Studies On The Mechanisms Of Compatibility Safflower Seed Oil To Enhance The Resistance Capacity Of Brain Cells And Mitochondria Against Free Oxygen Radical Mediated Cell Damage | | Posted on:2009-02-11 | Degree:Master | Type:Thesis | | Country:China | Candidate:R Han | Full Text:PDF | | GTID:2144360242499751 | Subject:Drug analysis | | Abstract/Summary: | PDF Full Text Request | | Objective:①To prepare of compatibility safflower seed oil composed ofα-linolenic acid and linoleic acid in different proportion;②Establishment of a brain cell(PC12 cell line) damage model(apoptosis) induced by H2O2 stimulation,and studies on the mechanisms of compatibility safflower seed oil to enhance the resistance capacity of brain cells against free oxygen radical mediated cell damage.③To study the capacity of compatibility safflower seed oil against lipid overoxidation in a mitichondrian damage system induced by H2O2/Fe2+.Methods:①To prepare compatibility safflower seed oil,and determine theα-linolenic acid and linoleic acid contents by GC method(gas phase chromatography);②To establish a free oxygen damage(apoptosis) model of PC12 brain cells,and to analyze the drug treatment of compatibility safflower seed oil in different dosage by methods of MTT,fluorescence imaging and flow cytometry to evaluate the relationship between cell activity and the dose-effect③To prepare mitochondria from rat brain by modified methods by Clark and establish an oxidative damage system with H2O2/Fe2+, and determine brownish lipid,membrane fluidity and ATPase activity before and after treatment of compatibility safflower seed oil.Results:①The contents ofα-linolenic acid and linoleic acid were about 62.49% and 22.91%,respectively,to meet the requirements of compatibility safflower seed oil;②The lowest dosage to establish the H2O2-induced cell damage was 200μM;the lowest dosage of compatibility safflower seed oil to make a significant resistance of PC12 cells against free oxygen mediated damage was 0.3mg/ml.③The ability of rat mitochondria to inhibit lipid overoxidation was significantly enhanced when the dosage of compatibility safflower seed oil kept at 0.3-0.5mg/ml.Conclusions:①The method to prepare compatibility safflower seed oil proved to be reproducible and feasible;②H2O2-induced cell damage model could be applied for the drug treatment with compatibility safflower seed oil,and was reproducible and stable.③The ability of compatibility safflower seed oil to resist free oxygen radical mediated cell damage maybe achieved by indirectly enhancing self-defense capacity of brain cells, instead of the direct contact between the drug and the free oxygen radicals. Compatibility safflower seed oil may work through the sub-cellular compartment-mitochondria by enhancing the anti-oxidation capacity of the cell. | | Keywords/Search Tags: | compatibility safflower seed oil (CSSO), cell model, anti-oxidation capacity, apoptosis, mitochondria | PDF Full Text Request | Related items |
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