Int J Angiol 2015; 24(01): 67-70
DOI: 10.1055/s-0034-1383433
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Effect of Cilostazol on the P50 of the Oxygen-Hemoglobin Dissociation Curve

Marshalyn McKoy
1   Department of Basic Medical Sciences, The University of the West Indies, Mona Campus, Kingston, Surrey, Jamaica
,
Kyomi Allen
1   Department of Basic Medical Sciences, The University of the West Indies, Mona Campus, Kingston, Surrey, Jamaica
,
Andrea Richards
1   Department of Basic Medical Sciences, The University of the West Indies, Mona Campus, Kingston, Surrey, Jamaica
,
Dagogo Pepple
1   Department of Basic Medical Sciences, The University of the West Indies, Mona Campus, Kingston, Surrey, Jamaica
› Author Affiliations
Further Information

Publication History

Publication Date:
03 September 2014 (online)

Abstract

Cilostazol is a drug used for the treatment of intermittent claudication caused by narrowing of the blood vessels and reduced oxygen supply, characterized by intense pain in the leg when walking. This study was designed to investigate the effect of cilostazol on the P50 of the oxygen hemoglobin dissociation curve. A total of eight healthy adult subjects were studied. Blood samples (0.5 mL) from each subject were mixed with 5, 10, and 20 μL of the 0.5 mg/mL stock solution of cilostazol to give concentrations of 10, 20, and 40 µg/mL equivalent to adult doses of 50, 100, and 200 mg, respectively. The control sample had no drug added. The oxygen hemoglobin dissociation curve of each sample was plotted and the P50 determined with a Hemox-Analyzer (TCS, Medical Products Division, Southampton, PA). The mean P50 for the control samples was 28.27 ± 0.43 mm Hg. The values of the samples exposed to 10, 20, and 40 µg/mL cilostozol were 29.63 ± 0.66, 30.15 ± 0.77, and 31.66 ± 0.62 mm Hg, respectively. There was a statistically significant difference (p < 0.01) between the control and samples exposed to 40 µg/mL cilostazol. This study suggests that cilostazol caused an increase in the release of oxygen from hemoglobin as shown in the P50 values. This effect was significant at the highest concentration of 40 µg/mL.

 
  • References

  • 1 Dawson DL, Zheng Q, Worthy SA, Charles B, Bradley Jr DV. Failure of pentoxifylline or cilostazol to improve blood and plasma viscosity, fibrinogen, and erythrocyte deformability in claudication. Angiology 2002; 53 (5) 509-520
  • 2 Adderley SP, Thuet KM, Sridharan M , et al. Identification of cytosolic phosphodiesterases in the erythrocyte: a possible role for PDE5. Med Sci Monit 2011; 17 (5) CR241-CR247
  • 3 Dunkerley HA, Tilley DG, Palmer D, Liu H, Jimmo SL, Maurice DH. Reduced phosphodiesterase 3 activity and phosphodiesterase 3A level in synthetic vascular smooth muscle cells: implications for use of phosphodiesterase 3 inhibitors in cardiovascular tissues. Mol Pharmacol 2002; 61 (5) 1033-1040
  • 4 Schrör K. The pharmacology of cilostazol. Diabetes Obes Metab 2002; 4 (Suppl. 02) S14-S19
  • 5 Hotta N, Nakamura J, Sakakibara F , et al. Electroretinogram in sucrose-fed diabetic rats treated with an aldose reductase inhibitor or an anticoagulant. Am J Physiol 1997; 273 (5 Pt 1) E965-E971
  • 6 MacDonald R. Red cell 2,3-diphosphoglycerate and oxygen affinity. Anaesthesia 1977; 32 (6) 544-553
  • 7 Guarnone R, Centenara E, Barosi G. Performance characteristics of Hemox-Analyzer for assessment of the hemoglobin dissociation curve. Haematologica 1995; 80 (5) 426-430
  • 8 Dawson DL, Cutler BS, Meissner MH, Strandness Jr DE. Cilostazol has beneficial effects in treatment of intermittent claudication: results from a multicenter, randomized, prospective, double-blind trial. Circulation 1998; 98 (7) 678-686