HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Role of κ-opioid receptor in hypoxic pulmonary artery hypertension and its underlying mechanism.

Abstract
The objective of this study were to determine the mechanism of action and role of the κ-opioid receptor (κ-OR) on hypoxic pulmonary artery hypertension (HPH) in the rat and its underlying mechanisms. The effect of U50,488H, a selective κ-OR agonist, on the proliferation of pulmonary arterial smooth muscle cells (PASMCs) under hypoxic conditions were measured by monotetrazolium assay and [H]-thymidine incorporation. Effects of U50,488H and nor-BNI, a highly selective κ-OR antagonist, on expression of κ-ORs were determined by Western blot technique. The results of our study demonstrated that U50,488H significantly lowered both mean pulmonary artery pressure and right ventricular pressure in HPH rats (P < 0.01). Further, this effect was abolished by nor-BNI (P < 0.01). Further, the effect of the agonist U50,488H was abolished by the antagonist nor-BNI (P < 0.01). mean pulmonary artery pressure and right ventricular pressure were both significantly upregulated in HPH rats treated with nor-BNI versus HPH control group rats (P < 0.01). Moreover, U50,488H inhibited proliferation of the PASMCs that were induced by hypoxia, and this inhibition lasted for 48 hours in a dose-dependent manner (P < 0.01). The inhibitory effect that U50,488H exerted on PASMC proliferation was also abolished by nor-BNI. During hypoxia, the expression of κ-ORs increased in the pulmonary artery. This increase of κ-OR expression was both enhanced by U50,488H and abolished by nor-BNI. The results demonstrate that U50,488H attenuates HPH through both the stimulation and upregulation of κ-ORs.
AuthorsLijun Zhang, Juan Li, Quanxing Shi, Rong Fan, Aaron Joshua Kaye, Yuemin Wang, Xin Sun, Franklin Bueno Rivera, Alan David Kaye, Jianming Pei
JournalAmerican journal of therapeutics (Am J Ther) 2013 Jul-Aug Vol. 20 Issue 4 Pg. 329-36 ISSN: 1536-3686 [Electronic] United States
PMID23838631 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antihypertensive Agents
  • Receptors, Opioid, kappa
  • 3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cyclohexyl)-benzeneacetamide, (trans)-Isomer
Topics
  • 3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cyclohexyl)-benzeneacetamide, (trans)-Isomer (administration & dosage, pharmacology)
  • Animals
  • Antihypertensive Agents (adverse effects, pharmacology)
  • Blood Pressure (drug effects)
  • Blotting, Western
  • Cell Proliferation (drug effects)
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Familial Primary Pulmonary Hypertension
  • Hypertension, Pulmonary (drug therapy, physiopathology)
  • Hypoxia (complications)
  • Male
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Opioid, kappa (drug effects, metabolism)
  • Time Factors
  • Up-Regulation (drug effects)
  • Vasodilation (drug effects)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: