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1.
Epilepsy Behav ; 36: 68-73, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24857811

ABSTRACT

Statins may act on inflammatory responses, decreasing oxidative stress and also reducing brain inflammation in several brain disorders. Epileptogenesis is a process in which a healthy brain becomes abnormal and predisposed to generating spontaneous seizures. We previously reported that lovastatin could prevent neuroinflammation in pilocarpine-induced status epilepticus (SE). In this context, this study investigated the long-lasting effects of lovastatin on mRNA expression of proinflammatory cytokines (interleukin-1ß, tumor necrosis factor α, interleukin-6) and the antiinflammatory cytokine IL-10 in the hippocampus during epileptogenesis by immunohistochemistry and real time polymerase chain reaction (RT-PCR) during the latent and chronic phases in the epilepsy model induced by pilocarpine in rats. For these purposes, four groups of rats were employed: saline (CONTROL), lovastatin (LOVA), pilocarpine (PILO), and pilocarpine plus lovastatin (PILO+LOVA). After pilocarpine injection (350mg/kg, i.p.), the rats were treated with 20mg/kg of lovastatin via an esophagic probe 2h after SE onset. All surviving rats were continuously treated during 15days, twice/day. The pilocarpine plus lovastatin group showed a significant decrease in the levels of IL-1ß, TNF-α, and IL-6 during the latent phase and a decreased expression of IL-1ß and TNF-α in the chronic phase when compared with the PILO group. Moreover, lovastatin treatment also induced an increased expression of the antiinflammatory cytokine, IL-10, in the PILO+LOVA group when compared with the PILO group in the chronic phase. Thus, our data suggest that lovastin may reduce excitotoxicity during epileptogenesis induced by pilocarpine by increasing the synthesis of IL-10 and decreasing proinflammatory cytokines in the hippocampus.


Subject(s)
Anticholesteremic Agents/pharmacology , Cytokines/metabolism , Epilepsy/pathology , Hippocampus/metabolism , Lovastatin/pharmacology , Animals , Anticholesteremic Agents/therapeutic use , Cytokines/genetics , Disease Models, Animal , Epilepsy/chemically induced , Epilepsy/drug therapy , Gene Expression Regulation/drug effects , Hippocampus/drug effects , Lovastatin/therapeutic use , Male , Muscarinic Agonists/toxicity , Pilocarpine/toxicity , RNA, Messenger/metabolism , Rats , Rats, Wistar
2.
Transl Psychiatry ; 2: e93, 2012 Mar 13.
Article in English | MEDLINE | ID: mdl-22832858

ABSTRACT

We find that a common mutation that increases angiotensin I-converting enzyme activity occurs with higher frequency in male patients suffering from refractory temporal lobe epilepsy. However, in their brains, the activity of the enzyme is downregulated. As an explanation, we surprisingly find that carbamazepine, commonly used to treat epilepsy, is an inhibitor of the enzyme, thus providing a direct link between epilepsy and the renin-angiotensin and kallikrein-kinin systems.


Subject(s)
Angiotensin-Converting Enzyme Inhibitors/pharmacology , Anticonvulsants/pharmacology , Carbamazepine/pharmacology , Epilepsy, Temporal Lobe/physiopathology , Peptidyl-Dipeptidase A/physiology , Alleles , Animals , Anterior Temporal Lobectomy , Disease Models, Animal , Dose-Response Relationship, Drug , Epilepsy, Temporal Lobe/genetics , Epilepsy, Temporal Lobe/pathology , Epilepsy, Temporal Lobe/surgery , Genotype , Humans , INDEL Mutation , Male , Mice , Mice, Inbred C57BL , Peptidyl-Dipeptidase A/genetics , Polymorphism, Genetic/genetics , Temporal Lobe/drug effects , Temporal Lobe/pathology
3.
Epilepsy Res ; 82(1): 46-56, 2008 Nov.
Article in English | MEDLINE | ID: mdl-18760902

ABSTRACT

Amado and Cavalheiro [Amado, D., Cavalheiro, E.A., 1998. Hormonal and gestational parameters in female rats submitted to the pilocarpine model of epilepsy. Epilepsy Res. 32, 266-274], studying the establishment of the pilocarpine epilepsy model in female rats observed that the estrous cycle was dramatically altered during the three periods of this experimental model. This work was delineated to study the function of sexual hormones in the development of the epilepsy model induced by pilocarpine in ovariectomized rats. Experimental groups were: (a) control animals during estrus phase of the estrous cycle (E) and ovariectomized female rats (OVX) treated with saline instead of pilocarpine in the same volume, (b) experimental animals, that developed status epilepticus (SE) and were studied during the chronic phase of this model: intact chronic rats (CHRON) and ovariectomized chronic rats (OVX+CHRON) and (c) ovariectomized chronic rats, that were submitted to hormonal replacement therapy treated with: medroxyprogesterone (OVX+CHRON+MPA); 17beta-estradiol (OVX+CHRON+E2), or both (OVX+CHRON+E2+MPA). All ovariectomized animals showed genital atrophy 4 days after the surgical procedure. Moreover, all animals that developed SE and survived showed spontaneous recurrent seizures during the chronic phase. Concerning to seizure frequency, animals receiving medroxyprogesterone associated with 17beta-estradiol showed decreased seizures' number. However, animals that received only medroxyprogesterone therapy also showed reduction in the number of seizures. In addition, hormonal treatment was also able to stabilize the mossy fibers sprouting process, showing the importance of these hormones in the development of the epilepsy in female rats.


Subject(s)
Epilepsy, Generalized/physiopathology , Estradiol/pharmacology , Gonadal Steroid Hormones/physiology , Hippocampus/drug effects , Hormone Replacement Therapy , Medroxyprogesterone/pharmacology , Animals , Epilepsy, Generalized/chemically induced , Estradiol/administration & dosage , Estradiol/therapeutic use , Estrus , Female , Hippocampus/physiopathology , Hypogonadism/complications , Hypogonadism/drug therapy , Hypogonadism/etiology , Medroxyprogesterone/administration & dosage , Medroxyprogesterone/therapeutic use , Mossy Fibers, Hippocampal/drug effects , Mossy Fibers, Hippocampal/ultrastructure , Ovariectomy/adverse effects , Pilocarpine/toxicity , Rats , Rats, Wistar
4.
Int Immunopharmacol ; 8(7): 1056-8, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18486918

ABSTRACT

Glossodynia or burning mouth syndrome is a multifunctional disorder. The oral mucosa is apparently normal but patients report burning and dried mouth and painful tongue and lips. The present study reports biochemical and physiological markers in saliva of patients presenting glossodynia compared to normal subjects. Saliva-buffering capacity and contents of protein and hyaluronic (HA) acid were similar in both groups. In contrast, chondroitin sulfate (CS) concentration was decreased in the saliva of patients with glossodynia when compared to control group (p=0.0036). On the other hand glandular kallikrein showed increased activity in the saliva of patients compared to normal subjects (p<0.0001). The data suggest involvement of the kinin system, possibly related to the low levels of CS. Depression could explain the low level of serotonin in patient serum (p=0.0478).


Subject(s)
Chondroitin Sulfates/analysis , Glossalgia/diagnosis , Kallikreins/analysis , Saliva/chemistry , Biomarkers , Glossalgia/metabolism , Humans
5.
Int Immunopharmacol ; 8(2): 197-9, 2008 Feb.
Article in English | MEDLINE | ID: mdl-18182226

ABSTRACT

Kinins may play a relevant role in epilepsy. In the present study, we evaluated the hippocampal expression of the remaining kinin receptor in B1 (B1KO) and B2 (B2KO) knockout mice strains during the development of pilocarpine epilepsy model. After pilocarpine injection, animals had their behavior parameters monitored to determine different phases of temporal lobe epilepsy (TLE) progression. Hippocampal mRNA expression was evaluated using specific primers for kinin receptors by Real Time-PCR. B1KO hippocampus from acute, silent and chronic phases showed no differences in B2 receptor mRNA expression when compared to control. An increased B1 receptor mRNA expression in treated B2KO hippocampus (0.97+/-0.12, acute; 0.86+/-0.09, silent; and 0.94+/-0.11, chronic phase; p<0,001) when compared to control (0.12+/-0.03) was observed. Behavioral and neurochemistry parameters suggest that kinin B1 receptor is fundamental to development of epilepsy on pilocarpine-induced model.


Subject(s)
Epilepsy, Temporal Lobe/etiology , Receptor, Bradykinin B1/physiology , Animals , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , RNA, Messenger/analysis , Receptor, Bradykinin B1/genetics , Receptor, Bradykinin B2/genetics , Receptor, Bradykinin B2/physiology
6.
Neurosci Res ; 51(3): 285-91, 2005 Mar.
Article in English | MEDLINE | ID: mdl-15710492

ABSTRACT

Nestin is an embryonic intermediate filament component protein, transiently expressed by the immediate precursor cells of neurons and glia, during brain development. We studied the nestin distribution in the hippocampal formation of rats submitted to pilocarpine model of epilepsy. Animals were studied during the acute, silent and chronic phases. Rats from control and acute groups presented absence of nestin-immunoreactivity (IR) in the hippocampal cells. In contrast, cells from this region presented strong nestin IR during the silent phase (3 and 7 days after status epilepticus (SE) onset), disappearing 14 days after SE. Nestin IR cells were scattered expressed in all hippocampal formation during the chronic phase. Almost all nestin IR cells exhibited glial fibrillary acidic protein (GFAP), which seems to revert to a more primitive glial form, as part of an adaptive response, transiently re-expressing phenotypic features typical of earlier stages of glial development. The re-expression of this developmental protein in the damaged cerebral tissue suggests that nestin may play an important role in the reconstruction of the glial cytoskeleton and/or remodeling events occurring in the pilocarpine model of epilepsy. Understanding how astrocytes influence network function in the injured hippocampus may, therefore, provide insight into epileptogenic mechanisms.


Subject(s)
Epilepsy/metabolism , Gene Expression Regulation/drug effects , Hippocampus/metabolism , Intermediate Filament Proteins/metabolism , Nerve Tissue Proteins/metabolism , Pilocarpine , Animals , Behavior, Animal , Disease Models, Animal , Epilepsy/chemically induced , Glial Fibrillary Acidic Protein/metabolism , Hippocampus/drug effects , Immunohistochemistry/methods , Male , Muscarinic Agonists , Nestin , Rats , Rats, Wistar
7.
Brain Res Bull ; 58(5): 509-16, 2002 Sep 15.
Article in English | MEDLINE | ID: mdl-12242104

ABSTRACT

Extracellular matrix proteoglycans (PGs) and glycosaminoglycans (GAGs) play a crucial role in cell differentiation and synaptogenesis by modulating neurite outgrowth. The chondroitin sulfate (CS)-rich PG, the receptor protein tyrosine phosphatase zeta/beta (RPTP zeta/beta), has been related to neural morphogenesis and axon guidance. Hippocampal sclerosis is the most frequent pathologic finding in patients with intractable mesial temporal lobe epilepsy (MTLE), which is associated with neuron loss, reactive gliosis, and mossy fiber sprouting. In the present study, we investigated the concentration of CS, heparan sulfate (HS) and hyaluronic acid (HA) in the hippocampus and temporal neocortex as well as RPTP zeta/beta expression in the hippocampus of patients with MTLE. Compared to autopsy control tissue, epileptic hippocampi showed a significantly increased concentration of CS (224%; p=0.0109) and HA (146%; p=0.039). HS was instead similar to control values. No differences were found in the concentration of CS, HS, or HA in the temporal neocortex of epileptic patients when compared to control values. In contrast, RPTP zeta/beta immunoreactivity was induced in astrocytes of the inner molecular layer of the dentate gyrus of the sclerotic hippocampus. Because matrix compounds have been associated with tissue injury and repair, the present findings suggest that changes in PGs and GAGs might be related to damage-induced gliosis and neuronal reorganization in the hippocampus of MTLE patients.


Subject(s)
Epilepsy, Temporal Lobe/metabolism , Glycosaminoglycans/metabolism , Hippocampus/metabolism , Proteoglycans/biosynthesis , Adult , Cerebral Cortex/metabolism , Cerebral Cortex/pathology , Chondroitin Sulfates/metabolism , Epilepsy, Temporal Lobe/pathology , Heparitin Sulfate/metabolism , Hippocampus/pathology , Humans , Hyaluronic Acid/metabolism , Nerve Tissue Proteins/biosynthesis , Protein Tyrosine Phosphatases/biosynthesis , Receptor-Like Protein Tyrosine Phosphatases, Class 5 , Sclerosis
8.
Epilepsia ; 43 Suppl 5: 159-61, 2002.
Article in English | MEDLINE | ID: mdl-12121313

ABSTRACT

PURPOSE: This work studied the profile of glycosaminoglycans (GAGs) in the hippocampus, cortex, and cerebrospinal fluid of patients with temporal lobe epilepsy (TLE). METHODS: The GAGs were analyzed by agarose gel electrophoresis, enzymatic degradation, and enzyme-linked immunosorbent assay (ELISA). RESULTS: The hippocampus of TLE patients showed increased levels of chondroitin sulfate and hyaluronic acid against normal levels of these GAGs in the neocortex and cerebrospinal fluid (CSF). CONCLUSIONS: These results suggest that these matrix components could be involved in the pathophysiology of TLE.


Subject(s)
Cerebral Cortex/metabolism , Cerebrospinal Fluid/metabolism , Epilepsy, Temporal Lobe/metabolism , Extracellular Matrix/metabolism , Glycosaminoglycans/metabolism , Hippocampus/metabolism , Chondroitin Sulfates/metabolism , Heparitin Sulfate/metabolism , Humans , Hyaluronic Acid/metabolism
9.
Epilepsia ; 43 Suppl 5: 227-9, 2002.
Article in English | MEDLINE | ID: mdl-12121326

ABSTRACT

PURPOSE: This study was performed to study the role of adenosine triphosphate (ATP) in the brain of pilocarpine-induced chronic epileptic rats. METHODS: ATP-mediated changes in intracellular calcium were studied by the fura-2 method. Immunohistochemistry and Western blotting methods were used to localize and quantify P2X7 receptors in these animals. RESULTS: The fluorimetric study in chronic rats revealed a biphasic response indicating the presence of P2X7 receptors. The Western blotting study showed an increase of 80% of P2X7 expression in chronic rats compared with the control group. P2X7 immunoreactivity resembled mossy fiber sprouting at the dentate gyrus of epileptic animals. CONCLUSIONS: These results suggest that purinergic receptors may participate in the pathophysiology of temporal lobe epilepsy.


Subject(s)
Adenosine Triphosphate/metabolism , Convulsants , Epilepsy, Temporal Lobe/chemically induced , Epilepsy, Temporal Lobe/physiopathology , Pilocarpine , Adenosine Triphosphate/pharmacology , Animals , Blotting, Western , Epilepsy, Temporal Lobe/pathology , Fluorometry , Hippocampus/drug effects , Hippocampus/pathology , Hippocampus/physiopathology , Immunohistochemistry , In Vitro Techniques , Rats , Receptors, Purinergic P2/metabolism , Receptors, Purinergic P2X7 , Reference Values
10.
Epilepsy Res ; 49(3): 181-8, 2002 May.
Article in English | MEDLINE | ID: mdl-12076839

ABSTRACT

Previous studies have shown that the susceptibility to pilocarpine-induced status epilepticus (SE) in female rats changes according to estrous cycle phases. These studies have also shown that following pilocarpine administration changes occur in gonadal, hypophyseal and hypothalamic hormones that could contribute for the sequence of the epileptic events. Accordingly, the present work aimed to investigate the role of sexual hormones withdrawal on the development of the pilocarpine model of epilepsy in female rats. With this purpose, castrated and non-castrated adult female Wistar rats were injected with pilocarpine and some characteristic parameters of the experimental model were observed. The results showed increased mortality after pilocarpine injection in the castrated rats when compared with non-castrated females. The latency period for SE onset and for the first spontaneous seizure was decreased in castrated when compared with non-castrated animals. The mossy fiber sprouting measured by neo-Timm scale during the chronic period, reached grade 3 for castrated epileptic rats while the non-castrated epileptic rats showed grade 2. Our results indicate that castration interferes with the epileptogenesis in the pilocarpine model of epilepsy suggesting that female sexual hormones could have protective effects against pilocarpine-induced SE.


Subject(s)
Disease Models, Animal , Epilepsy/chemically induced , Ovariectomy/adverse effects , Pilocarpine/adverse effects , Animals , Epilepsy/metabolism , Epilepsy/prevention & control , Female , Hippocampus/metabolism , Rats , Rats, Wistar
11.
Epilepsy Res ; 46(2): 121-8, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11463513

ABSTRACT

The relationship between free radical and scavenger enzymes has been found in the epileptic phenomena and reactive oxygen species have been implicated in seizure-induced neurodegeneration. Using the epilepsy model obtained by systemic administration of pilocarpine (PILO) in rats, we investigated the superoxide dismutase (SOD) and glutathione peroxidase (GPx) activities as well as the hydroperoxide (HPx) concentration in the hippocampus of rats during status epilepticus (SE), silent and chronic periods. The enzyme activities as well as the HPx concentration were measured using spectrophotometric methods and the results compared to values obtained from saline-treated animals. The SOD activity decreased after long-lasting SE period and during the chronic phase. In addition, HPx levels increased in same periods whereas the GPx activity increased only in the hippocampus of animals submitted to 1 h of SE. Animals presenting partial seizures, those submitted to 5 h of SE and animals from the silent period (seizure free) showed normal levels of SOD, GPx and HPx. These results show a direct evidence of lipid peroxidation during seizure activity that could be responsible for neuronal damage in the hippocampus of rats, during the establishment of PILO model of epilepsy.


Subject(s)
Epilepsy/metabolism , Glutathione Peroxidase/metabolism , Hippocampus/metabolism , Hydrogen Peroxide/metabolism , Superoxide Dismutase/metabolism , Animals , Chronic Disease , Epilepsy/chemically induced , Male , Muscarinic Agonists , Osmolar Concentration , Pilocarpine , Rats , Rats, Wistar , Status Epilepticus/chemically induced , Status Epilepticus/metabolism
12.
Braz J Med Biol Res ; 33(8): 913-8, 2000 Aug.
Article in English | MEDLINE | ID: mdl-10920433

ABSTRACT

The purpose of this study was to investigate the effect of the level of injury on the serum level of norepinephrine (Nor) and epinephrine (Epi) at rest and after maximal exercise in individuals with paraplegia. Twenty-six male spinal cord-injured subjects with complete paraplegia for at least 9 months were divided into two groups of 13 subjects each according to the level of injury, i.e., T1-T6 and T7-T12. Serum Nor and Epi concentrations were measured by HPLC-ECD, at rest (PRE) and immediately after a maximal ergospirometric test (POST). Statistical analysis was performed using parametric and non-parametric tests. Maximal heart rate, peak oxygen uptake, and PRE and POST Nor were lower in the T1-T6 than in the T7-T12 group (166 +/- 28 vs 188 +/- 10 bpm; 18.0 +/- 6.0 vs 25.8 +/- 4.1 ml kg(-1) min(-1); 0.54 +/- 0.26 vs 0.99 +/- 0.47 nM; 1.48 +/- 1. 65 vs 3.07 +/- 1.44 nM). Both groups presented a significant increase in Nor level after exercise, while only the T7-T12 group showed a significant increase in Epi after exercise (T1-T6: 0.98 +/- 0.72 vs 1.11 +/- 1.19 nM; T7-T12: 1.24 +/- 1.02 vs 1.89 +/- 1.57 nM). These data show that individuals with paraplegia above T6 have an attentuated catecholamine release at rest and response to exercise as compared to subjects with injuries below T6, which might prevent a better exercise performance in the former group.


Subject(s)
Epinephrine/blood , Norepinephrine/blood , Paraplegia/blood , Adolescent , Adult , Biomarkers/blood , Child , Chromatography, High Pressure Liquid , Exercise Test , Exercise Tolerance , Heart Rate , Humans , Male , Middle Aged , Rest , Severity of Illness Index , Spinal Cord Injuries/complications , Statistics, Nonparametric
13.
Braz. j. med. biol. res ; 33(8): 913-8, Aug. 2000. tab
Article in English | LILACS | ID: lil-265848

ABSTRACT

The purpose of this study was to investigate the effect of the level of injury on the serum level of norepinephrine (Nor) and epinephrine (Epi) at rest and after maximal exercise in individuals with paraplegia. Twenty-six male spinal cord-injured subjects with complete paraplegia for at least 9 months were divided into two groups of 13 subjects each according to the level of injury, i.e., T1-T6 and T7-T12. Serum Nor and Epi concentrations were measured by HPLC-ECD, at rest (PRE) and immediately after a maximal ergospirometric test (POST). Statistical analysis was performed using parametric and non-parametric tests. Maximal heart rate, peak oxygen uptake, and PRE and POST Nor were lower in the T1-T6 than in the T7-T12 group (166 Ý 28 vs 188 Ý 10 bpm; 18.0 Ý 6.0 vs 25.8 Ý 4.1 ml kg-1 min-1; 0.54 Ý 0.26 vs 0.99 Ý 0.47 nM; 1.48 Ý 1.65 vs 3.07 Ý 1.44 nM). Both groups presented a significant increase in Nor level after exercise, while only the T7-T12 group showed a significant increase in Epi after exercise (T1-T6: 0.98 Ý 0.72 vs 1.11 Ý 1.19 nM; T7-T12: 1.24 Ý 1.02 vs 1.89 Ý 1.57 nM). These data show that individuals with paraplegia above T6 have an attentuated catecholamine release at rest and response to exercise as compared to subjects with injuries below T6, which might prevent a better exercise performance in the former group


Subject(s)
Humans , Male , Child , Adolescent , Adult , Middle Aged , Catecholamines/blood , Epinephrine/blood , Exercise Test , Norepinephrine/blood , Paraplegia/blood , Rest , Chromatography, High Pressure Liquid , Exercise Tolerance , Heart Rate , Severity of Illness Index , Spinal Cord Injuries/complications , Statistics, Nonparametric
14.
Brain Res Bull ; 50(4): 229-39, 1999 Nov 01.
Article in English | MEDLINE | ID: mdl-10582521

ABSTRACT

Proteoglycans and glycosaminoglycans are elements of matrix. In the nervous system, glycosaminoglycans modulate neurite outgrowth and are co-receptors for growth factors playing a crucial role in cell differentiation and synaptogenesis. The receptor of protein tyrosine phosphatase beta (RPTPbeta) is a chondroitin sulphate proteoglycan which plays an important role in neural morphogenesis and axon guidance mechanisms. Pilocarpine-treated rats present status epilepticus, which is followed by a seizure-free period (silent), by a period of spontaneous recurrent seizures (chronic), and the hippocampus of these animals exhibits cell loss and mossy fiber sprouting. Thus, the synthesis of heparan sulphate and chondroitin sulphate and the time course of RPTPbeta immunoreactivity were studied in the hippocampus and cerebral cortex during these phases of pilocarpine-induced epilepsy. The results showed decreased synthesis of heparan sulphate during the acute phase and an increased synthesis of chondroitin sulphate during the silent period in the cortex and hippocampus. In control rats RPTPbeta immunoreactivity was detected only in glial cells. After 6 h of status epilepticus the RPTPbeta immunoreactivity was no longer detectable in the glial cells in both tissues and intense staining became evident in the matrix, surrounding CA3 and dentate gyrus and piriform cortex neurones. In the silent and chronic periods RPTPbeta immunoreactivity was mainly detected in neuronal somata and fibers of neurones of hippocampus and cortex. These changes show a selective variation of synthesis and expression of glycosaminoglycans and RPTPbeta in relation to epilepsy suggesting a molecular interplay between glia and neurones during seizures.


Subject(s)
Cerebral Cortex/metabolism , Epilepsy/metabolism , Glycosaminoglycans/biosynthesis , Hippocampus/metabolism , Pilocarpine/toxicity , Proteoglycans/biosynthesis , Animals , Chondroitin Sulfates/biosynthesis , Epilepsy/chemically induced , Heparitin Sulfate/biosynthesis , Male , Nerve Tissue Proteins/analysis , Protein Tyrosine Phosphatases/analysis , Rats , Rats, Wistar , Reaction Time/physiology , Receptor-Like Protein Tyrosine Phosphatases, Class 5 , Status Epilepticus/metabolism
15.
Neuroscience ; 91(2): 485-92, 1999.
Article in English | MEDLINE | ID: mdl-10366005

ABSTRACT

Neuroplasticity has been investigated considering the neuronal growth-associated phosphoprotein as a marker of neuronal adaptive capabilities. In the present work, studying the hippocampal reorganization observed in the epilepsy model induced by pilocarpine, we carried out quantitative western blotting associated with immunohistochemistry to determine the distribution of growth-associated phosphoprotein in the hippocampus of rats in acute, silent and chronic periods of this epilepsy model. The fibers and punctate elements from the inner molecular layer of the dentate gyrus were strongly immunostained in animals killed 5 h after status epilepticus, compared with the same region in control animals. Rats presenting partial seizures showed no alterations in the immunostaining pattern compared with saline-treated animals. The hippocampal dentate gyrus of animals during the seizure-free period and presenting spontaneous recurrent seizures was also characterized by strong growth-associated phosphoprotein immunostaining of fibers and punctate elements in the inner molecular layer, contrasting with the control group. As determined by western blotting analysis, growth-associated phosphoprotein levels increased following status epilepticus and remained elevated at the later time-points, both during the silent period and during the period of chronic recurring seizures. Pilocarpine-treated animals, which did not develop status epilepticus, showed no change in growth-associated phosphoprotein levels, indicating that status epilepticus is important to induce growth-associated phosphoprotein overexpression. The measurement of this overexpression could represent one of the early signals of hippocampal reorganization due to status epilepticus-induced damage.


Subject(s)
Dentate Gyrus/metabolism , Epilepsies, Partial/metabolism , GAP-43 Protein/metabolism , Phosphoproteins/metabolism , Pilocarpine/pharmacology , Seizures/metabolism , Animals , Dentate Gyrus/drug effects , Epilepsies, Partial/chemically induced , Immunohistochemistry , Male , Rats , Rats, Wistar , Reference Values , Seizures/chemically induced , Time Factors
16.
Brain Res Bull ; 47(3): 223-9, 1998 Oct.
Article in English | MEDLINE | ID: mdl-9865854

ABSTRACT

Systemic administration of pilocarpine (PILO) in adult rat produces acute limbic seizures leading to status epilepticus. Recent studies have shown the activation of mitogen-activated protein kinase (MAPK) cascades during experimentally induced seizures. MAPK activation may be triggered by glutamatergic stimulation and may play a key role in signal transduction pathways. In the present study, immunocytochemistry was used to analyze the spatiotemporal distribution pattern of the MAPK protein and its active form (A-MAPK) following PILO-induced status epilepticus. MAPK and A-MAPK immunoreactivities exhibited different patterns of distribution in the brain of normal and epileptic rats. The saline-treated rats, as well as the animals that received PILO but did not evolve to status epilepticus, showed a weak but selective MAPK immunoreactivity, detected in the hippocampal pyramidal neurons, dentate gyrus, hilus, CA3, CA1, and entorhinal, piriform, and cingulate cortices. A-MAPK immunoreactivity was instead observed only in neurites of the CA3 and hilus and in cells of the entorhinal and piriform cortices. In PILO-treated rats, between 30 and 60 min after status epilepticus there was an increase of the immunoreactivity to both antibodies, which were differently distributed throughout several structures of the limbic system. The immunostaining showed a slight decrease after 5 h of status epilepticus. However, MAPK and A-MAPK immunopositivities decreased markedly after 12 h of status epilepticus, returning almost to the basal expression. These findings are consistent with a spatial and time-dependent MAPK expression in selected limbic structures, and its activation could represent an initial trigger for neuronal modifications that may take part in the mechanism underlying acute epileptogenesis and in long-lasting neuropathological changes of the PILO model of epilepsy.


Subject(s)
Calcium-Calmodulin-Dependent Protein Kinases/metabolism , Limbic System/enzymology , Status Epilepticus/enzymology , Animals , Cell Count , Immunohistochemistry , Limbic System/pathology , Male , Neurons/enzymology , Neurons/pathology , Phosphorylation , Rats , Rats, Wistar , Status Epilepticus/pathology , Time Factors , Tissue Distribution
17.
Brain Res Bull ; 47(1): 87-93, 1998 Sep 01.
Article in English | MEDLINE | ID: mdl-9766394

ABSTRACT

Phosphorylation of tyrosine residue in proteins is an important modulatory process for membrane transduction and cell signaling and for several cellular functions. The concentration and distribution of phosphotyrosine proteins were analyzed in the hippocampi of rats in the model of epilepsy induced by pilocarpine using Western blotting and immunohistochemistry. The concentration of several phosphotyrosine proteins increased during status epilepticus. During the seizure-free period and the chronic period of this epilepsy model, the hippocampi of rats did not exhibit changes in the expression of these proteins. Immunohistochemistry showed an increased immunoreactivity throughout the hippocampal formation of rats 1 h after status epilepticus that was acutely induced by pilocarpine. Animals killed after 3 h of status epilepticus showed an increased expression of phosphotyrosine in the hippocampal hilus and CA3 regions. After 5 h of status epilepticus, phosphotyrosine immunoreactivity persisted only in the CA3 region. After 12 h of status epilepticus, the hippocampal formation exhibited a normal phosphotyrosine immunostaining, showing that the increased expression of these proteins is related to the acute phase and that several intracellular events could undergo modifications during the status epilepticus induced by pilocarpine.


Subject(s)
Hippocampus/drug effects , Pilocarpine/toxicity , Protein-Tyrosine Kinases/metabolism , Status Epilepticus/metabolism , Animals , Blotting, Western , Disease Models, Animal , Hippocampus/metabolism , Immunohistochemistry , Male , Phosphorylation , Rats , Rats, Wistar , Status Epilepticus/chemically induced
18.
Spinal Cord ; 36(1): 18-20, 1998 Jan.
Article in English | MEDLINE | ID: mdl-9471132

ABSTRACT

The purpose of this study was to evaluate the serum level of serotonin (5-HT) during rest and response to exercise in subjects with spinal cord injury (SCI) with different levels of physical activity. Twenty-five male subjects with traumatic paraplegia, the neurological levels being between T1 and T12, volunteered for the study. They were divided into two groups matched for age, weight and time since injury, according to the level of physical activity: 14 inactive and 11 subjects regularly involved in sports activity and considered active. They all performed a maximal spiroergometric test with an arm crank ergometer. Two samples of blood were collected for 5-HT determination, during rest (PRE) and immediately after exercise test (POST). Serum 5-HT concentration was measured by high performance liquid chromatography using electrochemical detection (HPLC-ED). The results showed that peak oxygen uptake (VO2peak) was higher in the active group (27.08 +/- 2.60 vs 18.89 +/- 5.58 mL.kg-1.min-1, P < 0.001). There were no significant differences between the inactive and active groups for the 5-HT PRE (respectively 176.96 and 193.73 ng.mL - 1, P > 0.05) or POST values (275.44 vs 311.05 ng.mL-1, P > 0.05). Both groups showed an increment in 5-HT after maximal exercise, but only in the active group it reached statistical significance (Wilcoxon test, P < 0.02). Our results show that chronic paraplegic individuals have normal resting serum serotonin levels and normal response to exercise. The relationship between training status, mood elevation and 5-HT in SCI could not be established in the present study, and further investigation is needed to clarify this issue.


Subject(s)
Exercise/physiology , Paraplegia/blood , Rest/physiology , Serotonin/blood , Adult , Chromatography, High Pressure Liquid , Electrochemistry , Ergometry , Exercise Test , Humans , Male , Oxygen Consumption/physiology
19.
Epilepsy Res ; 25(2): 133-7, 1996 Oct.
Article in English | MEDLINE | ID: mdl-8884171

ABSTRACT

The involvement of monoamines in the initiation or maintenance of epileptic phenomena has been extensively studied in cerebral tissues and in cerebrospinal fluid. The present work was undertaken to study monoamines and their metabolites in human spiking and non-spiking temporal cortex excised from patients with complex partial seizures unresponsive to available anticonvulsants. The same substances were also analyzed by HPLC-ED in cerebrospinal fluid obtained 24 h before the surgical procedure and compared with those from patients with chronic headache and normal neurological evaluation. The results show increased 5-HT, 5-HIAA and HVA levels in spiking compared with non-spiking cortex. Cerebrospinal fluid levels of 5-HIAA and HVA are concomitantly increased in epileptic compared with headache patients.


Subject(s)
Biogenic Monoamines/cerebrospinal fluid , Epilepsy, Complex Partial/metabolism , Temporal Lobe/metabolism , Adult , Biogenic Monoamines/metabolism , Female , Humans , Male
20.
Rev. Hosp. Säo Paulo Esc. Paul. Med ; 7(1/2): 40-4, Jan.-Jun. 1996. ilus
Article in English | LILACS | ID: lil-201441

ABSTRACT

The important of a large number of proteins involved in chronic diseases has been reported. In the present study the phosphoprotein GAP-43 was focused due to its relationship with chronic diseases such as epilepsy Alzheimer's disease, cerebral ischemia and phusiological events like long-term potentiation (LTP).


Subject(s)
Humans , Animals , Chronic Disease , Alzheimer Disease , Brain Ischemia , Epilepsy
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