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ischaemic preconditioning of the human heart. - Leicester Research ...

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4.2.5 Statistical Analysis<br />

All data are presented as mean ± SEM. All values were compared by ANOVA with<br />

application <strong>of</strong> a post hoc Tukey's test. Ap value <strong>of</strong> < 0.05 was considered statistically<br />

significant.<br />

4.3 RESULTS<br />

All samples entering <strong>the</strong> studies completed <strong>the</strong> applied experimental protocol and were<br />

included in <strong>the</strong> analysis. A dose-response analysis (0 to 5 mM) based on<br />

both CK leakage<br />

and MTT reduction, revealed that diazoxide and pinacidil were found to be most<br />

protective at a dose <strong>of</strong> 100 ýt! Vl and 0.5 mM respectively. Diazoxide lost its protective<br />

effect at doses > SOO ýLM and pinacidil at doses >- I mM (see Figures 4.2 and 4 3). At <strong>the</strong><br />

above optimal doses, <strong>the</strong> greatest degree <strong>of</strong> protection was afforded when <strong>the</strong> K, xui,<br />

openers was applied for 10 min before ischemia (pretreatment) followed by wash-out.<br />

Glibenclamide abolished <strong>the</strong> protective effects <strong>of</strong> <strong>preconditioning</strong> at doses > 10 pM (see<br />

Figure 4.4). A dose response analysis for 5-HD (Figure 4.5) was performed between<br />

concentrations <strong>of</strong> 0-10 mM. The minimal effective concentration for 5-HD which<br />

abolished protection afforded by <strong>preconditioning</strong> was I mM. The dose-response<br />

analysis<br />

for HMR 1883 (Figure 4.6) revealed that concentrations between <strong>the</strong> ranges 0 to 100 pM<br />

had no effect on <strong>the</strong> protection afforded by <strong>preconditioning</strong>. Again pretreatment with<br />

<strong>the</strong>se drugs for 10min before ischemia was <strong>the</strong> most effective protocol.<br />

95

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