Assays for the measurement of lipid peroxidation (CROSBI ID 48004)
Prilog u knjizi | izvorni znanstveni rad
Podaci o odgovornosti
Čipak Gašparović, Ana ; Jaganjac, Morana ; Mihaljević, Branka ; Borović Šunjic, Suzana ; Žarković, Neven
engleski
Assays for the measurement of lipid peroxidation
Physical and emotional stress, metabolic alterations, carcinogenesis or inflammation are conditions that cantrigger oxidative stress, which is defined as a balance shift of redox reactions towards oxidation, resulting in the increase of reactive oxygen species (ROS). The ROS are continuously formed in small quantities during the normal metabolism of cell, however overproduction of ROS is cytotoxic and damages macro-molecules (DNA, proteins, sugars and lipids). Polyunsaturated fatty acids (PUFA) that are esterified in membrane or storage lipids are subject to ROS-induced peroxidation resulting in the destruction of biomembranes. Final products of lipid peroxidation (LPO) are reactive aldehydes that are relatively stable and may diffuse far from the initial site of oxidative injury and act as second messengers of free radicals.The difference between physiological and pathological oxidative stress is often the occurrence of LPO and its final toxic products. In this chapter two classes of methods for measurement of LPO are described. Those first include assays for detection of the LPO on the level of the organism, while the second include molecular and cellular assays that reveal the mechanistic effects of LPO on functional morphology and viability of the cells.
ELISA ; HNE ; HPLC ; immunocyto ; histochemistry ; lipid derived aldehydes ; LOOH ; oxidative stress
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Podaci o prilogu
283-297.
objavljeno
10.1007/978-1-62703-239-1
Podaci o knjizi
Cell senescence
Galluzzi, Lorenzo ; Vitale, Ilio ; Kepp, Oliver ; Kroemer, Guido
Totowa (NJ): Humana Press
2013.
978-1-62703-238-4