Hydroxysafflor yellow A improves established monocrotaline-induced pulmonary arterial hypertension in rats

J Int Med Res. 2016 Jun;44(3):569-84. doi: 10.1177/0300060515597931. Epub 2016 Apr 8.

Abstract

Objective: To evaluate the beneficial effects of hydroxysafflor yellow A (HSYA) on monocrotaline (MCT)-induced pulmonary arterial hypertension (PAH) in rats, and to investigate the main pathophysiological mechanism of HSYA in preventing development of MCT-induced PAH.

Methods: Four groups (control, control with HSYA treatment, MCT-exposed, and MCT-exposed with HSYA treatment) were evaluated at day 28 following MCT exposure. Haemodynamic measurements, right ventricular hypertrophy, morphometry, inflammatory cytokines and oxidant expression were assessed.

Results: HSYA significantly reduced haemodynamic changes, right ventricular hypertrophy and morphometric changes induced by exposure to MCT. HYSA also suppressed MCT-induced inflammation and oxidative stress in rat pulmonary tissue.

Conclusions: Experimental MCT-induced PAH may be reduced by HSYA treatment, and the mechanism may involve suppression of inflammation and oxidative stress.

Keywords: Chinese medicine; hydroxysafflor; inflammation; monocrotaline; oxidant; pulmonary artery hypertension; safflower.

MeSH terms

  • 8-Hydroxy-2'-Deoxyguanosine
  • Animals
  • Chalcone / analogs & derivatives*
  • Chalcone / pharmacology
  • Chalcone / therapeutic use
  • Deoxyguanosine / analogs & derivatives
  • Deoxyguanosine / metabolism
  • Gene Expression Regulation / drug effects
  • Hemodynamics / drug effects
  • Hypertension, Pulmonary / complications
  • Hypertension, Pulmonary / drug therapy*
  • Hypertension, Pulmonary / genetics
  • Hypertension, Pulmonary / physiopathology
  • Hypertrophy, Right Ventricular / complications
  • Hypertrophy, Right Ventricular / drug therapy
  • Hypertrophy, Right Ventricular / genetics
  • Hypertrophy, Right Ventricular / physiopathology
  • Inflammation / pathology
  • Male
  • Malondialdehyde / metabolism
  • Monocrotaline
  • Oxidative Stress / drug effects
  • Quinones / pharmacology
  • Quinones / therapeutic use*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats, Wistar
  • Superoxide Dismutase / metabolism
  • Vascular Remodeling / drug effects

Substances

  • Quinones
  • RNA, Messenger
  • hydroxysafflor yellow A
  • Malondialdehyde
  • Chalcone
  • Monocrotaline
  • 8-Hydroxy-2'-Deoxyguanosine
  • Superoxide Dismutase
  • Deoxyguanosine