Related Experiment Videos
Lipid peroxidation causes an increase of lipid order and a decrease of 5'-nucleotidase activity in the liver plasma
C Pieri1, M Falasca, F Marcheselli
1Cytology Center, Gerontological Research Department of INRCA, Ancona, Italy.
Cellular and Molecular Biology
|July 1, 1992
Summary
Oxidative stress increases liver membrane microviscosity, which in turn reduces 5'-nucleotidase enzyme activity. This suggests membrane fluidity impacts enzyme function during peroxidation.
Area of Science:
- Biochemistry
- Cell Biology
- Membrane Biophysics
Background:
- 5'-nucleotidase is an ectoenzyme crucial for cellular signaling and nucleotide metabolism.
- Membrane microviscosity, a measure of lipid bilayer fluidity, influences protein function and membrane dynamics.
- Oxidative stress can alter membrane structure and enzyme activity.
Purpose of the Study:
- To investigate the impact of peroxidation on 5'-nucleotidase activity.
- To examine the effect of peroxidation on liver plasma membrane microviscosity.
- To determine the relationship between altered membrane microviscosity and 5'-nucleotidase activity.
Main Methods:
- Liver plasma membranes from Wistar rats were subjected to peroxidation using hydrogen peroxide (H2O2) and ferrous sulfate (FeSO4) or t-butylhydroperoxide.
- Membrane microviscosity was assessed using fluorescent lipid probes (DPH, PA-DPH) and a thiol reagent (1-PM).
- 5'-nucleotidase activity was measured following peroxidation treatments.
Main Results:
- Peroxidation significantly increased membrane microviscosity, indicated by elevated transition temperatures of fluorescent probes.
- The activity of 5'-nucleotidase was decreased following peroxidation.
- A correlation was observed between increased membrane microviscosity and reduced 5'-nucleotidase activity.
Conclusions:
- Peroxidation induces changes in liver plasma membrane structure, leading to increased microviscosity.
- The observed decrease in 5'-nucleotidase activity is likely regulated by the increased membrane microviscosity.
- These findings highlight the role of membrane biophysical properties in modulating enzyme function under oxidative stress.