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  1. Article: Natriuretic peptides in alcohol withdrawal: central and peripheral mechanisms.

    Kovács, G L

    Current medicinal chemistry

    2003  Volume 10, Issue 23, Page(s) 2559–2576

    Abstract: Abrupt cessation of long-term alcohol consumption produces well-defined symptoms called alcohol withdrawal (AW). The exact pathophysiological mechanisms involved in the appearance of AW symptoms and particularly those related to the precipitation of ... ...

    Abstract Abrupt cessation of long-term alcohol consumption produces well-defined symptoms called alcohol withdrawal (AW). The exact pathophysiological mechanisms involved in the appearance of AW symptoms and particularly those related to the precipitation of delirium tremens (DT), still await clarification in spite of the fact that the prediction of complicated AW is essential to guarantee that appropriate therapies may be planned in advance. Changes in central nervous system (CNS) glutamate- and GABA-transmission and a role of voltage-operated calcium channels are equally important elements of neuroadaptation to the chronic presence of alcohol. In addition to the CNS regulation, however, changes in peripheral fluid and electrolyte homeostasis may accompany, and are expected to modify the clinical symptoms of AW. In an early phase of acute withdrawal, plasma levels of atrial natriuretic peptide (ANP), plasma renin activity and aldosterone are high. In patients with DT, elevated levels of ANP were observed days before the actual onset of DT. It is concluded that the altered plasma ANP secretion might be associated with, and therefore used as an indicator of the onset of DT. However, ANP is present in and produced by the brain and thus it can be regarded as a neuropeptide. The role of CNS ANP was studied in mice, rendered tolerant to and physically dependent on alcohol. Intracerebroventricular injections of ANP attenuated, whereas those of an antiserum against ANP intensified hyperexcitability during AW. ANP in the brain - the content of which undergoes sensitive changes in the hippocampus during AW appears to interact primarily with glutamate transmission through the NMDA-receptors. This brain structure is of utmost importance for the generation of withdrawal-related hyperexcitability. It is concluded that peripheral secretion of ANP might be a diagnostics indicator, whereas ANP in the CNS might be a modulator of AW.
    MeSH term(s) Alcohol Withdrawal Delirium/blood ; Aldosterone/blood ; Amino Acid Sequence ; Animals ; Atrial Natriuretic Factor/blood ; Atrial Natriuretic Factor/metabolism ; Atrial Natriuretic Factor/pharmacology ; Atrial Natriuretic Factor/physiology ; Biomarkers/analysis ; Ethanol/adverse effects ; Humans ; Molecular Sequence Data ; Neurotransmitter Agents/metabolism ; Receptors, Atrial Natriuretic Factor/metabolism ; Renin/blood ; Substance Withdrawal Syndrome/etiology ; Substance Withdrawal Syndrome/metabolism
    Chemical Substances Biomarkers ; Neurotransmitter Agents ; Ethanol (3K9958V90M) ; Aldosterone (4964P6T9RB) ; Atrial Natriuretic Factor (85637-73-6) ; Renin (EC 3.4.23.15) ; Receptors, Atrial Natriuretic Factor (EC 4.6.1.2)
    Language English
    Publishing date 2003-09-29
    Publishing country United Arab Emirates
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 1319315-6
    ISSN 1875-533X ; 0929-8673
    ISSN (online) 1875-533X
    ISSN 0929-8673
    DOI 10.2174/0929867033456459
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Atrial natriuretic peptide modulates N-methyl-D-aspartate-induced hyperexcitability in ethanol-dependent mice.

    Kovács, G L

    European journal of pharmacology

    2000  Volume 401, Issue 3, Page(s) 343–347

    Abstract: The role of central nervous atrial natriuretic peptide was investigated for behavioral hyperexcitability in alcohol-dependent mice. Mice were made tolerant to and dependent on ethanol with an ethanol-liquid diet for 14 days. Five hours after withdrawal ... ...

    Abstract The role of central nervous atrial natriuretic peptide was investigated for behavioral hyperexcitability in alcohol-dependent mice. Mice were made tolerant to and dependent on ethanol with an ethanol-liquid diet for 14 days. Five hours after withdrawal from ethanol, withdrawal symptoms were analyzed by scoring handling-induced convulsions. N-methyl-D-aspartate (NMDA) induced behavioral seizures in a dose-dependent manner, an effect which was more intensive during the ethanol withdrawal period than in alcohol-naive animals. Intracerebroventricular (i.c.v.) injections of alpha-atrial natriuretic peptide (atrial natriuretic peptide) dose-dependently inhibited, whereas injection of an antiserum against atrial natriuretic peptide potentiated, the seizure-inducing effect of NMDA in ethanol-dependent mice. The main conclusion is that central nervous atrial natriuretic peptide plays a modulatory role in behavioral hyperexcitability during alcohol withdrawal.
    MeSH term(s) Animals ; Atrial Natriuretic Factor/immunology ; Atrial Natriuretic Factor/pharmacology ; Behavior, Animal/drug effects ; Dose-Response Relationship, Drug ; Drug Synergism ; Ethanol/pharmacology ; Immune Sera/adverse effects ; Injections, Intraventricular ; Male ; Mice ; N-Methylaspartate/adverse effects ; Seizures/chemically induced ; Seizures/prevention & control ; Substance-Related Disorders
    Chemical Substances Immune Sera ; Ethanol (3K9958V90M) ; N-Methylaspartate (6384-92-5) ; Atrial Natriuretic Factor (85637-73-6)
    Language English
    Publishing date 2000-08-11
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80121-5
    ISSN 1879-0712 ; 0014-2999
    ISSN (online) 1879-0712
    ISSN 0014-2999
    DOI 10.1016/s0014-2999(00)00474-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: The role of atrial natriuretic peptide in alcohol withdrawal: a peripheral indicator and central modulator?

    Kovács, G L

    European journal of pharmacology

    2000  Volume 405, Issue 1-3, Page(s) 103–112

    Abstract: Changes in fluid and electrolyte homeostasis may accompany and are likely to modify the clinical symptoms of alcohol-withdrawal reactions. It was of obvious theoretical and practical interest therefore to investigate the changes in the secretion of ... ...

    Abstract Changes in fluid and electrolyte homeostasis may accompany and are likely to modify the clinical symptoms of alcohol-withdrawal reactions. It was of obvious theoretical and practical interest therefore to investigate the changes in the secretion of hormones, which regulate the fluid and electrolyte homeostasis (atrial natriuretic peptide, aldosterone and plasma renin activity) during alcohol withdrawal in chronic alcoholic patients. In a phase of severe withdrawal, there were increased plasma renin activity and aldosterone levels observed. In a phase of partial recovery, on the other hand, the elevated plasma renin activity and aldosterone levels were back to the normal range. In 60% of the patients, delirium tremens was gradually developing during the observation period. In these patients, an elevated level of atrial natriuretic peptide was observed at the time of hospital admission, i.e. days before the actual onset of delirium tremens. It is concluded that the disturbed volume homeostasis and the consequently altered plasma atrial natriuretic peptide secretion might be associated with, and therefore used as an indicator of the onset of delirium tremens. To study the role of central nervous atrial natriuretic peptide, mice were rendered tolerant to and dependent on alcohol with an alcohol-liquid diet for 14 days. Five hours after withdrawal from alcohol, withdrawal hyperexcitability symptoms were analyzed. Intracerebroventricular (i.c.v.) injection of atrial natriuretic peptide attenuated, whereas that of an antiserum against atrial natriuretic peptide intensified the severity of handling-induced convulsions. N-methyl-D-aspartate induced behavioral seizures in a dose-dependent manner, whose effect was more intensive during the alcohol-withdrawal period than in alcohol-naive animals. I.c.v. injections of atrial natriuretic peptide dose-dependently inhibited, whereas that of antiserum against atrial natriuretic peptide potentiated the seizure-inducing effect of N-methyl-D-aspartate in alcohol-dependent mice. Although tentatively, it is concluded that peripheral secretion of atrial natriuretic peptide may be an indicator, whereas central nervous atrial natriuretic peptide a neuropeptide modulator of alcohol-withdrawal symptomatology.
    MeSH term(s) Animals ; Atrial Natriuretic Factor/blood ; Atrial Natriuretic Factor/physiology ; Biomarkers ; Central Nervous System Depressants/adverse effects ; Ethanol/adverse effects ; Humans ; Neurotransmitter Agents/physiology ; Substance Withdrawal Syndrome/metabolism ; Substance Withdrawal Syndrome/physiopathology
    Chemical Substances Biomarkers ; Central Nervous System Depressants ; Neurotransmitter Agents ; Ethanol (3K9958V90M) ; Atrial Natriuretic Factor (85637-73-6)
    Language English
    Publishing date 2000-09-29
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 80121-5
    ISSN 1879-0712 ; 0014-2999
    ISSN (online) 1879-0712
    ISSN 0014-2999
    DOI 10.1016/s0014-2999(00)00545-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: How much did that Band-Aid cost, really?

    Kovacs, G L

    Hospital material[dollar sign] management

    1997  Volume 22, Issue 10, Page(s) 2, 21

    MeSH term(s) Automatic Data Processing ; Bandages/economics ; Equipment and Supplies, Hospital/economics ; Hospital Costs ; Materials Management, Hospital/organization & administration ; Materials Management, Hospital/standards ; Total Quality Management ; United States
    Language English
    Publishing date 1997-10
    Publishing country United States
    Document type Journal Article
    ISSN 0888-3068
    ISSN 0888-3068
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Dose-dependent dual effect of corticosterone on cerebral 5-HT metabolism.

    Kovács, G L / Kishonti, J / Lissák, K / Telegdy, G

    Neurochemical research

    2013  Volume 2, Issue 3, Page(s) 311–322

    Abstract: The action of 1.0 and 10.0 mg/kg (i.p.) of corticosterone on serotonin (5-HT) and 5-hydroxyindoleacetic acid (5-HIAA) contents and on serotonin turnover, measured by an MAO-inhibitor method, was studied at 30 and 120 min after administration. A 1.0 mg/kg ...

    Abstract The action of 1.0 and 10.0 mg/kg (i.p.) of corticosterone on serotonin (5-HT) and 5-hydroxyindoleacetic acid (5-HIAA) contents and on serotonin turnover, measured by an MAO-inhibitor method, was studied at 30 and 120 min after administration. A 1.0 mg/kg dose of corticosterone increased the serotonin content and turnover in the hypothalamus and mesencephalon 30 min after administration; however, it was ineffective on dorsal hippocampus and frontal and parietal cortex. 5-HIAA content did not change significantly in any of the brain areas studied. A 10.0 mg/kg dose of corticosterone decreased the serotonin content and turnover in the hypothalamus and mesencephalon; it was ineffective in other brain areas investigated. 5-HIAA content significantly decreased in the hypothalamus while it increased in the mesencephalon and dorsal hippocampus. In the parietal and frontal cortex, 5-HIAA content did not change following administration of 10.0 mg/kg of corticosterone. At 120 min after corticosterone administration, neither 5-HT content and turnover nor 5-HIAA content showed any change in the brain areas investigated. The results suggest that corticosteroids might change the activity of the brain serotoninergic system in a dose- and time-dependent manner, and in this way the serotoninergic system might play an important role in mediation of the corticosteroid effect exerted on brain function.
    Language English
    Publishing date 2013-11-23
    Publishing country United States
    Document type Journal Article
    ZDB-ID 199335-5
    ISSN 1573-6903 ; 0364-3190
    ISSN (online) 1573-6903
    ISSN 0364-3190
    DOI 10.1007/BF00969361
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Alpha-atrial natriuretic peptide attenuates ethanol withdrawal symptoms.

    Kovács, G L

    European journal of pharmacology

    1993  Volume 238, Issue 2-3, Page(s) 417–419

    Abstract: Mice were rendered tolerant to and dependent on ethanol with an ethanol-liquid diet for 14 days. Five hours after withdrawal from ethanol, withdrawal symptoms were analyzed by scoring handling-induced convulsions. Intracerebroventricular (i.c.v.) ... ...

    Abstract Mice were rendered tolerant to and dependent on ethanol with an ethanol-liquid diet for 14 days. Five hours after withdrawal from ethanol, withdrawal symptoms were analyzed by scoring handling-induced convulsions. Intracerebroventricular (i.c.v.) injection of alpha-atrial natriuretic peptide (alpha-ANP) attenuated, whereas that of an antiserum against alpha-ANP (anti-ANP) intensified the severity of handling-induced convulsions.
    MeSH term(s) Animals ; Atrial Natriuretic Factor/administration & dosage ; Atrial Natriuretic Factor/pharmacology ; Dose-Response Relationship, Drug ; Ethanol/toxicity ; Injections, Intraventricular ; Male ; Mice ; Seizures/chemically induced ; Seizures/drug therapy ; Substance Withdrawal Syndrome/drug therapy
    Chemical Substances Ethanol (3K9958V90M) ; Atrial Natriuretic Factor (85637-73-6)
    Language English
    Publishing date 1993-07-20
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80121-5
    ISSN 1879-0712 ; 0014-2999
    ISSN (online) 1879-0712
    ISSN 0014-2999
    DOI 10.1016/0014-2999(93)90878-l
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  7. Article: Examination of the interaction of different lighting conditions and chronic mild stress in animal model.

    Muller, A / Gal, N / Betlehem, J / Fuller, N / Acs, P / Kovacs, G L / Fusz, K / Jozsa, R / Olah, A

    Acta physiologica Hungarica

    2015  Volume 102, Issue 3, Page(s) 301–310

    Abstract: We examined the effects of different shift work schedules and chronic mild stress (CMS) on mood using animal model. The most common international shift work schedules in nursing were applied by three groups of Wistar-rats and a control group with normal ... ...

    Abstract We examined the effects of different shift work schedules and chronic mild stress (CMS) on mood using animal model. The most common international shift work schedules in nursing were applied by three groups of Wistar-rats and a control group with normal light-dark cycle. One subgroup from each group was subjected to CMS. Levels of anxiety and emotional life were evaluated in light-dark box. Differences between the groups according to independent and dependent variables were examined with one- and two-way analysis of variance, with a significance level defined at p < 0.05. Interaction of lighting regimen and CMS was proved to be significant according to time spent in the light compartment and the average number of changes between the light and dark compartments. Results of our examination confirm that the changes of lighting conditions evocate anxiety more prominently than CMS. No significant differences were found between the results of the low rotating group and the control group, supposing that this schedule is the least harmful to health. Our results on the association between the use of lighting regimens and the level of CMS provide evidence that the fast rotating shift work schedule puts the heaviest load on the organism of animals.
    MeSH term(s) Animals ; Anxiety/etiology ; Anxiety/psychology ; Behavior, Animal ; Emotions ; Housing, Animal ; Lighting/methods ; Motor Activity ; Photoperiod ; Rats, Wistar ; Severity of Illness Index ; Stress, Psychological/diagnosis ; Stress, Psychological/etiology ; Stress, Psychological/psychology ; Time Factors
    Language English
    Publishing date 2015-09
    Publishing country Hungary
    Document type Comparative Study ; Journal Article
    ZDB-ID 802801-1
    ISSN 1588-2683 ; 0231-424X ; 0001-6756
    ISSN (online) 1588-2683
    ISSN 0231-424X ; 0001-6756
    DOI 10.1556/036.102.2015.3.8
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  8. Article: The involvement of catecholaminergic mechanisms in the behavioural action of vasopressin.

    Kovács, G L / Vécsei, L / Szabó, G / Telegdy, G

    Neuroscience letters

    2009  Volume 5, Issue 6, Page(s) 337–344

    Abstract: The effect of lysine-8-vasopressin (300 mU/kg b.w.) has been tested in a single-trial step-down passive avoidance test. Vasopressin treatment resulted in an improvement of step-down latency in normal rats, but this action disappeared when the animals ... ...

    Abstract The effect of lysine-8-vasopressin (300 mU/kg b.w.) has been tested in a single-trial step-down passive avoidance test. Vasopressin treatment resulted in an improvement of step-down latency in normal rats, but this action disappeared when the animals were pretreated with 80 mg/kg alpha-methyl-p-tyrosine (alpha-MT). Vasopressin treatment decreased the hypothalamic, septal and striatal dopamine (DA) levels. Following vasopressin, the turnover of norepinephrine (NE) increased in the hypothalamus, as did these of DA in the septum and striatum. The data suggest that the cerebral catecholaminergic system might be one of the important mediators of the behavioural action of vasopressin.
    Language English
    Publishing date 2009-07-07
    Publishing country Ireland
    Document type Journal Article
    ZDB-ID 194929-9
    ISSN 1872-7972 ; 0304-3940
    ISSN (online) 1872-7972
    ISSN 0304-3940
    DOI 10.1016/0304-3940(77)90110-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Inhibitory action of midbrain raphe stimulation on stress-induced elevation of plasma corticosterone level in rats.

    Kovács, G L / Kishonti, J / Lissák, K / Telegdy, G

    Neuroscience letters

    2009  Volume 3, Issue 5-6, Page(s) 305–310

    Abstract: Electric stimulation of rat midbrain raphe nuclei by means of chronically implanted bipolar electrodes was able to reduce the stress-induced increase in plasma corticosterone level by about 40-50%. A serotonin receptor blocker, methysergide, prevented ... ...

    Abstract Electric stimulation of rat midbrain raphe nuclei by means of chronically implanted bipolar electrodes was able to reduce the stress-induced increase in plasma corticosterone level by about 40-50%. A serotonin receptor blocker, methysergide, prevented the stimulation-induced inhibition of the stress response. The results support the possible existence of serotoninergic inhibition of hypothalamo-pituitary-adrenocortical activation in rats.
    Language English
    Publishing date 2009-07-07
    Publishing country Ireland
    Document type Journal Article
    ZDB-ID 194929-9
    ISSN 1872-7972 ; 0304-3940
    ISSN (online) 1872-7972
    ISSN 0304-3940
    DOI 10.1016/0304-3940(76)90059-8
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  10. Article: Peripheral oxytocin treatment modulates central dopamine transmission in the mouse limbic structures.

    Kovács, G L / Faludi, M / Falkay, G / Telegdy, G

    Neurochemistry international

    2009  Volume 9, Issue 4, Page(s) 481–485

    Abstract: The effects of subcutaneous (s.c.) oxytocin treatment have been investigated on various parameters of dopaminergic neurotransmission in basal forebrain structures (nucleus olfactorius posterior + nucleus accumbens + septum) of the mouse. Acute oxytocin ... ...

    Abstract The effects of subcutaneous (s.c.) oxytocin treatment have been investigated on various parameters of dopaminergic neurotransmission in basal forebrain structures (nucleus olfactorius posterior + nucleus accumbens + septum) of the mouse. Acute oxytocin treatment failed to influence dopamine utilization in the basal forebrain. Following chronic injections of oxytocin (0.2 mg/kg) for 8 8 days, the neuropeptide decreased dopamine utilization. Neither in vivo nor in vitro oxytocin treatment was capable of influencing the in vitro uptake of [(3)H]dopamine in basal forebrain slices. The spontaneous release of [(3)H]dopamine (in the presence of 4.2 mM K(+)) from basal forebrain tissue slices was not affected by in vitro or acute or chronic in vivo oxytocin treatment. The stimulated release of [(3)H]dopamine (in the presence of 30 mM K(+)) was significantly inhibited by chronic in vivo oxytocin administration. Chronic oxytocin treatment decreased the B(max) value of [(3)H]spiroperidol binding in the basal forebrain. The dissociation constant (K(d)) of [(3)H]spiroperidol binding was not influenced by oxytocin. The data indicate that peripheral oxytocin treatment is capable of modifying dopaminergic neurotransmission in mouse basal forebrain regions.
    Language English
    Publishing date 2009-11-16
    Publishing country England
    Document type Journal Article
    ZDB-ID 283190-9
    ISSN 1872-9754 ; 0197-0186
    ISSN (online) 1872-9754
    ISSN 0197-0186
    DOI 10.1016/0197-0186(86)90138-5
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