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1999 Fiscal Year Final Research Report Summary

Investigations for inhibition of arterial restenosis after metallic stent placement.

Research Project

Project/Area Number 09670922
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Radiation science
Research InstitutionFukui Medical University

Principal Investigator

SAKAI Toyohiko  Fukui Medical University, Faculty of Medicine, Assistant, 医学部, 助手 (40283189)

Project Period (FY) 1997 – 1999
KeywordsStent / Artery / Stenosis / Tranilast / Chitosan / Anticancer drug / Nitric oxide
Research Abstract

1) Effects of tranirast on inhibition of arterial restenosis
Ten rabbits were used for this experiment. Metallic stents were placed in the abdominal aorta in all rabbits. Four weeks after stent placement, all of them were sacrificed and the aortas were taken, and aortic specimen were made and microscopic obserbation was performed. For one week before and four weeks after the stent placemet, tranilast was orally treated for five of ten rabbits, and not for the other. Microscopically, all the specimen revealed intimal hyperplasia. The area of hyperplasia significantly decreased in the tranilast group than it in control.
2) Chitosan coating on metallic stent
Chitosan(1g) was solved in acetic acid(1N, 100ml). The metallic stent was placed into the solution and taken, and it was placed into the NaOH(1N, 100ml). Although some chitosan particles were attached on the surface of metallic stent, the coating seemed uneven and imcomplete. Further investigation would be necessary.
3) Effects of anticancer drugs on the vascular endotherial function.
Farmorbicin(EPIR), mitomycine(MMC), and fluorouracil(5-FU) were examined for this experiment. The rat thoracic aorta was removed and placed in the Krebs solution. The helical strips were made and the relaxation response to acetylcholine(Ach) and sodium nitroprusside (SNP) were evaluated. EPIR affected the relaxation response to Ach but did not it to SNP. MMC and 5-FU did not affect the relaxation response to Ach and SNP. These results reveal EPIR impairs endotherial function.

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Published: 2001-10-23  

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