TY - JOUR
T1 - Excitatory conditioning to the interoceptive nicotine stimulus blocks subsequent conditioning to an exteroceptive light stimulus
AU - Murray, Jennifer E.
AU - Bevins, Rick A.
N1 - Funding Information:
We thank Nicole R. Wells for her assistance. The research was supported by NIH grant DA018114 awarded to RAB and an American Psychological Association Dissertation Research Award awarded to JEM. JEM was supported by NIH F31-DA025399 and MRC 9536855 (the latter awarded to B.J. Everitt) while conducting the experiments and preparing the manuscript for submission, respectively. None of these sources had a role in the study design; the collection, analysis and interpretation of data; in writing the paper; or the decision to submit the paper for publication. MED-PC (for Windows, version IV) programs used in the present article are available in a slightly modified version upon request to Rick A. Bevins, Department of Psychology, University of Nebraska-Lincoln, Lincoln NE USA 68588-0308, or e-mail rbevins1@unl.edu . Correspondence related to this article should be addressed to Jennifer E. Murray, Department of Experimental Psychology, University of Cambridge, Cambridge UK, CB2 3EB, or e-mail jem98@cam.ac.uk .
PY - 2011/8/1
Y1 - 2011/8/1
N2 - Previous research has shown that a nicotine conditional stimulus (CS) can compete with (i.e., overshadow) a brief light CS. Another form of competition, blocking, has not yet been examined with the nicotine CS. Groups of rats were assigned to an element training condition. For the N+ group, during each daily 2. h element training session, there were ten intravenous nicotine infusions (0.03. mg/kg) followed 30. s later with 4. s access to sucrose. In the N- group, nicotine and sucrose presentations were explicitly unpaired. The chamber alone group (C alone) had no stimulus presentations. Element training was followed by compound training in all groups. A 30-s houselight was included during the time between the nicotine infusion and paired sucrose delivery. Non-reinforced element presentations assessed relative control of the goal tracking conditioned response (CR). The N+ group showed a higher proportion of CR control by the nicotine than the light. The opposite pattern was found in the N- and C alone groups indicating that nicotine CS controlled less of the CR than the light. Thus, excitatory conditioning with the nicotine CS blocked later conditioning to the light. This finding adds to literature examining the interaction between interoceptive drug CSs and other environmental stimuli.
AB - Previous research has shown that a nicotine conditional stimulus (CS) can compete with (i.e., overshadow) a brief light CS. Another form of competition, blocking, has not yet been examined with the nicotine CS. Groups of rats were assigned to an element training condition. For the N+ group, during each daily 2. h element training session, there were ten intravenous nicotine infusions (0.03. mg/kg) followed 30. s later with 4. s access to sucrose. In the N- group, nicotine and sucrose presentations were explicitly unpaired. The chamber alone group (C alone) had no stimulus presentations. Element training was followed by compound training in all groups. A 30-s houselight was included during the time between the nicotine infusion and paired sucrose delivery. Non-reinforced element presentations assessed relative control of the goal tracking conditioned response (CR). The N+ group showed a higher proportion of CR control by the nicotine than the light. The opposite pattern was found in the N- and C alone groups indicating that nicotine CS controlled less of the CR than the light. Thus, excitatory conditioning with the nicotine CS blocked later conditioning to the light. This finding adds to literature examining the interaction between interoceptive drug CSs and other environmental stimuli.
KW - Appetitive conditioning
KW - Blocking
KW - Drug discrimination
KW - Interoceptive cue competition
KW - Nicotine
KW - Overshadowing
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U2 - 10.1016/j.bbr.2011.03.020
DO - 10.1016/j.bbr.2011.03.020
M3 - Article
C2 - 21419807
AN - SCOPUS:79954632256
SN - 0166-4328
VL - 221
SP - 314
EP - 319
JO - Behavioural Brain Research
JF - Behavioural Brain Research
IS - 1
ER -