Showing posts with label TBARS. Show all posts
Showing posts with label TBARS. Show all posts

Saturday, 26 February 2011

LDL oxidation (test methods)

Taken from: http://ethesis.helsinki.fi/

2.2.5. Determination of lipoprotein oxidation


LDL oxidation is a lipid peroxidation chain reaction driven by free radical intermediates, which is accompanied by characteristic changes of chemical, physiochemical, and biological properties. Therefore, a variety of methods may be used for determining the rate and extent of oxidation in vitro (Puhl et al. 1994) and in vivo (Jialal and Devaraj 1996).

For in vivo LDL oxidation determination, the immunological method for autoantibody to Ox-LDL has been widely used (Jialal and Devaraj 1996), while a recent developed baseline diene conjugation measurement is a promising method for estimating LDL oxidation in vivo (Ahotupa et al. 1998). 

The in vitro estimation of LDL oxidation includes measurement of the increase of thiobarbituric acid-reactive substances (TBARS), total lipid hydroperoxides, defined lipid hydroperoxides, hydroxy- and hydroperoxy fatty acids, conjugated dienes (CD), oxysterols, lysophospholipids, aldehydes, fluorescent chromophores, measurement of disappearance of endogenous antioxidants and PUFA, oxygen uptake, and total peroxyl radical trapping potential (TRAP) (Puhl et al. 1994, Valkonen and Kuusi 1997). 

A convenient and very frequently used method for continuously monitoring the process of copper-induced LDL oxidation is to measure the conjugated diene formation at 234 nm as a time course in a UV spectrophotometer (Esterbauer et al. 1989).

LDL structure (detailed)

Taken from: http://ethesis.helsinki.fi/

2.2.8. LDL composition, oxidizability, and endogenous antioxidants


In LDL particle, cholesteryl linoleate represents quantitatively the single most important polyunsaturated fatty acid (PUFA) which is the substrate for peroxidation. If PUFA becomes oxidized to lipid hydroperoxides, their isolated carbon-carbon double bonds are converted to conjugated double bonds showing a strong UV-absorption at 234 nm, designated as conjugated diene (CD) formation (Esterbauer et al 1993). Therefore, its content in LDL may influence the determination of oxidation resistance measured by CD or TBARS formation (Ziouzenkova et al. 1996). 

Reaven et al. (1993) reported that LDL particles rich in PUFA are more readily oxidized than LDL particles enriched in saturated fatty acids or monounsaturated fatty acids. In addition, elevated levels of preformed lipid hydroperoxides and cholesterol in LDL were associated with increased oxidation susceptibility (Frei and Gaziano 1993). Studies have shown that monoenic fatty acids enriched LDL, for example oleic acid was remarkably resistant to oxidative modification as measured by decreased formation of CD and TBARS (Parthasarathy et al. 1990). 

The 3-hydroxy-3-methylglutaryl-coenzyme A (HMG CoA) reductase inhibitors reduced the susceptibility of LDL to oxidation by altering the LDL particle composition containing less lipid relative to protein (Lavy et al. 1991) or preserve endogenous antioxidants (Chen et al. 1997). In deed, most of these HMG-CoA reductase inhibitors themselves are antioxidants and could become bound to lipoprotein in the circulation to protect them against oxidation (Lennernas and Fager 1997, Girona et al. 1999). 

LDL particle size could also influence its oxidation susceptibility. For example, small, dense LDL particles displayed diminished resistance to oxidative stress in vitro (Tribble et al. 1992, de Graaf et al. 1991). 

Since LDL is the major extracellular transport vehicle for lipid-soluble antioxidants, it contains relatively large amounts of a-tocopherol, g-tocopherol, b-carotene, and ubiquinol-10 and among them a-tocopherol is the most important antioxidant known with 6 molecules per LDL particle (Esterbauer et al. 1995). As the oxidation goes on, a-tocopherol is the first and b-carotene is the last endogenous antioxidant in LDL particles to be depleted (Esterbauer et al. 1992). 

The endogenous antioxidants contained in LDL particles might influence oxidation resistance (Tribble et al. 1994). Dietary antioxidant supplementation could increase their content in LDL and therefore, increase oxidation resistance of lipoproteins (Nyyssonen et al. 1994, Jialal et al. 1995). The composition of native LDL and the antioxidants contained in LDL are listed in Tables 2 and 3.


Table 2. Composition of human LDL








Table 3. Antioxidants in native human LDL