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Functional Receptors for Atrial Natriuretic Peptide in the Rat Mammary Gland during Lactation1
The present study was undertaken: 1) to localize and characterize atrial natriuretic peptide (ANP) receptors in the rat mammary gland; and 2) to elucidate ANP-induced cellular formation of cyclic GMP (cGMP) and alterations in alveolar morphology during both early and late lactation. Receptor autorad...
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Published in: | Endocrinology (Philadelphia) 1998-05, Vol.139 (5), p.2615-2621 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
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Summary: | The present study was undertaken: 1) to localize and characterize
atrial natriuretic peptide (ANP) receptors in the rat mammary gland;
and 2) to elucidate ANP-induced cellular formation of cyclic GMP (cGMP)
and alterations in alveolar morphology during both early and late
lactation. Receptor autoradiography, employing rat-specific[
125I]ANP as radioligand, demonstrated binding sites in
the secretory tissue and larger blood vessels of the mammary gland.
Binding of [125I]rANP to membrane fractions was
completely displaced by unlabeled ANP and brain natriuretic peptide.
C-type natriuretic peptide and cANP(4–23) revealed limited
competition with radiolabeled ANP only during early lactation,
indicating a more heterogenous receptor population at that time.
Systemically administered ANP induced cGMP formation in the alveolar
epithelium, as shown with immunohistochemistry, and increased mammary
tissue cGMP concentrations in vivo throughout the
lactation period. Image analysis revealed enlargement of alveolar (but
not epithelial) cell area after ANP stimulation in late lactation,
suggesting altered alveolar filling or myoepithelial cell relaxation.
These results indicate that ANP induces biological effects in the rat
mammary gland through specific ANP-A receptor interaction with
subsequent intracellular cGMP formation. ANP may therefore play a
regulatory role in the control of mammary gland blood supply and
secretory function. |
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ISSN: | 0013-7227 1945-7170 |
DOI: | 10.1210/endo.139.5.5996 |