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Related Experiment Videos

Intravenous fat tolerance in hepatic schistosomiasis.

M H Ghanem, M H Fahmy, M Said

    Annals of Tropical Medicine and Parasitology
    |April 1, 1978
    PubMed
    Summary

    Schistosomal patients exhibit a significantly slower lipid elimination rate after intravenous fat emulsion compared to healthy controls. This impaired triglyceride clearance suggests altered lipid metabolism in schistosomiasis.

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    Revista de gastroenterologia de Mexico (English)·2020

    Area of Science:

    • Biochemistry
    • Clinical Medicine
    • Parasitology

    Background:

    • Schistosomiasis is a parasitic disease affecting millions globally.
    • Altered lipid metabolism is increasingly recognized in chronic infections.
    • The impact of schistosomiasis on exogenous lipid processing remains unclear.

    Purpose of the Study:

    • To investigate the in vivo elimination kinetics of an artificial fat emulsion in patients with schistosomiasis.
    • To compare lipid elimination rates between schistosomal patients and healthy controls.

    Main Methods:

    • A single intravenous dose of artificial fat emulsion was administered to 13 schistosomal patients and 13 controls.
    • Triglyceride (TG) levels were measured at various time points post-injection.
    • Lipid elimination curves were analyzed for kinetic differences.

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    Main Results:

    • Schistosomal patients showed significantly lower mean incremental TG values at 10 minutes post-injection compared to controls.
    • Lipid elimination followed zero-order kinetics in controls but exponential kinetics in schistosomal patients up to 120 minutes.
    • These findings indicate a delayed and altered clearance of exogenous lipids in schistosomiasis.

    Conclusions:

    • Schistosomiasis is associated with impaired elimination of intravenously administered fat emulsion.
    • The altered triglyceride kinetics suggest a significant impact of the disease on lipid metabolism.
    • Further research is warranted to elucidate the underlying mechanisms and clinical implications of these metabolic disturbances.