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Hepatic and lipoprotein lipases selectively assayed in postheparin plasma
A D Henderson1, W Richmond, R S Elkeles
1Unit of Metabolic Medicine, St. Mary's Hospital Medical School, Imperial College of Science, Technology and Medicine, London, UK.
Clinical Chemistry
|February 1, 1993
Summary
New assays accurately measure lipoprotein lipase (LPL) and hepatic lipase (HL) in plasma. Men showed higher HL and lower LPL activity than women, revealing a significant sex-based difference in enzyme levels.
Area of Science:
- Biochemistry
- Enzymology
- Clinical Chemistry
Background:
- Lipoprotein lipase (LPL) and hepatic lipase (HL) are key enzymes in lipid metabolism.
- Accurate measurement of LPL and HL activity is crucial for understanding lipid disorders.
- Existing assays may lack specificity or reliability for simultaneous LPL and HL determination.
Purpose of the Study:
- To develop and validate sensitive, reliable assays for the selective quantification of LPL and HL in postheparin plasma.
- To investigate potential sex differences in LPL and HL activity in healthy adults.
Main Methods:
- Developed a selective assay for HL by inhibiting LPL using high salt concentration (0.76 mol/L NaCl).
- Developed a selective assay for LPL by denaturing HL using sodium dodecyl sulfate.
- Validated the LPL assay against a method using an antiserum to inactivate HL.
- Quantified LPL and HL activity in plasma samples from 32 normal adults.
Main Results:
- Achieved selective measurement of LPL and HL activity.
- Demonstrated a clear sex difference in both enzyme activities.
- Men, on average, exhibited higher HL activity compared to women.
- Men, on average, exhibited lower LPL activity compared to women.
Conclusions:
- The developed assays provide sensitive and reliable methods for distinguishing LPL and HL activity.
- Significant sex-based differences in LPL and HL activity exist in the adult population.
- These findings contribute to a better understanding of lipase function in lipid metabolism and potential sex-specific variations.