Associations of ApoAI and ApoB-containing lipoproteins with AngII-induced abdominal aortic aneurysms in mice

Arterioscler Thromb Vasc Biol. 2015 Aug;35(8):1826-34. doi: 10.1161/ATVBAHA.115.305482. Epub 2015 Jun 4.

Abstract

Objective: Dyslipidemia is implicated in abdominal aortic aneurysms (AAAs) in humans and angiotensin (Ang) II-infused mice. This study determined effects of major lipoprotein classes on AngII-induced AAAs using multiple mouse strains with dietary and pharmacological manipulations.

Approach and results: Western diet had minor effects on plasma cholesterol concentrations and the low incidence of AngII-induced AAAs in C57BL/6J mice. Low incidence of AAAs in this strain was not attributed to protection from high-density lipoprotein, because apolipoprotein (apo) AI deficiency did not increase AngII-induced AAAs. ApoAI deletion also failed to alter AAA occurrence in hypercholesterolemic mice. Low-density lipoprotein receptor-/- mice fed normal diet had low incidence of AngII-induced AAAs. Western diet feeding of this strain provoked pronounced hypercholesterolemia because of increased apoB-containing lipoproteins with attendant increases of atherosclerosis in both sexes, but AAAs only in male mice. ApoE-deficient mice fed normal diet were modestly hypercholesterolemic, whereas this strain fed Western diet was severely hypercholesterolemic because of increased apoB-containing lipoprotein concentrations. The latter augmented atherosclerosis, but did not change the high incidence of AAAs in this strain. To determine whether reductions in apoB-containing lipoproteins influenced AngII-induced AAAs, ezetimibe was administered at a dose that partially reduced plasma cholesterol concentrations to ApoE-deficient mice fed Western diet. This decreased atherosclerosis, but not AAAs. This ezetimibe dose in ApoE-deficient mice fed normal diet significantly decreased plasma apoB-containing lipoprotein concentrations and reduced AngII-induced AAAs.

Conclusions: ApoB-containing lipoproteins contribute to augmentation of AngII-induced AAA in male mice. However, unlike atherosclerosis, AAA occurrence was not correlated with increases in plasma apoB-containing lipoprotein concentrations.

Keywords: angiotensins; aortic aneurysm; hypercholesterolemia; lipoproteins; receptors, LDL.

Publication types

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

MeSH terms

  • Angiotensin II*
  • Animals
  • Anticholesteremic Agents / pharmacology
  • Aorta, Abdominal / metabolism*
  • Aorta, Abdominal / pathology
  • Aortic Aneurysm, Abdominal / blood
  • Aortic Aneurysm, Abdominal / chemically induced*
  • Aortic Aneurysm, Abdominal / pathology
  • Aortic Aneurysm, Abdominal / prevention & control
  • Apolipoprotein A-I / blood*
  • Apolipoprotein A-I / deficiency
  • Apolipoprotein A-I / genetics
  • Apolipoprotein B-100
  • Apolipoproteins B / blood*
  • Apolipoproteins E / deficiency
  • Apolipoproteins E / genetics
  • Azetidines / pharmacology
  • Diet, Western
  • Disease Models, Animal
  • Ezetimibe
  • Female
  • Hypercholesterolemia / blood
  • Hypercholesterolemia / complications*
  • Hypercholesterolemia / drug therapy
  • Hypercholesterolemia / genetics
  • Male
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Receptors, LDL / deficiency
  • Receptors, LDL / genetics
  • Sex Factors

Substances

  • Anticholesteremic Agents
  • Apob protein, mouse
  • Apolipoprotein A-I
  • Apolipoprotein B-100
  • Apolipoproteins B
  • Apolipoproteins E
  • Azetidines
  • Receptors, LDL
  • Angiotensin II
  • Ezetimibe