Int J Angiol
DOI: 10.1055/s-0044-1779300
Review Article

Postoperative Intimal Hyperplasia: Review from My Research

Mitsuhiro Yamamura
1   Department of Cardiovascular Surgery, Hyogo Medical University, Nishinomiya-city, Hyogo, Japan
› Author Affiliations
Funding This study was supported by Grant-in-Aid for Scientific Research “KAKENHI” 2000, Japan; Grant-in-Aid for Researchers, Hyogo College of Medicine, 2003–2004, 2006–2007, Japan; Fujisawa Pharmaceutical Co., Ltd., Japan (FR-167653); and Mitsubishi Tanabe Pharma Co., Japan (Radicut®).[*]

Abstract

Postoperative intimal hyperplasia is the major cause of the vein graft occlusion. It is very important to establish an animal model for the start of research. After my vascular surgery residency in Japan, I started my research work on postoperative intimal hyperplasia at the University of Wisconsin-Madison. My research showed that endothelial injury and monocyte infiltration is the key for postoperative intimal hyperplasia, which is very similar to Ross' pathogenesis of atherosclerosis as an inflammatory disease. Focusing on postoperative intimal hyperplasia as an inflammatory disease, especially on tumor necrosis factor-α, FR-167653 (tumor necrosis factor-α suppressive agent, inhibitor of p38 mitogen-activated protein kinase; Fujisawa Pharmaceutical Co., Ltd., Japan) is found to suppress postoperative intimal hyperplasia in a rat model by reducing serum monocyte chemoattractant protein-1 levels. However, FR-167653 is not commercially available today. Because endothelial injury is the first step of postoperative intimal hyperplasia, I investigated whether the free radical scavenger, edaravone (Radicut, Mitsubishi Tanabe Pharma Co., Japan), which alleviates the endothelial injury in vitro, can also suppress postoperative intimal hyperplasia. Moreover, the free radical scavenger edaravone (Radicut®, Mitsubishi Tanabe Pharma Co.) is also found to suppress postoperative intimal hyperplasia, by alleviating endothelial injury. In clinical settings, it is very important to detect postoperative intimal hyperplasia before its establishment. Hepatocyte growth factor is not only a hepatic growth factor but also a vascular endothelial growth factor. Recently, serum hepatocyte growth factor level was found to be a candidate biomarker for postoperative intimal hyperplasia in our rat model.

Note

This review was presented at the 64th Annual World Congress, International College of Angiology in Davenport, Iowa, United States on September 15, 2023.


* Approved by FDA for the treatment of Amyotrophic Lateral Sclerosis (ALS), as RADICAVA® in United States.




Publication History

Article published online:
05 February 2024

© 2024. International College of Angiology. This article is published by Thieme.

Thieme Medical Publishers, Inc.
333 Seventh Avenue, 18th Floor, New York, NY 10001, USA

 
  • References

  • 1 Grondin CM, Campeau L, Lespérance J, Enjalbert M, Bourassa MG. Comparison of late changes in internal mammary artery and saphenous vein grafts in two consecutive series of patients 10 years after operation. Circulation 1984; 70 (3, Pt 2, suppl): I208-I212
  • 2 Hirsch GM, Karnovsky MJ. Inhibition of vein graft intimal proliferative lesions in the rat by heparin. Am J Pathol 1991; 139 (03) 581-587
  • 3 Hoch JR, Stark VK, Hullett DA, Turnipseed WD. Vein graft intimal hyperplasia: leukocytes and cytokine gene expression. Surgery 1994; 116 (02) 463-470 , discussion 470–471
  • 4 Yamamura M, Hoch JR, Strak VK. et al. The animal model of intimal hyperplasia after vein graft operation. Presented at: The 6th Annual Meeting of Asian Society for Cardiovascular Surgery; February 18–20, 1998; Tokyo, Japan
  • 5 Yamamura M, Miyamoto T, Hoch JR. Tumor necrosis factor-α expression in rat models of intimal hyperplasia. Int J Angiol 2001; 10: 77-79
  • 6 Yamamura M, Hoch JR, Strak VK, Malionowski RL, Nutt MP. Monocyte chemoattracted protein expression: difference in the development of vein graft and arterial intimal hyperplasia. Presented at: 47th Joint Annual Meeting of the Society for Vascular Surgery and the North American Chapter of the International Society for Cardiovascular Surgery; June 6–9, 1999; Washington, DC
  • 7 Ross R. Atherosclerosis: an inflammatory disease. N Engl J Med 1999; 340 (02) 115-126
  • 8 Yamamura M, Miyamoto Y. Postoperative Intimal Hyperplasia. J Jpn Coll Angiol 2007; 47: 421-427
  • 9 Yamamura M, Miyamoto T, Hoch JR. Monocyte chemoattractant protein-1 RNA expression in intimal hyperplasia of vein grafts in a rat model. Surg Today 2002; 20: 329-334
  • 10 Yamamoto N, Sakai F, Yamazaki H, Nakahara K, Okuhara M. Effect of FR167653, a cytokine suppressive agent, on endotoxin-induced disseminated intravascular coagulation. Eur J Pharmacol 1996; 314 (1–2): 137-142
  • 11 Yamamura M, Miyamoto T, Yao H. The effect of FR-167653 on postoperative intimal hyperplasia of the interposition vein graft in rat: 2nd Report. Jpn J Cardiovasc Surg 2003; 32: 75-78
  • 12 Yamamura M, Miyamoto Y, Mukai S. et al. Mechanism of FR-167653 against postoperative intimal hyperplasia. J Jpn Coll Angiol 2005; 45: 263-267
  • 13 Watanabe K, Watanabe K, Hayase T. Radical scavenging mechanism of MCI-186. Jpn Pharmacol Ther 1997; 25 (suppl): S1699-S1707
  • 14 Watanabe T, Morita I, Nishi H, Murota S. Preventive effect of MCI-186 on 15-HPETE induced vascular endothelial cell injury in vitro. Prostaglandins Leukot Essent Fatty Acids 1988; 33 (01) 81-87
  • 15 Yamamura M, Miyamoto Y, Mitsuno M. et al. Suppression of postoperative intimal hyperplasia of vein graft with edaravone in a rat model. Int J Angiol 2005; 14: 151-154
  • 16 Yamamura M, Miyamoto Y, Mitsuno M, Tanaka H, Kobayashi Y, Ryomoto M. Suppression of postoperative intimal hyperplasia of vein grafts with edaravone in rat models - a scanning electron microscope study. Int J Angiol 2007; 16 (04) 143-145
  • 17 Yamamura M, Mitsuno M, Tanaka H, Kobayashi Y, Fukui S, Miyamoto Y. Edaravone suppresses endothelial cell injury in vein grafts of a rat model. Int J Angiol 2008; 17 (04) 221-222
  • 18 Nakamura T, Nishizawa T, Hagiya M. et al. Molecular cloning and expression of human hepatocyte growth factor. Nature 1989; 342 (6248): 440-443
  • 19 Van Belle E, Witzenbichler B, Chen D. et al. Potentiated angiogenic effect of scatter factor/hepatocyte growth factor via induction of vascular endothelial growth factor: the case for paracrine amplification of angiogenesis. Circulation 1998; 97 (04) 381-390
  • 20 Harada M, Takenaka H, Ikenaga S. et al. Hepatocyte growth factor prevents intimal hyperplasia in rabbit carotid expanded polytetrafluoroethylene grafting. J Vasc Surg 2002; 35 (04) 786-791
  • 21 Morishita R, Nakamura S, Hayashi S. et al. Therapeutic angiogenesis induced by human recombinant hepatocyte growth factor in rabbit hind limb ischemia model as cytokine supplement therapy. Hypertension 1999; 33 (06) 1379-1384
  • 22 Shigematsu H, Yasuda K, Iwai T. et al. Randomized, double-blind, placebo-controlled clinical trial of hepatocyte growth factor plasmid for critical limb ischemia. Gene Ther 2010; 17 (09) 1152-1161
  • 23 Yamamura M, Ryomoto M, Sekiya N, Uemura H, Nishimyama M, Sakaguchi T. Serum hepatocyte growth factor level as the biomarker for postoperative intimal hyperplasia. J Vasc Surg 2020; 72 (Supplement e) e260