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Comparative biochemistry and physiology. B, Comparative biochemistry1987; 87(3); 501-506; doi: 10.1016/0305-0491(87)90044-7

Characterization of equine plasma lipoproteins after separation by density gradient.

Abstract: 1. Plasma lipoproteins from six thoroughbred horses were separated by density gradient ultracentrifugation. For each sample, lipoprotein bands were visualized by means of a prestained plasma control and characterized by electrophoretic, chemical and morphological analysis. 2. Very low density lipoproteins (VLDL) were isolated at d less than 1.018 g/ml. 3. Two clearly resolved bands were detected in the low density lipoprotein fraction (LDL). The density limits were evaluated as follows: LDL1(1.028 less than d less than 1.045 g/ml) and LDL2(1.045 less than d less than 1.070 g/ml). Marked differences were observed in the chemical composition and particle size of LDL1 and LDL2 fractions. 4. High density lipoprotein fraction (HDL) was usually isolated as a single band, distributed over the range 1.075 less than d less than 1.180 g/ml. However, chemical composition and particle size revealed heterogeneity in HDL subfractions. 5. The density limit of LDL and HDL bands varied in each animal, indicating differences in equine lipoprotein distribution.
Publication Date: 1987-01-01 PubMed ID: 3621911DOI: 10.1016/0305-0491(87)90044-7Google Scholar: Lookup
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Summary

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The research paper investigates the characterization of plasma lipoproteins in thoroughbred horses, where lipoproteins were separated by density gradient ultracentrifugation and studied for their various properties and differences among each other.

Density Gradient Ultracentrifugation

  • The researchers isolated plasma lipoproteins from six thoroughbred horses using a method known as density gradient ultracentrifugation. This is a method that utilizes differences in density to separate substances of interest, in this case, lipoproteins.
  • Post separation, lipoprotein bands were identified using a pre-stained plasma control and then further characterized by employing electrophoretic (a method to separate proteins based on their charge and size), chemical, and morphological (study of structure and form) analyses.

Characterization of Lipoproteins

  • The researchers focused on three types of lipoproteins: Very Low-Density Lipoproteins (VLDL), Low-Density Lipoproteins (LDL), and High-Density Lipoproteins (HDL).
  • VLDL was isolated at a density lesser than 1.018 g/ml, meaning it is lighter and thus floats at the top layer in the centrifugation process.
  • Two distinct bands were observed in LDL, classified as LDL1 and LDL2. Their density limits were also defined as LDL1 (1.028 < d < 1.045 g/ml) and LDL2 (1.045 < d < 1.070 g/ml). Further analysis showed significant differences between LDL1 and LDL2 in terms of their chemical composition and particle size.
  • HDL was typically isolated as one band across the range 1.075 < d < 1.180 g/ml. Despite appearing to be one band, chemical composition and particle size analyses revealed variety within the HDL, indicating the presence of subfractions.

Varied Density Limits and Lipoprotein Distribution

  • It was found that the density limit or range varied for each horse, indicating noticeable differences in lipoprotein distribution.
  • This variability could hint towards potential biological and physiological factors that may influence the presence and behavior of these lipoproteins in thoroughbred horses.

Cite This Article

APA
Le Goff D, Nouvelot A, Fresnel J, Silberzahn P. (1987). Characterization of equine plasma lipoproteins after separation by density gradient. Comp Biochem Physiol B, 87(3), 501-506. https://doi.org/10.1016/0305-0491(87)90044-7

Publication

ISSN: 0305-0491
NlmUniqueID: 2984730R
Country: England
Language: English
Volume: 87
Issue: 3
Pages: 501-506

Researcher Affiliations

Le Goff, D
    Nouvelot, A
      Fresnel, J
        Silberzahn, P

          MeSH Terms

          • Animals
          • Centrifugation, Density Gradient
          • Densitometry
          • Electrophoresis, Polyacrylamide Gel
          • Horses / blood
          • Lipoproteins / blood
          • Lipoproteins, HDL / blood
          • Lipoproteins, LDL / blood
          • Lipoproteins, VLDL / blood
          • Microscopy, Electron
          • Ultracentrifugation

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