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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Archives of gynecology and obstetrics 231 (1982), S. 315-320 
    ISSN: 1432-0711
    Keywords: Ovarian cycle ; Physiology ; Catecholestrogens ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Using highly stabilized catecholestrogen preparations-ascorbic acid added to the free alcohols or benzoic acid derivatives — 2- and 4-hydroxyestrogens were tested in simple, clearly defined animal models: As index for the peripheral action the influence on vaginal opening and uterus weight gain was monitored after continuous s.c. administration for 6 days (minipumps) in immature intact rats resulting in a relative estrogenic potency (estradiol = 100%) of 70–100% for 4-hydroxyestradiol and less than 30% for 2-hydroxyestradiol. As index for the central action LH levels were measured in adult ovx rats leading to the same relations in the relative potencies. As index for both central and peripheral actions LH levels and the formation of corpora lutea were investigated in animals with an intact but prepubertal feed-back loop, i.e. in 25-day-old immature rats. 4-Hydroxyestradiol in this model clearly triggered LH surges and induced ovulations, its potency being in the same range as that of estradiol. 2-Hydroxyestradiol, in comparable doses, again showed no significant effect. Finally, female immature animals known to ovulate 3 days after PMS injection were treated concomitantly with either primary or catecholestrogen-antibody preparations. Whereas the primary estrogen antibody significantly blocked ovulation, the 2- and 4-hydroxyestrogen antibodies were ineffective. If, however, PMS and estrogen-antibody treated animals were supplemented with 4-hydroxyestrogens, ovulations could be restored. Thereby, it was inferred that peripheral 4-hydroxyestrogens, though not essential for the physiology of reproduction, can completely replace the physiologically essential peripheral estradiol at central target sites.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 45 (1982), S. 217-229 
    ISSN: 1432-1106
    Keywords: Rat ; Thalamic reticular nucleus ; Lateral geniculate nucleus ; Electrophysiology ; HRP
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Electrophysiological and neuroanatomical techniques have been used to study the properties of cells in the reticular nucleus of the thalamus (RNT) responsive to photic stimuli. In the rat these cells are located in a discrete region of the nucleus lying immediately rostral to the dorsal lateral geniculate nucleus (LGNd), where the visual field is represented in a retinotopic fashion. After injections of horseradish peroxidase (HRP) into this area, neurones labelled with reaction product were found in the LGNd and not in other thalamic relay nuclei. After HRP injections into the LGNd, labelled RNT cells were found only within the region which contains neurones responsive to photic stimuli. These observations suggest that there is a precise reciprocal relation between the two areas. Studies and comparisons of the responses of relay cells (P cells) in LGNd and cells in RNT to electrical shocks lead us to conclude that RNT cells receive their excitation mainly via those relay cells in LGNd which are themselves excited by fast-conducting retinal ganglion cell axons. Such cells in LGNd have phasic responses and concentric receptive fields while RNT cells have phasic responses and on/off fields and a comparison of the receptive field sizes of P cells and RNT cells suggests that only a small number of LGNd relay cells converge on to each RNT cell. Further, although a particular functional class of relay cells in LGNd (Y-type) is shown to provide the major input to visually responsive RNT cells, both Y type and W type relay cells are subject to their inhibitory control. These results furnish evidence that cells in the RNT have an important role in modulating the flow of visual information from the LGNd to cortex.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 47 (1982), S. 270-276 
    ISSN: 1432-1106
    Keywords: Rat ; Turning ; Parafascicular nucleus ; Fasciculus retroflexus ; Apomorphine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Apomorphine, 2 mg/kg i.p., produced ipsilateral turning in rats with unilateral lesions in the parafascicular nucleus of the thalamus. The effect was completely blocked by the administration of haloperidol, 0.3 mg/kg i.p. There were no asymmetries by the lesions alone or after administration of haloperidol, 2 mg/kg i.p. to lesioned animals. In control experiments apomorphine produced a marked contralateral turning in animals with unilateral degeneration of the fasciculus retroflexus.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 78 (1982), S. 225-229 
    ISSN: 1432-2072
    Keywords: Diazepam ; Prenatal treatment ; Development ; Discrimination ; Motor behavior ; Learning retention ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract In the present study the effects of chronic treatment of pregnant rats with diazepam on the physical and behavioral development of their offspring were investigated. Rats that were diazepam-exposed prenatally were compared to age-matched controls in terms of the following: number of littermates; birth weight and weight gain until weaning; motor development and coordination; simple motor learning; open field activity; performance on learning tasks of varving complexity; retention of these tasks. Nulliparous Wistar rats were injected s.c. for 16 days of their pregnancy with either 2.5, 5, or 10 mg/kg diazepam or an equal volume of vehicle. Prenatal diazepam treatment did not alter litter size, birth weight, or the righting reflex, but seemed to retard early motor development transiently. Diazepam pups showed longer latencies and less rearing in the open field. There were no differences between animals exposed to drug and vehicle in simple motor learning or in acquiring a simple successive discrimination task. However, there were significant dosedependent differences on a complex six-choice simultaneous discrimination learning task, the diazepam-exposed rats making more errors and taking more time to reach the goal. A significant difference was seen again between diazepam-and vehicle-exposed rats on the retention test 10 days later. The results indicate that diazepam administered to pregnant rats has long-range effects on the behavior of the offspring, some becoming manifest even in maturity.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 76 (1982), S. 66-69 
    ISSN: 1432-2072
    Keywords: Experimental epilepsy ; Kindling ; Amygdala ; Acetylcholine ; Choline uptake ; Atropine ; Muscarinic receptors ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The effect of atropine on kindling the amygdala of rats was tested by administering the drug in a dose of 25 mg/kg 1 h before each stimulus was applied. Rats tested with atropine kindled at the same rate as saline-treated controls. Cholinergic activity in the amygdala of rats was assessed, 4 weeks after the completion of kindling, by measuring both muscarinic receptor numbers and sodium-dependent high affinity choline uptake in tissue homogenates. There was no change in either of these parameters attributable to kindling. These results suggest that changes in the cholinergic system are not fundamental either to the development or the maintenance of kindling in the rat amygdala.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 76 (1982), S. 114-117 
    ISSN: 1432-2072
    Keywords: Brain ; β-Adrenoceptors ; Serotonin synthesis ; Metoprolol ; ICI 118,551 ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Rats were treated subchronically (14 days) or acutely (single dose) with the β1-selective adrenoceptor antagonist metoprolol or the β2-selective adrenoceptor antagonist ICI 118,551. Metoprolol (350 mg/kg/day for 14 days, orally) significantly reduced the 5-hydroxytryptophan (5-HTP) accumulation when measured 30 min after inhibition of L-amino acid decarboxylase by NSD 1015 (100 mg/kg IP) in the limbic forebrain, the corpus striatum, the cerebral cortex, the brain stem, and in the cerebellum. ICI 118,551 (0.5 mg/kg, twice daily for 14 days, SC) also significantly reduced the 5-HTP accumulation in the same brain regions except in the corpus striatum and the brain stem. Simultaneously assayed tryptophan levels were largely unaffected. Thus sustained β-adrenoceptor blockade causes a decrease in the in vivo rate of tryptophan hydroxylation in various rat brain regions. The subchronic treatments with metoprolol or ICI 118,551 also significantly reduced the endogenous levels of 5-hydroxytryptamine (5-HT) in the various rat brain regions studied. Acute treatment with either metoprolol (2 mg/kg SC) or ICI 118,551 (0.5 mg/kg SC) did not affect the 5-HTP accumulation or the endogenous 5-HT levels in the brain regions studied. This inhibitory effect on brain 5-HT systems produced by sustained β-adrenoceptor blockade may be of significance both for the long-term cardiovascular action and for occasional neuropsychiatric side effects during β-blocking therapy.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 76 (1982), S. 160-162 
    ISSN: 1432-2072
    Keywords: Nicotine ; Withdrawal ; Plasma corticosterone ; Stress ; Adaptation ; 5-Hydroxytryptamine ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The effects of chronic nicotine administration (0.4 mg/kg for 40 days) and its withdrawal on the adrenocortical response to acute and repeated exposure to stress have been examined and related to changes in brain 5-hydroxyindole levels. No significant effects on the response to acute stress were observed. Repeated exposure to the stressful procedure resulted in complete adaptation of the adrenocortical response and the development of a significant (P〈0.01) positive correlation between the plasma corticosterone and hippocampal 5-HT concentrations. In nicotine-treated rats, complete adaptation did not occur and the plasma corticosterone showed a significant (P〈0.05) negative correlation with hippocampal 5-HT. Nicotine withdrawal was not associated with any reduction in plasma corticosterone, but did abolish its relationship with hippocampal 5-HT.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-2072
    Keywords: Turning behaviour ; Brain lesions ; 5-MeODMT ; Dopaminergic system ; Dopamine release ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The turning behaviour induced by 5-methoxy-N,N-dimethyltryptamine (5-MeODMT) has been investigated in rats with lesions of the dorsal raphé nucleus (DRN). 5-MeODMT caused a dose-related contralateral turning in rats with 5,7-dihydroxytrypamine (5,7-DHT) lesions of the substantia nigra and a similar effect was observed in DRN-lesioned rats. In contrast, a dose-related ipsilateral turning was observed when 5-MeODMT was injected into rats with 5,7-DHT lesions of the striatum. These results suggest that the effects of 5-MeODMT in DRN-lesioned rats are mediated via the substantia nigra. The contralateral turning induced by 5-MeODMT in rats with a 5,7-DHT lesion of the DRN was significantly reduced when a second 6-hydroxydopamine lesion was placed in the striatum, but not when it was placed in the nucleus accumbens. Thus the nigrostriatal dopaminergic system seems to be involved in 5-MeODMT-induced turning. The release of tritium from slices of substantia nigra previously labelled with [3H]-dopamine was inhibited by 5-MeODMT (10-7 to 10-5 M) and this effect was blocked by methysergide in a concentration-related manner. Tetrodotoxin (10-7M) failed to antagonise 5-MeODMT. These results suggest that 5-MeODMT can inhibit dopamine release from nigral dendrites, which could in turn enhance nigrostriatal activity by reducing the auto-inhibitory actions of dopamine, thereby causing contralateral turning in DRN-lesioned rats.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 78 (1982), S. 277-281 
    ISSN: 1432-2072
    Keywords: Conditioned taste aversion ; Scopolamine ; Prochlorperazine ; Lithium ; Amphetamine ; Morphine ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Two antiemetic drugs were tested on the expression of taste aversions previously conditioned in rats with lithium, amphetamine or morphine. Neither prochlorperazine nor scopolamine administered prior to testing attenuated established aversions, although both drugs are known to have antiemetic effects in other species. Negative findings were obtained with a range of doses of prochlorperazine and scopolamine, with strong and weak aversions, with one- and two-stimulus tests, in a repeated one-stimulus extinction procedure, with between- and within-group designs and with hooded, albino, male and female rats. The results do not support the widely accepted hypothesis that conditioned nausea mediates conditioned taste aversion.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1432-2072
    Keywords: Discriminative stimulus ; Diazepam ; Morphine ; Naloxone ; Endorphins ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Male Sprague-Dawley rats were trained in a two-lever food-reinforced procedure to discriminate between the effect of saline and diazepam (2.5 mg/kg). After acquisition of this discrimination, the ability of morphine to generalize, and naloxone to antagonize the diazepam discriminative stimulus was tested. The rats did not generalized the effect of morphine, and naloxone did not antagonize the diazepam discriminative stimulus whether it was given prior or subsequent to diazepam. These data suggest a lack of involvement of endorphins in mediating the discriminative stimulus property of diazepam.
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