Population
Neuronal and vascular smooth muscle (VSM) cells
Comparison
Adenoviral vector transferring AT1 receptor… vs Uninfected cells or cells infected with…
Design
Preclinical
Follow-up
up to 28 days
Authors
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Supports AT1R antisense gene therapy approach; leaves open in vivo validation and clinical translation for ANG-dependent hypertension.
Adenovirus-mediated delivery of AT1 receptor antisense cDNA successfully attenuates ANG II cellular actions in neuronal and VSM cells, demonstrating proof-of-concept for a potential gene therapy approach in ANG-dependent hypertension.
Lü et al. (1998) studied this question.
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