Literature DB >> 16200460

Cellular destruction following transmyocardial laser revascularization (TMR).

S M Cherian1, Y V Bobryshev, D Tran, A Sivaraman, R S A Lord, K M Cherian.   

Abstract

During transmyocardial revascularization, cellular destruction of cardiomyocytes occurs as a result of the high-energy laser. However, the features of myocardial cellular destruction are unclear. The present study was undertaken to examine the structural characteristics of cell death in the myocardium following transmyocardial revascularization. Myocardial specimens from 3 male patients who had died within 11 days following laser revascularization were collected within 1 h of death and were analyzed by immunohistochemistry and electron microscopy. For immunohistochemistry, antibodies to pro-apoptotic proteins CPP32 and BAX were used. Immunohistochemical examination demonstrated the presence of cells expressing both CPP32 and BAX along the laser channel. Electron microscopic analysis revealed that the lining surface of laser channels consisted of condensed acellular debris and dead cells. No endothelialization of channels was noted. The lumen of laser channels were surrounded by a rim of acellular debris with several outer concentric rims of cardiomyocytes showing features of cellular destruction. The present study identified features of both necrotic and apoptotic cellular death following laser revascularization.

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Year:  2005        PMID: 16200460     DOI: 10.1007/s10735-005-5343-7

Source DB:  PubMed          Journal:  J Mol Histol        ISSN: 1567-2379            Impact factor:   2.611


  30 in total

1.  Hyalin degeneration in the cardiomyopathy of overload.

Authors:  J T Beranek
Journal:  J Mol Cell Cardiol       Date:  1995-02       Impact factor: 5.000

2.  Channel patency and neovascularization after transmyocardial revascularization using an excimer laser: results and comparisons to nonlased channels.

Authors:  C A Mack; C J Magovern; R T Hahn; T Sanborn; L Lanning; W Ko; O W Isom; T K Rosengart
Journal:  Circulation       Date:  1997-11-04       Impact factor: 29.690

3.  New concepts in revascularization of the myocardium.

Authors:  M Mirhoseini; S Shelgikar; M M Cayton
Journal:  Ann Thorac Surg       Date:  1988-04       Impact factor: 4.330

4.  Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures.

Authors:  S M Hsu; L Raine; H Fanger
Journal:  J Histochem Cytochem       Date:  1981-04       Impact factor: 2.479

5.  Ultrastructural and immunohistochemical analysis of early myocardial changes following transmyocardial laser revascularization.

Authors:  S M Cherian; Y V Bobryshev; H Liang; N M Sankar; S J Inder; A Y Wang; R S Lord; K M Cherian
Journal:  J Card Surg       Date:  2000 Sep-Oct       Impact factor: 1.620

6.  Apoptosis. Death gets a brake.

Authors:  A H Wyllie
Journal:  Nature       Date:  1994-05-26       Impact factor: 49.962

7.  Transmyocardial laser revascularization. Anatomic evidence of long-term channel patency.

Authors:  D A Cooley; O H Frazier; K A Kadipasaoglu; S Pehlivanoglu; R L Shannon; P Angelini
Journal:  Tex Heart Inst J       Date:  1994

8.  Intraoperative arrhythmias and tissue damage during transmyocardial laser revascularization.

Authors:  K A Kadipaşaoglu; M Sartori; T Masai; H B Cihan; F J Clubb; J L Conger; O H Frazier
Journal:  Ann Thorac Surg       Date:  1999-02       Impact factor: 4.330

9.  Chondrocyte necrosis and apoptosis in impact damaged articular cartilage.

Authors:  C T Chen; N Burton-Wurster; C Borden; K Hueffer; S E Bloom; G Lust
Journal:  J Orthop Res       Date:  2001-07       Impact factor: 3.494

Review 10.  Apoptosis, oncosis, and necrosis. An overview of cell death.

Authors:  G Majno; I Joris
Journal:  Am J Pathol       Date:  1995-01       Impact factor: 4.307

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