Nitrous oxide with fentanyl and droperidol minimizes lipid peroxidation in the liver.

We have studied the level of lipid peroxidation in the liver of rats exposed to nitrous oxide plus oxygen or injected with droperidol of fentanyl. The effect of nitrous oxide used in combination with droperidol and fentanyl was also investigated. All the tested anaesthetics caused lipid peroxidation in the rat liver.

Polyamines as modulators of lipoperoxidation.

The polyamines spermine and spermidine and the diamine putrescine inhibit lipid peroxidation in phospholipid liposome suspensions and rat liver homogenates. Using the chemiluminescence technique the antioxidant activity of polyamines was found to be due to reactions with the free radical intermediates of lipid peroxidation and/or superoxide radicals. Also, the antioxidant action of polyamines correlated with the amount of their amino groups: the antioxidant activity increases from putrescine to spermine.

[Lipid peroxidation in emotional stress in rats: correlation with parameters of open field behavior].

TBA-reactive products were measured in the brain, liver, and heart of Wistar rats in control conditions and after 24 h immobilization. Animals were subjected to the open field test before and after the immobilization. Behavior patterns, gastric mucosa alterations and MDA accumulation in organs suggested that immobilization as well as food and water deprivation were all strong stressor stimuli.

Dynamics of lipid peroxidation in isoprenaline-induced myocardiopathy.

The dynamics of lipid peroxidation in isoprenaline-induced myocardiopathy was studied in rats. Spontaneous and Fe(II)- catalyzed generation of malondialdehyde (MDA)-like products and chemiluminescence in the heart, liver and brain homogenates were measured. The increase in the interval between treatment of rats with isoprenaline and their killing up to 48 hours led to an increase in MDA content in the heart.