Visceral cortex lesions block conditioned taste aversions induced by morphine
References (54)
- et al.
Efferent connections of the substantia nigra and ventral tegmental area in the rat
Brain Res
(1979) - et al.
Conditioned aversion by psychoactive drugs: Does it have significance for an understanding of drug dependence?
Addict Behav
(1975) - et al.
Conditioned taste aversions: Vagal and circulatory mediation of the toxic unconditioned stimulus
Behav Biol
(1978) - et al.
Cocaine-induced taste aversion in rats
Pharmacol Biochem Behav
(1978) - et al.
Cortical lesions: Flavour-illness and noise-shock conditioning
Behav Biol
(1974) - et al.
Direct connectivity between pontine taste areas and gustatory neocortex in rat
Brain Res
(1982) - et al.
Organization of catecholamine neurons projecting to the frontal cortex in rat
Brain Res
(1978) - et al.
Neuroleptics block the positive reinforcing effects of amphetamine but not of morphine as measured by place conditioning
Pharmacol Biochem Behav
(1985) - et al.
Noradrenergic innervation patterns in three regions of medial cortex: An immunofluorescence characterization
Brain Res Bull
(1979) - et al.
Drug reinforcement studied by the use of place conditioning in rat
Brain Res
(1982)
Projections from the nucleus of the solitary tract in the rat
Neuroscience
Projections of thalamic gustatory and lingual areas in the rat
Brain Res
Flavour aversions produced by contingent drug injection: Relative effectiveness of apomorphine, emetine, and lithium
Behav Res Ther
Absence of lithium-induced taste aversion after area postrema lesion
Brain Res
Attenuation of amphetamine-induced conditioned taste aversion following intraventricular 6-hydroxydopamine
Neurosci Lett
Reciprocal parabrachial-cortical connections in the rat
Brain Res
Efferent connections of the parabrachial nucleus in the rat
Brain Res
The organization of noradrenergic pathways from the brainstem to the paraventricular and the supraoptic nuclei in the rat
Brain Res Rev
Efferents and afferents of the ventral tegmental-A10 region studied after local injection of (3-H) leucine and horseradish peroxidase
Brain Res
Reinforcing effects of brain microinjections of morphine revealed by conditioned place preference
Brain Res
Temporal analysis of naloxone attenuation of morphine-induced taste aversion
Pharmacol Biochem Behav
The organization of the efferent projections of the parabrachial nucleus to the forebrain in the rat: A retrograde fluorescent double-labeling study
Brain Res
Action of drugs of abuse on brain reward systems
Pharmacol Biochem Behav
Catecholamine theories of reward: A critical review
Brain Res
Cortical neurons responding to tactile, thermal and taste stimulations of the rats tongue
Brain Res
On the central course of afferent fibers in the trigeminal, facial, glossopharyngeal, and vagal nerves and their nuclei in the mouse
Acta Physiol Scand (Suppl)
Endogenous opioids: Opposite motivational effects in brain and periphery
Nature
Cited by (60)
Insular Cortical circuits
2022, Neurocircuitry of AddictionPlace preferences induced by electrical stimulation of the external lateral parabrachial subnucleus in a sequential learning task: Place preferences induced by NLPBe stimulation
2020, Behavioural Brain ResearchCitation Excerpt :None of the animals received electrical stimulation during this phase. This procedure (phases 1, 2, and 3) is frequently used for place preference conditioning (sequential modality) in animal research on natural reinforcers [25,49–52] and drugs of abuse [31,33,35,36,38,39,41,43,44,53–56]. The sole objective of this second part was to classify the animals in groups according to the effect of stimulation, applying behavioral criteria widely used in previous studies [9–13,57–59].
Tolerance to rewarding brain electrical stimulation: Differential effects of contingent and non-contingent activation of parabrachial complex and lateral hypothalamus
2018, Behavioural Brain ResearchCitation Excerpt :However, this naloxone blockade is not observed when electrical stimulation is applied to the central nucleus of the amygdala [15] or lateral hypothalamus [13], indicating that the rewarding effects do not involve the opioid system in these cases [16]. Tolerance to rewarding stimulation was recently demonstrated; thus, animals subjected to daily activation sessions progressively reduced their stay in the stimulation-associated area after daily stimulation of the PB complex [9] or the related insular cortex (IC) [17], which is known to participate in various reward processes [18–22] and is compatible with reports on its involvement in processing drugs of abuse such as opiates [23,24] or stimulants [25–27]. The decay in rewarding effect found after daily electrical stimulation of the PB and insular cortex was not observed in animals receiving intermittent activation (day off/day on) [17,9].
Tolerance to repeated rewarding electrical stimulation of the insular cortex
2016, Brain ResearchMeasures of the aversive effects of drugs: A comparison of conditioned taste and place aversions
2015, Pharmacology Biochemistry and BehaviorCitation Excerpt :On PND 81 (the first day of conditioning), animals were again put in test bins and one of two novel tastes, i.e., unsweetened grape or cherry Kool-Aid (0.3% Kool-Aid solution) was presented instead of water. These two flavors have been shown to be discriminable and equally preferred by rats (see Mackey et al., 1986). Animals were immediately rank-ordered according to Kool-Aid consumption and assigned to one of five groups [0 (n = 8), 0.18 (n = 8), 0.32 (n = 8), 0.56 (n = 8) and 1.0 (n = 10) where group number indicates the dose of LiCl in mEq], such that mean consumption among groups was comparable.