Tags

Type your tag names separated by a space and hit enter

Activated protein C prevents deleterious effects of remote reperfusion injury caused by intestinal ischemia on wound healing in the left colonic anastomoses: an experimental study in the murine model.
Am J Surg. 2008 Nov; 196(5):774-87.AJ

Abstract

BACKGROUND

Activated protein C (APC) is a serine protease with anticoagulant and antiinflammatory activities. The delaying effects of remote reperfusion injury on the wound-healing process in colonic anastomoses have been previously shown. In this study, we aimed to investigate whether APC protects against deleterious systemic effects of intestinal ischemia/reperfusion (I/R) injury on colonic anastomotic wound healing process.

METHODS

Male Wistar-albino rats were randomly allocated into 4 groups, and a left colonic anastomosis was performed in all animals: (1) sham-operated group, simultaneously with left colonic anastomosis, the superior mesenteric artery and collateral branches were divided from the celiac axis, and the inferior mesenteric artery were isolated but not occluded (group 1, n = 12), (2) sham + APC group, identical to group 1 except for APC treatment (100 microg/kg, intravenously, 15 minutes before construction of the colonic anastomosis), (group 2, n = 12), (3) intestinal I/R group, 60 minutes of superior mesenteric ischemia followed by reperfusion (group 3, n = 12), and (4) APC-treated group, (100 microg/kg, intravenously, 15 minutes before reperfusion) (group 4, n = 12). All animals were sacrificed, and colonic anastomotic bursting pressures were measured in vivo on day 7. Tissue samples were obtained for analysis of hydroxyproline contents, nitrate/nitrite levels, and activities of oxidative and antioxidative enzymes. The plasma levels of proinflammatory cytokines and D-dimer were also measured.

RESULTS

Intestinal I/R led to significant decreases in colonic anastomotic bursting pressures, tissue hydroxyproline contents, and activities of antioxidative enzymes, along with increases in tissue nitrate/nitrite levels, activities of oxidative enzymes, and plasma levels of proinflammatory cytokines and D-dimer (P < .05). However, APC treatment led to significant increases in colonic anastomotic bursting pressures, tissue hydroxyproline contents, and activities of antioxidative enzymes, along with decreases in tissue nitrate/nitrite levels, activities of oxidative enzymes, and plasma levels of proinflammatory cytokines and D-dimer (P < .05).

CONCLUSION

This study clearly showed that APC treatment prevented the delaying effects of remote I/R injury on colonic anastomotic wound healing process. Further clinical studies are required to determine whether APC has a useful role in the enhancement of colonic anastomotic wound healing after particular operations in which I/R injury occurs.

Authors+Show Affiliations

Department of General Surgery, Pamukkale University, School of Medicine, 20070, Kinikli, Denizli, Turkey. zteke_md@yahoo.comNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

18466864

Citation

Teke, Zafer, et al. "Activated Protein C Prevents Deleterious Effects of Remote Reperfusion Injury Caused By Intestinal Ischemia On Wound Healing in the Left Colonic Anastomoses: an Experimental Study in the Murine Model." American Journal of Surgery, vol. 196, no. 5, 2008, pp. 774-87.
Teke Z, Sacar M, Yenisey C, et al. Activated protein C prevents deleterious effects of remote reperfusion injury caused by intestinal ischemia on wound healing in the left colonic anastomoses: an experimental study in the murine model. Am J Surg. 2008;196(5):774-87.
Teke, Z., Sacar, M., Yenisey, C., Atalay, A. O., Bicakci, T., & Erdem, E. (2008). Activated protein C prevents deleterious effects of remote reperfusion injury caused by intestinal ischemia on wound healing in the left colonic anastomoses: an experimental study in the murine model. American Journal of Surgery, 196(5), 774-87. https://doi.org/10.1016/j.amjsurg.2007.09.039
Teke Z, et al. Activated Protein C Prevents Deleterious Effects of Remote Reperfusion Injury Caused By Intestinal Ischemia On Wound Healing in the Left Colonic Anastomoses: an Experimental Study in the Murine Model. Am J Surg. 2008;196(5):774-87. PubMed PMID: 18466864.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Activated protein C prevents deleterious effects of remote reperfusion injury caused by intestinal ischemia on wound healing in the left colonic anastomoses: an experimental study in the murine model. AU - Teke,Zafer, AU - Sacar,Mustafa, AU - Yenisey,Cigdem, AU - Atalay,A Ozgur, AU - Bicakci,Tuncay, AU - Erdem,Ergun, Y1 - 2008/05/07/ PY - 2007/08/09/received PY - 2007/09/13/revised PY - 2007/09/13/accepted PY - 2008/5/10/pubmed PY - 2008/12/17/medline PY - 2008/5/10/entrez SP - 774 EP - 87 JF - American journal of surgery JO - Am J Surg VL - 196 IS - 5 N2 - BACKGROUND: Activated protein C (APC) is a serine protease with anticoagulant and antiinflammatory activities. The delaying effects of remote reperfusion injury on the wound-healing process in colonic anastomoses have been previously shown. In this study, we aimed to investigate whether APC protects against deleterious systemic effects of intestinal ischemia/reperfusion (I/R) injury on colonic anastomotic wound healing process. METHODS: Male Wistar-albino rats were randomly allocated into 4 groups, and a left colonic anastomosis was performed in all animals: (1) sham-operated group, simultaneously with left colonic anastomosis, the superior mesenteric artery and collateral branches were divided from the celiac axis, and the inferior mesenteric artery were isolated but not occluded (group 1, n = 12), (2) sham + APC group, identical to group 1 except for APC treatment (100 microg/kg, intravenously, 15 minutes before construction of the colonic anastomosis), (group 2, n = 12), (3) intestinal I/R group, 60 minutes of superior mesenteric ischemia followed by reperfusion (group 3, n = 12), and (4) APC-treated group, (100 microg/kg, intravenously, 15 minutes before reperfusion) (group 4, n = 12). All animals were sacrificed, and colonic anastomotic bursting pressures were measured in vivo on day 7. Tissue samples were obtained for analysis of hydroxyproline contents, nitrate/nitrite levels, and activities of oxidative and antioxidative enzymes. The plasma levels of proinflammatory cytokines and D-dimer were also measured. RESULTS: Intestinal I/R led to significant decreases in colonic anastomotic bursting pressures, tissue hydroxyproline contents, and activities of antioxidative enzymes, along with increases in tissue nitrate/nitrite levels, activities of oxidative enzymes, and plasma levels of proinflammatory cytokines and D-dimer (P < .05). However, APC treatment led to significant increases in colonic anastomotic bursting pressures, tissue hydroxyproline contents, and activities of antioxidative enzymes, along with decreases in tissue nitrate/nitrite levels, activities of oxidative enzymes, and plasma levels of proinflammatory cytokines and D-dimer (P < .05). CONCLUSION: This study clearly showed that APC treatment prevented the delaying effects of remote I/R injury on colonic anastomotic wound healing process. Further clinical studies are required to determine whether APC has a useful role in the enhancement of colonic anastomotic wound healing after particular operations in which I/R injury occurs. SN - 1879-1883 UR - https://www.unboundmedicine.com/medline/citation/18466864/Activated_protein_C_prevents_deleterious_effects_of_remote_reperfusion_injury_caused_by_intestinal_ischemia_on_wound_healing_in_the_left_colonic_anastomoses:_an_experimental_study_in_the_murine_model_ DB - PRIME DP - Unbound Medicine ER -