The Effect of a Synthetic Heparan Sulfate on the Healing of Colonic Anastomoses

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Standard

The Effect of a Synthetic Heparan Sulfate on the Healing of Colonic Anastomoses. / Nerstrøm, Malene; Krarup, Peter-Martin; Jorgensen, Lars Nannestad; Ågren, Magnus S.

I: Gastroenterology Research and Practice, Bind 2017, 1078062, 2017.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Nerstrøm, M, Krarup, P-M, Jorgensen, LN & Ågren, MS 2017, 'The Effect of a Synthetic Heparan Sulfate on the Healing of Colonic Anastomoses', Gastroenterology Research and Practice, bind 2017, 1078062. https://doi.org/10.1155/2017/1078062

APA

Nerstrøm, M., Krarup, P-M., Jorgensen, L. N., & Ågren, M. S. (2017). The Effect of a Synthetic Heparan Sulfate on the Healing of Colonic Anastomoses. Gastroenterology Research and Practice, 2017, [1078062]. https://doi.org/10.1155/2017/1078062

Vancouver

Nerstrøm M, Krarup P-M, Jorgensen LN, Ågren MS. The Effect of a Synthetic Heparan Sulfate on the Healing of Colonic Anastomoses. Gastroenterology Research and Practice. 2017;2017. 1078062. https://doi.org/10.1155/2017/1078062

Author

Nerstrøm, Malene ; Krarup, Peter-Martin ; Jorgensen, Lars Nannestad ; Ågren, Magnus S. / The Effect of a Synthetic Heparan Sulfate on the Healing of Colonic Anastomoses. I: Gastroenterology Research and Practice. 2017 ; Bind 2017.

Bibtex

@article{aba21210f3bd4edda202a1124c14ccbb,
title = "The Effect of a Synthetic Heparan Sulfate on the Healing of Colonic Anastomoses",
abstract = "BACKGROUND: The mimetic compound OTR4120 may replace endogenous-degraded heparan sulfates that normally maintain the bioactivity of growth factors that are important for tissue repair. Herein, we investigated the effect of OTR4120 on the healing of normal colonic anastomoses.METHODS: We evaluated the following two treatment groups of male Sprague Dawley rats (220-256 g): control-treated colonic anastomoses (n = 25) and OTR4120-treated colonic anastomoses (n = 25). We resected 10 mm of the left colon and then applied either saline alone (control) or OTR4120 (100 μg/mL) in saline to the colonic ends before an end-to-end single-layer anastomosis was constructed and again on the anastomosis before the abdomen and skin were closed.RESULTS: On postoperative day 3, the anastomotic breaking strengths were 1.47 ± 0.32 N (mean ± SD) in the control group and 1.52 ± 0.27 N in the OTR4120-treated animals (P = 0.622). We also found that the hydroxyproline concentration (indicator of collagen) in the anastomotic wounds did not differ (P = 0.571) between the two groups.CONCLUSIONS: Our data demonstrate that a single local application of OTR4120 intraoperatively did not increase the biomechanical strength of colonic anastomoses at the critical postoperative day 3 when the anastomoses are the weakest.",
author = "Malene Nerstr{\o}m and Peter-Martin Krarup and Jorgensen, {Lars Nannestad} and {\AA}gren, {Magnus S}",
year = "2017",
doi = "10.1155/2017/1078062",
language = "English",
volume = "2017",
journal = "Gastroenterology Research and Practice",
issn = "1687-6121",
publisher = "Hindawi Publishing Corporation",

}

RIS

TY - JOUR

T1 - The Effect of a Synthetic Heparan Sulfate on the Healing of Colonic Anastomoses

AU - Nerstrøm, Malene

AU - Krarup, Peter-Martin

AU - Jorgensen, Lars Nannestad

AU - Ågren, Magnus S

PY - 2017

Y1 - 2017

N2 - BACKGROUND: The mimetic compound OTR4120 may replace endogenous-degraded heparan sulfates that normally maintain the bioactivity of growth factors that are important for tissue repair. Herein, we investigated the effect of OTR4120 on the healing of normal colonic anastomoses.METHODS: We evaluated the following two treatment groups of male Sprague Dawley rats (220-256 g): control-treated colonic anastomoses (n = 25) and OTR4120-treated colonic anastomoses (n = 25). We resected 10 mm of the left colon and then applied either saline alone (control) or OTR4120 (100 μg/mL) in saline to the colonic ends before an end-to-end single-layer anastomosis was constructed and again on the anastomosis before the abdomen and skin were closed.RESULTS: On postoperative day 3, the anastomotic breaking strengths were 1.47 ± 0.32 N (mean ± SD) in the control group and 1.52 ± 0.27 N in the OTR4120-treated animals (P = 0.622). We also found that the hydroxyproline concentration (indicator of collagen) in the anastomotic wounds did not differ (P = 0.571) between the two groups.CONCLUSIONS: Our data demonstrate that a single local application of OTR4120 intraoperatively did not increase the biomechanical strength of colonic anastomoses at the critical postoperative day 3 when the anastomoses are the weakest.

AB - BACKGROUND: The mimetic compound OTR4120 may replace endogenous-degraded heparan sulfates that normally maintain the bioactivity of growth factors that are important for tissue repair. Herein, we investigated the effect of OTR4120 on the healing of normal colonic anastomoses.METHODS: We evaluated the following two treatment groups of male Sprague Dawley rats (220-256 g): control-treated colonic anastomoses (n = 25) and OTR4120-treated colonic anastomoses (n = 25). We resected 10 mm of the left colon and then applied either saline alone (control) or OTR4120 (100 μg/mL) in saline to the colonic ends before an end-to-end single-layer anastomosis was constructed and again on the anastomosis before the abdomen and skin were closed.RESULTS: On postoperative day 3, the anastomotic breaking strengths were 1.47 ± 0.32 N (mean ± SD) in the control group and 1.52 ± 0.27 N in the OTR4120-treated animals (P = 0.622). We also found that the hydroxyproline concentration (indicator of collagen) in the anastomotic wounds did not differ (P = 0.571) between the two groups.CONCLUSIONS: Our data demonstrate that a single local application of OTR4120 intraoperatively did not increase the biomechanical strength of colonic anastomoses at the critical postoperative day 3 when the anastomoses are the weakest.

U2 - 10.1155/2017/1078062

DO - 10.1155/2017/1078062

M3 - Journal article

C2 - 28620413

VL - 2017

JO - Gastroenterology Research and Practice

JF - Gastroenterology Research and Practice

SN - 1687-6121

M1 - 1078062

ER -

ID: 195541795