pubmed-article:6487893 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:6487893 | lifeskim:mentions | umls-concept:C0007450 | lld:lifeskim |
pubmed-article:6487893 | lifeskim:mentions | umls-concept:C0008010 | lld:lifeskim |
pubmed-article:6487893 | lifeskim:mentions | umls-concept:C0007277 | lld:lifeskim |
pubmed-article:6487893 | lifeskim:mentions | umls-concept:C0036751 | lld:lifeskim |
pubmed-article:6487893 | lifeskim:mentions | umls-concept:C0022616 | lld:lifeskim |
pubmed-article:6487893 | lifeskim:mentions | umls-concept:C1704632 | lld:lifeskim |
pubmed-article:6487893 | lifeskim:mentions | umls-concept:C1280500 | lld:lifeskim |
pubmed-article:6487893 | lifeskim:mentions | umls-concept:C0871261 | lld:lifeskim |
pubmed-article:6487893 | lifeskim:mentions | umls-concept:C2911692 | lld:lifeskim |
pubmed-article:6487893 | lifeskim:mentions | umls-concept:C1706817 | lld:lifeskim |
pubmed-article:6487893 | lifeskim:mentions | umls-concept:C0243076 | lld:lifeskim |
pubmed-article:6487893 | lifeskim:mentions | umls-concept:C0065809 | lld:lifeskim |
pubmed-article:6487893 | pubmed:issue | 1 | lld:pubmed |
pubmed-article:6487893 | pubmed:dateCreated | 1984-11-28 | lld:pubmed |
pubmed-article:6487893 | pubmed:abstractText | The effects of intracarotid (i.c.) injections of 5-hydroxytryptamine (5-HT; 1-50 micrograms) on carotid chemoreceptor activity recorded from the carotid sinus nerve have been studied in anaesthetized cats. Three separate components in the complex response of the chemoreceptors to injected 5-HT were identified. Firstly, a transient burst of activity was obtained during the injection period in 56% of the recordings. Secondly, in all the recordings a period of chemodepression commenced a few seconds after completing the injection and was usually dose-related. Thirdly, a delayed longer-lasting chemoexcitation occurred in many experiments, concomitant with a fall in systemic blood pressure. The neuronal 5-HT receptor antagonist MDL 72222 (10-100 micrograms kg-1, i.c.) virtually abolished the transient chemoexcitation evoked during 5-HT injections and also significantly increased the mean ID50 for 5-HT-induced chemodepression; in 37% of recordings 5-HT caused a dose-related chemoexcitation after the high dose of MDL 72222. Neither the delayed chemoexcitation nor the hypotension caused by 5-HT were much affected by the antagonist. MDL 72222 itself had a biphasic effect on chemosensory discharge, causing depression followed by a delayed excitation. The 5-HT2-receptor antagonist ketanserin (100 micrograms kg-1, i.c.) had no appreciable effect on the transient chemoexcitation evoked during 5-HT injections and caused a slight but significant increase in the mean ID50 for 5-HT-induced chemodepression. The delayed chemoexcitation and accompanying hypotension associated with 5-HT were both substantially reduced or abolished by the antagonist. Ketanserin itself caused a short-lasting period of chemoexcitation. All the effects of injected 5-HT on chemosensory discharge could be abolished by the combination of MDL 72222 and ketanserin (100 micrograms kg-1, i.c.). Neither MDL 72222 nor ketanserin had any significant effect upon the response of the carotid chemoreceptors to hypoxia. The rate at which discharge increased, and also the steady-state discharge before and during hypoxia, were unaffected by the antagonists, alone or in combination. At least two types of 5-HT receptor appeared to be involved in the response of carotid body chemoreceptors to 5-HT. Transient excitation and chemodepression were mediated via MDL 72222-sensitive (peripheral neuronal) receptors whereas the delayed chemoexcitation and associated hypotension involved a ketanserin-sensitive, presumably 5-HT2-, receptor. It appears unlikely that 5-HT plays a crucial role in chemoreception. | lld:pubmed |
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pubmed-article:6487893 | pubmed:language | eng | lld:pubmed |
pubmed-article:6487893 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:6487893 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:6487893 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:6487893 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:6487893 | pubmed:month | Sep | lld:pubmed |
pubmed-article:6487893 | pubmed:issn | 0007-1188 | lld:pubmed |
pubmed-article:6487893 | pubmed:author | pubmed-author:KirbyG CGC | lld:pubmed |
pubmed-article:6487893 | pubmed:author | pubmed-author:McQueenD SDS | lld:pubmed |
pubmed-article:6487893 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:6487893 | pubmed:volume | 83 | lld:pubmed |
pubmed-article:6487893 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:6487893 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:6487893 | pubmed:pagination | 259-69 | lld:pubmed |
pubmed-article:6487893 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:6487893 | pubmed:year | 1984 | lld:pubmed |
pubmed-article:6487893 | pubmed:articleTitle | Effects of the antagonists MDL 72222 and ketanserin on responses of cat carotid body chemoreceptors to 5-hydroxytryptamine. | lld:pubmed |
pubmed-article:6487893 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:6487893 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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