Receptor subtype that mediates the neuronal effects of angiotensin ii in the rat dorsal medulla

We have shown previously that many neurons in the caudal medial nucleus tractus solitarii (nTS) are excited by angiotensin (Ang) II. The selective Ang II receptor antagonists losartan (AT 1; DuP 753) and CGP 42112A or PD 123177 (AT 2) were used to evaluate the receptor subtype that mediates excitati...

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Veröffentlicht in:Brain research bulletin 1993, Vol.31 (1), p.195-200
Hauptverfasser: Barnes, Karen L., McQueeney, Allison J., Ferrario, Carlos M.
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Ferrario, Carlos M.
description We have shown previously that many neurons in the caudal medial nucleus tractus solitarii (nTS) are excited by angiotensin (Ang) II. The selective Ang II receptor antagonists losartan (AT 1; DuP 753) and CGP 42112A or PD 123177 (AT 2) were used to evaluate the receptor subtype that mediates excitation of medial nTS neurons by Ang II (1 μM) in rat medulla in vitro slices. Neither losartan nor the AT 2 antagonists altered the baseline firing of either Ang II-sensitive or Ang II-unresponsive neurons. However, in six cells with low-frequency spontaneous activity that remained above baseline after excitation by Ang II, subsequent administration of losartan reversed the firing pattern to the initial low-frequency activity. Losartan (10 μM) blocked the excitation by Ang II in 29 medial nTS neurons. The Ang II-induced excitation recovered from Type I blockade in 1 h. In contrast, both CGP 42112A (10 and 100 μM, n = 12) and PD 123177 (100 μM, n = 7) failed to block excitation by Ang II in all neurons tested. Furthermore, the AT 2 antagonists were ineffective in preventing Ang Il-induced neuronal excitation both when they were the first antagonist tested and when they were evaluated after the neuron had recovered from AT 1 receptor blockade. These studies suggest that the Ang II-induced excitation of caudal medial nTS neurons is mediated by AT 1 Ang II receptors.
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The selective Ang II receptor antagonists losartan (AT 1; DuP 753) and CGP 42112A or PD 123177 (AT 2) were used to evaluate the receptor subtype that mediates excitation of medial nTS neurons by Ang II (1 μM) in rat medulla in vitro slices. Neither losartan nor the AT 2 antagonists altered the baseline firing of either Ang II-sensitive or Ang II-unresponsive neurons. However, in six cells with low-frequency spontaneous activity that remained above baseline after excitation by Ang II, subsequent administration of losartan reversed the firing pattern to the initial low-frequency activity. Losartan (10 μM) blocked the excitation by Ang II in 29 medial nTS neurons. The Ang II-induced excitation recovered from Type I blockade in 1 h. In contrast, both CGP 42112A (10 and 100 μM, n = 12) and PD 123177 (100 μM, n = 7) failed to block excitation by Ang II in all neurons tested. Furthermore, the AT 2 antagonists were ineffective in preventing Ang Il-induced neuronal excitation both when they were the first antagonist tested and when they were evaluated after the neuron had recovered from AT 1 receptor blockade. These studies suggest that the Ang II-induced excitation of caudal medial nTS neurons is mediated by AT 1 Ang II receptors.</description><subject>Angiotensin II</subject><subject>Angiotensin II - antagonists &amp; inhibitors</subject><subject>Angiotensin II - pharmacology</subject><subject>Angiotensin Receptor Antagonists</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biphenyl Compounds - pharmacology</subject><subject>Central nervous system</subject><subject>Central neurotransmission. Neuromudulation. Pathways and receptors</subject><subject>CGP 42112A</subject><subject>Electrophysiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glutamates - pharmacology</subject><subject>Glutamic Acid</subject><subject>Imidazoles - pharmacology</subject><subject>In vitro brain slice</subject><subject>In Vitro Techniques</subject><subject>L-glutamate</subject><subject>Losartan</subject><subject>Losartan potassium</subject><subject>Medulla Oblongata - cytology</subject><subject>Medulla Oblongata - drug effects</subject><subject>Neuronal recording</subject><subject>Neurons - drug effects</subject><subject>Nucleus tractus solitarii</subject><subject>Oligopeptides - pharmacology</subject><subject>PD 123177</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Angiotensin - physiology</subject><subject>Subtype-selective Ang II receptor antagonists</subject><subject>Tetrazoles - pharmacology</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0361-9230</issn><issn>1873-2747</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9r3DAQxUVISTdpvkELOoSSHtyOJFuyL4ES-g8ChdKchSyNWhWvtZHkQr595eyyx_SiQcxvHo_3CHnN4D0DJj-AkKwZuIDrQbwbAHjXqBOyYb0SDVetOiWbI_KSnOf8BwBk38kzctbD0PUt3xD9Ay3uSkw0L2N53CEtv02hW3TBFMz1h3TGJcXZTBS9R1syjZ6a-VeIBeccZhoCre9KpnrqYsqVrQrLNJlX5IU3U8bLw7wg958__bz92tx9__Lt9uNdY1umSuO86by3zDo-Vrtq4Moqx7vRKiP61oKzsh-FV7xte2-Mw06oEQXgqEYnuLggb_e6uxQfFsxFb0O2WB3MGJesVSeFFCD_CzLZAeN8VWz3oE0x54Re71LYmvSoGei1AL2mq9d09SD0UwFa1bM3B_1lrBkcjw6J1_3VYW-yNZNPZrYhH7FWQq8YVOxmj2EN7W_ApLMNONvaS6odaBfD8z7-AUF3opw</recordid><startdate>1993</startdate><enddate>1993</enddate><creator>Barnes, Karen L.</creator><creator>McQueeney, Allison J.</creator><creator>Ferrario, Carlos M.</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>1993</creationdate><title>Receptor subtype that mediates the neuronal effects of angiotensin ii in the rat dorsal medulla</title><author>Barnes, Karen L. ; McQueeney, Allison J. ; Ferrario, Carlos M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-dfa5ffc1cd2b2307927c7d25bc7a384c0dc68b3f72448faade537be30eb7bd323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Angiotensin II</topic><topic>Angiotensin II - antagonists &amp; inhibitors</topic><topic>Angiotensin II - pharmacology</topic><topic>Angiotensin Receptor Antagonists</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biphenyl Compounds - pharmacology</topic><topic>Central nervous system</topic><topic>Central neurotransmission. Neuromudulation. Pathways and receptors</topic><topic>CGP 42112A</topic><topic>Electrophysiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glutamates - pharmacology</topic><topic>Glutamic Acid</topic><topic>Imidazoles - pharmacology</topic><topic>In vitro brain slice</topic><topic>In Vitro Techniques</topic><topic>L-glutamate</topic><topic>Losartan</topic><topic>Losartan potassium</topic><topic>Medulla Oblongata - cytology</topic><topic>Medulla Oblongata - drug effects</topic><topic>Neuronal recording</topic><topic>Neurons - drug effects</topic><topic>Nucleus tractus solitarii</topic><topic>Oligopeptides - pharmacology</topic><topic>PD 123177</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, Angiotensin - physiology</topic><topic>Subtype-selective Ang II receptor antagonists</topic><topic>Tetrazoles - pharmacology</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Barnes, Karen L.</creatorcontrib><creatorcontrib>McQueeney, Allison J.</creatorcontrib><creatorcontrib>Ferrario, Carlos M.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Brain research bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Barnes, Karen L.</au><au>McQueeney, Allison J.</au><au>Ferrario, Carlos M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Receptor subtype that mediates the neuronal effects of angiotensin ii in the rat dorsal medulla</atitle><jtitle>Brain research bulletin</jtitle><addtitle>Brain Res Bull</addtitle><date>1993</date><risdate>1993</risdate><volume>31</volume><issue>1</issue><spage>195</spage><epage>200</epage><pages>195-200</pages><issn>0361-9230</issn><eissn>1873-2747</eissn><coden>BRBUDU</coden><abstract>We have shown previously that many neurons in the caudal medial nucleus tractus solitarii (nTS) are excited by angiotensin (Ang) II. The selective Ang II receptor antagonists losartan (AT 1; DuP 753) and CGP 42112A or PD 123177 (AT 2) were used to evaluate the receptor subtype that mediates excitation of medial nTS neurons by Ang II (1 μM) in rat medulla in vitro slices. Neither losartan nor the AT 2 antagonists altered the baseline firing of either Ang II-sensitive or Ang II-unresponsive neurons. However, in six cells with low-frequency spontaneous activity that remained above baseline after excitation by Ang II, subsequent administration of losartan reversed the firing pattern to the initial low-frequency activity. Losartan (10 μM) blocked the excitation by Ang II in 29 medial nTS neurons. The Ang II-induced excitation recovered from Type I blockade in 1 h. In contrast, both CGP 42112A (10 and 100 μM, n = 12) and PD 123177 (100 μM, n = 7) failed to block excitation by Ang II in all neurons tested. Furthermore, the AT 2 antagonists were ineffective in preventing Ang Il-induced neuronal excitation both when they were the first antagonist tested and when they were evaluated after the neuron had recovered from AT 1 receptor blockade. These studies suggest that the Ang II-induced excitation of caudal medial nTS neurons is mediated by AT 1 Ang II receptors.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>8095842</pmid><doi>10.1016/0361-9230(93)90025-7</doi><tpages>6</tpages></addata></record>
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identifier ISSN: 0361-9230
ispartof Brain research bulletin, 1993, Vol.31 (1), p.195-200
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source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Angiotensin II
Angiotensin II - antagonists & inhibitors
Angiotensin II - pharmacology
Angiotensin Receptor Antagonists
Animals
Biological and medical sciences
Biphenyl Compounds - pharmacology
Central nervous system
Central neurotransmission. Neuromudulation. Pathways and receptors
CGP 42112A
Electrophysiology
Fundamental and applied biological sciences. Psychology
Glutamates - pharmacology
Glutamic Acid
Imidazoles - pharmacology
In vitro brain slice
In Vitro Techniques
L-glutamate
Losartan
Losartan potassium
Medulla Oblongata - cytology
Medulla Oblongata - drug effects
Neuronal recording
Neurons - drug effects
Nucleus tractus solitarii
Oligopeptides - pharmacology
PD 123177
Rats
Rats, Sprague-Dawley
Receptors, Angiotensin - physiology
Subtype-selective Ang II receptor antagonists
Tetrazoles - pharmacology
Vertebrates: nervous system and sense organs
title Receptor subtype that mediates the neuronal effects of angiotensin ii in the rat dorsal medulla
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