Feeding and drinking interactions after acute butyrophenone administration
The effects on feeding and drinking of various doses of droperidol, haloperidol and spiroperidol were studied in a number of paradigms. All three butyrophenones produced generally similar effects. After food deprivation, feeding was slightly increased at low doses but was decreased at the higher dos...
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Veröffentlicht in: | Pharmacology, biochemistry and behavior biochemistry and behavior, 1977-10, Vol.7 (4), p.295-301 |
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description | The effects on feeding and drinking of various doses of droperidol, haloperidol and spiroperidol were studied in a number of paradigms. All three butyrophenones produced generally similar effects. After food deprivation, feeding was slightly increased at low doses but was decreased at the higher doses; the concomitant postprandial drinking was attenuated at all doses. Desalivate rats showed a marked attenuation of feeding (and prandial drinking) at low doses, but when wet mash was given instead of pellets and water a normal dose-response relationship was obtained. After water deprivation drinking was attenuated at all doses, and when food was also available during the drinking test the food intake was decreased in proportion to the drinking. Drinking was blocked more when food was present than in its absence. Insulin and 2-deoxyglucose induced feeding in sated rats was attenuated but not abolished by haloperidol. The findings are discussed relative to the role of activation and brain catecholamines in feeding and drinking. |
doi_str_mv | 10.1016/0091-3057(77)90223-4 |
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All three butyrophenones produced generally similar effects. After food deprivation, feeding was slightly increased at low doses but was decreased at the higher doses; the concomitant postprandial drinking was attenuated at all doses. Desalivate rats showed a marked attenuation of feeding (and prandial drinking) at low doses, but when wet mash was given instead of pellets and water a normal dose-response relationship was obtained. After water deprivation drinking was attenuated at all doses, and when food was also available during the drinking test the food intake was decreased in proportion to the drinking. Drinking was blocked more when food was present than in its absence. Insulin and 2-deoxyglucose induced feeding in sated rats was attenuated but not abolished by haloperidol. The findings are discussed relative to the role of activation and brain catecholamines in feeding and drinking.</description><identifier>ISSN: 0091-3057</identifier><identifier>EISSN: 1873-5177</identifier><identifier>DOI: 10.1016/0091-3057(77)90223-4</identifier><identifier>PMID: 928487</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>2-Deoxyglucose ; Animals ; Brain catecholamines ; Butyrophenones ; Butyrophenones - pharmacology ; Deoxyglucose - pharmacology ; Deprivation ; Drinking ; Drinking Behavior - drug effects ; Droperidol - pharmacology ; Feeding ; Feeding Behavior - drug effects ; Food Deprivation ; Haloperidol - pharmacology ; Hunger - drug effects ; Insulin ; Insulin - pharmacology ; Male ; Rats ; Salivarectomy ; Salivary Glands - physiology ; Spiperone - pharmacology ; Thirst - drug effects ; Water Deprivation</subject><ispartof>Pharmacology, biochemistry and behavior, 1977-10, Vol.7 (4), p.295-301</ispartof><rights>1977</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-979271475abec27386c8058df9bc8b7c9751c7e81eadfa18947de532232808f73</citedby><cites>FETCH-LOGICAL-c356t-979271475abec27386c8058df9bc8b7c9751c7e81eadfa18947de532232808f73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0091-3057(77)90223-4$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/928487$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rowland, Neil</creatorcontrib><creatorcontrib>Engle, David J.</creatorcontrib><title>Feeding and drinking interactions after acute butyrophenone administration</title><title>Pharmacology, biochemistry and behavior</title><addtitle>Pharmacol Biochem Behav</addtitle><description>The effects on feeding and drinking of various doses of droperidol, haloperidol and spiroperidol were studied in a number of paradigms. All three butyrophenones produced generally similar effects. After food deprivation, feeding was slightly increased at low doses but was decreased at the higher doses; the concomitant postprandial drinking was attenuated at all doses. Desalivate rats showed a marked attenuation of feeding (and prandial drinking) at low doses, but when wet mash was given instead of pellets and water a normal dose-response relationship was obtained. After water deprivation drinking was attenuated at all doses, and when food was also available during the drinking test the food intake was decreased in proportion to the drinking. Drinking was blocked more when food was present than in its absence. Insulin and 2-deoxyglucose induced feeding in sated rats was attenuated but not abolished by haloperidol. The findings are discussed relative to the role of activation and brain catecholamines in feeding and drinking.</description><subject>2-Deoxyglucose</subject><subject>Animals</subject><subject>Brain catecholamines</subject><subject>Butyrophenones</subject><subject>Butyrophenones - pharmacology</subject><subject>Deoxyglucose - pharmacology</subject><subject>Deprivation</subject><subject>Drinking</subject><subject>Drinking Behavior - drug effects</subject><subject>Droperidol - pharmacology</subject><subject>Feeding</subject><subject>Feeding Behavior - drug effects</subject><subject>Food Deprivation</subject><subject>Haloperidol - pharmacology</subject><subject>Hunger - drug effects</subject><subject>Insulin</subject><subject>Insulin - pharmacology</subject><subject>Male</subject><subject>Rats</subject><subject>Salivarectomy</subject><subject>Salivary Glands - physiology</subject><subject>Spiperone - pharmacology</subject><subject>Thirst - drug effects</subject><subject>Water Deprivation</subject><issn>0091-3057</issn><issn>1873-5177</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1977</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtPwzAQhC3EqxT-QQ85ITgE_Ei6zgUJVZSHKnGBs-XYGzA0TrETpP57ElJx5LQa7cxI8xEyY_SKUTa_prRgqaA5XABcFpRzkWZ7ZMIkiDRnAPtk8mc5JicxflBKMz6HI3JYcJlJmJCnJaJ1_i3R3iY2OP85COdbDNq0rvEx0VUvEm26FpOya7eh2byjbzwm2tbOu9gGPThPyUGl1xHPdndKXpd3L4uHdPV8_7i4XaVG5PM2LaDgwDLIdYmGg5BzI2kubVWURpZgCsiZAZQMta00k0UGFnPRr-OSygrElJyPvZvQfHUYW1W7aHC91h6bLioQABQo743ZaDShiTFgpTbB1TpsFaNqIKgGPGrAowDUL0GV9bHZrr8ra7R_oRFZ_74Z39hv_HYYVDQOvekxBjStso37v_8HpQGAEQ</recordid><startdate>197710</startdate><enddate>197710</enddate><creator>Rowland, Neil</creator><creator>Engle, David J.</creator><general>Elsevier Inc</general><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>7X8</scope></search><sort><creationdate>197710</creationdate><title>Feeding and drinking interactions after acute butyrophenone administration</title><author>Rowland, Neil ; Engle, David J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-979271475abec27386c8058df9bc8b7c9751c7e81eadfa18947de532232808f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1977</creationdate><topic>2-Deoxyglucose</topic><topic>Animals</topic><topic>Brain catecholamines</topic><topic>Butyrophenones</topic><topic>Butyrophenones - pharmacology</topic><topic>Deoxyglucose - pharmacology</topic><topic>Deprivation</topic><topic>Drinking</topic><topic>Drinking Behavior - drug effects</topic><topic>Droperidol - pharmacology</topic><topic>Feeding</topic><topic>Feeding Behavior - drug effects</topic><topic>Food Deprivation</topic><topic>Haloperidol - pharmacology</topic><topic>Hunger - drug effects</topic><topic>Insulin</topic><topic>Insulin - pharmacology</topic><topic>Male</topic><topic>Rats</topic><topic>Salivarectomy</topic><topic>Salivary Glands - physiology</topic><topic>Spiperone - pharmacology</topic><topic>Thirst - drug effects</topic><topic>Water Deprivation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rowland, Neil</creatorcontrib><creatorcontrib>Engle, David J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Pharmacology, biochemistry and behavior</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rowland, Neil</au><au>Engle, David J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Feeding and drinking interactions after acute butyrophenone administration</atitle><jtitle>Pharmacology, biochemistry and behavior</jtitle><addtitle>Pharmacol Biochem Behav</addtitle><date>1977-10</date><risdate>1977</risdate><volume>7</volume><issue>4</issue><spage>295</spage><epage>301</epage><pages>295-301</pages><issn>0091-3057</issn><eissn>1873-5177</eissn><abstract>The effects on feeding and drinking of various doses of droperidol, haloperidol and spiroperidol were studied in a number of paradigms. All three butyrophenones produced generally similar effects. After food deprivation, feeding was slightly increased at low doses but was decreased at the higher doses; the concomitant postprandial drinking was attenuated at all doses. Desalivate rats showed a marked attenuation of feeding (and prandial drinking) at low doses, but when wet mash was given instead of pellets and water a normal dose-response relationship was obtained. After water deprivation drinking was attenuated at all doses, and when food was also available during the drinking test the food intake was decreased in proportion to the drinking. Drinking was blocked more when food was present than in its absence. Insulin and 2-deoxyglucose induced feeding in sated rats was attenuated but not abolished by haloperidol. The findings are discussed relative to the role of activation and brain catecholamines in feeding and drinking.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>928487</pmid><doi>10.1016/0091-3057(77)90223-4</doi><tpages>7</tpages></addata></record> |
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subjects | 2-Deoxyglucose Animals Brain catecholamines Butyrophenones Butyrophenones - pharmacology Deoxyglucose - pharmacology Deprivation Drinking Drinking Behavior - drug effects Droperidol - pharmacology Feeding Feeding Behavior - drug effects Food Deprivation Haloperidol - pharmacology Hunger - drug effects Insulin Insulin - pharmacology Male Rats Salivarectomy Salivary Glands - physiology Spiperone - pharmacology Thirst - drug effects Water Deprivation |
title | Feeding and drinking interactions after acute butyrophenone administration |
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