“…Four hours of ischemia was chosen to induce substantial flap ischemia–reperfusion injury without exceeding the critical ischemia time of musculocutaneous flaps and thereby risking microcirculatory failure. Our previous study confirmed that the flaps were exposed to ischemia–reperfusion injury shown by histological and immunological analyses (Krag et al, ). We administered RIC after onset of flap ischemia and before reperfusion, so‐called remote ischemic perconditioning (Schmidt et al, ) to study an isolated effect on coagulation after flap ischemia–reperfusion injury and to avoid a perconditioning effect on the flaps.…”
Section: Discussionsupporting
confidence: 85%
“…The systemic coagulation marker response to flap ischemia–reperfusion injury was investigated by comparing measurements obtained before flap reperfusion with 5 h of reperfusion, because flap inflammation peaked at 5 h of reperfusion in the same model (Krag et al, ). Musculocutaneous flap ischemia–reperfusion injury reduced thrombin generation lag time and time‐to‐peak thrombin indicating hypercoagulation, but it also reduced peak thrombin and ETP indicating hypocoagulation.…”
Section: Discussionmentioning
confidence: 99%
“…Sixteen female Danish Landrace pigs were included in the study (mean weight 39 kg, range 35–42 kg). Following the principles of replacement, reduction, and refinement for animal studies, we used pigs that were also part of a previously published study (Krag et al, ).…”
Section: Methodsmentioning
confidence: 99%
“…The animals were anesthetized and euthanized as previously described (Krag et al, ). After induction of general anesthesia, the large neck vessels were dissected on the left side.…”
Section: Methodsmentioning
confidence: 99%
“…This experimental treatment reduced infarct size after angioplasty in a randomized controlled trial on acute myocardial infarction (Botker et al, ). Furthermore, RIC reduced infarct size (Addison et al, ) and attenuated acute inflammation (Krag et al, ) in porcine latissimus dorsi flaps subjected to ischemia–reperfusion injury. The tissue‐protective mechanisms behind RIC are multifactorial with humoral and neural pathways being investigated (Addison et al, ).…”
The local coagulation marker response to musculocutaneous flap ischemia-reperfusion could be measured systemically by moderate hypercoagulation. RIC did not substantially influence coagulation markers following musculocutaneous flap ischemia-reperfusion injury.
“…Four hours of ischemia was chosen to induce substantial flap ischemia–reperfusion injury without exceeding the critical ischemia time of musculocutaneous flaps and thereby risking microcirculatory failure. Our previous study confirmed that the flaps were exposed to ischemia–reperfusion injury shown by histological and immunological analyses (Krag et al, ). We administered RIC after onset of flap ischemia and before reperfusion, so‐called remote ischemic perconditioning (Schmidt et al, ) to study an isolated effect on coagulation after flap ischemia–reperfusion injury and to avoid a perconditioning effect on the flaps.…”
Section: Discussionsupporting
confidence: 85%
“…The systemic coagulation marker response to flap ischemia–reperfusion injury was investigated by comparing measurements obtained before flap reperfusion with 5 h of reperfusion, because flap inflammation peaked at 5 h of reperfusion in the same model (Krag et al, ). Musculocutaneous flap ischemia–reperfusion injury reduced thrombin generation lag time and time‐to‐peak thrombin indicating hypercoagulation, but it also reduced peak thrombin and ETP indicating hypocoagulation.…”
Section: Discussionmentioning
confidence: 99%
“…Sixteen female Danish Landrace pigs were included in the study (mean weight 39 kg, range 35–42 kg). Following the principles of replacement, reduction, and refinement for animal studies, we used pigs that were also part of a previously published study (Krag et al, ).…”
Section: Methodsmentioning
confidence: 99%
“…The animals were anesthetized and euthanized as previously described (Krag et al, ). After induction of general anesthesia, the large neck vessels were dissected on the left side.…”
Section: Methodsmentioning
confidence: 99%
“…This experimental treatment reduced infarct size after angioplasty in a randomized controlled trial on acute myocardial infarction (Botker et al, ). Furthermore, RIC reduced infarct size (Addison et al, ) and attenuated acute inflammation (Krag et al, ) in porcine latissimus dorsi flaps subjected to ischemia–reperfusion injury. The tissue‐protective mechanisms behind RIC are multifactorial with humoral and neural pathways being investigated (Addison et al, ).…”
The local coagulation marker response to musculocutaneous flap ischemia-reperfusion could be measured systemically by moderate hypercoagulation. RIC did not substantially influence coagulation markers following musculocutaneous flap ischemia-reperfusion injury.
We assessed the effects and potential mechanism of romote ischemic preconditioning (RIPC) on leukocytes‐endothelium cell adhesion in the flap microvessel after ischemia‐reperfusion (I/R) injury. Eight hours after reperfusion, edema and intravascular leukocyte aggregation were reduced and microvessels were more obvious in the group with superficial inferior epigastric artery (SIEA) perforator flap (SIEA‐flap) subjected to RIPC than in the I/R group. Zinc finger protein 667 (ZNF667) was significantly increased but P‐selectin was decreased in the flaps subjected to RIPC, compared to those in the I/R group. The low expression of P‐selectin was associated with ZNF667 expression and activation in human dermal microvascular endothelial cells in response to hypoxic preconditioning. ZNF667 bound to the P‐selectin promoter region, suppressing its transcription through a special core sequence. The ablation of P‐selectin by small interfering RNA effectively prevented the leukocytes‐endothelium cell adhesion effect of ZNF667‐knockdown. ZNF667 upregulation attenuates leukocyte‐endothelial cell adhesion by negatively regulating the expression of P‐selectin in SIEA‐flap subjected to RIPC.
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