Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1982 Aug 12;245(2):317-25.
doi: 10.1016/0006-8993(82)90814-9.

Angiotensin-converting enzyme in discrete areas of the rat forebrain and pituitary gland

Angiotensin-converting enzyme in discrete areas of the rat forebrain and pituitary gland

J M Saavedra et al. Brain Res. .

Abstract

With the use of a sensitive radioisotopic method we have examined the activity of the angiotensin-converting enzyme (ACE, E.C. 3.4.15.1) in specific nuclei of the rat forebrain and in the anterior, intermediate and posterior lobes of the pituitary gland of the rat. We reported that ACE activity is heterogeneously distributed in the rat forebrain, with a 200-fold difference between the lowest and the highest values. Highest enzyme activities were found in the subfornical organ and in the posterior lobe of the pituitary gland. High ACE activity was also detected in the intermediate and anterior lobes of the pituitary gland, the caudate nucleus, and the medial habenular nucleus. Substantial activity also existed in the globus pallidus, the median eminence, the supraoptic and paraventricular nuclei, the lateral habenular nucleus and the organon vasculosum laminae terminalis. Our results demonstrate that one of the components of the renin-angiotensin system, the angiotensin-converting enzyme, is highly localized to a few discrete brain structures and the pituitary gland. These findings suggest that angiotensin II could be formed locally in some of these structures, supporting previous immunohistochemical data.

PubMed Disclaimer

Similar articles

Cited by

Publication types

Substances

LinkOut - more resources