Serum concentration of high density lipoproteins (HDLs) in leishmaniotic dogs

Fabrizio Ibba1, Gabriele Rossi2, Sara Meazzi2

  • 1Department of Veterinary Sciences and Public Health, University of Milan, Via Celoria 10, 20133, Milan, Italy; Veterinary Clinic Poggio di Pini, Capoterra (CA), Italy.

Insights

High density lipoproteins (HDLs) and antioxidant paraoxonase-1 (PON-1) levels were low in leishmaniotic dogs but increased after treatment. These findings suggest HDLs may help monitor oxidation in canine leishmaniasis.

Area of Science:

  • Veterinary Medicine
  • Biochemistry
  • Immunology

Background:

  • Canine leishmaniasis is a significant parasitic disease with complex pathophysiological changes.
  • Oxidative stress and inflammation are implicated in the progression of leishmaniasis.
  • High density lipoproteins (HDLs) possess antioxidant and anti-inflammatory properties.

Purpose of the Study:

  • To investigate changes in HDL cholesterol (HDL-Chol, HDL%), C-reactive protein (CRP), and paraoxonase-1 (PON-1) in dogs with leishmaniasis before and after treatment.
  • To explore the relationship between HDL parameters, inflammation markers, and oxidative stress in affected dogs.

Main Methods:

  • Sera from 10 control dogs and 10 leishmaniotic dogs were analyzed.
  • Leishmaniotic dogs were sampled before and at multiple time points after treatment with antimonials and allopurinol.
  • Measurements included HDL-Chol, HDL%, CRP, and PON-1 activity.

Main Results:

  • Leishmaniotic dogs exhibited lower HDL-Chol and PON-1 levels compared to controls.
  • HDL-Chol and PON-1 levels significantly increased after treatment.
  • HDL-Chol and HDL% showed positive correlations with PON-1 and negative correlations with CRP.

Conclusions:

  • HDL levels and PON-1 activity are reduced in canine leishmaniasis, indicating increased oxidative stress.
  • Treatment reverses these changes, suggesting a role for HDLs in disease recovery.
  • HDLs may serve as a valuable biomarker for monitoring oxidative stress and inflammation in leishmaniotic dogs.