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              <text>&lt;a href="http://doi.org/10.1016/0031-9384(95)02119-1" target="_blank" rel="noreferrer noopener"&gt;http://doi.org/10.1016/0031-9384(95)02119-1&lt;/a&gt;</text>
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              <text>597–604</text>
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              <text>4</text>
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          <name>Volume</name>
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            <elementText elementTextId="41022">
              <text>59</text>
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            <name>Title</name>
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                <text>Olfactory bulbectomy disrupts the expression of cocaine-induced conditioned place preference.</text>
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            <name>Publisher</name>
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              <elementText elementTextId="41011">
                <text>Physiology &amp; behavior</text>
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            <name>Date</name>
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                <text>1996</text>
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                <text>1996-05</text>
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          <element elementId="49">
            <name>Subject</name>
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                <text>Animals; Body Weight/drug effects/physiology; Cocaine/*pharmacology; Conditioning; Male; Narcotics/*pharmacology; Olfaction Disorders/psychology; Olfactory Bulb/anatomy &amp; histology/*physiology; Operant/*drug effects; Rats; Reward; Smell/drug effects/*physiology; Sulfates/pharmacology; Zinc Compounds/pharmacology; Zinc Sulfate</text>
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            <elementTextContainer>
              <elementText elementTextId="41015">
                <text>Calcagnetti D J; Quatrella L A; Schechter M D</text>
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                <text>The role of the olfactory sense in the expression of cocaine-induced conditioned place preference (CPP) was examined in adult male rats (n = 35) of the N/Nih strain. Consistent with the scientific literature, rats were observed to significantly (p \textless 0.05) increase (double) the seconds spent in their least-preferred chamber following cocaine-chamber pairings. Subsequently, groups of rats underwent one of three treatments: 1) olfactory bulbectomy (BULBX), 2) sham surgery (SHAM), or 3) sham surgery plus intranasal zinc sulfate perfusion (ZnSO4). Zinc sulfate was used to produce a temporary loss of olfaction. In a separate behavioral measure of olfactory acuity, both BULBX and ZnSO4-treated rats performed at an equally deficient level, in contrast to SHAM-treated rats that were not rendered anosmic. A second conditioned place preference test revealed that the ZnSO4-perfused and SHAM groups did not differ from their original postcocaine preference measurements. In contrast, the BULBX group spent significantly fewer seconds in the cocaine-paired chamber. After a 14-day interval, a third preference test revealed that SHAM and ZnSO4-treated rats displayed an equivalent preference for the cocaine-paired chamber (at 2.7 times above baseline). Interestingly, the seconds spent in the cocaine-paired chamber by BULBX rats did not differ from their baseline (e.g., precocaine exposure). These results suggest that bulbectomy disrupts the expression of cocaine-induced place preference. Interpretations of data from BULBX rats involving the production of an anhedonic condition and the relevance of olfactory bulbectomy as an animal model of anhedonic depression are discussed.</text>
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                <text>&lt;a href="http://doi.org/10.1016/0031-9384(95)02119-1" target="_blank" rel="noreferrer noopener"&gt;10.1016/0031-9384(95)02119-1&lt;/a&gt;</text>
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            <description>Information about rights held in and over the resource</description>
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                <text>Article information provided for research and reference use only. All rights are retained by the journal listed under publisher and/or the creator(s).</text>
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        <name>Body Weight/drug effects/physiology</name>
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      <tag tagId="4226">
        <name>Calcagnetti D J</name>
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      <tag tagId="22772">
        <name>Cocaine/*pharmacology</name>
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        <name>Conditioning</name>
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        <name>Male</name>
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        <name>Narcotics/*pharmacology</name>
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        <name>Olfaction Disorders/psychology</name>
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        <name>Olfactory Bulb/anatomy &amp; histology/*physiology</name>
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        <name>Physiology &amp; behavior</name>
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        <name>Quatrella L A</name>
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        <name>Rats</name>
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        <name>Reward</name>
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        <name>Schechter M D</name>
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        <name>Smell/drug effects/*physiology</name>
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        <name>Sulfates/pharmacology</name>
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        <name>Zinc Compounds/pharmacology</name>
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        <name>Zinc Sulfate</name>
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              <text>&lt;a href="http://doi.org/10.1016/0024-3205(94)00414-n" target="_blank" rel="noreferrer noopener"&gt;http://doi.org/10.1016/0024-3205(94)00414-n&lt;/a&gt;</text>
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              <text>475–483</text>
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              <text>7</text>
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              <text>56</text>
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          <element elementId="50">
            <name>Title</name>
            <description>A name given to the resource</description>
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              <elementText elementTextId="40906">
                <text>Blockade of cocaine-induced conditioned place preference: relevance to cocaine abuse therapeutics.</text>
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            <name>Date</name>
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                <text>1995</text>
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                <text>1905-06</text>
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            <description>The topic of the resource</description>
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              <elementText elementTextId="40910">
                <text>Animals; Calcium Channel Blockers/pharmacology/therapeutic use; Cocaine/*antagonists &amp; inhibitors; Conditioning (Psychology)/*drug effects; Humans; Narcotic Antagonists/pharmacology; Serotonin Antagonists/pharmacology; Substance-Related Disorders/*drug therapy</text>
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                <text>Calcagnetti D J; Keck B J; Quatrella L A; Schechter M D</text>
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            <description>An account of the resource</description>
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                <text>Conditioned place preference/aversion testing is a behavioral method believed capable of measuring the affective (positive, neutral or negative) properties of psychoactive drugs. Cocaine injections in rats reliably produces a positive place preference. Drugs that attenuate or block this effect of cocaine have obvious potential for developing treatments to address cocaine addiction as well as to add to the scientific understanding of the mechanism of cocaine's action at the cellular level. To date, six drugs have been reported to block the expression of a cocaine-induced conditioned place preference (CPP) and this review evidences the cocaine-induced CPP blockage by the two potent L-type calcium channel blockers, isradipine and nifedipine, the two serotonin-3 receptor antagonists, MDL72222 and ICS205-930, the delta opioid receptor selective antagonist naltrindole, and lastly, a mixed opioid agonist-antagonist buprenorphine. Additional evidence relating to the blockade of other cocaine behavioral effects by these putative blockers is addressed, where appropriate, from studies employing other procedures such as drug stimulus discrimination, self-administration, electrical brain stimulation and increases in locomotor activity. The significance of these findings is discussed in the context of their relevance to the development of treatment regimens to allow for cessation of cocaine abuse.</text>
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                <text>&lt;a href="http://doi.org/10.1016/0024-3205(94)00414-n" target="_blank" rel="noreferrer noopener"&gt;10.1016/0024-3205(94)00414-n&lt;/a&gt;</text>
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            <name>Rights</name>
            <description>Information about rights held in and over the resource</description>
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              <elementText elementTextId="40915">
                <text>Article information provided for research and reference use only. All rights are retained by the journal listed under publisher and/or the creator(s).</text>
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