Key result
Lisinopril did not significantly change mean junctional resistance in guinea pig ventricular myocytes compared to baseline (15.0 vs 14.5 M omega; p > 0.05).
Why the study?
Does lisinopril modulate intercellular resistance in guinea pig ventricular myocytes?
Does lisinopril modulate intercellular resistance in guinea pig ventricular myocytes?
Absolute Event Rate: 15% vs 14.5%
p-value: p=> 0.05
Lisinopril does not modulate junctional resistance independent of ACE inhibition in guinea pig ventricular myocytes.
No effect of lisinopril on junctional resistance in guinea pig myocytes; leaves open potential modulation in other models or species.
Previous reports have suggested that angiotensin converting enzyme (ACE) inhibitors are able to modulate intercellular resistance through an ACE-independent action. Therefore, the aim of our study was to determine whether the ACE inhibitor lisinopril would modulate intercellular resistance of guinea pig ventricular myocytes. Junctional resistance was measured using the double patch-clamp technique in eight cell pairs at baseline and during superfusion with 10(-4) M lisinopril. In these cell pairs, mean junctional resistance (+/-SEM) measured at baseline (14.5 +/- 3.8 M omega) was unchanged (15.0 +/- 3.6 M omega; p > 0.05) during lisinopril even after a 25-min exposure to the drug (n = 3). As well, a 20-min exposure to 10(-6) M lisinopril from the intracellular milieu did not modify the junctional resistance. In conclusion, this study demonstrates that modulation of junctional resistance independent of drug-related ACE inhibition is not observed with lisinopril.
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Daleau et al. (1997) studied this question. Lisinopril vs. Baseline was evaluated on Junctional resistance (p=> 0.05). Lisinopril did not significantly change mean junctional resistance in guinea pig ventricular myocytes compared to baseline (15.0 vs 14.5 M omega; p > 0.05).
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