Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

e0232 The change of ventricular INa at different time of simulated ischaemia and the effect of atorvastatin

View through CrossRef
Objective To observe time dependent effects of simulated ischaemia on transient sodium currents (INa) of rat left ventricular myocytes, and the effects of atorvastatin on ischaemia INa. Methods 30 Wistar rats were used for isolating left ventricular myocytes, which were randomly divided into two groups: ischaemia group (normal → simulated ischaemia) and statin group (normal → simulated ischaemia with 5 μmol/l atorvastatin). INa were recorded in normal condition (for control) by whole-cell patchclamp. Then in simulated ischaemia condition, INa were recorded from 3 to 21 min, monitored normalised peak currents every 2 min, and compared gate parameters between normal and simulated ischaemia (3 min) condition. Results a. Normalised currents (at −40 mV), in ischaemia group, compared with normal (0.95±0.04), the currents in simulated ischaemia were increased to peak at 3 min (1.15±0.08, p 0.05, respectively), and decreased at 21 min (0.56±0.13, p 0.05). b. Gate parameters, from normal to simulated ischaemia condition at 3 min, membrane potential at 50% maximal activation (V1/2,a), offsetting of activation curve (Ka), membrane potential at 50% maximal inactivation (V1/2,i) and deinactivation constant (τ) were decreased (p<0.01, respectively) in ischaemia group, but offsetting of inactivation curve (Ki) were not changed; compared between two groups, Ki of statin group were decreased (p<0.05) and the decrease of τ value in statin group were less than ischaemia group (p<0.05). Conclusions The effects of simulated ischaemia on INa are time dependent, while INa is transient increased at 3 min, and atorvastatin can depress this process.
Title: e0232 The change of ventricular INa at different time of simulated ischaemia and the effect of atorvastatin
Description:
Objective To observe time dependent effects of simulated ischaemia on transient sodium currents (INa) of rat left ventricular myocytes, and the effects of atorvastatin on ischaemia INa.
Methods 30 Wistar rats were used for isolating left ventricular myocytes, which were randomly divided into two groups: ischaemia group (normal → simulated ischaemia) and statin group (normal → simulated ischaemia with 5 μmol/l atorvastatin).
INa were recorded in normal condition (for control) by whole-cell patchclamp.
Then in simulated ischaemia condition, INa were recorded from 3 to 21 min, monitored normalised peak currents every 2 min, and compared gate parameters between normal and simulated ischaemia (3 min) condition.
Results a.
Normalised currents (at −40 mV), in ischaemia group, compared with normal (0.
95±0.
04), the currents in simulated ischaemia were increased to peak at 3 min (1.
15±0.
08, p 0.
05, respectively), and decreased at 21 min (0.
56±0.
13, p 0.
05).
b.
Gate parameters, from normal to simulated ischaemia condition at 3 min, membrane potential at 50% maximal activation (V1/2,a), offsetting of activation curve (Ka), membrane potential at 50% maximal inactivation (V1/2,i) and deinactivation constant (τ) were decreased (p<0.
01, respectively) in ischaemia group, but offsetting of inactivation curve (Ki) were not changed; compared between two groups, Ki of statin group were decreased (p<0.
05) and the decrease of τ value in statin group were less than ischaemia group (p<0.
05).
Conclusions The effects of simulated ischaemia on INa are time dependent, while INa is transient increased at 3 min, and atorvastatin can depress this process.

Related Results

Effects of simulated ischemia-reperfusion and atorvastatin on INa in rat left ventricular myocytes.
Effects of simulated ischemia-reperfusion and atorvastatin on INa in rat left ventricular myocytes.
Objective To observe time dependent effects of simulated ischemia-reperfusion on transient sodium currents (INa) in rat left ventricular myocytes, and effects of ...
e0078 The effect of acute atorvastatin on cardioprotection of ischaemic postconditioning in diabetes mellitus
e0078 The effect of acute atorvastatin on cardioprotection of ischaemic postconditioning in diabetes mellitus
Objective This study was to investigate if the low dose of acute atorvastatin treatment could affect the cardioprotection of ischaemic post-conditioning (Ipost) i...
Identify and Assess Drug Interactions with Atorvastatin in Inpatient Care
Identify and Assess Drug Interactions with Atorvastatin in Inpatient Care
Background: Atorvastatin is a recent HMG-COA reductase inhibitor used to treat primary hypercholesterolemia, homozygous familial hypercholesterolemia, and mixed dyslipidemias. It i...
e0034 Inhibition of atorvastatin on the autophagy of vascular endothelial cells
e0034 Inhibition of atorvastatin on the autophagy of vascular endothelial cells
Objective To explore the mechanism of atorvastatin's protection on vascular endothelial cells, we conducted the research of impact of atorvastatin on vascular end...
Profil Klinik dan Farmakoterapi Anti-Dislipidemia Diabetes di Rumah Sakit Gunawan Mangunkusumo Ambarawa
Profil Klinik dan Farmakoterapi Anti-Dislipidemia Diabetes di Rumah Sakit Gunawan Mangunkusumo Ambarawa
Dyslipidemia is characterized by increased plasma TG, low HDL-c, and high LDL-c, which is commonly found in patients with diabetes mellitus (DM) and is one of the main causes of is...

Back to Top