Literature DB >> 8056012

Accumulation of macrophages in the arterial vessel wall following experimental balloon angioplasty.

H Hanke1, S Hassenstein, A Ulmer, J Kamenz, M Oberhoff, K K Haase, A Baumbach, A M Gown, K R Karsch.   

Abstract

Smooth muscle cell (SMC) proliferation is a key event in the development of restenosis after balloon angioplasty, and it is thought that macrophages play an important role in the complex process of activation of SMCs after vascular injury induced by balloon angioplasty. The study was designed to determine the time course of the accumulation of macrophages in the intimal layer following experimental balloon angioplasty. To determine the extent and time course of the accumulation of macrophages after experimental balloon angioplasty, an intimal atheroma was produced by repeated weak electrical stimulation of the right carotid artery of 45 male New Zealand White rabbits. Additionally, the animals received an 0.5% cholesterol diet during the 28 days of plaque development. Transluminal balloon angioplasty was subsequently performed. At 3, 7, 14, 21, 28 and 42 days after balloon treatment the vessels from at least five animals from each group were excised and analysed for the presence of macrophages using immunocytochemical techniques. In one group of five animals plaque development occurred without subsequent balloon angioplasty; the animals were killed after 21 days (sham group). SMCs were identified by immunohistological staining of alpha-actin. Intimal thickening increased after dilatation from 137 +/- 62 microns (control group without balloon treatment) to 244 +/- 47 microns in the 42 days after angioplasty (P < 0.05). The percentage of macrophages in the intimal layer displayed a significant increase (P < 0.01) at 14 days after angioplasty (9.1 +/- 4.3% vs 2.0 +/- 1.7% in the control group).(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1994        PMID: 8056012     DOI: 10.1093/oxfordjournals.eurheartj.a060569

Source DB:  PubMed          Journal:  Eur Heart J        ISSN: 0195-668X            Impact factor:   29.983


  7 in total

1.  Attenuated herpes simplex virus 1 blocks arterial apoptosis and intimal hyperplasia induced by balloon angioplasty and reduced blood flow.

Authors:  Christopher L Skelly; Amito Chandiwal; James E Vosicky; Ralph R Weichselbaum; Bernard Roizman
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2.  Liposomal simvastatin attenuates neointimal hyperplasia in rats.

Authors:  Eyal Afergan; Meital Ben David; Hila Epstein; Nickolay Koroukhov; Dalia Gilhar; Keren Rohekar; Haim D Danenberg; Gershon Golomb
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3.  [Endovascular Ir-192 HDR brachytherapy for avoidance of intimal hyperplasia in peripheral vessels after PTA and stent implantation. A 6-year experience].

Authors:  H D Böttcher; B Schopohl
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4.  Enhanced neointimal growth in cultured rabbit aorta following in vivo balloon angioplasty.

Authors:  W E Dale; P S Batra; E H Blaine
Journal:  In Vitro Cell Dev Biol Anim       Date:  1998 Nov-Dec       Impact factor: 2.416

5.  Modulating vascular intimal hyperplasia using HSV-1 mutant requires activated MEK.

Authors:  C L Skelly; Q He; L Spiguel; S McCormick; R Weichselbaum
Journal:  Gene Ther       Date:  2012-03-15       Impact factor: 5.250

6.  Evidence for the Use of Multiple Mechanisms by Herpes Simplex Virus-1 R7020 to Inhibit Intimal Hyperplasia.

Authors:  Susan McCormick; Qi He; Jordan Stern; Nikolai Khodarev; Ralph Weichselbaum; Christopher L Skelly
Journal:  PLoS One       Date:  2015-07-01       Impact factor: 3.240

7.  Macrophage-stimulated microRNA expression in mural cells promotes transplantation-induced neointima formation.

Authors:  Xiaotong Guo; Mengyao Sun; Chaochao Dai; Xun Zhang; Qihui Yin; Jiaqi Ling; Xinyue Li; Xiao Wu; Fan Jiang; Jianli Wang
Journal:  Oncotarget       Date:  2017-05-02
  7 in total

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