Literature DB >> 18287663

Histological and morphometric analyses for rat carotid balloon injury model.

David A Tulis1.   

Abstract

Experiments aimed at analyzing the response of blood vessels to mechanical injury and ensuing remodeling responses often employ the highly characterized carotid artery balloon injury model in laboratory rats. This approach utilizes luminal insertion of a balloon embolectomy catheter into the common carotid artery with inflation and withdrawal resulting in an injury characterized by vascular endothelial cell (EC) denudation and medial wall distension. The adaptive response to this injury is typified by robust vascular smooth muscle cell (SMC) replication and migration, SMC apoptosis and necrosis, enhanced synthesis and deposition of extracellular matrix (ECM) components, partial vascular EC regeneration from the border zones, luminal narrowing, and establishment of a neointima in time-dependent fashion. Evaluation of these adaptive responses to blood vessel injury can include acute and longer term qualitative and quantitative measures including expression analyses, activity assays, immunostaining for a plethora of factors and signals, and morphometry of neointima formation and gross mural remodeling. This chapter presents a logical continuation of Chapter 1 that offers details for performing the rat carotid artery balloon injury model in a standard laboratory setting by providing commonly used protocols for performing histological and morphometric analyses in such studies. Moreover, procedures, caveats, and considerations included in this chapter are highly relevant for alternative animal vascular physiology/pathophysiology studies and in particular those related to mechanisms of vascular injury and repair. Included in this chapter are specifics for in situ perfusion-fixation, tissue harvesting and processing for both snap-frozen and paraffin-embedded protocols, specimen embedding and sectioning, slide preparation, several standard histological staining steps, and routine morphological assessment.

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Year:  2007        PMID: 18287663      PMCID: PMC2831536          DOI: 10.1007/978-1-59745-571-8_2

Source DB:  PubMed          Journal:  Methods Mol Med        ISSN: 1543-1894


  4 in total

1.  YC-1, a benzyl indazole derivative, stimulates vascular cGMP and inhibits neointima formation.

Authors:  D A Tulis; W Durante; K J Peyton; G B Chapman; A J Evans; A I Schafer
Journal:  Biochem Biophys Res Commun       Date:  2000-12-20       Impact factor: 3.575

2.  Kinetics of cellular proliferation after arterial injury. III. Endothelial and smooth muscle growth in chronically denuded vessels.

Authors:  A W Clowes; M M Clowes; M A Reidy
Journal:  Lab Invest       Date:  1986-03       Impact factor: 5.662

3.  Mechanisms of stenosis after arterial injury.

Authors:  A W Clowes; M A Reidy; M M Clowes
Journal:  Lab Invest       Date:  1983-08       Impact factor: 5.662

4.  Heme oxygenase-1 attenuates vascular remodeling following balloon injury in rat carotid arteries.

Authors:  D A Tulis; W Durante; K J Peyton; A J Evans; A I Schafer
Journal:  Atherosclerosis       Date:  2001-03       Impact factor: 5.162

  4 in total
  16 in total

1.  Response gene to complement 32 promotes vascular lesion formation through stimulation of smooth muscle cell proliferation and migration.

Authors:  Jia-Ning Wang; Ning Shi; Wei-Bing Xie; Xia Guo; Shi-You Chen
Journal:  Arterioscler Thromb Vasc Biol       Date:  2011-06-02       Impact factor: 8.311

2.  A Rat Carotid Artery Pressure-Controlled Segmental Balloon Injury with Periadventitial Therapeutic Application.

Authors:  Nicholas E Buglak; Edward S M Bahnson
Journal:  J Vis Exp       Date:  2020-07-09       Impact factor: 1.355

3.  Manganese superoxide dismutase inhibits neointima formation through attenuation of migration and proliferation of vascular smooth muscle cells.

Authors:  Jia-Ning Wang; Ning Shi; Shi-You Chen
Journal:  Free Radic Biol Med       Date:  2011-10-24       Impact factor: 7.376

4.  Soluble guanylyl cyclase-activated cyclic GMP-dependent protein kinase inhibits arterial smooth muscle cell migration independent of VASP-serine 239 phosphorylation.

Authors:  Andrew W Holt; Danielle N Martin; Patti R Shaver; Shaquria P Adderley; Joshua D Stone; Chintamani N Joshi; Jake T Francisco; Robert M Lust; Douglas A Weidner; Brian M Shewchuk; David A Tulis
Journal:  Cell Signal       Date:  2016-06-11       Impact factor: 4.315

5.  Label-free imaging of atherosclerotic plaques using third-harmonic generation microscopy.

Authors:  David M Small; Jason S Jones; Irwin I Tendler; Paul E Miller; Andre Ghetti; Nozomi Nishimura
Journal:  Biomed Opt Express       Date:  2017-12-13       Impact factor: 3.732

6.  The soluble guanylate cyclase stimulator BAY 41-2272 inhibits vascular smooth muscle growth through the cAMP-dependent protein kinase and cGMP-dependent protein kinase pathways.

Authors:  Chintamani N Joshi; Danielle N Martin; Jonathan C Fox; Natalia N Mendelev; Trisha A Brown; David A Tulis
Journal:  J Pharmacol Exp Ther       Date:  2011-08-08       Impact factor: 4.030

7.  Tissue vibration induces carotid artery endothelial dysfunction: a mechanism linking snoring and carotid atherosclerosis?

Authors:  Jin-Gun Cho; Paul K Witting; Manisha Verma; Ben J Wu; Anu Shanu; Kristina Kairaitis; Terence C Amis; John R Wheatley
Journal:  Sleep       Date:  2011-06-01       Impact factor: 5.849

8.  Periostin mediates vascular smooth muscle cell migration through the integrins alphavbeta3 and alphavbeta5 and focal adhesion kinase (FAK) pathway.

Authors:  Guohong Li; Rong Jin; Russell A Norris; Lin Zhang; Shiyong Yu; Fusheng Wu; Roger R Markwald; Anil Nanda; Simon J Conway; Susan S Smyth; D Neil Granger
Journal:  Atherosclerosis       Date:  2009-07-30       Impact factor: 5.162

9.  A microstructurally motivated model of arterial wall mechanics with mechanobiological implications.

Authors:  C Bellini; J Ferruzzi; S Roccabianca; E S Di Martino; J D Humphrey
Journal:  Ann Biomed Eng       Date:  2013-11-07       Impact factor: 3.934

10.  AMP-activated protein kinase inhibits vascular smooth muscle cell proliferation and migration and vascular remodeling following injury.

Authors:  Joshua D Stone; Avinash Narine; Patti R Shaver; Jonathan C Fox; Jackson R Vuncannon; David A Tulis
Journal:  Am J Physiol Heart Circ Physiol       Date:  2012-11-30       Impact factor: 4.733

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