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1. |
Perinatal Distress and Prognosis of Psychotic Illness |
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Neuropsychobiology,
Volume 17,
Issue 4,
1987,
Page 173-175
James A. Wilcox,
Henry A. Nasrallah,
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摘要:
The medical histories of a group of 511 patients hospitalized for schizophrenia were examined for the occurrence of perinatal distress. These patients were part of a 40-year follow-up study, so that their prognostic outcome was known at the time of this study. In this way, 200 cases of chronic schizophrenia were compared with 311 cases of psychotics with good prognosis. It was found that a history of perinatal distress was much more common in the poor prognosis group than in the good prognosis group. This difference could not be accounted for by age or family history of psychiatric illness.
ISSN:0302-282X
DOI:10.1159/000118359
出版商:S. Karger AG
年代:1987
数据来源: Karger
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2. |
Total Biopterin Levels of Plasma in Patients with Depression |
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Neuropsychobiology,
Volume 17,
Issue 4,
1987,
Page 176-177
R. Hashimoto,
N. Ozaki,
T. Ohta,
Y. Kasahara,
N. Kaneda,
T. Nagatsu,
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摘要:
The total biopterin levels of plasma in 12 patients with depression were measured. They were elevated significantly as compared with those in normal controls. The plasma biopterin levels in 6 of 12 patients were measured both in the depressive and in the remissive phases. In the depressive phase the total biopterin levels were increased, whereas in the remission phase they did not differ from those in normal controls. Antidepressants did not affect the plasma biopterin levels. We speculate that the elevation of the plasma biopterin levels in patients with depression was related to the depressive state itself.
ISSN:0302-282X
DOI:10.1159/000118360
出版商:S. Karger AG
年代:1987
数据来源: Karger
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3. |
Prostaglandin Synthesis among Alcoholic Suicide Attempters and Nonattempters |
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Neuropsychobiology,
Volume 17,
Issue 4,
1987,
Page 178-181
James P. MacMurray,
Louis P. Bozzetti,
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摘要:
Serum PGF2α titers were examined in 8 sober alcoholic males who had attempted suicide and 19 nonattempting alcoholic males. Two of the 8 attempters had used violent means and the remaining 6 had used nonviolent means. The suicide attempters had significantly lower PGF2α titers, relative to the nonattempters (p < 0.005), with the violent attempters expressing maximally reduced titers. There were no significant differences between the groups with respect to age, alcohol consumption patterns, or admission scores on the Beck Depression Inventor
ISSN:0302-282X
DOI:10.1159/000118361
出版商:S. Karger AG
年代:1987
数据来源: Karger
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4. |
Platelet3H-Imipramine Binding and Familial Transmission of Affective Disorders |
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Neuropsychobiology,
Volume 17,
Issue 4,
1987,
Page 182-186
Miron Baron,
Amiram Barkai,
Rhoda Gruen,
Eric Peselow,
Ronald F. Fieve,
Frederic Quitkin,
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摘要:
We studied platelet 3H-imipramine binding and family history of affective illness in 26 patients with bipolar affective disorder and 24 patients with unipolar affective disorder. The density of platelet 3H-imipramine binding sites (Bmax) was significantly lower in bipolar patients with family history of affective illness than in healthy controls; however, there was a considerable overlap in Bmax values between the familial cases and the normal controls. A similar trend was observed in familial cases of unipolar disorder but the differences fell short of statistical significance. The nonfamilial cases of affective disorder did not differ from the healthy controls. The possible role of reduced platelet 3H-imipramine binding as a genetic vulnerability ‘marker’ in affective disorder was discus
ISSN:0302-282X
DOI:10.1159/000118362
出版商:S. Karger AG
年代:1987
数据来源: Karger
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5. |
Chronic Treatment with Imipramine Does Not Reverse the Effects of 3 Anxiogenic Compounds in a Test of Anxiety in the Rat |
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Neuropsychobiology,
Volume 17,
Issue 4,
1987,
Page 187-192
Sandra E. File,
Amanda L. Johnston,
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摘要:
The ability of chronic treatment with imipramine (an antidepressant with anti-panic activity) to antagonise the anxiogenic effects of 3 different compounds was investigated in the elevated plus-maze. The compounds chosen are likely to produce anxiety by activity at different sites in the central nervous system: yohimbine, by blocking the α2-adrenoceptor; FG 7142, by action at the β-carboline site on the GABA-benzodiazepine receptor complex and pentylenetetrazole, by acting at the picrotoxinin site on this complex. Administration of imipramine following 21 days pre-treatment did not produce a significant consistent anxiolytic effect alone and was unable to reverse the anxiety produced by any of the 3 anxiogenic compounds. Our results are discussed in terms of the nature of the anxiety produced by the anxiogenic drugs and the sensitivity of tests of anxiety to anti-panic agent
ISSN:0302-282X
DOI:10.1159/000118363
出版商:S. Karger AG
年代:1987
数据来源: Karger
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6. |
The Effect of Ethanol (Alcohol) and Stress on Plasma Catecholamine Levels in Individual Female and Male Rats |
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Neuropsychobiology,
Volume 17,
Issue 4,
1987,
Page 193-198
G.T. Livezey,
N. Balabkins,
W.H. Vogel,
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摘要:
Individual male and female Sprague-Dawley rats with indwelling jugular catheters were subjected to restraint stress both without and with pretreatment with 1 g/kg ethanol (i.p., 20% w/v in water). Plasma norepinephrine (NE) and epinephrine (E) were determined prior to restraint and at 5, 15 and 30 min after the onset of immobilization. Overall, ethanol increased the baseline levels of both catecholamine slightly and transiently but markedly decreased the stress response of both NE and E. The extent of the stress response alone and its reduction by ethanol varied markedly among animals and between the sexes. Female rats showed more varied and higher stress responses and a slightly different response to ethanol. Individual baseline values of NE or E without or after ethanol did not predict the intensity or duration of the stress response or its reduction by ethanol. The total stress response over the entire stress period without ethanol was mostly determined by the 5-min stress response, whereas the total stress response with ethanol was mostly determined by the 15- and 30-min stress responses. The stress response without ethanol predicted strongly its reduction by ethanol; the greater the stress response without ethanol the greater its reduction by ethanol. Our data obtained in rats support the ‘tension reduction hypothesis’ of human alcoholism and would place individuals with a high stress response at greatest risk to abuse alco
ISSN:0302-282X
DOI:10.1159/000118364
出版商:S. Karger AG
年代:1987
数据来源: Karger
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7. |
Effects of Scopolamine (0.25–0.75 mg i.m.) on the Quantitative EEG and the Neuropsychological Status of Healthy Volunteers |
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Neuropsychobiology,
Volume 17,
Issue 4,
1987,
Page 199-205
Walter G. Sannita,
Lino Maggi,
Guido Rosadini,
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摘要:
There has been clinical and experimental evidence that cholinergic compounds and precursors of choline are potentially useful in the treatment of dementia. Anticholinergic compounds have also been proposed as a possible acute model for pharmaco-EEG studies focussed on CNS aging. Single doses of scopolamine (0.25–0.75 mg i.m.) and a matching placebo were administered to 8 young healthy volunteers. Quantitative EEG recordings and neuropsychological testing were performed in baseline conditions prior to and 30, 90 and 120 min after drug administration. Scopolamine induced a dose-related increase of relative power in low- and high-frequency components and a decrease in the range 8.0–13.5 Hz and in total signal power. These modifications were found to be limited to the posterior scalp electrode derivations and were observed from the 90-min control onwards. Concomitantly, there was a significant impairment in the subjects’ response to neuropsychological testing after the administration of 0.50 and 0.75 mg of scopolamine. At a dose of 0.75 mg, volunteers complained about subjective symptoms which were definitely unpleasant. The effects of this dose on the EEG and the neuropsychological status did not differ significantly from those observed after a dose of 0.50 mg. As regards dose and tolerance, 0.50 mg of scopolamine administered intramuscularly appears to be a suitable dose for pharmaco-EEG st
ISSN:0302-282X
DOI:10.1159/000118365
出版商:S. Karger AG
年代:1987
数据来源: Karger
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8. |
Effects of the Selective 5-Hydroxytryptamine Uptake Inhibitors Paroxetine and Zimeldine on EEG Sleep and Waking Stages in the Rat |
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Neuropsychobiology,
Volume 17,
Issue 4,
1987,
Page 206-212
Horst Kleinlogel,
Hans R. Burki,
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摘要:
The effects of oral paroxetine and zimeldine on EEG sleep-waking phases in the rat were investigated over a wide dose range. To ascertain that at the doses used for the EEG studies paroxetine and zimeldine selectively affect the serotoninergic system, their effects on brain 5-hydroxytryptamine (5-HT), dopamine and noradrenaline were determined. It was found that paroxetine and zimeldine at doses of 1–18 mg/kg dose-dependently prolonged waking and shortened slow-wave sleep and paradoxical sleep. In the same dose range cortical 5-HT turnover was significantly reduced, whereas the other aminergic systems were not influenced. These results suggest that 5-HT uptake inhibitors increase vigilance in rats at oral doses which selectively stimulate the serotoninergic syste
ISSN:0302-282X
DOI:10.1159/000118366
出版商:S. Karger AG
年代:1987
数据来源: Karger
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9. |
International Pharmaco-EEG Group (IPEG) |
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Neuropsychobiology,
Volume 17,
Issue 4,
1987,
Page 213-218
G. Dumermuth,
G. Ferber,
W.M. Herrmann,
H. Hinrichs,
H. Künkel,
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ISSN:0302-282X
DOI:10.1159/000118367
出版商:S. Karger AG
年代:1987
数据来源: Karger
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10. |
IPEG Symposium 1988 Japan |
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Neuropsychobiology,
Volume 17,
Issue 4,
1987,
Page 218-218
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PDF (145KB)
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ISSN:0302-282X
DOI:10.1159/000118368
出版商:S. Karger AG
年代:1987
数据来源: Karger
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