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1.
Infection ; 42(4): 775-8, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24531907

ABSTRACT

Etravirine is metabolized by three cytochrome P450 enzymes that are in turn induced by rifampin. Consequently, co-administration of etravirine and rifampin is not recommended. To date, however, no clinical studies exploring the drug-drug interaction of this combination have been conducted. Here we report two cases of off-label etravirine use concurrently with antitubercular treatment, dictated by the unavailability of other treatments. Plasma drug concentrations were monitored by regular measurements. Our results appear to confirm the increased metabolism of etravirine through the induction of cytochrome P450 enzymes, but the adequacy of drug levels in all of the measurements and subsequent virological suppression suggest that this drug interaction may not be clinically relevant.


Subject(s)
Anti-HIV Agents/pharmacokinetics , Antitubercular Agents/therapeutic use , HIV Infections/drug therapy , Pyridazines/pharmacokinetics , Rifampin/therapeutic use , Tuberculosis/drug therapy , Adult , Anti-HIV Agents/therapeutic use , Drug Interactions , Female , HIV Infections/complications , Humans , Nitriles , Plasma/chemistry , Pyridazines/therapeutic use , Pyrimidines , Tuberculosis/complications
3.
J Thromb Haemost ; 3(7): 1414-20, 2005 Jul.
Article in English | MEDLINE | ID: mdl-15978097

ABSTRACT

In order to assess whether the HR2 haplotype of the factor V gene (HR2) increases the risk of venous thromboembolism (VTE) in carriers of antithrombin (AT), protein C (PC) or S (PS) defects, we performed this determination in 336 subjects, who were family members of 66 symptomatic patients with clotting inhibitors defects. We first assessed the presence of previous VTE, and then followed prospectively subjects without prior VTE. VTE episodes had occurred in 26 individuals: 18 in 139 carriers of clotting inhibitors defects alone (annual incidence, 0.55%), four in 33 carriers of clotting inhibitors defects combined with HR2 (0.52%) and four in 151 non-carriers (0.1%), resulting in a relative risk (RR) for VTE of 4.9 (95% CI: 1.7-14.4) and 4.62 (95% CI: 1.2-18.4), respectively. After an overall follow-up of 2557 patient-years, VTE episodes developed in 12 subjects: nine in 121 carriers of clotting inhibitors defects alone (annual incidence, 0.92%), three in 29 carriers of clotting inhibitors defects combined with HR2 (1.0%) and none in 147 non-carriers. In family members of patients with AT, PC or PS defects the coinheritance of HR2 haplotype does not seem to increase the thromboembolic risk.


Subject(s)
Antithrombins/genetics , Factor V/genetics , Protein C Deficiency/genetics , Protein C/genetics , Protein S Deficiency/genetics , Venous Thrombosis/epidemiology , Venous Thrombosis/genetics , Adult , Age Factors , Aged , Antithrombins/deficiency , Blood Coagulation Disorders/genetics , Cohort Studies , Disease-Free Survival , Family Health , Female , Haplotypes , Heterozygote , Humans , Incidence , Male , Middle Aged , Prospective Studies , Pulmonary Embolism/genetics , Retrospective Studies , Risk , Thrombosis , Time Factors
4.
MAGMA ; 17(3-6): 109-16, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15614516

ABSTRACT

Although ischemic stroke has higher incidence and severity in aged than in young humans, the age factor is generally neglected in ischemia animal models. This study was aimed at comparing age-dependent effects at early stages of transient global cerebral ischemia (TGCI) in rats. TGCI was induced in two groups of rats (3-6 and 20-24 months old, respectively) by exposure to 15% oxygen and 15 min occlusion of the two common carotid arteries. Brains were analysed in vivo by MRI-apparent diffusion coefficient (ADC) and T2 maps--at 1-3 h post-TGCI and in vitro by histochemical examination of triphenyltetrazolium chloride (TTC)-stained slices. At 1-3 h post-TGCI, a higher incidence of lesions was found in aged than in young rats especially in the hippocampus and cortex (occipital plus parietal) but not in the thalamus. The lesioned regions showed lower ADC values in aged than in younger rats. The most substantial ADC decreases were associated with enhanced spin-spin relaxation and lower TTC staining. The different responses of the two age groups support the use of aged animals for investigations on different ischemia models. Our model of brain ischemia appears appropriate for further studies including drug effects.


Subject(s)
Aging , Disease Models, Animal , Image Interpretation, Computer-Assisted/methods , Ischemic Attack, Transient/diagnosis , Magnetic Resonance Imaging/methods , Stroke/diagnosis , Animals , Brain/blood supply , Brain/pathology , Ischemic Attack, Transient/complications , Ischemic Attack, Transient/pathology , Male , Rats , Rats, Inbred F344 , Reproducibility of Results , Sensitivity and Specificity , Severity of Illness Index , Stroke/etiology , Stroke/pathology
5.
Med Secoli ; 13(1): 47-57, 2001.
Article in Italian | MEDLINE | ID: mdl-12361058

ABSTRACT

In the preface of his Greek edition of Hippocrates, published in Basle in 1538, Janus Cornarius of Zwickau mentions a manuscript of the French physician Nicolas Kopp among the textual sources used by him to review the preceding edition. It is known that Nicolas inherited the library of his father Wilhelm, who made the translations of two Hippocratic treatises, Prognostikon and De victus ratione in morbis acutis, published in Paris in 1511. It is suggested that the manuscript used by Cornarius for his edition and earlier by Wilhelm Kopp for his translations can be identified with the Par. gr. 2254 and 2255. This proposal is verified in the present article by an examination of the translation by Wilhelm Kopp of the treatise De victus ratione in morbis acutis, which is contained in the original part of the manuscript Par. gr. 2254.


Subject(s)
Manuscripts, Medical as Topic/history , Medicine , Publishing/history , Translations , France , Greece , History, 16th Century , History, Ancient , Switzerland
6.
Ann Ist Super Sanita ; 36(4): 453-7, 2000.
Article in English | MEDLINE | ID: mdl-11367924

ABSTRACT

Neuronal damage and phosphoinositide hydrolysis stimulated by neurotransmitter receptor agonists in cerebral cortex of 3- and 24-month Fischer 344 rats, following an episode of brain ischemia, were compared. Transient global ischemia was induced by occlusion of common carotid arteries for 15 minutes in conditions of moderate hypoxia. Seven days after, histological examination of cerebral cortex showed cell loss, neurons with nuclear pyknosis, cytoplasmatic degeneration, and glial proliferation. Ischemic lesions appeared moderate to severe in young rats and intermediate in all the aged animals. In young rats inositol phosphates accumulation stimulated by excitatory amino acids (ACPD, ibotenate and quisqualate), but not by norepinephrine or carbachol, was enhanced significantly with respect to sham-operated animals. No potentiation at all was observed in aged rats. This finding suggests that the events leading to the increased metabotropic response in the post-ischemia period is impaired by the ageing process.


Subject(s)
Brain Ischemia/metabolism , Phosphatidylinositols/metabolism , Receptors, Metabotropic Glutamate/physiology , Age Factors , Animals , Male , Rats , Rats, Inbred F344
7.
Exp Toxicol Pathol ; 51(4-5): 392-6, 1999 Jul.
Article in English | MEDLINE | ID: mdl-10445403

ABSTRACT

The aim of this study was to identify the effects of widely used laboratory anaesthetics on cytochrome (CYP) activity in male Sprague Dawley rats in vivo. The anaesthetics used were urethane and ketamine. 7-Ethoxyresorufin (EROD), 7-pentoxyresorufin (PROD), aniline and ethylmorphine were used as substrates for CYP 1A, CYP 2B, CYP 2E1 and CYP 3A, respectively. Urethane increased EROD (CYP 1A) activity by 40 % (p < 0.01), and hydroxylation of aniline (CYP 2E1) by 14 % in the early phase of anaesthesia and by 60 % (p < 0.01) in the later one. Urethane also reduced the demethylation of ethylmorphine by 37 % (p < 0.01), but did not affect CYP 2B activity significantly. Ketamine did not significantly affect CYP 1A, 2B or 2E1. However, it reduced the demethylation of ethylmorphine (i.e. CYP 3A) by 32 % (p < 0.01). From these data, we concluded that a single dose of urethane inhibits CYP 3A but increases CYP 2E1 and CYP 1A, and that a single dose of ketamine inhibits the activity of CYP 3A.


Subject(s)
Anesthetics/pharmacology , Aryl Hydrocarbon Hydroxylases , Cytochrome P-450 Enzyme System/metabolism , Ketamine/pharmacology , Liver/enzymology , Urethane/pharmacology , Animals , Cytochrome P-450 CYP1A1/metabolism , Cytochrome P-450 CYP2B1/metabolism , Cytochrome P-450 CYP2E1/metabolism , Cytochrome P-450 CYP3A , Cytochrome P-450 Enzyme Inhibitors , Enzyme Inhibitors/pharmacology , Kinetics , Male , Oxidoreductases, N-Demethylating/metabolism , Rats , Rats, Sprague-Dawley
8.
Med Secoli ; 11(1): 9-28, 1999.
Article in Italian | MEDLINE | ID: mdl-11624204

ABSTRACT

The Anatomical Procedures is Galen's most complete treatise on anatomy, which the Western culture came to know only in the Renaissance. Its first Latin translation was made by Demetrius Chalcondylas (1423-1511). He was a teacher of some translators of the ancient Greek physicians, and an owner of many Greek medical manuscripts. The translation by Chalcondylas was revised and published by Berengario da Carpi in 1529, and was reprinted only once, in 1531. Its philological analysis proves that it depends on a Greek manuscript, a copy of Par. gr. 1849, which is now lost. The humanist physician Nicolo Leoniceno knew the translation by Calchondylas before it was published, for he quoted it in his Apologia printed in 1522. Therefore, this translation circulated as a manuscript, which was so far ignored.


Subject(s)
Anatomy/history , Manuscripts, Medical as Topic/history , Publishing/history , Translations , Greek World , History, 16th Century , History, Ancient , Italy
9.
MAGMA ; 7(1): 28-34, 1998 Nov.
Article in English | MEDLINE | ID: mdl-9877457

ABSTRACT

A model of transient global brain ischemia consisting of bilateral occlusion of common carotid arteries for 10 min and mild hypoxia (15% O2-85% N2) for 20 min was studied by means of MRI in young and aged Fischer 344 rats (3-4 and 24-26 months, respectively). Ischemia was assessed by full suppression of spontaneous EEG activity, which reappeared and normalized similarly in the two age-groups. The survival of young with respect to aged rats was considerably higher both at 24 h (20/20, i.e. 100% vs 12/16, i.e. 75%) and at 48 h (16/20, i.e. 80% vs 6/16, i.e. 38%). The localisation of brain lesions, their severity and progression were evaluated by a diffusion-weighted MRI (DWI) sequence at 24 and 48 h post-ischemia. There were no DWI-detectable lesions in eight out of 20 young and two out of 12 aged rats. The localisation of DWI-detected lesions was rather similar in rats of the two age-groups. In fact, the cerebral cortex, mainly parietal, occipital and temporal lobes were damaged in 83% of young and 90% of aged rats. The respective percentages for the thalamus were 83 and 60%, for the striatum 58 and 50%, and for the hippocampus 25 and 30%. The lesions present in the cerebral cortex and the thalamus were considerably more severe in aged than in young rats. In conclusion, in spite of similar localisation of ischemic lesions in the two age-groups, their incidence was higher, appearance more rapid and severity more pronounced in aged with respect to young rats. This resulted in a considerably higher mortality of the former. The overall data indicate that the age issue is very important in experimental ischemia research.


Subject(s)
Aging/physiology , Ischemic Attack, Transient/diagnosis , Animals , Behavior, Animal/physiology , Disease Models, Animal , Disease Progression , Electrophysiology , Hypoxia/chemically induced , Hypoxia/pathology , Ischemic Attack, Transient/pathology , Magnetic Resonance Imaging/methods , Male , Rats , Rats, Inbred F344
10.
Neurochem Int ; 31(4): 563-9, 1997 Oct.
Article in English | MEDLINE | ID: mdl-9308006

ABSTRACT

A model of ischemic-hypoxic brain injury which combines bilateral occlusion of common carotid arteries for 10 min and mild hypoxia (15% O2 for 10 min before and during occlusion) was developed. Global ischemia was assessed by a simplified EEG recording indicating isoelectric line, i.e. full arrest of cortical electrical activity. Histological examination of brain 7 days after ischemic insult showed from moderate to severe damage, mainly in the cerebral cortex (layers III, V and VI) and hippocampus (mainly CA1 subfield). The injury consisted of neuronal degeneration and necrosis with nuclear pyknosis and karyorrhexis. Immunohistochemical staining for gliofibrillar acidic protein showed a marked glial proliferation in the cerebral cortex and hippocampus. In the cortical slices, inositol phosphates accumulation stimulated by excitatory amino acid agonists (ACPD, ibotenate and quisqualate), as well as by norepinephrine and carbachol, was enhanced significantly (p < 0.01) with respect to sham-operated rats 7 days, but not 24 h, after the ischemic insult. The overall data show that the relatively simple transient brain hypoxia/ischemia rat model produces full arrest of cortical EEG, histopathological alterations and those relative to post-receptor neurochemical mechanisms characteristic of four-vessel occlusion model.


Subject(s)
Brain Diseases/metabolism , Brain Diseases/pathology , Hypoxia/metabolism , Hypoxia/pathology , Ischemic Attack, Transient/metabolism , Ischemic Attack, Transient/pathology , Animals , Behavior, Animal/physiology , Brain Diseases/physiopathology , Cell Division , Cerebral Cortex/metabolism , Cerebral Cortex/pathology , Cerebral Cortex/physiopathology , Electroencephalography , Glial Fibrillary Acidic Protein/metabolism , Hydrolysis , Hypoxia/physiopathology , Immunohistochemistry , Ischemic Attack, Transient/physiopathology , Male , Neuroglia/pathology , Neurons/pathology , Phosphatidylinositols/metabolism , Rats , Rats, Sprague-Dawley , Receptors, Metabotropic Glutamate/agonists
11.
MAGMA ; 5(2): 139-49, 1997 Jun.
Article in English | MEDLINE | ID: mdl-9268078

ABSTRACT

A newly developed model of transient global ischemia in the rat was evaluated by magnetic resonance imaging (MRI) in terms of localization of brain lesions, their extent and severity, and temporal evolution. Such a model, consisting of bilateral occlusion of common carotid arteries for 10 minutes and mild hypoxia (15% O2) for 20 minutes induces delayed neuronal degeneration, necrosis, and gliosis (detected histologically and immunohistochemically). Ischemia was assessed by full suppression of spontaneous electroencephalographic activity. A "hybrid" T2-/diffusion-weighted MR sequence enhancing more effectively the contrast between injured and intact tissues as compared to T2-weighted MRI was used at 24, 48, 72, and 96 hours and at 7 days postischemia. Twenty hypoxic-ischemic rats showed a considerable variability in brain damage. In 8, there were no MRI-detectable lesions at any interval. In the other 12 rats, the severity and extension of neuronal damage varied markedly, but the lesions were always localized (monolaterally in 8 and bilaterally in 4 rats) in the occipital, temporal, or parietal cerebral cortex. Mainly, they were of intermediate severity or were severe (as assessed by MRI hyperintensity) and were accompanied by usually less severe lesions in the thalamus and/or caudate putamen. The hippocampus was affected moderately or severely in 4 of 12 rats. In most cases, there was at 48 hours a considerable growth in severity and/or extension of lesions, which usually remained stable at later intervals. In conclusion, MRI allowed us to follow brain lesions during the first week in this relatively simple and noninvasive model of transient global ischemia.


Subject(s)
Ischemic Attack, Transient/diagnosis , Magnetic Resonance Imaging/methods , Animals , Brain/anatomy & histology , Electroencephalography , Electrophysiology , Hypoxia/complications , Hypoxia/diagnosis , Hypoxia/physiopathology , Ischemic Attack, Transient/complications , Ischemic Attack, Transient/physiopathology , Longitudinal Studies , Male , Rats , Rats, Inbred F344 , Time Factors
12.
Neurochem Res ; 22(1): 93-100, 1997 Jan.
Article in English | MEDLINE | ID: mdl-9021769

ABSTRACT

Ubiquitin (Ub) is a small 76-residue protein, involved in intracellular protein degradation through a specific ATP-dependent system, which uses Ub as a tag to label proteins committed to be hydrolyzed by a specific 26 S protease. PGP-9.5 is another important component of the Ub system, i.e. a neuron-specific carboxyl-terminal hydrolase, which recycles Ub from Ub-polypeptide complexes. We have investigated the expression of Ub and PGP-9.5 in rat hippocampal neurons in an early phase of reperfusion in a model of transient global brain ischemia/hypoxia (bilateral occlusion of common carotid arteries for 10 min accompanied by mild hypoxia-15% O2-for 20 min), by means of immunohistochemical methods using light and electron microscopy. The intensity of Ub and PGP-9.5 immunoreactivity was evaluated by image analysis. We have detected a marked increase of Ub immunoreactivity (UIR) in neurons of CA1, CA2, CA3, CA4, and dentate gyrus subfields 1 hr after ischemia/hypoxia (but not after hypoxia only), statistically significant as confirmed by image analysis. Such increase in immunoreactivity in ischemic/hypoxic rats was localized essentially in the nuclei of hippocampal neurons. There were no changes in PGP-9.5 immunoreactivity. The data suggest that in the present model of rat brain ischemia/hypoxia Ub is involved in the neuronal stress response.


Subject(s)
Hippocampus/physiopathology , Hypoxia, Brain/physiopathology , Nerve Tissue Proteins/physiology , Reperfusion Injury/physiopathology , Thiolester Hydrolases/metabolism , Ubiquitins/physiology , Animals , Disease Models, Animal , Electroencephalography , Hippocampus/blood supply , Hippocampus/enzymology , Hypoxia, Brain/enzymology , Image Processing, Computer-Assisted , Immunohistochemistry , Male , Microscopy, Electron , Pyramidal Cells/ultrastructure , Rats , Rats, Sprague-Dawley , Reperfusion Injury/enzymology , Ubiquitin Thiolesterase
13.
Neurochem Res ; 21(5): 541-5, 1996 May.
Article in English | MEDLINE | ID: mdl-8726960

ABSTRACT

The influence of hypothyroidism (HO) induced by treatment with propylthiouracil on lipid composition, receptor responsiveness of M1-muscarinic receptors (M1AChRs) and metabotropic glutamate receptors (mGluRs) as well as on protein kinase C (PKC) activity was investigated in the cerebral cortex of Lewis rats. HO did not influence the lipid composition. There was a significant 2-fold increase of efficacy and 6-fold decrease of potency of carbachol-induced inositol phosphate (IP) accumulation in HO, with respect to control rats. The efficacy of trans-(1S,3R)-1-amino-1,3-cyclopentanedicarboxylic acid (ACPD)-induced IP accumulation was also higher in HO (by 50%), without differences in EC50 values. The activities of soluble calcium-dependent and calcium-independent PKC were higher in HO than in control rats (both roughly 30%); membrane-associated PKCs were not modified. The data indicate that HO induces an increased responsiveness of M1AChRs and mGluRs and a rise in the soluble PKC activity that could be available and ready for translocation.


Subject(s)
Cerebral Cortex/metabolism , Hypothyroidism/metabolism , Inositol Phosphates/metabolism , Inositol/metabolism , Protein Kinase C/metabolism , Receptors, Metabotropic Glutamate/physiology , Receptors, Muscarinic/physiology , Animals , Carbachol/pharmacology , Cerebral Cortex/drug effects , Cycloleucine/analogs & derivatives , Cycloleucine/pharmacology , Male , Neurotoxins/pharmacology , Pirenzepine/metabolism , Rats , Rats, Inbred Lew
14.
Neurochem Res ; 21(3): 323-9, 1996 Mar.
Article in English | MEDLINE | ID: mdl-9139238

ABSTRACT

The effects of metabotropic glutamate receptor (mGluR) agonists on inositol phosphates (IP) accumulation were investigated in slices of the cerebral cortex, hippocampus, striatum and cerebellum of adult Sprague-Dawley rats. EC(50) values for 1S, 3R-1-aminocyclopentane-1, 3-dicarboxylic acid (ACPD) did not differ significantly between various brain areas (range 10(-5) M), quisqualate was the most potent in all the brain areas (range 10(-7) - 10(-6) M), except the cerebellum (10(-5) M), ibotenate was the most potent in the striatum (range 10(-6) M) and the least potent in the cerebral cortex and hippocampus (range 10(-4) M). The efficacy in the four brain areas showed the following trend of ranking order for ACPD and quisqualate: hippocampus > striatum > cerebral cortex > cerebellum, and for ibotenate: hippocampus > cerebral cortex > striatum > cerebellum, although the observed differences reached the level of statistical significance only in the case of ACPD (hippocampus and striatum vs cerebellum) and ibotenate (hippocampus vs cerebellum). Co-incubation of the agonists at maximally effective concentrations in any pairwise combination resulted in no substantial additivity of IP accumulation. D,L-1-amino-3-phosphonopropionic acid (AP3) and D,L-2-amino-4-phosphonobutyric acid (AP4) at 0.5 mM concentration antagonized ACPD-induced IP accumulation by about 70 and 45 percent, respectively, without differences between brain areas. On the other hand, the antagonistic effects of L-serine-o-phosphate (SOP) at 1 mM concentration were the highest in the hippocampus (75 percent) and the lowest in the cerebellum (25 percent). The comparative data indicate considerable regional receptor heterogeneity, in terms of different ratios of response to the agonists (but not antagonists, except SOP). There is a robust responsiveness of mGluRs not only in the hippocampus and cerebral cortex, but also in the striatum which exhibits the highest affinity to both quisqualate and ibotenate.


Subject(s)
Brain/metabolism , Cycloleucine/analogs & derivatives , Ibotenic Acid/pharmacology , Neuroprotective Agents/pharmacology , Phosphatidylinositols/metabolism , Quisqualic Acid/pharmacology , Receptors, Metabotropic Glutamate/physiology , Animals , Brain/drug effects , Cerebellum/metabolism , Cerebral Cortex/metabolism , Corpus Striatum/metabolism , Cycloleucine/pharmacology , Dose-Response Relationship, Drug , Hippocampus/metabolism , Hydrolysis , In Vitro Techniques , Kinetics , Male , Organ Specificity , Rats , Rats, Sprague-Dawley , Receptors, Metabotropic Glutamate/drug effects
15.
Brain Res Bull ; 41(4): 193-200, 1996.
Article in English | MEDLINE | ID: mdl-8924028

ABSTRACT

The electric synaptic efficacy, in terms of extracellular electrical potentials, and the intracellular postsynaptic efficacy, in terms of inositol phosphate (IP) accumulation, were evaluated in rat hippocampal slices exposed for a brief period (10 min) to a high concentration of calcium (+2.7 mM). In addition, the effects of N-methyl-D-asparate (NMDA) ionotropic and metabotropic glutamate receptor (mGluR) antagonists on the induction and the establishment or maintenance of enhanced synaptic efficacy of CA1 pyramidal neurons due to high-calcium exposure were also tested. Elevation of the calcium concentration from 1.3-4 mM in the medium bathing hippocampal slices produced a long-lasting (80 over 90 min) increase in the slope of the CA1 somatic excitatory postsynaptic potential and the amplitude of the population spike (PS). Slice perfusion with NMDA antagonists cyclazocine and cis-4-phosphonomethyl-2-piperidine-carboxylic acid (CGS 19755) or with mGluR antagonists L-2-amino-3-phosphonopropionic acid (AP3) or alpha-methyl-4-carboxyphenyl-glycine (all 0.1 mM), during the 10-min period of exposure to high-calcium prevented the induction of such changes. By contrast, slice perfusion with the same concentration of CGS 19755 or L-AP3 did not affect the already established long-lasting increase in amplitude of CA1 PS induced by high-calcium. Moreover, high-calcium failed to produce any significant modification of the basal IP accumulation or of the IP accumulation elicited by mGluR agonist 1S,3R-trans-amino cyclo-pentane-1,3-dicarboxylic acid (ACPD). In conclusion, the results confirm that high-calcium induces a long-lasting increase in synaptic efficacy in rat hippocampal slices. Both NMDA ionotropic and mGluR receptors are involved in the induction, but not in the maintenance, of this phenomenon. In line with these data no modifications of basal or ACPD-induced phosphoinositide hydrolysis have been found during the maintenance stage.


Subject(s)
Calcium/physiology , Glutamic Acid/physiology , Long-Term Potentiation/physiology , Alanine/analogs & derivatives , Alanine/pharmacology , Animals , Brain Chemistry/drug effects , Brain Chemistry/physiology , Cyclazocine/pharmacology , Electrophysiology , Excitatory Amino Acid Agonists/pharmacology , Excitatory Amino Acid Antagonists/pharmacology , In Vitro Techniques , Male , N-Methylaspartate/antagonists & inhibitors , Narcotic Antagonists/pharmacology , Pipecolic Acids/pharmacology , Pyramidal Cells/drug effects , Pyramidal Cells/physiology , Rats , Rats, Sprague-Dawley , Synaptic Transmission/drug effects , Synaptic Transmission/physiology
16.
Neurochem Res ; 19(10): 1311-7, 1994 Oct.
Article in English | MEDLINE | ID: mdl-7891849

ABSTRACT

The effects of a subacute intoxication with diisopropyl fluorophosphate (DPF) on total muscarinic acetylcholine receptor sites (mAChRs) and M-1 AChRs were evaluated in the cerebral cortex of young (2-4 months) and aged (22-24 months) Fischer 344 rats. Since M-1 AChRs are coupled to the metabolism of phosphoinositides, carbachol-induced accumulation of inositol phosphates (IP) and its inhibition by glutamate and NMDA was also measured in the cortical slices. DFP treatment caused about 75% inhibition of cholinesterase and 35% down-regulation of mAChRs (measured as [3H]quinuclidinyl benzylate binding) in both young and aged rats. The down-regulation of M-1-ACHRs (measured as [3H]pirenzepine binding) was more pronounced in aged (30%) than in young (17%) DFP-treated rats. There was a significant increase in carbachol-induced IP accumulation in aged, with respect to young, untreated rats. DFP treatment caused a considerable decrease in such IP accumulation in aged but not in young rats. Glutamate and NMDA antagonized carbachol-induced IP accumulation in untreated young and aged rats (and the effects of NMDA were reversed by carboxy-piperazinyl-propyl phosphonic acid). In DFP-treated rats such antagonism was somewhat less pronounced. The data appear of interest in relation to the use of anticholinesterase compounds in the therapy of senile dementia of Alzheimer's type. They suggest that beside their primary action (increasing brain ACh levels) such compounds also act on post-receptor mechanisms and on the interactions between cholinergic and glutamatergic neurotransmitter systems.


Subject(s)
Aging/metabolism , Carbachol/pharmacology , Cerebral Cortex/drug effects , Excitatory Amino Acids/metabolism , Inositol Phosphates/metabolism , Receptors, Muscarinic/drug effects , Analysis of Variance , Animals , Carbachol/antagonists & inhibitors , Cerebral Cortex/metabolism , Down-Regulation/drug effects , Glutamic Acid/pharmacology , In Vitro Techniques , Isoflurophate/poisoning , Male , N-Methylaspartate/pharmacology , Rats , Rats, Inbred F344 , Syndrome
17.
Neurochem Res ; 19(9): 1181-6, 1994 Sep.
Article in English | MEDLINE | ID: mdl-7824072

ABSTRACT

The effect of hypothyroidism on the lipid composition of synaptosomes, density and affinity of muscarinic receptor sites, and acetylcholinesterase activity in the cerebral cortex of young and aged rats was investigated. The animals were made hypothyroid by adding 0.05% propyl-2-thiouracil to their drinking water for four weeks. This pathological state induced an increase in the relative percentage of sphingomyelin in young rats. In aged rats hypothyroidism induced a decrease of sphingomyelin and glycerophosphocholine and an increase of cholesterol. The effect of hypothyroid state on cerebral cortex resulted in an increase of acethylcholinesterase activity both in young and aged rats and was also reflected in an increase of density of M1-AChRs but only in the former.


Subject(s)
Acetylcholinesterase/metabolism , Cerebral Cortex/metabolism , Hypothyroidism/metabolism , Lipid Metabolism , Receptors, Muscarinic/metabolism , Synaptosomes/metabolism , Acetylcholinesterase/drug effects , Aging/metabolism , Animals , Cerebral Cortex/drug effects , Cerebral Cortex/ultrastructure , Hypothyroidism/chemically induced , Male , Propylthiouracil , Rats , Rats, Inbred Lew , Receptors, Muscarinic/drug effects , Synaptosomes/drug effects
18.
Neurotoxicology ; 15(3): 735-9, 1994.
Article in English | MEDLINE | ID: mdl-7854614

ABSTRACT

The effects of glutamate and N-methyl aspartate (NMDA) on carbachol-induced inositol phosphate (IP) accumulation were evaluated in slices of the cerebral cortex of rats treated with diisopropyl fluorophosphate (DFP) for 2 weeks. This induced an about 75% inhibition of cholinesterases. The IP accumulation induced by carbachol (expressed as ratio stimulated/basal IP content) was lower in DFP rats than in controls when incorporation of [3H]-myoinositol into membrane phospholipids and their hydrolysis were measured (no washing step between labeling and hydrolytic incubation). There were no differences in carbachol induced IP accumulation between control and DFP rats when only phosphoinositide hydrolysis was determined (hydrolytic incubation of prelabeled washed slices). When both incorporation of [3H]-myoinositol and the hydrolysis were measured, 0.5 mM glutamate and 0.1 mM NMDA caused a significant, about 40%, decrease of carbachol-induced IP accumulation in control rats; the inhibitory effects of glutamate and NMDA were not significant in DFP rats. When only hydrolytic IP accumulation by carbachol was studied, the inhibitory effects of glutamate and NMDA were very similar in control and DFP rats. Additional experiments on inositol phospholipid synthesis showed a significantly lesser [3H]-myoinositol incorporation (by about 30%) in DFP rats. This may explain the differences between the results obtained by the two methods. The overall data suggest that the attenuation of glutamate and NMDA effects in DFP-rats depends on a decrease of carbachol-induced IP accumulation or phosphoinositide synthesis rather than on the EAA specific action.


Subject(s)
Carbachol/pharmacology , Cerebral Cortex/drug effects , Glutamic Acid/pharmacology , Isoflurophate/poisoning , N-Methylaspartate/pharmacology , Phosphatidylinositols/metabolism , Animals , Cerebral Cortex/metabolism , In Vitro Techniques , Male , Rats , Rats, Sprague-Dawley
19.
Neurochem Res ; 18(5): 585-9, 1993 May.
Article in English | MEDLINE | ID: mdl-8097298

ABSTRACT

The effects of glutamate, NMDA and quisqualate on carbachol- and norepinephrine-elicited formation of inositol phosphate (IP) were evaluated in slices prepared from the cerebral cortex of 3- and 24-month Sprague-Dawley rats. Glutamate, NMDA, and quisqualate antagonized the IP response to carbachol in a concentration-dependent fashion. This antagonism was more pronounced in aged than in young rats, both for glutamate (IC5O 0.114 and 0.210 mM) and NMDA (IC5O 0.0029 and 0.127 mM), but not for quisqualate. Glutamate (but not NMDA) also antagonized in a concentration-dependent fashion the IP response to norepinephrine, IC50s were 0.061 and 0.126 mM for aged and young rats, respectively; quisqualate had an inhibitory effect only at 1 mM concentration in the two age-groups, while in aged rats some stimulatory effect was present at 0.1 mM concentration. Glutamate, NMDA and quisqualate (1 mM) did not affect basal IP accumulation in either young or aged rats; quisqualate, however, at 0.1 mM concentration had some stimulatory effect, more pronounced in aged rats. This effect was probably responsible for the biphasic effect of quisqualate in this age-group. The most important finding consists of the demonstration of an age-related increase in the inhibitory effects of NMDA on carbachol-induced IP accumulation. This implies an altered modulation of cholinergic post-receptor mechanisms by glutamatergic mechanisms.


Subject(s)
Aging/metabolism , Amino Acids/pharmacology , Cerebral Cortex/metabolism , Inositol Phosphates/metabolism , Animals , Carbachol/pharmacology , Cerebral Cortex/drug effects , Glutamates/pharmacology , Glutamic Acid , Male , N-Methylaspartate/pharmacology , Norepinephrine/pharmacology , Quisqualic Acid/pharmacology , Rats , Rats, Sprague-Dawley
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