Protective effects of aloperin on monocroline-induced pulmonary hypertension via regulation of Rho A/Rho kinsase pathway in rats

Biomed Pharmacother. 2017 Nov:95:1161-1168. doi: 10.1016/j.biopha.2017.08.126. Epub 2017 Sep 15.

Abstract

Pulmonary hypertension (PH) is fatal disease which closely involves Rho A/ Rho kinsase (ROCK) pathway. Aloperine is a main active alkaloid extracted from Sophora alopecuroides, which is a traditional Chinese herbal medicine that has been used widely. However, the effects of this alkaloid on pulmonary hypertension and its mechanisms remain unclear. Therefore, this study is designed to investigate whether aloperine has protective effects on PH induced by monocrotaline, whether these effects may be related to regulation of RhoA/ROCK pathway in rats. Pulmonary hypertension was induced by monocrotaline (60mg/kg), and subsequently oral administration of aloperine (25, 50, 100mg/kg/day) for 21 days. At the end of the experiment, rats were underwent hemodynamic and morphologic assessments. At same time, the expression of Rho A, ROCK1, ROCK2, as well as activities of ROCK in the lung of rat has been detected. Afterwards, the expression of p27kip1, Bax, Bcl-2, which was the downstream proliferation and apoptosis factors of ROCK, were tested. The result indicted that aloperine treatment showed significantly improvement in hemodynamic and pathomorphologic data. Moreover, the reduction in expression of Rho A, ROCK1, ROCK2, and suppression in activities of ROCK were found in rat lungs after aloperine treatment. Furthermore, aloperine also alleviated the MCT-induced changes of p27kip1, Bax and Bcl-2. In summary, this study indicates that aloperine have protective effects on monocrotaline-induced PH. And these effects may be partially related to RhoA/ROCK pathway. Thus, aloperine could be considered a possible therapeutic strategy for PH.

Keywords: Aloperine; Monocrotaline; Pulmonary hypertension; Rho A; Rho kinase.

MeSH terms

  • Animals
  • Cardiomegaly / complications
  • Cardiomegaly / drug therapy
  • Cardiomegaly / physiopathology
  • Cyclin-Dependent Kinase Inhibitor p27 / metabolism
  • Electrocardiography
  • Hemodynamics / drug effects
  • Hypertension, Pulmonary / chemically induced*
  • Hypertension, Pulmonary / diagnostic imaging
  • Hypertension, Pulmonary / drug therapy*
  • Hypertension, Pulmonary / physiopathology
  • Lung / drug effects
  • Lung / pathology
  • Lung / physiopathology
  • Male
  • Monocrotaline
  • Piperidines / pharmacology
  • Piperidines / therapeutic use*
  • Proliferating Cell Nuclear Antigen / metabolism
  • Protective Agents / pharmacology
  • Protective Agents / therapeutic use*
  • Pulmonary Artery / drug effects
  • Pulmonary Artery / pathology
  • Pulmonary Artery / physiopathology
  • Quinolizidines
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats, Sprague-Dawley
  • Vascular Remodeling / drug effects
  • bcl-2-Associated X Protein / metabolism
  • rho-Associated Kinases / genetics
  • rho-Associated Kinases / metabolism*
  • rhoA GTP-Binding Protein / genetics
  • rhoA GTP-Binding Protein / metabolism*

Substances

  • Piperidines
  • Proliferating Cell Nuclear Antigen
  • Protective Agents
  • Quinolizidines
  • RNA, Messenger
  • bcl-2-Associated X Protein
  • Cyclin-Dependent Kinase Inhibitor p27
  • aloperine
  • Monocrotaline
  • rho-Associated Kinases
  • rhoA GTP-Binding Protein