto S, Ogura M, Inoue A, Marumo F. Plasma endothelin levels in hypertension and chronic renal failure. Hypertension Dallas 1990; 15: 493-496
  • 7 Ohlstein EH, Storer BL, Butcher JA, DeBouck C, Feuerstein G. Platelets stimulate expression of endothelin mRNA and endothelin biosynthesis in cultured endothelial cells. Circ Res 1991; 69: 832-841
  • 8 Maruyama I, Tokunaga O, Soejima Y, Osame M, Saito H. ET-1 is synthesized in megakaryocyte and megakaryoblastic leukemia cells and contained in platelets. Blood 1991; 78 (10) Suppl (Suppl. 01) 1580a
  • 9 Thiemermann C, Lidbury P, Thomas R, Vane J. Endothelin inhibits ex vivo platelet aggregation in the rabbit. Eur J Pharmacol 1988; 158: 181-182
  • 10 Thiemermann C, Lidbury PS, Thomas GR, Vane JR. Endothelin-1 releases prostacyclin and inhibits ex vivo platelet aggregation in the anesthetized rabbit. J Cardiovasc Pharmacol 1989; 13 Suppl (Suppl. 05) S138-S41
  • 11 Thiemermann C, May GR, Page PC, Vane JR. Endothelin-1 inhibits platelet aggregation in vivo: a study with111indium-labelled platelets. Br J Pharmacol 1990; 99: 303-308
  • 12 Herman F, Magyar K, Chabrier P-E, Braquet P, Filep J. Prostacyclin mediates antiaggregatory and hypotensive actions of endothelin in anesthetized beagle dogs. Br J Pharmacol 1989; 98: 38-40
  • 13 deNucci G, Thomas R, D’Orleans-Juste P, Antunes E, Walder C, Warner TD, Vane JR. Pressor effects of circulating endothelin are limited by its removal in the pulmonary circulation and by the release of prostacyclin and endothelium-derived relaxing factor. Proc Natl Acad Sci USA 1988; 85: 9797-9800
  • 14 Bush LR, Shebuski RJ. In vivo models of arterial thrombosis and thrombolysis. FASEB J 1990; 4: 3087-3098
  • 15 Coller BS, Folts JD, Scudder LE, Smith SR. Antithrombotic effect of a monoclonal antibody to the platelet glycoprotein IIb/IIIa receptor in an experimental animal model. Blood 1986; 68: 783-786
  • 16 Anderson HV, Kirkeeide RL, Krishnaswami A, Weigellt LA, Revana M, Weisman HF, Willerson JT. Cyclic flow variations after coronary angioplasty in humans: clinical and angiographic characteristics and elimination with 7E3 monoclonal antibody. J Am Coll Cardiol 1994; 23: 1031-1037
  • 17 Rote WE, Mu DX, Bates ER, Nedelman MA, Lucchesi BR. Prevention of rethrombosis after coronary thrombolysis in a chronic canine model. I. Adjunctive therapy with monoclonal antibody 7E3 F(ab’)2 fragment J Cardiovasc Pharmacol 1994; 23: 194-202
  • 18 Mickelson JK, Simpson PJ, Cronin M, Homeister JW, Lay well E, Kitzen J, Lucchesi BR. Antiplatelet antibody [7E3 F(ab’)2] prevents rethrombosis after recombinant tissue-type plasminogen activator-induced coronary artery thrombolysis in a canine model. Circulation 1990; 81: 617-627
  • 19 Topol EJ, Califf RM, Weisman HF, Ellis SG, Tcheng JE, Worley S, Ivan- hoe R, George BS, Fintel D, Weston M, Sigmon K, Anderson KM, Lee KL. Willerson JT on behalf of The EPIC Investigators. Randomised trial of coronary intervention with antibody against platelet IIb/IIIa integrin for reduction of clinical restenosis: results at six months Lancet 1994; 343: 881-886
  • 20 Aiken JW, Shebuski RJ. Comparison in anesthetized dogs of the antiaggregatory and hemodynamic effects of prostacyclin and a chemically stable prostacyclin analog, 6a-CARBA-PGI2(Carbacyclin). Prostaglandins 1980; 19: 629-643
  • 21 Aiken JW, Shebuski RJ, Gorman RR. Blockage of partially obstructed coronary arteries with platelet thrombi: Comparison between its prevention with cyclooxygenase inhibitors versus prostacyclin. Adv Prostaglandin Thromboxane Leukot Res 1980; 7: 635-639
  • 22 Filep JG, Herman F, Battistini B, Chabrier P-E, Braquet P, Sirois P. Antiaggregatory and hypotensive effects of endothelin in beagle dogs: Role for prostacyclin. J Cardiovasc Pharmacol 1991; 17 Suppl (Suppl. 07) S216-218
  • 23 Joseph R, Scicli AG, Han E, Grunfeld S, Carretero OA, Welch KM A. ET-1 and human platelet activity. Thromb Res 1991; 61: 529-536
  • 24 Ohlstein EH, Storer B, Nambi P, Given M, Lippton H. Endothelin and platelet function. Thromb Res 1990; 57: 967-974
  • 25 Patel A, Fairbanks L, Gordge MP, Neild GH. Failure of endothelin to influence in vitro platelet responses. Thromb Res 1989; 56: 769-770
  • 26 Astarie-Dequeker C, Iouzalen L, David-Dufilho M, Devynck M-A. In vitro inhibition by endothelins of thrombin-induced aggregation and Ca2+mobilization in human platelets. Brit J Pharmacol 1992; 106: 966-971
  • 27 Touyz RM, Schiffrin EL. Effects of angiotensin II and endothelin-1 on platelet aggregation and cytosolic pH and free Ca2+concentrations in essential hypertension. Hypertension 1993; 22: 853-862
  • 28 Leadley RJ Jr, Lee P, Erickson LA, Shebuski RJ. The snake venom peptide sarafotoxin S6b inhibits repetitive platelet thrombus formation in the stenosed canine coronary artery. J Cardiovasc Pharmacol 1993; 22 Suppl (Suppl. 08) S199-203
  • 29 Clozel M, Gray GA, Breu V, Loffler BM, Osterwalder R. The endothelin ETB receptor mediates both vasodilation and vasoconstriction in vivo. Bio-chem Biophys Res Comm 1992; 186: 867-873
  • 30 Bodin P, Milner P, Winter R, Bumstock G. Chronic hypoxia changes the ratio of endothelin to ATP release from rat aortic endothelial cells exposed to high flow. Proc R Soc Lond B Biol Sci 1992; 247: 131-135
  • 31 Emori T, Hirata Y, Ohta K, Shichiri M, Marumo F. Secretory mechanism of immunoreactive endothelin in cultured bovine endothelial cells. Biochem Biophys Res Commun 1989; 162 (01) 217-223