Literature DB >> 11231463

Nitric oxide synthase isoform expression in a porcine model of granulation tissue formation.

J S Pollock1, W Webb, D Callaway, W O'Brien, T R Howdieshell.   

Abstract

BACKGROUND: This study was designed to determine whether the nitric oxide (NO) pathway is involved in wound granulation tissue formation.
METHODS: A section of the pig abdominal wall (excluding the skin) was excised, creating an incisional hernia. The resulting defect was repaired with silicone sheeting in a manner that mimics a temporary abdominal wall closure. During the 14-day experimental period, porcine omentum adhered to the peritoneal edges of the defect and a highly vascularized granulation tissue formed on both sides of the sheeting. Granulation tissue thickness and wound fluid volume were monitored by ultrasonography and epigastric artery flow velocity was monitored by color Doppler flow analysis at days 2, 4, 7, 9, 11, and 14. Fluid was serially harvested from the wound compartment at days 2, 4, 7, 9, 11, and 14 for nitrite/ nitrate (NOx) analysis. Finally, granulation tissue was harvested at day 14 for immunohistochemical and molecular analyses.
RESULTS: There was a significant increase in granulation tissue thickness and wound fluid volume during the 14-day study period. Blood flow to the wound increased significantly by day 4 and returned toward baseline by day 14. Wound fluid NOx levels significantly increased from days 7 to 11 and then decreased to near baseline values by day 14. Wound fluid arginine levels significantly decreased when compared with peritoneal fluid and plasma levels at day 14, while wound fluid ornithine levels significantly increased. Immunohistochemical analysis of granulation tissue at day 14 revealed nitric oxide synthase (NOS) 2 was present in the majority of the cells in the granulation tissue. NOS 3 was expressed in endothelial cells only, and NOS 1 expression was not observed in the granulation tissue.
CONCLUSIONS: This study suggests that NO, NOS 2, and arginine may play critical roles in granulation tissue formation and wound healing. Arginase and NOS 2 may compete for available arginine as a substrate, thereby limiting later NO production in favor of sustained ornithine synthesis.

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Year:  2001        PMID: 11231463     DOI: 10.1067/msy.2001.111700

Source DB:  PubMed          Journal:  Surgery        ISSN: 0039-6060            Impact factor:   3.982


  4 in total

1.  Upregulation of arginase-II contributes to decreased age-related myocardial contractile reserve.

Authors:  Mehnaz Khan; Jochen Steppan; Karl H Schuleri; Karl Schuleri; Sungwoo Ryoo; Eric Tuday; Lukasz Bugaj; Lakshmi Santhanam; Tal Berkowitz; Daniel Nyhan; Artin A Shoukas; Dan E Berkowitz
Journal:  Eur J Appl Physiol       Date:  2011-12-08       Impact factor: 3.078

2.  Novel nitric oxide producing probiotic wound healing patch: preparation and in vivo analysis in a New Zealand white rabbit model of ischaemic and infected wounds.

Authors:  Mitchell Jones; Jorge G Ganopolsky; Alain Labbé; Mirko Gilardino; Christopher Wahl; Christopher Martoni; Satya Prakash
Journal:  Int Wound J       Date:  2012-01-06       Impact factor: 3.315

3.  Hyperbaric oxygen therapy mediates increased nitric oxide production associated with wound healing: a preliminary study.

Authors:  Joseph V Boykin; Chris Baylis
Journal:  Adv Skin Wound Care       Date:  2007-07       Impact factor: 2.347

4.  Effect of L-arginine supplement on liver regeneration after partial hepatectomy in rats.

Authors:  Tsuyoshi Kurokawa; Jun An; Koji Tsunekawa; Yoshiharu Shimomura; Shunsuke Kazama; Naohisa Ishikawa; Toshiaki Nonami; Satoru Sugiyama
Journal:  World J Surg Oncol       Date:  2012-05-31       Impact factor: 2.754

  4 in total

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