Literature DB >> 10549575

Effect of ursodeoxycholic acid on ischemia/reperfusion injury in isolated rat heart.

W Y Lee1, S H Han, T S Cho, Y H Yoo, S M Lee.   

Abstract

In this study, the effects of ursodeoxycholic acid (UDCA) on ischemia/reperfusion injury were investigated on isolated heart perfusion model. Hearts were perfused with oxygenated Krebs-Henseleit solution (pH 7.4, 37 degrees C) on a Langendorff apparatus. After equilibration, isolated hearts were treated with UDCA 20 to 160 microM or vehicle (0.04% DMSO) for 10 min before the onset of ischemia. After global ischemia (30 min), ischemic hearts were reperfused and allowed to recover for 30 min. The physiological (i.e. heart rate, left ventricular developed pressure, coronary flow, double product and time to contracture formation) and biochemical (lactate dehydrogenase; LDH) parameters were evaluated. In vehicle-treated group, time to contracture formation was 21.4 min during ischemia, LVDP was 18.5 mmHg at the endpoint of reperfusion and LDH activity in total reperfusion effluent was 54.0 U/L. Cardioprotective effects of UDCA against ischemia/reperfusion consisted of a reduced TTC (EC25=97.3 microM), reduced LDH release and enhanced recovery of cardiac contractile function during reperfusion. Especially, the treatments of UDCA 80 and 160 microM significantly increased LVDP and reduced LDH release. Our findings suggest that UDCA ameliorates ischemia/reperfusion-induced myocardial damage.

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Year:  1999        PMID: 10549575     DOI: 10.1007/bf02979156

Source DB:  PubMed          Journal:  Arch Pharm Res        ISSN: 0253-6269            Impact factor:   4.946


  7 in total

1.  KP-102 (growth hormone-releasing peptide-2) attenuates ischemia/reperfusion injury in isolated rat hearts.

Authors:  Sadayoshi Furuta; Toshimitsu Hori; Tadashi Ohyama
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2006-06-14       Impact factor: 3.000

2.  Systemic gut microbial modulation of bile acid metabolism in host tissue compartments.

Authors:  Jonathan R Swann; Elizabeth J Want; Florian M Geier; Konstantina Spagou; Ian D Wilson; James E Sidaway; Jeremy K Nicholson; Elaine Holmes
Journal:  Proc Natl Acad Sci U S A       Date:  2010-09-13       Impact factor: 11.205

3.  Chenodeoxycholic and deoxycholic acids induced positive inotropic and negative chronotropic effects on rat heart.

Authors:  Jie Gao; Guanyin Yuan; Zhan Xu; Luyao Lan; Wenkuan Xin
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2020-08-18       Impact factor: 3.000

4.  Ursodeoxycholic acid prevents ventricular conduction slowing and arrhythmia by restoring T-type calcium current in fetuses during cholestasis.

Authors:  Oladipupo Adeyemi; Anita Alvarez-Laviada; Francisca Schultz; Effendi Ibrahim; Michael Trauner; Catherine Williamson; Alexey V Glukhov; Julia Gorelik
Journal:  PLoS One       Date:  2017-09-21       Impact factor: 3.240

5.  Prolonged ursodeoxycholic acid administration reduces acute ischaemia-induced arrhythmias in adult rat hearts.

Authors:  Elisa Ferraro; Lidia Pozhidaeva; David S Pitcher; Catherine Mansfield; Jia Han Benjamin Koh; Catherine Williamson; Oleg Aslanidi; Julia Gorelik; Fu Siong Ng
Journal:  Sci Rep       Date:  2020-09-17       Impact factor: 4.379

6.  Bile acids in treatment of ocular disease.

Authors:  Jeffrey H Boatright; John M Nickerson; Anisha G Moring; Machelle T Pardue
Journal:  J Ocul Biol Dis Infor       Date:  2009-08-27

Review 7.  Overview of Bile Acids Signaling and Perspective on the Signal of Ursodeoxycholic Acid, the Most Hydrophilic Bile Acid, in the Heart.

Authors:  Noorul Izzati Hanafi; Anis Syamimi Mohamed; Siti Hamimah Sheikh Abdul Kadir; Mohd Hafiz Dzarfan Othman
Journal:  Biomolecules       Date:  2018-11-27
  7 in total

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