The anti-inflammatory effects of Pseudorlaric acid D on atherosclerosis

Biomed Pharmacother. 2020 May:125:109993. doi: 10.1016/j.biopha.2020.109993. Epub 2020 Feb 12.

Abstract

Atherosclerosis is regarded as a chronic inflammatory disease which immune response is regulated by multiple factors. Pseudorlaric acid D (PLAD) is the main bioactive component of Pseudolarix kaempferi Gorden, but little of its property has been found in the literature. We aimed to investigate the anti-inflammatory activity and the underlying mechanisms of PLAD on atherosclerosis. In this study, atherosclerosis model was established by feeding with a high-fat diet in ApoE-/- mice. PLAD was administered intragastrically at a dose of 5 mg/kg for four weeks. We found that PLAD could significantly improve the lipid metabolism and decrease atherosclerotic lesion areas as well as mitigate atherosclerotic changes on vessel walls. Besides, PLAD could markedly inhibit the inflammatory response by down-regulating the levels of Ly6Chi monocytes and NETs, and restraining NETs formation. The expression of pro-inflammatory cytokines IL-1β and IL-18 was also evidently reduced by PLAD. These results indicated that modulating the activation and recruitment of Ly6Chi monocytes and NETs could be the potential anti-inflammatory mechanisms of PLAD on atherosclerosis. PLAD might be a promising therapeutic strategy for the treatment of atherosclerosis and inflammation-related diseases.

Keywords: Atherosclerosis; Inflammation; Monocytes; NETs; Pseudolaric acid D.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / chemistry
  • Anti-Inflammatory Agents / pharmacology*
  • Aortic Diseases / diagnosis
  • Aortic Diseases / drug therapy
  • Aortic Diseases / etiology
  • Apolipoproteins E / deficiency
  • Atherosclerosis / diagnosis
  • Atherosclerosis / drug therapy
  • Atherosclerosis / etiology
  • Cytokines / genetics
  • Cytokines / metabolism
  • Disease Models, Animal
  • Echocardiography
  • Extracellular Traps / drug effects
  • Gene Expression
  • Immunohistochemistry
  • Lipids / blood
  • Male
  • Mice
  • Mice, Knockout
  • Molecular Structure
  • Monocytes / immunology
  • Monocytes / metabolism
  • Monocytes / pathology
  • Phytochemicals / chemistry
  • Phytochemicals / pharmacology*
  • Plaque, Atherosclerotic / diagnosis
  • Plaque, Atherosclerotic / drug therapy
  • Plaque, Atherosclerotic / etiology

Substances

  • Anti-Inflammatory Agents
  • Apolipoproteins E
  • Cytokines
  • Lipids
  • Phytochemicals