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Thermodynamic measurements on the organic system of (DI-DCNQI)(2)(Ag(1-x)Cu(x)) (x = 0,0.05, 0.71, 0.90) were performed to study the change from the charge-ordered (CO) insulating state to the π-d hybridized metallic state. A thermal anomaly associated with the antiferromagnetic transition that occurred in the charge-ordered lattice was observed at 6.2 K from the temperature dependence of the heat capacity of (DI-DCNQI)(2)Ag. We have found that the magnetic entropy around the peak is only 1.5% of Rln2, corresponding to the full entropy expected for the formula unit of (DI-DCNQI)(2)Ag. This anomaly is suppressed down to about 3 K in the x = 0.05 sample owing to the disorders induced in the CO lattice. In the metallic concentration of x = 0.90, the low-temperature electronic heat capacity coefficient, γ was found to be enhanced by up to about 63.6 mJ K(-2) mol(-1) probably owing to the cooperative effect of π-d hybridization and intersite Coulomb interaction (V).
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Isobaric heat capacities C p of benzene confined in silica MCM-41 mesopores with average diameters equal to and smaller than 2.9 nm were measured by precise adiabatic calorimetry. The confined benzene samples revealed no thermal anomaly due to crystallization/fusion and vitrified at low temperatures. The C p curves displayed a hump and a considerably quick decrease on the low-temperature side of the hump as the pore diameter increased. The enthalpy-relaxation effects observed on intermittent heating showed that the anomaly of the C p hump and quick decrease is not assigned to a glass transition. The bend in the temperature dependence of density reported previously was interpreted as corresponding to the quick decrease in C p . We concluded that the anomalous C p and density behaviors originated from the ordering/excitation in the configurational state, close to the ground state, of confined molecular aggregate and proposed a scenario that explains the general C p curves of ordinary bulk supercooled liquids in equilibrium at low temperatures below the glass-transition temperatures.
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PURPOSE: To investigate possible associations between the gene number and allelic forms of glutathione S-transferase M1 (GSTM1) and the occurrence of nucleic and cortical age-related cataracts. METHODS: Patients with cortical cataract, nuclear cataract, mixed and cortical cataract, and no cataract were sytematically selected from subjects evaluated in the Italian-American Study of the Natural History of Age-Related Cataract. The patients were typed for the A, B, and null alleles of GSTM1 using a variation of the amplification refractory mutation system. RESULTS: Forty-nine percent of patients (50/102) with cortical cataracts, 45% (13/29) with nuclear cataracts, 51% (36/71) with mixed nuclear and cortical cataracts, and 50% of controls (49/98) were homozygous for the null GSTM1 allele. Twenty-five percent of patients (26/102) with cortical cataracts, 24% (7/29) with nuclear cataracts, 31% with mixed nuclear and cortical cataracts, and 27% of controls (26/98) displayed only the A allele for GSTM1. Twenty-four percent of patients (24/102) with cortical cataract, 24% (7/29) with nuclear cataracts, 14% (10/71) with mixed nuclear and cortical cataract, and 18% of controls showed only the B allele for GSTM1. Two percent of patients (2/102) with cortical cataracts, 7% (2/29) with nuclear cataracts, 4% (3/71) with mixed nuclear and cortical cataracts, and 5% of controls (5/98) showed both A and B alleles for GSTM1. CONCLUSIONS: No associations between the GSTM1 alleles, including the null allele, and cataracts were detected in this study.
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Envelhecimento , Catarata/genética , Glutationa Transferase/genética , Isoenzimas/genética , Idoso , Idoso de 80 Anos ou mais , Alelos , Sequência de Bases , Catarata/etnologia , Catarata/etiologia , Primers do DNA/química , Feminino , Frequência do Gene , Teste de Complementação Genética , Genótipo , Humanos , Itália/etnologia , Masculino , Pessoa de Meia-Idade , Dados de Sequência Molecular , Reação em Cadeia da Polimerase , Fatores de Risco , Estados Unidos/epidemiologiaRESUMO
Recently ultraviolet light (UV) reaching the Earth's surface has been gradually increasing in amounts by the destruction of the ozone layers. Large parts of UV are absorbed in the cornea and lens, and only a few amounts reached the retina; however, the effect on the retina is not fully elucidated. 38 rats were irradiated 0.5-5.0 J/cm2 UV from 6 to 50 times every 24 hours, and immunohistochemically and immunochemically for superoxide dismutases (SOD). Morphologically, the destruction of rod outer segments (ROS) and dissociation of cell membranes between the pigment epithelial cells (PE) were already observed by 6 times 0.5 J/cm2 UV irradiations. As the doses of UV increased, heterochromatins and lipid droplets increased in the PE. In normal retina, Cu/Zn SOD were mainly distributed from the inner limiting membrane (ILM) to the ganglion cell layer, and the PE; however, after 6 times 0.5 J/cm2 UV irradiations, the distribution became widened from inner to outer plexiform layer (OPL). At that time, the concentrations of Cu/Zn and Mn SOD increased in the retina. The present study reveals that the morphological damage caused by UV irradiation is observed in the ROS and PE, where no immunoreactivities could be detected to Cu/Zn and Mn SOD. However, morphological damage was not from the ILM to OPL, where the immunoreactivities to both Cu/Zn and Mn SOD were observed.
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Retina/enzimologia , Retina/efeitos da radiação , Superóxido Dismutase/efeitos da radiação , Animais , Radicais Livres/metabolismo , Heterocromatina/metabolismo , Imuno-Histoquímica , Epitélio Pigmentado Ocular/enzimologia , Epitélio Pigmentado Ocular/efeitos da radiação , Ratos , Ratos Wistar , Células Ganglionares da Retina/enzimologia , Células Ganglionares da Retina/efeitos da radiação , Segmento Externo da Célula Bastonete/enzimologia , Segmento Externo da Célula Bastonete/efeitos da radiação , Superóxido Dismutase/metabolismo , Raios UltravioletaRESUMO
PURPOSE: To report an 8-month-old infant with choroidal osteoma. METHOD: Case report. RESULTS: The patient, who had bilateral yellow stippling at the posterior pole, was followed up for 8 years. Both fundi developed creamy, irregular scalloped lesions. Computed tomography showed a bony plate at the posterior pole bilaterally. CONCLUSION: We believe that this is the youngest patient reported to have choroidal osteoma.
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Neoplasias Ósseas/patologia , Neoplasias da Coroide/patologia , Osteoma/patologia , Corioide/diagnóstico por imagem , Corioide/patologia , Feminino , Seguimentos , Fundo de Olho , Humanos , Lactente , Tomografia Computadorizada por Raios XRESUMO
To identify the major risk factors for the increased incidence of congenital malformations in offspring of mothers being treated for epilepsy with antiepileptic drugs (AEDs) during pregnancy and, to determine the relative teratogenic risk of AEDs, we prospectively analyzed 983 offspring born in Japan, Italy, and Canada. The incidence of congenital malformations in offspring without drug exposure was 3.1%, versus an incidence with drug exposure of 9.0%. The highest incidence in offspring exposed to a single AED occurred with primidone (PRM; 14.3%), which was followed by valproate (VPA; 11.1%), phenytoin (PHT; 9.1%), carbamazepine (CBZ; 5.7%), and phenobarbital (PB; 5.1%). The VPA dose and level positively correlated with the incidence of malformations. This study first determined a cut-off value of VPA dose and level at 1000 mg/day and 70 microg/ml, respectively, to avoid the occurrence of malformations. The incidence of malformations increases as the number of drugs increases, and as the total daily dose increases. Specific combinations of AEDs such as VPA + CBZ and PHT + PRM + PB produced a higher incidence of congenital malformations. The incidence of malformations was not associated with any background factors studied except for the presence of malformations in siblings. These results indicate that the increased incidence of congenital malformations was caused primarily by AEDs, suggesting that malformations can be prevented by improvements in drug regimen, and by avoiding polypharmacy and high levels of VPA (more than 70 microg/ml) in the treatment of epileptic women of childbearimg age.
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Anormalidades Induzidas por Medicamentos , Anticonvulsivantes/efeitos adversos , Anormalidades Induzidas por Medicamentos/epidemiologia , Adulto , Anticonvulsivantes/uso terapêutico , Canadá , Anormalidades Congênitas/epidemiologia , Relação Dose-Resposta a Droga , Quimioterapia Combinada , Feminino , Humanos , Incidência , Itália , Japão , Gravidez , Estudos ProspectivosRESUMO
The aim of the present study was to evaluate the risk of intrauterine growth delay in the offspring of epileptic mothers and to quantify the risks of intrauterine exposure to antiepileptic drugs (AEDs). Data concerning 870 newborns, prospectively collected in Canada, Japan and Italy, using the same study design, were pooled and analyzed. The overall proportion of newborns whose body weight (7.8%) or head circumference (11.1%) at birth were below the 10th percentile was not increased. However, logistic regression analysis showed that the risk of small head circumference was significantly higher in Italian than in Japanese (RR 4.2; 95% CI: 2.2-8.0) or Canadian children (RR 2.6; 95% CI: 1.1-6.5), and in children exposed to polytherapy (RR 2.7; 95% CI: 1.2-6.3), phenobarbital (PB) (RR 3.6; 95% CI: 1.4-9.4) and primidone (PRM) (RR 4.5; 95% CI: 1.5-13.8). Country was also the only factor affecting low body weight, with Italian children having a higher risk than Japanese (RR 5.2; 95% CI: 2.6-10.4) or Canadian (RR 8.8; 95% CI: 2.0-38.1) children. Due to the small categories, the influence of AED doses and plasma concentrations was studied for each individual AED, without adjustment for the other potential confounding factors. A clear dose-dependent effect was found for PB and PRM in terms of both small head circumference and low body weight, and a concentration-dependent effect for PB in terms of small head circumferences. The size of the difference between the Italian and the other two populations, which is only partially explained by differences in therapeutic regimens, suggests that genetic, environmental and ethnic factors also need to be taken into account when considering possible explanations.
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Desenvolvimento Embrionário e Fetal/fisiologia , Epilepsia/fisiopatologia , Complicações na Gravidez/fisiopatologia , Anticonvulsivantes/uso terapêutico , Peso Corporal , Canadá , Quimioterapia Combinada , Epilepsia/tratamento farmacológico , Feminino , Cabeça/anatomia & histologia , Humanos , Recém-Nascido , Itália , Japão , Gravidez , Estudos Prospectivos , Análise de Regressão , Fatores de RiscoRESUMO
We report here a patient with frequent nocturnal attacks, characterized by paroxysmal dystonic posturing of the left arm and contraction of the lower face, lasting 20-30 seconds. The attacks occurred in clusters of up to 20 spasms during the NREM stage of sleep. Interictal EEG showed clear-cut epileptic discharges in the right frontal region. Repeated ictal video-EEG recordings revealed only arousal pattern immediately before and during seizures except in those which evolved to left sided clonic hemiconvulsions. The dystonic attacks here described share many features of nocturnal paroxysmal dystonia (NPD) of Lugaresi and Cirignotta in common, including nocturnal periodic occurrence, absence of ictal EEG changes during attacks, and favorable response to CBZ, except for their unilateral nature. It was assumed that our case may be a lateralized variant of NPD and would further support the hypothesis that NPD is one particular form of frontal lobe epilepsy.
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Distonia/fisiopatologia , Epilepsia do Lobo Frontal/fisiopatologia , Criança , Distonia/complicações , Eletroencefalografia , Epilepsia do Lobo Frontal/complicações , Feminino , Lateralidade Funcional , Humanos , Sono/fisiologiaRESUMO
A study of epileptic drop attacks (EDA) by simultaneous video-polygraphic recordings was carried out in one epileptic patient with myoclonic astatic seizures (Doose syndrome). EDA was shown to correspond to a burst of generalized bilaterally synchronous spike and wave complexes (GBSSW) at 3 Hz. Absence seizures were also observed with a burst of GBSSW with similar characteristics. The amplitudes of the corresponding slow wave component of GBSSW among the three intensities of atonia, i.e. complete atonia, minor atonia and no discernible atonia (control), was compared. A high amplitude was demonstrated to correspond with more pronounced atonia and a lower amplitude with reduced or absent atonia. These findings suggest that EDA corresponding to GBSSW have a neurophysiological mechanism in common with absence seizures, and that if the GBSSW is intense, it may be sufficient to cause immediate loss of global muscle tone.
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Eletroencefalografia , Epilepsia Tipo Ausência/fisiopatologia , Epilepsia Generalizada/fisiopatologia , Mioclonia/fisiopatologia , Pré-Escolar , Eletromiografia , Epilepsia Tipo Ausência/complicações , Epilepsia Generalizada/complicações , Humanos , Masculino , Músculos/fisiopatologia , Mioclonia/complicações , Gravação em VídeoRESUMO
The prevalence of abnormal pregnancy outcomes in the offspring of 103 epileptic women, followed prospectively during pregnancy between 1982 and 1989, was compared with that in the previous study of 119 pregnancies by Dansky et al from the same institution. Our results have shown a significant decrease in the prevalence of major malformations, as compared with the previous study: 8.8% vs 24.1% (P < 0.01). Monotherapy was more frequent and the mean number of drugs used during pregnancy was significantly smaller in the present study. Phenytoin, phenobarbital and primidone were prescribed less frequently in the present study, whereas carbamazepine and valproic acid were used more frequently. Plasma levels of valproic acid during pregnancy were higher in mothers of malformed babies. In the present study, plasma folate levels were significantly higher, and more patients were taking folate supplements during pregnancy. In conclusion, the type and number of drugs used during pregnancy, as well as the plasma concentrations and serum folate levels, may determine the frequency of abnormal outcomes.
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Anticonvulsivantes/uso terapêutico , Epilepsia/tratamento farmacológico , Complicações na Gravidez/tratamento farmacológico , Resultado da Gravidez , Anormalidades Induzidas por Medicamentos/epidemiologia , Aborto Espontâneo/epidemiologia , Adulto , Anticonvulsivantes/efeitos adversos , Anticonvulsivantes/sangue , Epilepsia/complicações , Feminino , Humanos , Gravidez , Estudos Prospectivos , Fatores de RiscoRESUMO
PURPOSE: Calbindin-D 28K (CaD) and parvalbumin (PV) are calcium-binding proteins thought to act as an intraneural calcium ion buffering system in the central nervous system. We previously reported that PV appears at birth in some cells in the outer portion of the nuclear layer of the retina that can differentiate into horizontal cells. CaD is also distributed in horizontal cells; however, it is not clear at which developmental stage CaD appears. METHODS: The development of horizontal cells and the distribution of CaD and PV was examined ultrastructurally and immunohistochemically in rat retinas from birth (P0) to postnatal day 50 (P50). RESULTS: Our ultrastructural data showed clear differentiation of horizontal cells from other retinal cells in the early postnatal days. These cells became nearly mature around P10 to P12. PV appeared in the outer nuclear layer at birth (P0) and, by P7, was observed in the ganglion cell layer, amacrine cells, and horizontal cells. CaD-immunoreactive cells, however, were not seen in any portions of the retina until P7. At P10, CaD-immunoreactivity was faintly observed in horizontal cells, and its immunoreactivity gradually increased in the horizontal cells from P10 to P15 when the eyes of the rats opened. CaD was not found in the ganglion cell layer or in amacrine cells at any period examined. CONCLUSION: In the horizontal cells, PV appeared when they were ultrastructurally distinguished from other retinal cells, while CaD appeared when they already had some structure for endocytosis and synaptic transmission, suggesting that PV and CaD may be good morphological and functional markers for horizontal cells, respectively.
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Proteínas do Olho/análise , Proteínas do Tecido Nervoso/análise , Neurônios/química , Parvalbuminas/análise , Retina/crescimento & desenvolvimento , Animais , Calbindinas , Feminino , Técnicas Imunoenzimáticas , Masculino , Neurônios/ultraestrutura , Ratos , Ratos Wistar , Retina/química , Retina/ultraestrutura , Proteína G de Ligação ao Cálcio S100/análiseRESUMO
Patients with brain damage, especially under malnutrition, sometimes show a disordered thermoregulation. Our case was an 11 year-3-month-old boy with severe brain damage probably of prenatal origin, who was physically extremely small in size for age and showed difficulty of taking food. Low body temperature ranging from 34.0 degrees C to 36.0 degrees C became outstanding since 9 years of age. Continuous rectum temperature monitoring was starged, when he was admitted in our department of pediatrics in Tokyo Women's Medical College Hospital for the therapy of acute infection. Before hospitalization, he took orally only 150 to 200 kcal/day. After the recovery from the infection, a higher calorie diet appropriate for his body weight was given through a nasal tube. Dramatic improvement was observed in terms of sleep pattern, body temperature and thermoregulation after the administration of higher calorie nutrients. It is suggested that the circadian rhythm of the body temperature would be disturbed by chronic malnutrition in children with brain damage.
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Regulação da Temperatura Corporal/fisiologia , Dano Encefálico Crônico/complicações , Hipotermia/terapia , Distúrbios Nutricionais/terapia , Criança , Nutrição Enteral , Humanos , Hipotermia/etiologia , MasculinoRESUMO
The glass transition behavior of hydroxylamine (HA) aqueous solutions in bulk and confined in silica-gel nanopores with average width of 1.1 nm was studied by means of differential scanning calorimetry measurements and adiabatic calorimetry. The glass transition temperature (Tg) of the confined solution with high HA mole-fraction (xHA) was essentially the same as the value of the bulk. This suggests that the nano-size confinement affects the Tg of HA aqueous solution little. Meanwhile, the bulk solution with xHA < 0.3 revealed partial crystallization on cooling and, on the other hand, the confined solution with the same xHA did not crystallize. The Tg of the xHA = 0.076 confined solution was 174 K which is higher than the value of 160 K for pure water confined in the same silica-gel pores. This demonstrates that HA doping leads to no abrupt Tg-decrease, unlike doping of all the other second components reported so far, suggesting that HA is set neatly in a hydrogen-bond network formed by water molecules. We discuss the xHA dependence of Tg for the HA aqueous solutions from a viewpoint related to peculiar phase-behavior of pure water. Considering that the xHA = 0.076 aqueous solution revealed no anomaly compared with pure water, it was recognized as corresponding to the high-temperature phase of pure water.