Effects of High Fat Feeding and Diabetes on Regression of Atherosclerosis Induced by Low-Density Lipoprotein Receptor Gene Therapy in LDL Receptor-Deficient Mice

PLoS One. 2015 Jun 5;10(6):e0128996. doi: 10.1371/journal.pone.0128996. eCollection 2015.

Abstract

We tested whether a high fat diet (HFD) containing the inflammatory dietary fatty acid palmitate or insulin deficient diabetes altered the remodeling of atherosclerotic plaques in LDL receptor knockout (Ldlr-/-) mice. Cholesterol reduction was achieved by using a helper-dependent adenovirus (HDAd) carrying the gene for the low-density lipoprotein receptor (Ldlr; HDAd-LDLR). After injection of the HDAd-LDLR, mice consuming either HFD, which led to insulin resistance but not hyperglycemia, or low fat diet (LFD), showed regression compared to baseline. However there was no difference between the two groups in terms of atherosclerotic lesion size, or CD68+ cell and lipid content. Because of the lack of effects of these two diets, we then tested whether viral-mediated cholesterol reduction would lead to defective regression in mice with greater hyperglycemia. In both normoglycemic and streptozotocin (STZ)-treated hyperglycemic mice, HDAd-LDLR significantly reduced plasma cholesterol levels, decreased atherosclerotic lesion size, reduced macrophage area and lipid content, and increased collagen content of plaque in the aortic sinus. However, reductions in anti-inflammatory and ER stress-related genes were less pronounced in STZ-diabetic mice compared to non-diabetic mice. In conclusion, HDAd-mediated Ldlr gene therapy is an effective and simple method to induce atherosclerosis regression in Ldlr-/- mice in different metabolic states.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adenoviridae / genetics
  • Animals
  • Aorta / metabolism
  • Aorta / pathology
  • Atherosclerosis / complications
  • Atherosclerosis / genetics
  • Atherosclerosis / pathology
  • Atherosclerosis / therapy*
  • Cholesterol, Dietary / administration & dosage
  • Collagen / genetics
  • Collagen / metabolism
  • Diabetes Mellitus, Experimental / chemically induced
  • Diabetes Mellitus, Experimental / complications
  • Diabetes Mellitus, Experimental / genetics*
  • Diabetes Mellitus, Experimental / pathology
  • Diet, High-Fat*
  • Gene Expression
  • Genetic Therapy / methods*
  • Genetic Vectors
  • Hyperglycemia / complications
  • Hyperglycemia / genetics
  • Hyperglycemia / pathology
  • Hyperglycemia / therapy*
  • Insulin Resistance
  • Macrophages / metabolism
  • Macrophages / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Plaque, Atherosclerotic / complications
  • Plaque, Atherosclerotic / genetics
  • Plaque, Atherosclerotic / pathology
  • Plaque, Atherosclerotic / therapy*
  • Receptors, LDL / deficiency
  • Receptors, LDL / genetics*
  • Streptozocin

Substances

  • Cholesterol, Dietary
  • Receptors, LDL
  • Streptozocin
  • Collagen