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Journal ArticleDOI

Differential effects of the novel kappa opioid receptor antagonist, JDTic, on reinstatement of cocaine-seeking induced by footshock stressors vs cocaine primes and its antidepressant-like effects in rats

TLDR
Depression and stress are two states during cocaine abstinence which users identify as precipitating relapse, and JDTic may have properties which attenuate both.
Abstract
Stress and depression have been linked to relapse of cocaine abuse Antagonism of the kappa opioid receptor (KOR) has been reported to attenuate some effects of stressors, and antagonism of the KOR has been reported to have antidepressant-like properties Our objective was to determine whether the potent and selective KOR antagonist, (3R)-7-hydroxy-N-{(1S)-1-{[(3R,4R)-4-(3-hydroxyphenyl)-3,4-dimethyl-1-piperidinyl]methyl}-2-methylpropyl}-1,2,3,4-tetrahydro-3-isoquinoline-carboxamide (JDTic), can reduce the ability of a stressor (intermittent footshock) to reinstate cocaine-seeking behavior and to have antidepressant-like effects in the forced swim test (FST) Male Long–Evans hooded rats were trained to lever-press, reinforced with 05 mg/kg iv infusion of cocaine, according to fixed ratio 1 reinforcement schedules during daily 2-h experimental sessions After performance had stabilized, lever pressing was extinguished for 12 consecutive sessions, and doses of 0 (vehicle), 3, 10, and 30 mg/kg JDTic were then administered ig to separate groups of 12 rats Twenty four hours later, the rats were given 15 min of intermittent footshock (087 mA, 05 s activation time, average interactivation interval of 40 s) or a 17-mg/kg ip administration of cocaine prime followed by a 2-h reinstatement test session JDTic was also evaluated for its ability to block diuresis induced by the KOR agonist, U50,488H (10 mg/kg, sc), during 5-h test sessions beginning 1 h after footshock reinstatement tests to verify its KOR antagonist activity In the FST, male Sprague–Dawley rats were treated with either nor-binaltorphimine (nor-BNI) or JDTic (both at 03, 1, 3, or 10 mg/kg, injected sc 23 h before), or desipramine (56, 10, or 17 mg/kg, injected ip 23, 5, and 1 h before) and placed in a cylinder of water, during which the predominance of immobility, swimming, and climbing were scored during 5-s intervals for 5 min The 10- and 30-mg/kg doses of JDTic significantly reduced footshock-induced reinstatement of responding previously reinforced by cocaine and significantly attenuated U50,488H-induced diuresis In contrast, JDTic did not affect cocaine-prime-induced reinstatement Both nor-BNI and JDTic decreased immobility and increased swimming time in the FST, similar to the antidepressant desipramine Depression and stress are two states during cocaine abstinence which users identify as precipitating relapse, and JDTic may have properties which attenuate both

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Journal ArticleDOI

A Role for Brain Stress Systems in Addiction

TL;DR: The role of brain stress systems and brain antistress systems in addiction provides novel targets for treatment and prevention of addiction and insights into the organization and function of basic brain emotional circuitry.
Journal ArticleDOI

The Dysphoric Component of Stress Is Encoded by Activation of the Dynorphin κ-Opioid System

TL;DR: The convergence of stress-induced aversive inputs on the Dynorphin system was unexpected, implicates dynorphin as a key mediator of dysphoria, and emphasizes κ-receptor antagonists as promising therapeutics.
Journal ArticleDOI

The dynorphin/kappa opioid system as a modulator of stress-induced and pro-addictive behaviors

TL;DR: Results suggest that activation of the dynorphin/kappa opioid receptor (KOR) system is likely to play a major role in the pro-addictive effects of stress and novel insight to neuropeptide systems that regulate affective state is provided.
Journal ArticleDOI

Opioid receptors: distinct roles in mood disorders

TL;DR: To date, both human and animal studies have mainly examined MORs in the etiology of depressive disorders, and future studies will address DOR and KOR function in established and emerging neurobiological aspects of depression, including neurogenesis, neurodevelopment, and social behaviors.
Journal ArticleDOI

Dynorphin, stress, and depression

TL;DR: This review summarizes current data on how KOR systems contribute to the acute, delayed, and cumulative molecular and behavioral effects of stress and focuses on behavioral paradigms that provide insight on interactions between stress and KOR function within each of these temporal categories.
References
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Journal ArticleDOI

Depression: a new animal model sensitive to antidepressant treatments

R D Porsolt, +2 more
- 21 Apr 1977 - 
TL;DR: Results presented below indicate that immobility is reduced by different treatments known to be therapeutic in depression including three drugs, iprindole, mianserin and viloxazine which although clinically active show little or no ‘antidepressant’ activity in the usual animal tests.
Journal ArticleDOI

A psychomotor stimulant theory of addiction

TL;DR: A new attempt at a general theory of addiction is offered, based on the common denominator of the psychomotor stimulants---amphetamine, cocaine, and related drugs---rather than on thecommon denominators of the socalled depressant drugs~opiates, barbiturates, alcohol, and others.
Journal ArticleDOI

Active behaviors in the rat forced swimming test differentially produced by serotonergic and noradrenergic antidepressants.

TL;DR: This study demonstrated that distinct patterns of active behaviors are produced by antidepressants that selectively inhibit norepinephrine (NE) or serotonin (5-HT) uptake in the rat forced swimming test (FST), and showed that SSRIs are not false negatives in the FST.
Journal ArticleDOI

Abstinence Symptomatology and Psychiatric Diagnosis in Cocaine Abusers: Clinical Observations

TL;DR: Longitudinal evaluations showed a three-phase sequence of post-cocaine abuse abstinence symptoms, and over half the sample also met criteria for ed 3 DSM-III, axis I psychiatric disorders.
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