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1.
J Clin Neurosci ; 16(4): 601-2, 2009 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-19201613

RESUMEN

Aneurysms of the penetrating branches of the middle cerebral artery are rare. Previous reports have concentrated on aneurysms that arise from the distal lenticulostriate artery where the natural history is unclear. Here, we report a case of a ruptured aneurysm located at the insular penetrating branch of the right middle cerebral artery, which was associated with an external capsular haematoma. The aneurysm persisted as shown by angiography at one month and the patient refused surgical treatment at that stage. Follow-up angiography two years later showed resolution of the aneurysm. The aetiologies and treatment options are reviewed.


Asunto(s)
Aneurisma Roto/patología , Aneurisma Intracraneal/patología , Arteria Cerebral Media/patología , Adulto , Aneurisma Roto/complicaciones , Angiografía Cerebral/métodos , Humanos , Aneurisma Intracraneal/complicaciones , Masculino , Tomografía Computarizada por Rayos X/métodos
2.
Ann Trop Med Parasitol ; 99(1): 61-70, 2005 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-15701257

RESUMEN

The histomorphology of granuloma formation and gelatinase production were investigated in the brains, hearts, lungs and livers of Sprague-Dawley rats infected with Angiostrongylus cantonensis. The relationships between two gelatinases and granulomatous fibrosis were explored, following infection of each rat with 60 infective larvae of the nematode. Worm recovery from the brain was maximal on day 15 post-inoculation whereas peak recovery from the lungs was maximal 75 days later, on day 90. The granulomatous reactions and fibrosis were marked in the lungs but only mild, if present at all, in the brain, heart and liver. Gelatin zymography revealed that matrix metalloproteinase2 (MMP-2) was present, at all time-points, in the heart and lungs, although only in the lungs was there partial conversion of the 72-kDa pro-enzyme to the 64-kDa active form during granulomatous fibrosis. The activity of the MMP-9 pro-enzyme was significantly higher at the time-points when granuloma formation was observed than at other times. Immuno-histochemistry revealed MMP-2 and MMP-9 within the lung granulomas, around infiltrating leucocytes and the epithelial cells of the alveoli. As the granulomatous fibrosis appeared to be strongly associated with MMP-2 and MMP-9, these enzymes may be useful markers in the lungs of rats infected with A. cantonensis.


Asunto(s)
Angiostrongylus cantonensis/enzimología , Granuloma/enzimología , Metaloproteinasa 2 de la Matriz/análisis , Metaloproteinasa 9 de la Matriz/análisis , Angiostrongylus cantonensis/aislamiento & purificación , Animales , Encéfalo/enzimología , Encéfalo/parasitología , Fibrosis , Corazón/parasitología , Hígado/enzimología , Hígado/parasitología , Pulmón/enzimología , Pulmón/parasitología , Masculino , Miocardio/enzimología , Fibrosis Pulmonar/enzimología , Fibrosis Pulmonar/parasitología , Ratas , Ratas Sprague-Dawley , Infecciones por Strongylida/enzimología , Infecciones por Strongylida/patología
3.
Parasitol Res ; 94(5): 321-8, 2004 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-15449178

RESUMEN

Induction of gelatinase in eosinophilic meningitis of BALB/c-strain mice was caused by Angiostrongylus cantonensis. Time-course studies showed that the molecular weight of 94-kDa gelatinase was detected at day 10 post-inoculation (PI), and reached a high intensity from days 15 to 25 PI. The 94-kDa gelatinase activity was clearly inhibited by EDTA and 1,10-phenanthroline, but not by leupeptin and phenylmethanesulphonyl fluoride. When immunoblots were performed using specific antiserums against the 94-kDa gelatinase B (matrix metalloproteinase-9; MMP-9) with cerebrospinal fluid (CSF), the 94-kDa immunopositive band was MMP-9. Immunohistochemistry studies demonstrated MMP-9 localisation within eosinophils and macrophages. The increased MMP-9 activity was closely associated with the rapid rise of CSF eosinophils, and the inflammatory reaction of the subarachnoid space. In contrast to changes in MMP-9, MMP-2 activity was constitutive and unaffected in this parasitic meningitis. These results show that MMP-9 was associated with eosinophilic meningitis, and that the enzyme may be a useful marker for angiostrongyliasis meningitis.


Asunto(s)
Angiostrongylus cantonensis/patogenicidad , Eosinofilia/parasitología , Metaloproteinasa 9 de la Matriz/metabolismo , Meningitis/parasitología , Infecciones por Strongylida/parasitología , Animales , Masculino , Ratones , Ratones Endogámicos BALB C , Espacio Subaracnoideo/inmunología , Espacio Subaracnoideo/metabolismo
4.
Ann Trop Med Parasitol ; 98(8): 831-41, 2004 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-15667715

RESUMEN

Matrix metalloproteinase-9 (MMP-9) has been implicated in the pathogenesis of eosinophilic meningitis caused by Angiostrongylus cantonensis. In the present study, such meningitis in mice was found to be associated with elevated expression of MMP-9 mRNA, elevated MMP-9 concentrations and enhanced MMP-9 activity in the cerebrospinal fluid (CSF). Immunocytochemistry showed that an anti-MMP-9 antibody reacted with macrophages, neutrophils and eosinophils from the CSF. As eosinophils are generally considered to be effector cells in host defence against A. cantonensis infection, high-resolution immuno-electron microscopy was then used to confirm the localization of MMP-9 in the eosinophils from the CSF. The method used, which was based on immunogold, indicated that the eosinophilic MMP-9 was mostly localized in the 'small' granules in the cytoplasm and along the cell membrane, and not in the crystalloid-containing secretory granules observed. It therefore appears that MMP-9 is synthesised and/or stored in the small granules of the eosinophils, and is released into the subarachnoid space of the host's brain by secretion or cell rupture.


Asunto(s)
Angiostrongylus cantonensis , Líquido Cefalorraquídeo/enzimología , Eosinofilia/enzimología , Eosinófilos/enzimología , Metaloproteinasa 9 de la Matriz/análisis , Meningitis/enzimología , Infecciones por Strongylida/complicaciones , Animales , Líquido Cefalorraquídeo/citología , Eosinofilia/etiología , Eosinofilia/patología , Eosinófilos/ultraestructura , Masculino , Meningitis/etiología , Meningitis/patología , Ratones , Ratones Endogámicos BALB C , Microscopía Electrónica/métodos , Microscopía Inmunoelectrónica/métodos , Infecciones por Strongylida/enzimología , Infecciones por Strongylida/patología
5.
Shock ; 16(2): 153-8, 2001 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-11508869

RESUMEN

The authors tested the hypothesis in a rat model that hypervolemic hemodilution during heatstroke affected the mean arterial pressure (MAP), striatal dopamine (DA) release, and local cerebral blood flow and neuronal damage score in different brain structures. The heatstroke was induced by exposing the urethane-anesthetized rats to an ambient temperature of 42 degrees C. Hypervolemic hemodilution was produced by intravenous administration of 10% human albumin. Relative and absolute blood flow in the corpus striatum were determined using the laser Doppler flowmetry and the autoradiography diffusible tracer technique, respectively. The DA release in the striatum was estimated using the in vivo microdialysis technique. After onset of heatstroke, animals with hypervolemic state alone, produced by saline or heparinized blood injection, displayed higher values of DA release, as well as neuronal damage score in the striatum, hypothalamus, or cortex, but lower values of MAP and blood flow in the striatum, hypothalamus, or cortex compared to normothermic controls. However, the heatstroke-induced arterial hypotension, cerebral ischemia, increased striatal DA overload, and increased neuronal damage score were attenuated by induction of both hypervolemic and hemodilution state with 10% albumin either before or after the onset of heatstroke. In addition, constant infusions of a vasopressor agent phenylephrine (2 microg kg(-1) min(-1)) after the onset of heatstroke failed to maintain appropriate levels of MAP and resulted in no protection against heatstroke. Thus, it appears that the observed benefit of the 10% albumin is secondary to hemodilution and/or maintenance of MAP.


Asunto(s)
Golpe de Calor/fisiopatología , Hemodilución , Análisis de Varianza , Animales , Temperatura Corporal , Dióxido de Carbono/sangre , Cuerpo Estriado/irrigación sanguínea , Cuerpo Estriado/patología , Modelos Animales de Enfermedad , Haloperidol/uso terapéutico , Golpe de Calor/sangre , Golpe de Calor/prevención & control , Monitoreo Fisiológico , Neuronas/patología , Oxígeno/sangre , Presión Parcial , Ratas , Ratas Wistar , Flujo Sanguíneo Regional , Tasa de Supervivencia , Factores de Tiempo
6.
J Biochem ; 110(5): 732-6, 1991 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-1783603

RESUMEN

The effects of melittin on the bilayer-to-inverted hexagonal (HII) phase transition of egg phosphatidylethanolamine (EPE) and the influence of the phase state of membrane matrix on hydrolysis of EPE by phospholipases have been studied. The phase transitions were measured using the fluorescent probe N-(7-nitro-2,1,3-benzoxadiazol-4-yl)phosphatidylethanolamine (N-NBD-PE) and differential scanning calorimetry. In the presence of melittin at a lipid-to-melittin molar ratio (R1) of 200, 100, and 20, the phase transition of EPE disappeared, indicating that melittin stabilizes the bilayer structure. In the presence of 10 mol% of cholesterol, the phase transition temperature (TH) decreased and TH was observed even in the presence of melittin at R1 of 200 and 100. The fluorescence intensity of the tryptophan residue of melittin is sensitive to the phase transition and the wavelength of emission maxima shift from 352 to 337 nm upon addition of EPE and EPE-cholesterol (10 mol%) at R1 of 200. Kinetic parameters for phospholipase-catalyzed hydrolysis of EPE in bilayer and HII phases showed that HII phase of EPE is a poorer substrate for phospholipases and that cholesterol decreases the susceptibility of EPE to phospholipases.


Asunto(s)
Meliteno/farmacología , Fosfatidiletanolaminas/química , Fosfolipasas/química , Estabilidad de Enzimas/efectos de los fármacos , Hidrólisis , Cinética , Membrana Dobles de Lípidos/antagonistas & inhibidores , Fosfatidiletanolaminas/farmacología , Fosfolipasas/efectos de los fármacos , Espectrometría de Fluorescencia
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