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  • Digitale Medien  (7)
  • Place conditioning  (4)
  • Microelectrophoresis  (3)
Materialart
  • Digitale Medien  (7)
Erscheinungszeitraum
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Psychopharmacology 98 (1989), S. 203-206 
    ISSN: 1432-2072
    Schlagwort(e): Place conditioning ; Motivation ; Aversion ; Opioids, μ-, δ- and κ-receptors ; Rat
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract The role of central versus peripheral opioid receptors in mediating the aversive effects of opioids was examined by use of an unbiased place preference conditioning procedure in rats. The non-selective opioid antagonist naloxone (NLX) produced conditioned aversions for the drug-associated place after subcutaneous (SC) as well as intracerebroventricular (ICV) administration. Place aversions were also observed in response to the ICV administration of the selective μ-antagonist CTOP. In contrast, the selective δ-antagonist ICI 174,864 and the selective κ-antagonist norbinaltorphimine (nor-BNI) (ICV) were without effect. Place aversions were also produced by central applications of the selective κ-agonist U50,488H and the dynorphin derivative E-2078. For those opioid ligands tested, the doses required to produce place aversions were substantially lower following ICV as compared to SC administration. These data confirm that κ-agonists and opioid antagonists produce aversive states in the drug-naive animal and demonstrate that this effect is centrally mediated. Furthermore, the ability of NLX and CTOP, in contrast to both ICI 174,864 and nor-BNI, to produce place aversions suggests that the aversive effects of opioid antagonists result from the blockade of μ-receptors.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 338 (1988), S. 392-396 
    ISSN: 1432-1912
    Schlagwort(e): β-Endorphin-(1-27) ; Opioids ; Place conditioning ; β-Endorphin ; μ-, δ-, κ-, ε-Receptors ; Motivation
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary A place preference conditioning procedure was used to characterize the motivational effects of β-endorphin-(1-27), a naturally occurring fragment of β-endorphin (β-EP). The intracerebroventricular (ICV) administration of β-EP, selective μ-(DAGO) or δ-(DPDPE) opioid receptor agonists to rats produced marked preferences for the drug-associated place, whereas the selective κ-opioid receptor agonist, U-50488H produced conditioned aversions. ICV injections of the β-EP-(1-27) (5–20 μg), however, resulted in no preference for either the drug- or vehicle-associated place. Pretreatment with β-EP-(1-27) (10 μg) eliminated the place preference produced by β-EP. It abolished the place preferences induced by both DAGO and DPDPE but did not modify the effects of either U-50488H or the psychostimulant d-amphetamine. These data demonstrate that β-EP-(1-27) selectively antagonizes the motivational effects of μ- and β-opioid agonists and suggest that this fragment may function as an endogenous antagonist of the reinforcing effects of opioid agonists in vivo.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Experimental brain research 9 (1969), S. 221-235 
    ISSN: 1432-1106
    Schlagwort(e): Microelectrophoresis ; Glutamatic acid ; GABA ; Spread in brain tissue
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary The spread of microelectrophoretically applied substances was investigated in the cortex and in the caudate nucleus by means of double-multi-barrelled electrodes with tip separations varying from 12–300 μ. Spike activity induced in non-spontaneously firing neurones by application of glutamate and inhibition of spontaneously firing neurones by GABA were interpreted as an effect of the substances diffusing into the immediate neighbourhood of the neurone. This interpretation seems to be acceptable, since in only a small number of tests could an indication for trans-neuronally induced firing be found. The data obtained from dosage-response-curves, when adequately corrected, correspond to curves deduced from the diffusion equation for a diffusion coefficient of about 1.0×10−5 (cm2/sec). The mean threshold dosage for activation of spike activity by glutamate was found to be 0.25 mM. When glutamate was applied from the remote electrode the threshold concentration was achieved with comparatively lower dosages. This discrepancy is interpreted in terms of different areas of distribution. The mean distance between neurone and electrode was found to be about 20 μ when neurones with a satisfactory spike/noise ratio were recorded. This field was found to often be smaller than that occupied by the substances, even at low dosages.
    Materialart: Digitale Medien
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  • 4
    ISSN: 1432-1106
    Schlagwort(e): Cutaneous Receptive Fields ; Microelectrophoresis ; Amino Acids ; Inhibitory Interneurones
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary Extracellular recording of 320 neurones in the dorsal horn (L 7) were performed in cats by means of multibarrelled electrodes. Changes of cutaneous receptive field size and responsiveness to tactile stimulation induced by microelectrophoretic application of exciting (glutamic acid — GLA; homocysteic acid — HCA) and depressing (glycine — GY; and gamma-amino-butyric acid — GABA) amino acids were studied on cells giving origin to the spino-cervical tract (SCT) as well as on other unidentified dorsal horn cells (NON-SCT-neurones). Two types of SCT-neurones were distinguished. An unexpected finding was that in most type I SCT-neurones low doses of GLA induced increased excitability but higher doses of GLA could not induce a depolarization block and very often led to a decrease in cell excitability. Recordings obtained with double-multibarrelled electrodes are very suggestive that this biphasic effect of GLA is mediated via inhibitory interneurones induced by the spreading of GLA. In almost all type II SCT-neurones and NON-SCT-neurones GLA induced increase of excitability leading to a depolarization block at high doses. Such changes were accompanied by a considerable increase of receptive field size and responsiveness to mechanical stimulation. In all types of cells GY induced a shrinkage of the receptive field and also reduced sensitivity. In most dorsal horn cells encountered in this study cooling at thoracic level produced an increase in field size and sensitivity. GLA could induce a further increase when applied at the same time, however.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    Springer
    Psychopharmacology 103 (1991), S. 209-214 
    ISSN: 1432-2072
    Schlagwort(e): Place conditioning ; SCH-23390 ; A-69024 ; D-1 receptor ; N. accumbens ; Mesolimbic system ; Rat
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract An unbiased place preference conditioning procedure was used to examine the secondary reinforcing effects of selective D-1 dopamine (DA) receptor antagonists and the neuroanatomical substrates mediating these effects. Systemic administration of SCH-23390 or the non-benzazepine D-1 receptor antagonist A-69024 produced dose-related conditioned aversions for the drug-associated place. In contrast, the D-2 antagonists spiperone and (−)sulpiride were without effect. SCH-23390-induced place aversions were also observed after intracerebroventricular administration. The minimum dose producing this effect was significantly lower than that after systemic injection. Aversive effects were also observed after microinjection of SCH-23390 into the n. accumbens. In contrast, microinjections of this antagonist into the ventral tegmental area, caudate putamen or medial prefrontal cortex were without effect. These data confirm that the blockade of D-1 but not D-2 DA receptors induces aversive states. Furthermore, they suggest that D-1 receptors in the n. accumbens may play an important role in the regulation of non-drug induced affective states.
    Materialart: Digitale Medien
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  • 6
    ISSN: 1432-2013
    Schlagwort(e): Glutamic Acid ; GABA ; Microelectrophoresis ; Corpus striatum ; Neurone Discharges ; Glutaminsäure ; GABA ; Mikroelektrophorese ; Corpus striatum ; Neuronentladungen
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary The antagonistic effect of microelectrophoretically applied glutamic acid (Gl) and gamma-amino-butyric-acid (GABA) upon the synaptically induced discharge activity of neurones of the corpus striatum was investigated in unanesthetized rabbits. 1. In the caudate nucleus (NC) only a small number of neurones fired spontaneously, but following application of Gl, many neurones could be activated. In the putamen spontaneous discharge activity was much higher. Electrical stimulation of the thalamus evoked discharge activity in the NC only in some of the neurones. Additional application of Gl however, mostly induced a characteristic discharge pattern, consisting of primary activation (PA), followed by after-discharges after a discharge-free interval. 2. The latency of the PA was shortened from approximately 20 msec (maximum) to about 4–6 msec when increasing doses of Gl were applied. High anionic currents had a similar effect. This “net-latency” points to the activation of an oligosynaptic pathway. The discharge-free interval of about 160–300 msec was shortened to some extent by Gl, but only in some neurones large Gl doses abolished the discharge-free pause completely. It is concluded, that the discharge-free interval represents an inhibitory phase, basing on hyperpolarization. 3. The effects of GABA were antagonistic towards Gl. With submaximal doses of GABA the latency of the PA highly increased. Gl reversed the GABA-inhibition and normalized the latency of the PA. High cationic (hyperpolarizing) currents showed similar effects as GABA. It is concluded that in the Gl/GABA-antagonism depolarization and repolarization of the neuronal membrane is involved.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    Springer
    Psychopharmacology 96 (1988), S. 110-115 
    ISSN: 1432-2072
    Schlagwort(e): Tolerance ; Opioids ; Reinforcement ; Place conditioning ; Morphine ; U-69593 ; d-Amphetamine ; Rat
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract The issue of whether tolerance develops to the motivational effects of opioids was addressed by use of an unbiased place preference conditioning procedure. Administration of the μ-opioid agonists morphine or fentanyl produced dose-related preferences for the drug-associated place in control rats. In contrast, the κ-opioid agonist, U-69593 produced conditioned place aversions. Non-contingent administration of morphine (5.0 mg/kg/12 h) for 4 days prior to conditioning resulted in tolerance to its reinforcing effects, and cross-tolerance to the effects of fentanyl. No cross-tolerance to the motivational effects of the psychostimulantd-amphetamine or the κ-opioid agonist U-69593 was observed. Chronic administration of U-69593 prior to conditioning produced tolerance to its aversive effects. This treatment did not, however, modify the reinforcement produced by morphine. These data demonstrate that tolerance develops to both the reinforcing and aversive properties of opioids and suggest that differential cross-tolerance may provide a useful method for determining the pharmacological basis underlying drug-induced motivational effects.
    Materialart: Digitale Medien
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