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August 1, 1997Circulation Research

Adenoviral Gene Transfer of Phospholamban in Isolated Rat Cardiomyocytes

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Population

Neonatal rat cardiomyocytes

Comparison

Recombinant adenovirus designed to overexpress… vs Uninfected or control cardiomyocytes

Design

Preclinical

Follow-up

48 hours

Key result

Adenovirus-mediated overexpression of phospholamban in rat cardiomyocytes prolonged the relaxation phase (710 vs 344 ms, P<0.01) and decreased peak intracellular calcium (630 vs 967 nmol/L, P<0.01).

Authors

RHRoger J. HajjarUSUlrich SchmidtJKJing X. Kang

Discussion

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Overview

Does not inform clinical practice; leaves open phospholamban targeting in human HF models.

Structured PICO

P
Population
Neonatal rat cardiomyocytes used to study the effects of phospholamban overexpression on intracellular calcium handling.
I
Intervention
Recombinant adenovirus designed to overexpress phospholamban (Ad.RSV.PL) at a multiplicity of infection (MOI) of 10.0 pfu/cell
C
Comparator
Uninfected or control cardiomyocytes
O
Outcome
Intracellular Ca2+ transients (relaxation phase, peak [Ca2+]i, and resting [Ca2+]i)surrogate

Main Result

p-value: p=<.01

Overexpression of phospholamban in rat cardiomyocytes impairs intracellular Ca2+ handling, mimicking abnormalities seen in heart failure, which can be partially corrected by simultaneous SERCA2a overexpression.

Cite This Study

Hajjar et al. (1997) studied Heart failure. Adenoviral gene transfer of phospholamban (Ad.RSV.PL) vs. Uninfected control cells was evaluated on Intracellular Ca2+ transients (relaxation phase, peak [Ca2+]i, resting [Ca2+]i) (p=<.01). Adenovirus-mediated overexpression of phospholamban in rat cardiomyocytes prolonged the relaxation phase (710 vs 344 ms, P<0.01) and decreased peak intracellular calcium (630 vs 967 nmol/L, P<0.01).

synapsesocial.com/papers/6a5dee7e488486c5eff67912https://doi.org/10.1161/01.res.81.2.145
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