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Title: New developments in the assessment of weight-related experiential avoidance (AAQW-Revised)

Authors:
; ; ; ;
Publication Date:
Sponsoring Org.:
USDOE Office of Nuclear Energy (NE), Fuel Cycle Technologies (NE-5)
OSTI Identifier:
1359265
Grant/Contract Number:
SFRH/BD/84452/2012
Resource Type:
Journal Article: Publisher's Accepted Manuscript
Journal Name:
Journal of Contextual Behavioral Science
Additional Journal Information:
Journal Volume: 5; Journal Issue: 3; Related Information: CHORUS Timestamp: 2017-05-28 10:01:44; Journal ID: ISSN 2212-1447
Publisher:
Elsevier
Country of Publication:
Country unknown/Code not available
Language:
English

Citation Formats

Palmeira, Lara, Cunha, Marina, Pinto-Gouveia, José, Carvalho, Sérgio, and Lillis, Jason. New developments in the assessment of weight-related experiential avoidance (AAQW-Revised). Country unknown/Code not available: N. p., 2016. Web. doi:10.1016/j.jcbs.2016.06.001.
Palmeira, Lara, Cunha, Marina, Pinto-Gouveia, José, Carvalho, Sérgio, & Lillis, Jason. New developments in the assessment of weight-related experiential avoidance (AAQW-Revised). Country unknown/Code not available. doi:10.1016/j.jcbs.2016.06.001.
Palmeira, Lara, Cunha, Marina, Pinto-Gouveia, José, Carvalho, Sérgio, and Lillis, Jason. Fri . "New developments in the assessment of weight-related experiential avoidance (AAQW-Revised)". Country unknown/Code not available. doi:10.1016/j.jcbs.2016.06.001.
@article{osti_1359265,
title = {New developments in the assessment of weight-related experiential avoidance (AAQW-Revised)},
author = {Palmeira, Lara and Cunha, Marina and Pinto-Gouveia, José and Carvalho, Sérgio and Lillis, Jason},
abstractNote = {},
doi = {10.1016/j.jcbs.2016.06.001},
journal = {Journal of Contextual Behavioral Science},
number = 3,
volume = 5,
place = {Country unknown/Code not available},
year = {Fri Jul 01 00:00:00 EDT 2016},
month = {Fri Jul 01 00:00:00 EDT 2016}
}

Journal Article:
Free Publicly Available Full Text
Publisher's Version of Record at 10.1016/j.jcbs.2016.06.001

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  • When histamine (Hi) and other agonists were applied intraventricularly, Hi caused a dose-dependent inhibition of the avoidance response in rats; its ED50 was 3.60 ..mu..g. l-methylHi, l-methylimidazole acetic acid and imidazole acetic acid which are major metabolites of Hi produced no inhibitory effect even at 50 ..mu..g. H/sub 1/-agonists (2-methylHi and 2-thiazolylethylamine) also depressed the avoidance response; their dose-response lines run parallel to that of Hi. The depressant effects of H/sub 2/-agonists (4-methylHi and dimaprit) were relatively weak; their dose-response lines were not parallel to that of Hi. When antagonists were pretreated intravenously, Hi action was clearly antagonized by diphehydraminemore » and pyrilamine, but not by cimetidine or ranitidine. Intraventricular injection of Hi mixed with cimetidine or ranitidine did not change the effect induced by Hi alone. The avoidance response was not affected by noradrenaline, dopamine or 5-hydroxytryptamine. Although acetylcholine (ACh) suppressed the avoidance response dose-dependently, its effect was much weaker than that of Hi. Pretreatment with cholinergic blocking drugs (atropine and scopolamine) antagonized ACh action but not Hi action. From these results, it is assumed that the inhibitory effect of Hi on the avoidance response is preferentially linked to the H/sub 1/-receptor. After intraventricular application of /sup 3/H-Hi, the highest radioactivity was determined in the hypothalamus. 21 references, 4 figures, 4 tables.« less
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