Why the study?
Does ACE inhibition with MK 422 alter the metabolism of Ang I to Ang-(1-7) in dog brainstem homogenates?
Population
Dog brainstem and spinal cord (microdissected regions)
Comparison
In vitro metabolism of 125I-angiotensin I in the… vs Absence of MK 422
Design
Preclinical
Authors
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Highlights potential ACE-independent Ang-(1-7) production in brainstem; leaves open relevance to central autonomic regulation.
Does ACE inhibition with MK 422 alter the metabolism of Ang I to Ang-(1-7) in dog brainstem homogenates?
The study demonstrates high ACE activity in monoamine regions of the dog brainstem and identifies Ang-(1-7) as the major metabolite of Ang I regardless of ACE inhibition.
Santos et al. (1988) studied this question.
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