2 242

Cited 18 times in

Pharmacodynamic characteristics and cardioprotective effects of new NHE1 inhibitors

Authors
 Juno Kim  ;  Yi-Sook Jung  ;  Kyung Hwan Kim  ;  Min Goo Lee  ;  Sung-eun Yoo  ;  Kyu Yang Yi  ;  Byung Ho Lee  ;  Wan Namkung  ;  Mi-Young Kim  ;  WonSun Han 
Citation
 EUROPEAN JOURNAL OF PHARMACOLOGY, Vol.567(1-2) : 131-138, 2007 
Journal Title
 EUROPEAN JOURNAL OF PHARMACOLOGY 
ISSN
 0014-2999 
Issue Date
2007
MeSH
Animals ; Animals, Newborn ; Cardiotonic Agents/pharmacology* ; Cell Hypoxia ; Cell Survival/drug effects ; Cells, Cultured ; Furans/pharmacology ; Guanidines/pharmacology* ; Humans ; Kinetics ; Myocytes, Cardiac/drug effects ; Rats ; Rats, Sprague-Dawley ; Sodium-Hydrogen Exchanger 1 ; Sodium-Hydrogen Exchangers/antagonists & inhibitors* ; Structure-Activity Relationship ; Submandibular Gland/cytology ; Sulfones/pharmacology ; Thiophenes/pharmacology
Abstract
Inhibitors of Na+/H+ exchanger (NHE) 1 have been shown to exert protective effects on various myocardial injuries. In this study, we characterized the pharmacodynamic properties of new guanidine NHE1 inhibitors (cariporide, sabiporide, KR-32511, KR-32570, and KR-33028) to analyze their myocardial protective effects. Although NHE1 is the major NHE isoform in cardiomyocytes, IC50values of these chemicals tested in rat cardiomyocytes were significantly different from those in PS120/hNHE1 cells where human NHE1 is heterologously expressed. In rat cardiomyocytes, KR-32570 and KR-33028 exhibited the highest potencies and their IC50values were 7 ± 2 nM and 9 ± 3 nM, respectively. The IC50values of all the chemicals tested on rat submandibular gland NHE2 were in the micromolar range, and they showed no inhibitory effects on hNHE3 and epithelial Na+ channels up to 30 μM, suggesting a high selectivity toward NHE1. Sabiporide and KR-32570 exhibited slow dissociation kinetics with NHE1 inhibition persisting even after rinsing-out. When the cytoprotective effects of chemicals against hypoxic damage of rat cardiomyocytes were examined, the order of potency was KR-32570 ≥ KR-33028 > sabiporide > cariporide > KR-32511. This order was exactly the same as that for the NHE1 inhibition in rat cardiomyocytes and did not correlate with any other properties, including the slow dissociation kinetics. Taken together, these results suggest that KR-32570 and KR-33028 are potent candidates for cardioprotective agents, and that the IC50 in the target organ is the most critical factor governing the cytoprotective effects of NHE1 inhibitors.
Full Text
http://www.sciencedirect.com/science/article/pii/S0014299907004402
DOI
10.1016/j.ejphar.2007.03.056
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pharmacology (약리학교실) > 1. Journal Papers
Yonsei Authors
Kim, Kyung Hwan(김경환)
Lee, Min Goo(이민구) ORCID logo https://orcid.org/0000-0001-7436-012X
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/96007
사서에게 알리기
  feedback

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse