Literature DB >> 16201264

Effects of diazoxide treatments on electrophysiologyic properties in guinea pig papillary muscles undergoing ischemia/reperfusion.

Yunhai Yang1, Zhaomin Han, Zhiwei Hu, Kailun Zhang.   

Abstract

The effects of diazoxide treatments on electrophysiologyic properties in guinea pig papillary muscles undergoing ischemia/reperfusion was studied using intracellular microelectrode technique. Twenty-four guinea pigs were randomly divided into three groups (n=8 in each group). In control group, St. Thomas solution was given. In experimental group, St. Thomas solution with diazoxide (100 mol/L) was given. In pretreatment group, the muscle was treated with diazoxide 20 min before arrested with St. Thomas cardioplegia. The results showed that the APD50 and APD90 in experimental and pretreatment groups were significantly shorter after 5 and 10 min reperfusion (P <0.01, P<0.05), but longer after 30 min reperfusion (P<0.01, P<0.05) than in control group. In experimental and pretreatment groups, APA, OS, Vmax recovered more quickly than those in control group. The time to re-systole after reperfusion in control group was longer than that in experimental and pretreatment groups. There was no significant difference in RP among three groups. The time of arrest in pretreatment group was longer than that in experimental and pretreatment group (P<0.05). This study indicates that protective effects of St. Thomas solution with diazoxide is better than that of pretreatment with diazoxide or St. Thomas solution alone.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16201264     DOI: 10.1007/bf02828135

Source DB:  PubMed          Journal:  J Huazhong Univ Sci Technolog Med Sci        ISSN: 1672-0733


  6 in total

1.  Molecular composition of mitochondrial ATP-sensitive potassium channels probed by viral Kir gene transfer.

Authors:  J Seharaseyon; A Ohler; N Sasaki; H Fraser; T Sato; D C Johns; B O'Rourke; E Marbán
Journal:  J Mol Cell Cardiol       Date:  2000-11       Impact factor: 5.000

2.  Cardioprotective effect of diazoxide and its interaction with mitochondrial ATP-sensitive K+ channels. Possible mechanism of cardioprotection.

Authors:  K D Garlid; P Paucek; V Yarov-Yarovoy; H N Murray; R B Darbenzio; A J D'Alonzo; N J Lodge; M A Smith; G J Grover
Journal:  Circ Res       Date:  1997-12       Impact factor: 17.367

3.  Myocardial protection afforded by nicorandil and ischaemic preconditioning in a rabbit infarct model in vivo.

Authors:  J Imagawa; G F Baxter; D M Yellon
Journal:  J Cardiovasc Pharmacol       Date:  1998-01       Impact factor: 3.105

4.  Pharmacological plasticity of cardiac ATP-sensitive potassium channels toward diazoxide revealed by ADP.

Authors:  N D'hahan; C Moreau; A L Prost; H Jacquet; A E Alekseev; A Terzic; M Vivaudou
Journal:  Proc Natl Acad Sci U S A       Date:  1999-10-12       Impact factor: 11.205

5.  Cardioprotective effect of diazoxide is mediated by activation of sarcolemmal but not mitochondrial ATP-sensitive potassium channels in mice.

Authors:  Masashi Suzuki; Tomoaki Saito; Toshiaki Sato; Masaji Tamagawa; Takashi Miki; Susumu Seino; Haruaki Nakaya
Journal:  Circulation       Date:  2003-02-11       Impact factor: 29.690

6.  Mitochondrial ATP-dependent potassium channels: novel effectors of cardioprotection?

Authors:  Y Liu; T Sato; B O'Rourke; E Marban
Journal:  Circulation       Date:  1998-06-23       Impact factor: 29.690

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.