NPY modulates neurotransmission of CGRP-containing vasodilator nerves in rat mesenteric arteries

H. Kawasaki, C. Nuki, A. Saito and K. Takasaki Department of Pharmacology, Miyazaki Medical College, Japan. The effect of neuropeptide Y (NPY) in neurotransmission of calcitonin gene-related peptide (CGRP)-containing vasodilator nerves was investigated in rats. In perfused mesenteric vascular beds w...

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Veröffentlicht in:American journal of physiology. Heart and circulatory physiology 1991-09, Vol.261 (3), p.H683-H690
Hauptverfasser: Kawasaki, H, Nuki, C, Saito, A, Takasaki, K
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container_end_page H690
container_issue 3
container_start_page H683
container_title American journal of physiology. Heart and circulatory physiology
container_volume 261
creator Kawasaki, H
Nuki, C
Saito, A
Takasaki, K
description H. Kawasaki, C. Nuki, A. Saito and K. Takasaki Department of Pharmacology, Miyazaki Medical College, Japan. The effect of neuropeptide Y (NPY) in neurotransmission of calcitonin gene-related peptide (CGRP)-containing vasodilator nerves was investigated in rats. In perfused mesenteric vascular beds with active tone, perivascular nerve stimulation (PNS; 1-8 Hz) caused a frequency-dependent vasodilator response, which was abolished by 300 nM tetrodotoxin (TTX), 500 nM capsaicin, 1 microM human CGRP-(8-37), or cold storage denervation (4 degrees C for 72 h). NPY (5, 10, and 50 nM) concentration dependently inhibited the vasodilator response to PNS, whereas NPY had little effect on vasodilation induced by exogenous CGRP (10 and 100 pmol) or 1 nmol acetylcholine (ACh). NPY (10 nM) inhibited the neurogenic release of CGRP-like immunoreactivity induced by PNS (4 and 8 Hz), which was abolished by 300 nM TTX and the removal of Ca2+ from the medium. Combined perfusion with 5 nM NPY and 10 nM norepinephrine additively inhibited the vasodilator response to PNS but not to exogenous CGRP and ACh. Immunohistochemistry showed the distinct distribution of CGRP- and NPY-like immunoreactivity-containing fibers in rat mesenteric arteries. These results suggest that NPY modulates presynaptically the release of CGRP from CGRP-containing vasodilator nerves in rat mesenteric arteries.
doi_str_mv 10.1152/ajpheart.1991.261.3.h683
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Kawasaki, C. Nuki, A. Saito and K. Takasaki Department of Pharmacology, Miyazaki Medical College, Japan. The effect of neuropeptide Y (NPY) in neurotransmission of calcitonin gene-related peptide (CGRP)-containing vasodilator nerves was investigated in rats. In perfused mesenteric vascular beds with active tone, perivascular nerve stimulation (PNS; 1-8 Hz) caused a frequency-dependent vasodilator response, which was abolished by 300 nM tetrodotoxin (TTX), 500 nM capsaicin, 1 microM human CGRP-(8-37), or cold storage denervation (4 degrees C for 72 h). NPY (5, 10, and 50 nM) concentration dependently inhibited the vasodilator response to PNS, whereas NPY had little effect on vasodilation induced by exogenous CGRP (10 and 100 pmol) or 1 nmol acetylcholine (ACh). NPY (10 nM) inhibited the neurogenic release of CGRP-like immunoreactivity induced by PNS (4 and 8 Hz), which was abolished by 300 nM TTX and the removal of Ca2+ from the medium. Combined perfusion with 5 nM NPY and 10 nM norepinephrine additively inhibited the vasodilator response to PNS but not to exogenous CGRP and ACh. Immunohistochemistry showed the distinct distribution of CGRP- and NPY-like immunoreactivity-containing fibers in rat mesenteric arteries. 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Heart and circulatory physiology</title><addtitle>Am J Physiol</addtitle><description>H. Kawasaki, C. Nuki, A. Saito and K. Takasaki Department of Pharmacology, Miyazaki Medical College, Japan. The effect of neuropeptide Y (NPY) in neurotransmission of calcitonin gene-related peptide (CGRP)-containing vasodilator nerves was investigated in rats. In perfused mesenteric vascular beds with active tone, perivascular nerve stimulation (PNS; 1-8 Hz) caused a frequency-dependent vasodilator response, which was abolished by 300 nM tetrodotoxin (TTX), 500 nM capsaicin, 1 microM human CGRP-(8-37), or cold storage denervation (4 degrees C for 72 h). NPY (5, 10, and 50 nM) concentration dependently inhibited the vasodilator response to PNS, whereas NPY had little effect on vasodilation induced by exogenous CGRP (10 and 100 pmol) or 1 nmol acetylcholine (ACh). NPY (10 nM) inhibited the neurogenic release of CGRP-like immunoreactivity induced by PNS (4 and 8 Hz), which was abolished by 300 nM TTX and the removal of Ca2+ from the medium. Combined perfusion with 5 nM NPY and 10 nM norepinephrine additively inhibited the vasodilator response to PNS but not to exogenous CGRP and ACh. Immunohistochemistry showed the distinct distribution of CGRP- and NPY-like immunoreactivity-containing fibers in rat mesenteric arteries. These results suggest that NPY modulates presynaptically the release of CGRP from CGRP-containing vasodilator nerves in rat mesenteric arteries.</description><subject>Acetylcholine - pharmacology</subject><subject>Animals</subject><subject>Calcitonin Gene-Related Peptide - pharmacology</subject><subject>Calcitonin Gene-Related Peptide - physiology</subject><subject>Capsaicin - pharmacology</subject><subject>Denervation</subject><subject>Electric Stimulation</subject><subject>Guanethidine - pharmacology</subject><subject>In Vitro Techniques</subject><subject>Male</subject><subject>Mesenteric Arteries - innervation</subject><subject>Methoxamine - pharmacology</subject><subject>Muscle, Smooth, Vascular - innervation</subject><subject>Neuropeptide Y - pharmacology</subject><subject>Peptide Fragments - pharmacology</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Sympathetic Nervous System - drug effects</subject><subject>Sympathetic Nervous System - physiology</subject><subject>Synaptic Transmission - drug effects</subject><subject>Tetrodotoxin - pharmacology</subject><subject>Vasodilation - drug effects</subject><issn>0363-6135</issn><issn>0002-9513</issn><issn>1522-1539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkN1KwzAAhYMoc04fQcgLtDbJkjaXMtQJQ4fohVcxf10z1mYk3WRvb0aVeXUuDt_h8AEAUZEjRPGdXG8bK0OfI85RjhnKSd6wipyBcapxhijh52BcEEYyhgi9BFcxrouioCUjIzBCjBJKyjH4ell-wtab3Ub2NsLO7oLvg-xi62J0voO-hrOnt2WmfddL17luBfcyeuMS4EMCwj5xroNB9rC10Xa9DU7DdC6ljdfgopabaG9-cwI-Hh_eZ_Ns8fr0PLtfZHo6RX3Gaoy1rkxZcjatK45ZTXnFDcVGa0K5qphkFVK6UJiUimmsEDXMqtIwonhNJqAadnXwMQZbi21wrQwHgQpxdCb-nImjM5GcCSLmyVlCbwd0u1OtNSdwkJT6fOgbt2q-XbBi2xySnI1fHU6r_wZ_AMWHfbg</recordid><startdate>19910901</startdate><enddate>19910901</enddate><creator>Kawasaki, H</creator><creator>Nuki, C</creator><creator>Saito, A</creator><creator>Takasaki, K</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19910901</creationdate><title>NPY modulates neurotransmission of CGRP-containing vasodilator nerves in rat mesenteric arteries</title><author>Kawasaki, H ; Nuki, C ; Saito, A ; Takasaki, K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-6f22cc8d77964f8926f5989d52dcc359b86a681bc0b237b6c2b15d6eb7d63b9f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Acetylcholine - pharmacology</topic><topic>Animals</topic><topic>Calcitonin Gene-Related Peptide - pharmacology</topic><topic>Calcitonin Gene-Related Peptide - physiology</topic><topic>Capsaicin - pharmacology</topic><topic>Denervation</topic><topic>Electric Stimulation</topic><topic>Guanethidine - pharmacology</topic><topic>In Vitro Techniques</topic><topic>Male</topic><topic>Mesenteric Arteries - innervation</topic><topic>Methoxamine - pharmacology</topic><topic>Muscle, Smooth, Vascular - innervation</topic><topic>Neuropeptide Y - pharmacology</topic><topic>Peptide Fragments - pharmacology</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Sympathetic Nervous System - drug effects</topic><topic>Sympathetic Nervous System - physiology</topic><topic>Synaptic Transmission - drug effects</topic><topic>Tetrodotoxin - pharmacology</topic><topic>Vasodilation - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kawasaki, H</creatorcontrib><creatorcontrib>Nuki, C</creatorcontrib><creatorcontrib>Saito, A</creatorcontrib><creatorcontrib>Takasaki, K</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kawasaki, H</au><au>Nuki, C</au><au>Saito, A</au><au>Takasaki, K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>NPY modulates neurotransmission of CGRP-containing vasodilator nerves in rat mesenteric arteries</atitle><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle><addtitle>Am J Physiol</addtitle><date>1991-09-01</date><risdate>1991</risdate><volume>261</volume><issue>3</issue><spage>H683</spage><epage>H690</epage><pages>H683-H690</pages><issn>0363-6135</issn><issn>0002-9513</issn><eissn>1522-1539</eissn><abstract>H. Kawasaki, C. Nuki, A. Saito and K. Takasaki Department of Pharmacology, Miyazaki Medical College, Japan. The effect of neuropeptide Y (NPY) in neurotransmission of calcitonin gene-related peptide (CGRP)-containing vasodilator nerves was investigated in rats. In perfused mesenteric vascular beds with active tone, perivascular nerve stimulation (PNS; 1-8 Hz) caused a frequency-dependent vasodilator response, which was abolished by 300 nM tetrodotoxin (TTX), 500 nM capsaicin, 1 microM human CGRP-(8-37), or cold storage denervation (4 degrees C for 72 h). NPY (5, 10, and 50 nM) concentration dependently inhibited the vasodilator response to PNS, whereas NPY had little effect on vasodilation induced by exogenous CGRP (10 and 100 pmol) or 1 nmol acetylcholine (ACh). NPY (10 nM) inhibited the neurogenic release of CGRP-like immunoreactivity induced by PNS (4 and 8 Hz), which was abolished by 300 nM TTX and the removal of Ca2+ from the medium. Combined perfusion with 5 nM NPY and 10 nM norepinephrine additively inhibited the vasodilator response to PNS but not to exogenous CGRP and ACh. Immunohistochemistry showed the distinct distribution of CGRP- and NPY-like immunoreactivity-containing fibers in rat mesenteric arteries. These results suggest that NPY modulates presynaptically the release of CGRP from CGRP-containing vasodilator nerves in rat mesenteric arteries.</abstract><cop>United States</cop><pmid>1653537</pmid><doi>10.1152/ajpheart.1991.261.3.h683</doi></addata></record>
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subjects Acetylcholine - pharmacology
Animals
Calcitonin Gene-Related Peptide - pharmacology
Calcitonin Gene-Related Peptide - physiology
Capsaicin - pharmacology
Denervation
Electric Stimulation
Guanethidine - pharmacology
In Vitro Techniques
Male
Mesenteric Arteries - innervation
Methoxamine - pharmacology
Muscle, Smooth, Vascular - innervation
Neuropeptide Y - pharmacology
Peptide Fragments - pharmacology
Rats
Rats, Inbred Strains
Sympathetic Nervous System - drug effects
Sympathetic Nervous System - physiology
Synaptic Transmission - drug effects
Tetrodotoxin - pharmacology
Vasodilation - drug effects
title NPY modulates neurotransmission of CGRP-containing vasodilator nerves in rat mesenteric arteries
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