63 research outputs found

    Cellular Mechanisms Participating in Brain Repair of Adult Zebrafish and Mammals after Injury

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    Adult neurogenesis is an evolutionary conserved process occurring in all vertebrates. However, striking differences are observed between the taxa, considering the number of neurogenic niches, the neural stem cell (NSC) identity, and brain plasticity under constitutive and injury-induced conditions. Zebrafish has become a popular model for the investigation of the molecular and cellular mechanisms involved in adult neurogenesis. Compared to mammals, the adult zebrafish displays a high number of neurogenic niches distributed throughout the brain. Furthermore, it exhibits a strong regenerative capacity without scar formation or any obvious disabilities. In this review, we will first discuss the similarities and differences regarding (i) the distribution of neurogenic niches in the brain of adult zebrafish and mammals (mainly mouse) and (ii) the nature of the neural stem cells within the main telencephalic niches. In the second part, we will describe the cascade of cellular events occurring after telencephalic injury in zebrafish and mouse. Our study clearly shows that most early events happening right after the brain injury are shared between zebrafish and mouse including cell death, microglia, and oligodendrocyte recruitment, as well as injury-induced neurogenesis. In mammals, one of the consequences following an injury is the formation of a glial scar that is persistent. This is not the case in zebrafish, which may be one of the main reasons that zebrafish display a higher regenerative capacity

    QF2011: a protocol to study the effects of the Queensland flood on pregnant women, their pregnancies, and their children's early development

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    Effet protecteur des HDL en phase aiguë d’AVC ischémique en condition d’hyperglycémie

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    Ischemic stroke is a major public health problem. Currently, available therapies are based on a vascular approach. The advent of mechanical thrombectomy as a routine treatment for stroke exposes the patient to reperfusion injury such as hemorrhagic transformation (HT). Acute hyperglycemia increases this risk. We have developed a relevant and reproducible preclinical model in mice to study the mechanisms of these HT. High density lipoproteins (HDL) are molecular complexes with protective properties. We demonstrated that during the acute phase of stroke, these HDLs become dysfunctional. One of the mechanisms of this alteration is represented by the oxidation of surface proteins including apoA-1 by myeloperoxidase (MPO) released by neutrophils recruited into the ischemic zone. The MPO plasmatic level determination in the acute phase of stroke could be relevant. The injection of HDL has already proved effective in reducing the size of infarct and in the occurrence of HT in murine models of stroke. The hypothesis of a lack of efficiency of HDL in this particular pathological condition leads us to consider an improvement of their functions thanks to their vector property of protective molecules. These HDLs would then be used as a transporter of molecules increasing their neuro- and endothelio-protective potential in the treatment of ischemic stroke.Les accidents vasculaires cérébraux (AVC) ischémiques sont un problème majeur de santé publique. Les thérapies actuellement disponibles se fondent sur une approche vasculaire de la prise en charge. L’arrivée de la thrombectomie mécanique comme traitement de routine de l’AVC, expose le patient à des lésions de reperfusion comme les transformations hémorragiques (TH). L’hyperglycémie aiguë, augmente ce risque. Nous avons mis au point un modèle préclinique pertinent et reproductible chez la souris permettant d’étudier les mécanismes de ces TH. Les lipoprotéines de haute densité (HDL) sont des complexes moléculaires ayant des propriétés protectrices. Nous avons démontré que lors de la phase aiguë de l’AVC, ces HDL subissaient des modifications structurelles et devenaient dysfonctionnelles. Un des mécanismes de cette altération est représenté par l’oxydation des protéines de surface notamment l’apoA-1 par la myéloperoxydase (MPO) libérée par les neutrophiles recrutés dans la zone ischémiée. Le dosage du taux plasmatique de MPO en phase aiguë d’AVC pourrait permettre de mieux caractériser ce mécanisme. L’injection de HDL a déjà prouvé son efficacité dans la diminution de la taille des infarctus cérébraux ainsi que dans la survenue des complications hémorragiques sur des modèles murin d’ischémie cérébrale. L’hypothèse d’un défaut d’efficacité des HDL dans cette condition pathologique particulière nous conduit à envisager une amélioration de leurs fonctions grâce à leur propriété de vecteur de molécules protectrices. Ces HDL seraient alors utilisées comme transporteur de molécules augmentant leur potentiel neuro- et endothélio-protecteur dans le traitement de l’AVC ischémique

    Protective effect of HDL during acute stroke under hyperglycemic condition

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    Les accidents vasculaires cérébraux (AVC) ischémiques sont un problème majeur de santé publique. Les thérapies actuellement disponibles se fondent sur une approche vasculaire de la prise en charge. L’arrivée de la thrombectomie mécanique comme traitement de routine de l’AVC, expose le patient à des lésions de reperfusion comme les transformations hémorragiques (TH). L’hyperglycémie aiguë, augmente ce risque. Nous avons mis au point un modèle préclinique pertinent et reproductible chez la souris permettant d’étudier les mécanismes de ces TH. Les lipoprotéines de haute densité (HDL) sont des complexes moléculaires ayant des propriétés protectrices. Nous avons démontré que lors de la phase aiguë de l’AVC, ces HDL subissaient des modifications structurelles et devenaient dysfonctionnelles. Un des mécanismes de cette altération est représenté par l’oxydation des protéines de surface notamment l’apoA-1 par la myéloperoxydase (MPO) libérée par les neutrophiles recrutés dans la zone ischémiée. Le dosage du taux plasmatique de MPO en phase aiguë d’AVC pourrait permettre de mieux caractériser ce mécanisme. L’injection de HDL a déjà prouvé son efficacité dans la diminution de la taille des infarctus cérébraux ainsi que dans la survenue des complications hémorragiques sur des modèles murin d’ischémie cérébrale. L’hypothèse d’un défaut d’efficacité des HDL dans cette condition pathologique particulière nous conduit à envisager une amélioration de leurs fonctions grâce à leur propriété de vecteur de molécules protectrices. Ces HDL seraient alors utilisées comme transporteur de molécules augmentant leur potentiel neuro- et endothélio-protecteur dans le traitement de l’AVC ischémique.Ischemic stroke is a major public health problem. Currently, available therapies are based on a vascular approach. The advent of mechanical thrombectomy as a routine treatment for stroke exposes the patient to reperfusion injury such as hemorrhagic transformation (HT). Acute hyperglycemia increases this risk. We have developed a relevant and reproducible preclinical model in mice to study the mechanisms of these HT. High density lipoproteins (HDL) are molecular complexes with protective properties. We demonstrated that during the acute phase of stroke, these HDLs become dysfunctional. One of the mechanisms of this alteration is represented by the oxidation of surface proteins including apoA-1 by myeloperoxidase (MPO) released by neutrophils recruited into the ischemic zone. The MPO plasmatic level determination in the acute phase of stroke could be relevant. The injection of HDL has already proved effective in reducing the size of infarct and in the occurrence of HT in murine models of stroke. The hypothesis of a lack of efficiency of HDL in this particular pathological condition leads us to consider an improvement of their functions thanks to their vector property of protective molecules. These HDLs would then be used as a transporter of molecules increasing their neuro- and endothelio-protective potential in the treatment of ischemic stroke

    Influence du médecin généraliste dans le stress et l'anxiété des familles de patients hospitalisés en Réanimation

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    AIX-MARSEILLE2-BU MĂ©d/Odontol. (130552103) / SudocSudocFranceF

    Romiplostim for the Emergency Management of Severe Immune Thrombocytopenia with Intracerebral Hemorrhage

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    Currently, we lack well-established guidelines for the emergency management of severe immune thrombocytopenia (ITP) with life-threatening bleeding. We now report the management of two patients with severe ITP, complicated by substantial cerebral hemorrhage, requiring urgent surgery due to refractory intracranial hypertension. To rapidly boost platelet counts (PCs), corticosteroids, intravenous immunoglobulin, and iterative platelet transfusions were given; all were ineffectual. Romiplostim, a thrombopoietin receptor agonist, was then administered as an “on demand therapy,” with the result that a rapid and sustained increase of PCs was achieved, thus allowing for postoperative hemostasis. Both patients recovered good neurological condition, suggesting the potential utility of romiplostim, in combined therapy, for the emergency management of severe ITP

    High-Density Lipoproteins Are Bug Scavengers

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    Lipoproteins were initially defined according to their composition (lipids and proteins) and classified according to their density (from very low- to high-density lipoproteins—HDLs). Whereas their capacity to transport hydrophobic lipids in a hydrophilic environment (plasma) is not questionable, their primitive function of cholesterol transporter could be challenged. All lipoproteins are reported to bind and potentially neutralize bacterial lipopolysaccharides (LPS); this is particularly true for HDL particles. In addition, HDL levels are drastically decreased under infectious conditions such as sepsis, suggesting a potential role in the clearance of bacterial material and, particularly, LPS. Moreover, "omics" technologies have unveiled significant changes in HDL composition in different inflammatory states, ranging from acute inflammation occurring during septic shock to low-grade inflammation associated with moderate endotoxemia such as periodontal disease or obesity. In this review, we will discuss HDL modifications associated with exposure to pathogens including bacteria, viruses and parasites, with a special focus on sepsis and the potential of HDL therapy in this context. Low-grade inflammation associated with atherosclerosis, periodontitis or metabolic syndrome may also highlight the protective role of HDLs in theses pathologies by other mechanisms than the reverse transport of cholesterol
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