ISSN : 1301-5680
e-ISSN : 2149-8156
Turkish Journal of Thoracic and Cardiovascular Surgery     
The effects of clopidogrel, acetyl salicylic acid and tirofiban on acetylcholine-induced dilation in rat thoracic aorta segments
Erdem Ali Özkısacık, Berent Dişcigil, Tünay Kurtoğlu, Selim Durmaz, Uğur Gürcün, Mehmet Boğa, M. İsmail Badak
Department of Cardiovascular Surgery, Medical Faculty of Adnan Menderes University, Aydın, Turkey
DOI : 10.5606/tgkdc.dergisi.2012.111

Abstract

Background: In this article, we aimed to investigate the effects of antithrombotic agents, including acetyl salicylic acid (ASA), clopidogrel, and tirofiban on the acetylcholine (ACh)- induced dilation responses in rat thoracic aorta segments.

Methods: Twenty-eight Wistar albino male rats weighing between 250-300 g were included in the study. The rats were randomly divided into four groups: the ASA group (n=7), the clopidogrel group (n=7), the tirofiban group (n=7), and the control group (n=7). Intraperitoneal (IP) injection of ASA (1.5 mg/kg) or clopidogrel (1 mg/kg) was administered 12 hours before the experiment. In the tirofiban group, 150 μgr/kg tirofiban IP was given twice at one and 12 hours before the experiment. The rats in the control group did not receive any medication. After the rats were decapitated, the segments of the thoracic aorta were removed and suspended in an oxygenated Krebs solution in a tissue bath, and the dose dependency in the responses to the ACh-induced dilation in the aortic rings were studied.

Results: The dilation responses of the aortic rings to ACh in the lowest molar concentration (10-9) were found to be reduced in the ASA (94.3%±3.3) and clopidogrel (94.6%±3.1) groups when compared with the control group (86.7%±8.1) (p<0.05). The responses to higher concentrations of ACh were observed to be similar in all of the groups.

Conclusion: Acetyl salicylic acid and clopidogrel treatments resulted in a slight delay of endotheliummediated relaxation while tirofiban had no significant effect. These findings suggest that ASA and clopidogrel may have a limited effect on endothelium-mediated vasodilation.

Thrombocytes play a key role in the pathogenesis of atherothrombotic diseases such as myocardial infarction, stroke, and peripheral vascular occlusions. Acetyl salicylic acid (ASA) and clopidogrel are widely administered antiplatelet agents that play an essential part in therapy for these diseases. These antiaggregant drugs prevent vascular disorders with well-known indications, which have also been implicated in the guidelines.[1-4] Tirofiban is a parenteral a ntiplatelet drug which is frequently used in patients undergoing percutaneous coronary intervention (PCI) in the setting of acute coronary syndrome.[5]

The endothelium is a selective, permeable barrier between the circulating blood and the vessel wall. Physiologically, it controls the capillary transportation of water and water-soluble compounds along with the levels of plasma lipids. Endothelial cells are sensitive to hemodynamic and humoral alterations and are activated to release endothelium-derived factors and biologicallyactive substances.

Beyond these functions, the endothelium bears anticoagulant, antiaggregant and fibrinolytic properties and regulates the production of vascular reactive molecules. Endothelial cells also interact with various types of other cells, including platelets, through numerous biochemical pathways which display complex and diverse actions. As an example, adenosine diphosphate (ADP), which stimulates platelet aggregation, leads to the release of vasodilator prostacyclin from the endothelial cells.[6,7] Therefore, the endothelium plays an important role in maintaining homeostasis by providing regular blood flow and adjusting the diameter of the vessel lumen.

The aim of this experimental study was to investigate the effects of antiaggregant pretreatment (ASA, clopidogrel, and tirofiban) on the acetylcholine-induced relaxation response of the endothelium in rat thoracic aorta segments in vitro.

Methods

The animal ethics and research committee of Adnan Menderes University approved all protocols prior to the commencement of the study. The experiments were carried out on 28 adult male Wistar albino rats (250-300 g) obtained from the experimental animal laboratory of the Medical Faculty of Adnan Menderes University. The rats were fed a standard laboratory diet and water ad libitum and housed in cages in a temperature-controlled (22±2 °C) room with a 12-hour dark-light cycle before the experiments. The study was conducted at the Electrophysiology and Cardiovascular Research Laboratory of Adnan Menderes University. The rats were randomly assigned into four experimental groups.

Tablets of ASA (Coraspin® 100 mg tb-Bayer, Turkey) and clopidogrel (Plavix® 75mg tb-Sanofi Aventis, Turkey) were crushed in sterile containers, and each tablet was dissolved in distilled water to obtain a homogenous mixture. Tirofiban (Aggrastat® 0.25 mg/ml-Merck Sharp Dohme, Turkey) was obtained in sterile vials.

ASA group (n=7): Acetyl salicilic acid (1.5 mg/kg) was administered intraperitoneally 12 hours before the experiment.

Clopidogrel group (n=7): Clopidogrel (1 mg/kg) was administered intraperitoneally 12 hours before the experiment.

Tirofiban group (n=7): Tirofiban (150 μgr/kg) was administered intraperitoneally twice, once at the first hour and again 12 hours before the experiment.

Control group (n=7): No medication was administered before the experiment.

Under high-dose ether anesthesia, a median sternotomy was performed, the heart and lungs were retracted, and the arcus and thoracic aortic segments, adjacent to the thoracic vertebrae, were removed. The rats were then sacrificed by decapitation. The aorta was carefully dissected free from the adipose and connective tissue remnants with the help of surgical binocular loupes (x3.5) by paying meticulous attention to avoid damage to the endothelium, and segments of the aortic rings, each 3-4 mm in length, were quickly prepared. The rings were then suspended in four parallel bath organ chamber systems (May IOBS 99, COMMAT Pharmacolgy and Physiology Instruments, Ankara, Turkey) each containing 25 ml Krebs solution [118.3 mM sodium chloride (NaCl), 4.7 mM potassium chloride (KCl), 1.2 mM magnesium sulfate (MgSO4), 1.22 mM monopotassium phosphate (KH2PO4), 2.5 mM calcium chloride (CaCl2), 25.0 mM sodium bicarbonate (NaHCO3), and 11.1.mM glucose (Sigma- Aldrich, St. Louis, Missouri, USA) maintained at 37 °C and bubbled with 95% oxygen (O2), 5% carbon dioxide (CO2). Two stainless steel clips were passed through the lumen of each ring. One was anchored to the bottom of the chamber while the other was suspended in order to connect with a transducer system (May GTA030, and Biopac Systems Inc. Model MP 100, COMMAT, Ankara, Turkey).[8,9] The data was obtained by means of the AcqKnowledge 3.8.2 hardware system (COMMAT, Ankara, Turkey).

After maintaining a state of equilibrium, the aortic rings were distended under a force of 1 gram (gr) and progressively stretched by increasing the force by 1 gr every 10 minutes until a tension of 3 gr was reached. At the end of this cycle, a period of 10 minutes had passed, and the rings were contracted by the addition of norepinephrine (Sigma-Aldrich) (0.1 mlx10-4M) to the baths. The responses were recorded, and a plateau level was then achieved. The baths were washed with Krebs solution, and the rings were distended with a final force of 4 g. Provided a stable state was reached, contraction was stimulated again by adding norepinephrine (0.1 mlx10-4M) into the baths, which was subsequently followed by acetylcholine (ACh) (Sigma- Aldrich) (0.1 mlx10-4M) (Figure 1). The relaxation responses of the aortic rings to the ACh were recorded, and then the baths were washed twice and allowed to equilibrate in Krebs solution for 45 minutes before starting the experiment. The baths in which an absence of contraction or relaxation was observed were excluded from the study, suggesting that the endothelium of the aortic rings in these baths may have been damaged during the harvest, causing them to fail to respond properly.[10]

Figure 1: An example of the contraction response to norepinephrine, followed by acetylcholine induced relaxation of the aortic ring.

The experiment was started by stimulating the contractile response with the addition of an equal amount of norepinephrine (0.1 mlx10-4M) to each bath. When a stable plateau level was achieved, an initial dose of 0.1 mlx10-9M ACh was given. After each given concentration of ACh, the relaxation response was recorded. When a plateau level was reached, subsequent doses (each 0.1ml. in volume) were administered. In this manner, the concentration of ACh was gradually increased, and a final dose of 0.1mlx10-4M was achieved as depicted in Table 1.

Table 1: Concentrations of acetylcholine doses

The change in the tonus of the ring with each relaxation from the maximum tonus as a response to given doses of acetylcholine was calculated and expressed in percentages. The data was analyzed statistically by analysis of variance (ANOVA) and by Student’s t-test. The differences were considered to be statistically significant when p<0.05.

Results

The relationship between the percentage of relaxation and concentration of ACh in the baths for each group is shown in Figure 2. The relaxation response to the lowest concentration of Ach (10-9) in the ASA (94.3%±3.3) and clopidogrel (94.6%±3.1) groups was found to be significantly decreased when compared with the control (86.7%±8.1) group (p<0.05). However, the relaxation responses for all the remaining concentrations of Ach were similar between the groups, and no statistical significance was present (p>0.05).

Figure 2: The relationship between the acetylcholine concentration and the percentage of decrement in the tonus from the maximum tonus is shown. The vertical axis represents the relaxation response, and the horizontal axis represents the subsequent acetylcholine doses. * p<0.5; ASA: Acetyl salicylic acid.

Discussion

Antiplatelet therapy has a pivotal role in the treatment of ischemic vascular diseases; however, the mechanisms by which the antiplatelet agents inhibit thrombocytes may also interfere with physiological processes elsewhere and cause adverse effects. The protection and preservation of normal endothelial functions are important issues to be considered during the management of thrombotic disorders. Therefore, we aimed to assess the effects of aspirin, clopidogrel and tirofiban, commonly employed antiplatelet drugs, on endothelial functions by examining the Ach-induced dilatation responses of the aortic rings, obtained from pretreated rats, in a tissue bath.

The inhibition of cyclooxygenase by ASA results in an irreversible blockage of the thrombocyte aggregation, which is the principal therapeutic action. Although ASA inhibits both the thromboxane and prostacyclin pathways, the effect on the former is more evident in low doses.[11] The members of prostaglandin family may exhibit vasodilator or vasoconstrictor properties and, therefore, counteract to form a balance, which is an important factor in the determination of the vascular tonus. Aspirin, when applied in antiaggregant doses, strongly inhibits cyclooxygenase-1 (Cox-1) and blocks the synthesis of thromboxane A2 (TXA2), thereby preventing the aggregation of thrombocytes and vasoconstriction.[12] However, the inhibitory effect of the antiaggregant doses of ASA on cyclooxygenase-2 (Cox-2), which is associated with the synthesis of the vasodilator prostacyclin, is less evident.[13] In experimental studies, ASA has been reported to decrease the dilation response to ACh in rat aorta segments.[14,15] On the other hand, in vivo studies have demonstrated that ASA induces a reduction in vascular resistance and augments coronary blood flow. [16] In this study, the dilation responses of the aortic rings to minimum ACh concentration (10-9), harvested from the rats pretreated with ASA, were observed to be significantly reduced when compared with the responses in the control group. Nevertheless, we did not observe a blunting of the dilation response in the ASA group with higher concentrations of ACh used in this study. This suggests that this state reflects a limited latency of the endothelium to respond to ACh. In addition, we did not note any remarkable augmentation of the Ach-induced dilation response with the ASA treatment in comparison with the control group.

Clopidogrel is a thienopyridine derivative and a selective inhibitor of the P2Y12 type of ADP receptors that is expressed by platelets which cause the secretion of thromboxane A2 (TXA2).[17,18] These receptors have also been found to exist in cells other than platelets, including the rat and human vascular smooth muscle cells.[19] Adenosine diphosphate has been shown to induce vasoconstriction via P2Y12 receptors; however, it is also believed to cause arterial relaxation by increasing the synthesis of endothelium-derived nitric oxide (NO).[19-21] Thus, the effect of ADP-mediated pathways on the endothelium is currently unclear.[22] Clopidogrel has been reported to exhibit vasomodulatory activity[23] and direct endothelial effects independent from antiplatelet actions,[24] which are still not fully understood. Recently, Froldi et al.[25] reported that the clopidogrel pretreatment of rats resulted in only a slight decrement of the constriction response of the aortic tissues to phenylephrine in vitro. In the present study, although the dilation response to the lowest ACh (10-9) concentration in the clopidogrel group was observed to be reduced in comparison with the response in the control group, there was no significant difference in the responses between the two groups for increased ACh concentrations.

Glycoprotein IIb/IIIa (GPIIb/IIIa) receptors are integrins expressed on platelets, and the activation of these receptors leads to firm binding to fibrinogen and platelet aggregation.[26] Vascular injury is a trigger for vascular cells for the expression of such integrins, which results in the platelet-endothelium adhesion among other hazardous effects.[27] Tirofiban is a competitive inhibitor of GPIIb/IIIa receptors,[28] and it has been suggested that it has protective effects on the endothelium, acute coronary syndrome, and symptomatic coronary artery disease.[29,30] Warnholtz et al.[31] reported improvement in the flow-mediated dilation of the brachial artery after PCI with tirofiban treatment. However, these studies were all performed in clinical settings where there was obvious endothelial damage, and the vascular effects of tirofiban on an intact endothelium is uncertain. Kintscher et al.[32] found that tirofiban had no direct effect on cultured human vascular endothelial cells and suggested that it acts on the endothelium via indirect mechanisms. In this study, we observed no statistically significant difference in the dilation response between the control and tirofiban groups at any given concentration of Ach.

In conclusion, ASA and clopidogrel pretreatments resulted in a slight delay of the dilation response to ACh in rat thoracic aorta segments while the tirofiban pretreatment had no significant effect. These findings suggest that ASA and clopidogrel may have a limited effect on endothelium-induced vasodilation, but further investigations are necessary to understand the influence of these agents on endothelial functions and the underlying mechanisms.

Declaration of conflicting interests
The authors declared no conflicts of interest with respect to the authorship and/or publication of this article.

Funding
The authors received no financial support for the research and/or authorship of this article.

References

1) Braunwald E, Antman EM, Beasley JW, Califf RM, Cheitlin MD, Hochman JS, et al. ACC/AHA guideline update for the management of patients with unstable angina and non-STsegment elevation myocardial infarction-2002: summary article: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee on the Management of Patients With Unstable Angina). Circulation 2002;106:1893-900.

2) Antman EM, Anbe DT, Armstrong PW, Bates ER, Green LA, Hand M, et al. ACC/AHA guidelines for the management of patients with ST-elevation myocardial infarctionexecutive summary: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Writing Committee to Revise the 1999 Guidelines for the Management of Patients With Acute Myocardial Infarction). Circulation 2004;110:588-636.

3) Norgren L, Hiatt WR, Dormandy JA, Nehler MR, Harris KA, Fowkes FG,et al. Inter-Society Consensus for the Management of Peripheral Arterial Disease (TASC II). J Vasc Surg 2007;45 Suppl S:S5-67.

4) Chaturvedi S, Bhattacharya P. New insights in antiplatelet therapy for patients with ischemic stroke. Neurologist 2011;17:255-62.

5) Ueno M, Kodali M, Tello-Montoliu A, Angiolillo DJ. Role of platelets and antiplatelet therapy in cardiovascular disease. J Atheroscler Thromb 2011;18:431-42.

6) Vane JR, Anggård EE, Botting RM. Regulatory functions of the vascular endothelium. N Engl J Med 1990;323:27-36.

7) Jaffe EA. Cell biology of endothelial cells. Hum Pathol 1987;18:234-9.

8) Discigil B, Evora PR, Pearson PJ, Viaro F, Rodrigues AJ, Schaff HV. Ionic radiocontrast inhibits endotheliumdependent vasodilation of the canine renal artery in vitro: possible mechanism of renal failure following contrast medium infusion. Braz J Med Biol Res 2004;37:259-65.

9) Evora PR, Pearson PJ, Discigil B, Oeltjen MR, Schaff HV. Pharmacological studies on internal mammary artery bypass grafts. Action of endogenous and exogenous vasodilators and vasoconstrictors. J Cardiovasc Surg (Torino) 2002;43:761-71.

10) Evora PR, Pearson PJ, Chua YL, Discigil B, Schaff HV. Exogenous hyaluronidase induces release of nitric oxide from the coronary endothelium. J Thorac Cardiovasc Surg 2000;120:707-11.

11) Lee TK, Chen YC, Lien IN, Liu MC, Huang ZS. Inhibitory effect of acetylsalicylic acid on platelet function in patients with completed stroke or reversible ischemic neurologic deficit. Stroke 1988;19:566-70.

12) Yasuda O, Takemura Y, Kawamoto H, Rakugi H. Aspirin: recent developments. Cell Mol Life Sci 2008;65:354-8.

13) Schrör K. Aspirin and platelets: the antiplatelet action of aspirin and its role in thrombosis treatment and prophylaxis. Semin Thromb Hemost 1997;23:349-56.

14) Bilgen I, Oner G, Eren E. Dietary L-arginine restores aspirin-induced endothelial dysfunction in rat aorta. Arch Physiol Biochem 2003;111:232-8.

15) Iida H, Iida M, Takenaka M, Fukuoka N, Dohi S. Comparative effects of cilostazol and aspirin on the impairment of endothelium-dependent cerebral vasodilation caused by acute cigarette smoking in rats. J Thromb Thrombolysis 2010;29:483-8.

16) Magen E, Viskoper JR, Mishal J, Priluk R, London D, Yosefy C. Effects of low-dose aspirin on blood pressure and endothelial function of treated hypertensive hypercholesterolaemic subjects. J Hum Hypertens 2005;19:667-73.

17) Dorsam RT, Kunapuli SP. Central role of the P2Y12 receptor in platelet activation. J Clin Invest 2004;113:340-5.

18) Storey RF, Judge HM, Wilcox RG, Heptinstall S. Inhibition of ADP-induced P-selectin expression and platelet-leukocyte conjugate formation by clopidogrel and the P2Y12 receptor antagonist AR-C69931MX but not aspirin. Thromb Haemost 2002;88:488-94.

19) Wihlborg AK, Wang L, Braun OO, Eyjolfsson A, Gustafsson R, Gudbjartsson T, et al. ADP receptor P2Y12 is expressed in vascular smooth muscle cells and stimulates contraction in human blood vessels. Arterioscler Thromb Vasc Biol 2004;24:1810-5.

20) Buvinic S, Briones R, Huidobro-Toro JP. P2Y(1) and P2Y(2) receptors are coupled to the NO/cGMP pathway to vasodilate the rat arterial mesenteric bed. Br J Pharmacol 2002;136:847-56.

21) Guns PJ, Korda A, Crauwels HM, Van Assche T, Robaye B, Boeynaems JM, et al. Pharmacological characterization of nucleotide P2Y receptors on endothelial cells of the mouse aorta. Br J Pharmacol 2005;146:288-95.

22) Hess CN, Kou R, Johnson RP, Li GK, Michel T. ADP signaling in vascular endothelial cells: ADP-dependent activation of the endothelial isoform of nitric-oxide synthase requires the expression but not the kinase activity of AMPactivated protein kinase. J Biol Chem 2009;284:32209-24.

23) Yang LH, Hoppensteadt D, Fareed J. Modulation of vasoconstriction by clopidogrel and ticlopidine. Thromb Res 1998;92:83-9.

24) Jakubowski A, Chlopicki S, Olszanecki R, Jawien J, Lomnicka M, Dupin JP, et al. Endothelial action of thienopyridines and thienopyrimidinones in the isolated guinea pig heart. Prostaglandins Leukot Essent Fatty Acids 2005;72:139-45.

25) Froldi G, Bertin R, Dorigo P, Montopoli M, Caparrotta L. Endothelium-independent vasorelaxation by ticlopidine and clopidogrel in rat caudal artery. J Pharm Pharmacol 2011;63:1056-62. doi: 10.1111/j.2042-7158.2011.01313.x.

26) Offermanns S. Activation of platelet function through G protein-coupled receptors. Circ Res 2006;99:1293-304.

27) Sajid M, Stouffer GA. The role of alpha(v)beta3 integrins in vascular healing. Thromb Haemost 2002;87:187-93.

28) Kleiman NS. Pharmacokinetics and pharmacodynamics of glycoprotein IIb-IIIa inhibitors. Am Heart J 1999;138:263-75.

29) Iliodromitis EK, Andreadou I, Markantonis-Kyroudis S, Mademli K, Kyrzopoulos S, Georgiadou P, et al. The effects of tirofiban on peripheral markers of oxidative stress and endothelial dysfunction in patients with acute coronary syndromes. Thromb Res 2007;119:167-74.

30) Heitzer T, Ollmann I, Köke K, Meinertz T, Munzel T. Platelet glycoprotein IIb/IIIa receptor blockade improves vascular nitric oxide bioavailability in patients with coronary artery disease. Circulation 2003;108:536-41.

31) Warnholtz A, Ostad MA, Heitzer T, Goldmann BU, Nowak G, Munzel T. Effect of tirofiban on percutaneous coronary intervention-induced endothelial dysfunction in patients with stable coronary artery disease. Am J Cardiol 2005;95:20-3.

32) Kintscher U, Kappert K, Schmidt G, Doerr G, Grill M, Wollert-Wulf B, et al. Effects of abciximab and tirofiban on vitronectin receptors in human endothelial and smooth muscle cells. Eur J Pharmacol 2000;390:75-87.

Keywords : Acetylsalicylic acid; clopidogrel; endothelium; tirofiban
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