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 |
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container_title | American journal of physiology. Heart and circulatory physiology |
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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 |
format | Article |
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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><identifier>ISSN: 0363-6135</identifier><identifier>ISSN: 0002-9513</identifier><identifier>EISSN: 1522-1539</identifier><identifier>DOI: 10.1152/ajpheart.1991.261.3.h683</identifier><identifier>PMID: 1653537</identifier><language>eng</language><publisher>United States</publisher><subject>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</subject><ispartof>American journal of physiology. Heart and circulatory physiology, 1991-09, Vol.261 (3), p.H683-H690</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-6f22cc8d77964f8926f5989d52dcc359b86a681bc0b237b6c2b15d6eb7d63b9f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1653537$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kawasaki, H</creatorcontrib><creatorcontrib>Nuki, C</creatorcontrib><creatorcontrib>Saito, A</creatorcontrib><creatorcontrib>Takasaki, K</creatorcontrib><title>NPY modulates neurotransmission of CGRP-containing vasodilator nerves in rat mesenteric arteries</title><title>American journal of physiology. 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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source | MEDLINE; Alma/SFX Local Collection |
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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