Skip to main content
Log in

Effect of Probucol on Smooth Muscle Cell Proliferation and Dedifferentiation After Vascular Injury in Rabbits: Possible Role of PDGF

  • Published:
Cardiovascular Drugs and Therapy Aims and scope Submit manuscript

Abstract

We previously reported a clinical study in which probucol reduced the restenosis rate. The mechanism of this effect is unclear. Restenosis is characterized by neointimal hyperplasia caused by proliferation of smooth muscle cells (SMCs), which increases the expression of Platelet-derived growth factor (PDGF)-A and SMemb. SMemb, a non–muscle-type myosin heavy chain most predominantly expressed in embryonic smooth muscle, can be used as a good molecular marker for dedifferentiated SMC. The aim of this study was to analyze the effect of probucol on neointimal proliferation and the level of expression of PDGF-A and SMemb after balloon injury in rabbits. Probucol was given orally 1.3 g/d from 2 weeks prior to carotid balloon injury to the time of killing (2 or 4 weeks after balloon injury). Intimal area was determined histologically using a computerized morphometry program. For quantification of SMC proliferation, alpha-actin–positive cells and proliferating cell nuclear antigen (PCNA)-labeled cells were counted. The expression of PDGF-A and SMemb mRNA was analyzed by the RNase protection assay. SMemb expression was also examined by immunohistochemistry. Probucol remarkably decreased intimal area by 70% and the number of SMC and PCNA-labeled cells in the intima. The expression of PDGF-A mRNA was significantly increased after balloon injury in untreated rabbits, whereas it was markedly suppressed with probucol treatment. The expression of SMemb was significantly increased in injured arteries at mRNA and protein levels. However, probucol did not suppress SMemb expression. Probucol is effective in preventing SMC proliferation, which is possibly due to a decrease in the expression of PDGF.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Popma JJ, Topol EJ. Factors influencing restenosis after coronary angioplasty. Am J Med 1990;88:1N-16N.

    Google Scholar 

  2. Beatt KJ, Serruys PW, Hugenholtz PG. Restenosis after coronary angioplasty: New standards for clinical studies. J Am Coll Cardiol 1990;15:491-498.

    Google Scholar 

  3. Liu MW, Roubin GS, King SB III. Restenosis after coronary angioplasty: Potential biologic determinants and role of intimal hyperplasia. Circulation 1989;79:1374-1387.

    Google Scholar 

  4. Popma JJ, Califf RM, Topol EJ. Clinical trials of restenosis after coronary angioplasty. Circulation 1991;84:1426-1436

    Google Scholar 

  5. Schwartz RS, Holmes DR, Topol EJ. The restenosis paradigm revisited: An alternative proposal for cellular mechanism. J Am Coll Cardiol 1992;20:1284-1293

    Google Scholar 

  6. Lee YJ, Yamaguchi H, Daida H, et al. PTCA: Pharmacological interventions to modify restenosis (abstr). Circulation 1991;84:II-298.

    Google Scholar 

  7. Kisanuki A, Asada Y, Hatakeyama K, Hayashi T, Sumiyoshi A. Contribution of the endothelial to intimal thickening in normocholesterolemic and hypercholesterolemic rabbits. Arterioscler Thromb 1992;88:628-637

    Google Scholar 

  8. Shinomiya M, Shirai K, Saito Y, Yoshida S. Inhibition of intimal thickening of the carotid artery of rabbits and of outgrowth of explants of aorta by probucol. Atherosclerosis 1992;97:143-148

    Google Scholar 

  9. Ferns GAA, Forster L, Stewart-Lee A, Konneh M, Nourooz-Zadeh J, Anggard EE. Probucol inhibits neointimal thickening and macrophage accumulation after balloon injury in the cholesterol-fed rabbit. Proc Natl Acad Sci 1992;89:11312-11316

    Google Scholar 

  10. Schneider JE, Berk BC, Gravanis MB, et al. Probucol decreases neointimal formation in a swine model of coronary artery balloon injury. A possible role for antioxidant in restenosis. Circulation 1993;88:628-637

    Google Scholar 

  11. Akeson AL, Woods CW, Mosher LB, Thomas CE, Jackson RL. Inhibition of IL-1 β expression in THP-1 cells by probucol and tocopherol. Atherosclerosis 1991;86:261-270

    Google Scholar 

  12. Ku G, Doherty NS, Schmidt LF, Jackson RL, Dinerstein RJ. Ex vivo lipopolysaccharide-induced interleukin-1 secretion from murine peritoneal macrophages inhibited by probucol, a hypocholesterolemic agent with antioxidant properties. FASEB J 1990;4:1645-1653

    Google Scholar 

  13. Hanke H, Strohschneider T, Oberhoff M, Betz E, Karsch KR. Time course of smooth muscle cell proliferation in the intima and media of arteries following experimental angioplasty. Circ Res 1990;67:651-659

    Google Scholar 

  14. Ueda M, Becker AE, Tsukada T, Numano F, Fujimoto T. Fibrocellular tissue response after percutaneous transluminal coronary angioplasty. An immunocytochemical analysis of the cellular composition. Circulation 1991;83:1327- 1332

    Google Scholar 

  15. Kuro-o M, Nagai R, Nakahara K, et al. cDNA cloning of a myosin heavy chain isoform in embryonic smooth muscle and expression during vascular development and in arteriosclerosis. J Biol Chem 1991;266:3768-3773

    Google Scholar 

  16. Nagai R, Kuro-o M, Babij P, Periasamy M. Identification of two types of smooth muscle myosin heavy chain isoforms by cDNA cloning and immunoblot analysis. J Biol Chem 1989;264:9734-9737.

    Google Scholar 

  17. Kuro-o M, Nagai R, Tsuchimochi H, et al. Developmentally regulated expression of vascular smooth muscle myosin heavy chain isoforms. J Biol Chem 1989;264:18272-18275

    Google Scholar 

  18. Hedin U, Thyberg J. Plasma fibronectin promotes modulation of arterial smooth-muscle cells from contractile to the synthetic phenotype. Differentiation 1987;33:239-346

    Google Scholar 

  19. Hedin U, Bottger BA, Forsberg E, Johansson S, Thyberg J. Diverse effects of fibronectin and laminin on phenotypic properties of cultured arterial smooth muscle cells. J Cell Biol 1988;107:307-319

    Google Scholar 

  20. Weissberg PL, Grainger DJ, Shanahan CM, Metcalfe JC. Approaches to the development of selective inhibitors of vascular smooth muscle cell proliferation. Cardiovascular Res 1993;27:1191-1198

    Google Scholar 

  21. Ross R. The pathogenesis of atherosclerosis-an update. N Engl J Med 1986;314:488-500

    Google Scholar 

  22. Mao SJT, Yates MT, Rechtin AE, Jackson RL, Van Sickle WA. Antioxidant activity of probucol and its analogies in hypercholesterolemic Watanabe rabbits. J Med Chem 1991; 34:299-302

    Google Scholar 

  23. Kim HS, Aikawa M, Kimura K, et al. Ductus arteriosus: Advanced differentiation of smooth muscle cell demonstrated by myosin heavy chain isoform expression in rabbits. Circulation 1993;88:1804-1810

    Google Scholar 

  24. Anderson PG. Restenosis: Animal models and morphometric techniques in studies of the vascular response to injury. Cardiovasc Pathol 1992;1:263-278.

    Google Scholar 

  25. Chomezynski P, Saccini N. Single step method of RNA isolation by acid guanidinium thiocyanate-phenol chloroform extraction. Anal Biochem 1987;162:156-159

    Google Scholar 

  26. Nakahara K, Nishimura H, Kuro-o M, et al. Identification of three types of PDGF-A chain gene transcripts in rabbit vascular smooth muscle and their regulated expression during development and by angiotensin II. Biochem Biophys Res Commun 1992;184:811-818

    Google Scholar 

  27. Aikawa M, Sivam PN, Kuro-o M, et al. Human smooth muscle myosin heavy chain isoforms as molecular markers for vascular development and atherosclerosis. Circ Res 1993;73:1000-1012

    Google Scholar 

  28. Sabath D, Broome HE, Prystowsky MB. Glyceraldehyde-3-phosphate dehydrogenase mRNA is a major interleukin 2-induced transcript in a cloned T-helper lymphocyte. Gene 1990;91:185-191.

    Google Scholar 

  29. Godfried SL, Deckelbaum LI. Natural antioxidants and restenosis after percutaneous transluminal coronary angioplasty. Am Heart J 1995;129:203-210

    Google Scholar 

  30. Simons M, Leclerc G, Safian RD, Isner JM, Weir L, Baim DS. Relation between activated smooth-muscle cells in coronary-artery lesions and restenosis after atherectomy. N Engl J Med 1993;328:608-613

    Google Scholar 

  31. Suzuki J, Isobe M, Aikawa M, et al. Nonmuscle and smooth muscle myosin heavy chain expression in rejected cardiac allografts. Circulation 1996;94:1118-1124

    Google Scholar 

  32. Kurki P, Ogata K, Tan EM. Monoclonal antibodies to proliferating cell nuclear antigen PCNA/cyclin as probes for proliferating cells by immunofluorecence microscopy and flow cytometry. J Immunol Methods 1988;109:49-55

    Google Scholar 

  33. Majesky MW, Reidy MA, Bowen Pope DF, Hart CE, Wicox JN, Schwarz SM. PDGF ligand and receptor gene expression during repair of arterial injury. J Cell Biol 1990; 111:2149-2158

    Google Scholar 

  34. Ross R, Glomset JA. The pathogenesis of atherosclerosis (part 2). N Engl J Med 1976;295:420-425

    Google Scholar 

  35. Ku G, Doherty NS, Wolos JA, Jackson RL, Schmidt LF, Hendricks D. Inhibition by probucol of interleukin 1 secretion and its implication in atherosclerosis. Am J Cardiol 1988;62:77B-81B

    Google Scholar 

  36. Raines EW, Dower SK, Ross R. Interleukin-1 mitogenic activity for fibroblast and smooth muscle cell is due to PDGF-AA. Science 1989;243:393-396

    Google Scholar 

  37. Powell JS, Clozel JP, Muller RKM, et al. Inhibitors of angiotensin-converting enzyme prevent myointimal proliferation after vascular injury. Science 1989;245:186-188

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Miyauchi, K., Aikawa, M., Tani, T. et al. Effect of Probucol on Smooth Muscle Cell Proliferation and Dedifferentiation After Vascular Injury in Rabbits: Possible Role of PDGF. Cardiovasc Drugs Ther 12, 251–260 (1998). https://doi.org/10.1023/A:1007761631674

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1007761631674

Navigation