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      KCI등재 SCOPUS SCIE

      Different Regulation of Atrial ANP Release through Neuropeptide Y <sub>2</sub> and Y <sub>4</sub> Receptors

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      https://www.riss.kr/link?id=A107562852

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      <P>Neuropeptide Y (NPY) receptors are present in cardiac membranes. However, its physiological roles in the heart are not clear. The aim of this study was to define the direct effects of pancreatic polypeptide (PP) on atrial dynamics and atrial natriuretic peptide (ANP) release in perfused beating atria. Pancreatic polypeptides, a NPY Y<SUB>4</SUB> receptor agonist, decreased atrial contractility but was not dose-dependent. The ANP release was stimulated by PP in a dose-dependent manner. GR 23118, a NPY Y<SUB>4</SUB> receptor agonist, also increased the ANP release and the potency was greater than PP. In contrast, peptide YY (3-36) (PYY), an NPY Y<SUB>2</SUB> receptor agonist, suppressed the release of ANP with positive inotropy. NPY, an agonist for Y<SUB>1, 2, 5</SUB> receptor, did not cause any significant changes. The pretreatment of NPY (18-36), an antagonist for NPY Y<SUB>3</SUB> receptor, markedly attenuated the stimulation of ANP release by PP but did not affect the suppression of ANP release by PYY. BIIE0246, an antagonist for NPY Y<SUB>2</SUB> receptor, attenuated the suppression of ANP release by PYY. The responsiveness of atrial contractility to PP or PYY was not affected by either of the antagonists. These results suggest that NPY Y<SUB>4</SUB> and Y<SUB>2</SUB> receptor differently regulate the release of atrial ANP.</P>
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      <P>Neuropeptide Y (NPY) receptors are present in cardiac membranes. However, its physiological roles in the heart are not clear. The aim of this study was to define the direct effects of pancreatic polypeptide (PP) on atrial dynamics and atrial ...

      <P>Neuropeptide Y (NPY) receptors are present in cardiac membranes. However, its physiological roles in the heart are not clear. The aim of this study was to define the direct effects of pancreatic polypeptide (PP) on atrial dynamics and atrial natriuretic peptide (ANP) release in perfused beating atria. Pancreatic polypeptides, a NPY Y<SUB>4</SUB> receptor agonist, decreased atrial contractility but was not dose-dependent. The ANP release was stimulated by PP in a dose-dependent manner. GR 23118, a NPY Y<SUB>4</SUB> receptor agonist, also increased the ANP release and the potency was greater than PP. In contrast, peptide YY (3-36) (PYY), an NPY Y<SUB>2</SUB> receptor agonist, suppressed the release of ANP with positive inotropy. NPY, an agonist for Y<SUB>1, 2, 5</SUB> receptor, did not cause any significant changes. The pretreatment of NPY (18-36), an antagonist for NPY Y<SUB>3</SUB> receptor, markedly attenuated the stimulation of ANP release by PP but did not affect the suppression of ANP release by PYY. BIIE0246, an antagonist for NPY Y<SUB>2</SUB> receptor, attenuated the suppression of ANP release by PYY. The responsiveness of atrial contractility to PP or PYY was not affected by either of the antagonists. These results suggest that NPY Y<SUB>4</SUB> and Y<SUB>2</SUB> receptor differently regulate the release of atrial ANP.</P>

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