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Pretreatment with a dual antiplatelet and anticoagulant (APAC) reduces ischemia-reperfusion injury in a mouse model of temporary middle cerebral artery occlusion-implications for neurovascular procedures.
Denorme, Frederik; Frösen, Juhana; Jouppila, Annukka; Lindgren, Antti; Resendiz-Nieves, Julio C; Manninen, Hannu; De Meyer, Simon F; Lassila, Riitta.
Afiliação
  • Denorme F; Laboratory for Thrombosis Research, KU Leuven Campus Kulak Kortrijk, Kortrijk, Belgium.
  • Frösen J; Hemorrhagic Brain Pathology Research Group, Dept. of Neurosurgery, Kuopio University Hospital, Kuopio, Finland.
  • Jouppila A; Department of Neurosurgery, Tampere University Hospital, Tampere, Finland.
  • Lindgren A; Helsinki University Central Hospital Clinical Research Institute, Helsinki, Finland.
  • Resendiz-Nieves JC; Department of Clinical Radiology, Kuopio University Hospital, Kuopio, Finland.
  • Manninen H; Institute of Clinical Medicine, School of Medicine, Faculty of Health Sciences, University of Eastern Finland, Kuopio, Finland.
  • De Meyer SF; Department of Neurosurgery, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
  • Lassila R; Department of Radiology, Kuopio University Hospital, Kuopio, Finland.
Acta Neurochir (Wien) ; 166(1): 137, 2024 Mar 15.
Article em En | MEDLINE | ID: mdl-38485848
ABSTRACT

BACKGROUND:

Several neurovascular procedures require temporary occlusion of cerebral arteries, leading to ischemia of unpredictable length, occasionally causing brain infarction. Experimental models of cerebral ischemia-reperfusion injury have established that platelet adhesion and coagulation play detrimental roles in reperfusion injury following transient cerebral ischemia. Therefore, in a model of cerebral ischemia-reperfusion injury (IRI), we investigated the therapeutic potential of a dual antiplatelet and anticoagulant (APAC) heparin proteoglycan mimetic which is able to bind to vascular injury sites.

METHODS:

Brain ischemia was induced in mice by transient occlusion of the right middle cerebral artery for 60 min. APAC, unfractionated heparin (UFH) (both at heparin equivalent doses of 0.5 mg/kg), or vehicle was intravenously administered 10 min before or 60 min after the start of ischemia. At 24 h later, mice were scored for their neurological and motor behavior, and brain damage was quantified.

RESULTS:

Both APAC and UFH administered before the onset of ischemia reduced brain injury. APAC and UFH pretreated mice had better neurological and motor functions (p < 0.05 and p < 0.01, respectively) and had significantly reduced cerebral infarct sizes (p < 0.01 and p < 0.001, respectively) at 24 h after transient occlusion compared with vehicle-treated mice. Importantly, no macroscopic bleeding complications were observed in either APAC- or UFH-treated animals. However, when APAC or UFH was administered 60 min after the start of ischemia, the therapeutic effect was lost, but without hemorrhaging either.

CONCLUSIONS:

Pretreatment with APAC or UFH was safe and effective in reducing brain injury in a model of cerebral ischemia induced by transient middle cerebral artery occlusion. Further studies on the use of APAC to limit ischemic injury during temporary occlusion in neurovascular procedures are indicated.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Lesões Encefálicas / Traumatismo por Reperfusão / Isquemia Encefálica Limite: Animals Idioma: En Revista: Acta Neurochir (Wien) Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Bélgica

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Lesões Encefálicas / Traumatismo por Reperfusão / Isquemia Encefálica Limite: Animals Idioma: En Revista: Acta Neurochir (Wien) Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Bélgica