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Astaxanthin Complexes to Attenuate Muscle Damage after In Vivo Femoral Ischemia-Reperfusion ; Astaxanthin Complexes to Attenuate Muscle Damage after In Vivo Femoral Ischemia-Reperfusion.

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  • معلومة اضافية
    • Contributors:
      Univ Paris Diderot, INSERM, Lab Vasc Translat Sci U1148, Paris, France; Département d'Anatomo-Pathologie Hôpital Bichat; AP-HP - Hôpital Bichat - Claude Bernard Paris; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP); Laboratoire de Recherche Vasculaire Translationnelle (LVTS (UMR_S_1148 / U1148)); Université Paris 13 (UP13)-Université Paris Diderot - Paris 7 (UPD7)-Institut National de la Santé et de la Recherche Médicale (INSERM); Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP); Université Joseph Fourier - Grenoble 1 - Institut universitaire de formation des maîtres - Académie de Grenoble (UJF IUFM Grenoble); Université Joseph Fourier - Grenoble 1 (UJF); Université Paris Nord (Paris 13)
    • بيانات النشر:
      HAL CCSD
      MDPI
    • الموضوع:
      2019
    • Collection:
      Université Paris 13: HAL
    • نبذة مختصرة :
      International audience ; (1) Background: Reperfusion injury refers to the cell and tissue damage induced, when blood flow is restored after an ischemic period. While reperfusion reestablishes oxygen supply, it generates a high concentration of radicals, resulting in tissue dysfunction and damage. Here, we aimed to challenge and achieve the potential of a delivery system based on astaxanthin, a natural antioxidant, in attenuating the muscle damage in an animal model of femoral hind-limb ischemia and reperfusion. (2) Methods: The antioxidant capacity and non-toxicity of astaxanthin was validated before and after loading into a polysaccharide scaffold. The capacity of astaxanthin to compensate stress damages was also studied after ischemia induced by femoral artery clamping and followed by varied periods of reperfusion. (3) Results: Histological evaluation showed a positive labeling for CD68 and CD163 macrophage markers, indicating a remodeling process. In addition, higher levels of Nrf2 and NQO1 expression in the sham group compared to the antioxidant group could reflect a reduction of the oxidative damage after 15 days of reperfusion. Furthermore, non-significant differences were observed in non-heme iron deposition in both groups, reflecting a cell population susceptible to free radical damage. (4) Conclusions: Our results suggest that the in situ release of an antioxidant molecule could be effective in improving the antioxidant defenses of ischemia/reperfusion (I/R)-damaged muscles.
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/31207871; hal-03022423; https://hal.science/hal-03022423; https://hal.science/hal-03022423/document; https://hal.science/hal-03022423/file/marinedrugs-17-00354%20Astaxanthin%20Complexes%20to%20Attenuate%20Muscle%20Damage%20after%20In%20Vivo%20Femoral%20Ischemia-Reperfusion%20.pdf; PUBMED: 31207871; PUBMEDCENTRAL: PMC6627496
    • الرقم المعرف:
      10.3390/md17060354
    • Rights:
      info:eu-repo/semantics/OpenAccess
    • الرقم المعرف:
      edsbas.7F64C606