• DocumentCode
    2781201
  • Title

    Nanocapsulated flavonoid: Effect on cerebral ischemia-reperfusion induced mitochondrial oxidative damage in rat brain

  • Author

    Ghosh, Swarupa ; Sarkar, Sibani ; Das, Nirmalendu

  • Author_Institution
    Biomembrane Div., Indian Inst. of Chem. Biol., Kolkata, India
  • fYear
    2010
  • fDate
    16-18 Dec. 2010
  • Firstpage
    203
  • Lastpage
    208
  • Abstract
    Mitochondria are the most important source of Reactive Oxygen species. Superoxide anion produced by mitochondria leads to damage to membranes impairing the ability of mitochondria to synthesize ATP and to carry out their wide range of metabolic functions. Thus mitochondria are both the source as well as the target for ROS. Oxidative stress generated in ischemia-reperfusion and other neurodegenerative disorders, distorts the homeostasis between ROS generation in mitochondria and its antioxidant defense for ROS detoxification. The weakened cellular antioxidant level in ageing accelerates mitochondrial oxidative damage also and this contributes to the decrease in efficiency of oxidative phosphorylation associated with ageing. Quercetin (QC), the naturally occurring flavonoid has immense free radical scavenging properties but its clinical application is restricted mostly due to its insoluble nature and inability to circumvent the Blood Brain Barrier like most of the common therapeutics. Nanocapsulated QC (NQC) is an effective approach in combating ischemia- reperfusion induced neurodegeneration. Cerebral ischemia subsequent reperfusion causes a massive damage in rat brain, both for young and aged. NQC treatment exerted a substantial protection against cerebral ischemia reperfusion induced mitochondrial damage. Higher conjugated diene and ROS level in neuronal mitochondria accompanied with a lower GSH were found in aged, compared to sham control young rats. Further loss of those parameters was observed in aged rat brain by cerebral ischemia and reperfusion. NQC treatment resulted a significant protection both in young and old rats, where as, no significant protection was noticed when aged rats were treated with QC. The marked damage in neuronal mitochondrial respiratory enzymes due to ischemia-reperfusion in all age grouped rats was prevented by NQC and protected mitochondria to restore its normal functions.
  • Keywords
    biomembranes; brain; cellular biophysics; enzymes; haemorheology; medical disorders; molecular biophysics; nanomedicine; neurophysiology; patient treatment; NQC treatment; ROS detoxification; ageing; blood brain barrier; cellular antioxidant level; cerebral ischemia-reperfusion induced mitochondrial oxidative damage; common circumvent therapeutics; conjugated diene; homeostasis; immense free radical scavenging property; ischemia-reperfusion induced neurodegeneration; membranes; metabolic functions; nanocapsulated QC; nanocapsulated flavonoid; neurodegenerative disorders; neuronal mitochondria; neuronal mitochondrial respiratory dropping enzymes; phosphorylation; quercetin; rat brain; reactive oxygen species; young rats; Aging; Encapsulation; Image color analysis; Nanoparticles; Polymers; Proteins; Rats; Nanocapsules; Quercetin; cerebral ischemia reperfusion; cytochrome c; mitochondria; oxidative stress;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Systems in Medicine and Biology (ICSMB), 2010 International Conference on
  • Conference_Location
    Kharagpur
  • Print_ISBN
    978-1-61284-039-0
  • Type

    conf

  • DOI
    10.1109/ICSMB.2010.5735372
  • Filename
    5735372