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Auton Neurosci ; 105(1): 1-7, 2003 Apr 30.
Artigo em Inglês | MEDLINE | ID: mdl-12742185

RESUMO

Urodynamic and pharmacological studies were performed to investigate the effect of crystalluria on the micturition reflex and the involvement of glutamatergic transmission. The rats, which were given LP-805 (100 mg/kg/day) orally for 12 days, voided crystalluria. The pH of these crystalluria (LP-805 urine) was the same as normal urine. The amount of crystals was 70-100/division magnified 400 x. The end of the crystals was sharp. Intravesical administration of LP-805 urine induced hyperreflexia of the micturition reflex in normal rats. When the infusion solution was changed to LP-805 urine from saline, the latency was reduced to 57.6+/-2.1% of control in single cystometrogram (CMG) or was reduced to 51.4+/-0.9% of control in continuous CMG. The voiding volume was reduced to 52.1+/-3.6% of control in single CMG or was reduced to 62.5+/-0.8% of control in continuous CMG. These parameters were recovered after LP-805 urine was removed. Intravesical administration of acetic acid did not induce hyperreflexia of the micturition reflex in LP-805-treated rats. These data suggest that the chronic irritation by aculeate crystals might induce hyperreflexia of the micturition reflex, which increase afferent neuronal activity. Intravenous administration of MK-801 (0.001 to 1 mg/kg) inhibited the micturition reflex in a dose-dependent manner. The ID50 in LP-805-treated rats (0.03 mg/kg i.v.) was lower than that in normal rats (0.56 mg/kg i.v.). After chronic irritation of the bladder epithelium, MK-801 sensitivity was enhanced for the micturition reflex. These data suggested that crystalluria elicit hyperreflexia in the micturition reflex that mediated with NMDA glutamatergic receptors.


Assuntos
Cistite Intersticial/tratamento farmacológico , Maleato de Dizocilpina/uso terapêutico , Micção/efeitos dos fármacos , Animais , Doença Crônica , Cristalização , Cistite Intersticial/induzido quimicamente , Maleato de Dizocilpina/farmacologia , Relação Dose-Resposta a Droga , Feminino , Pirazóis/toxicidade , Pirimidinas/toxicidade , Ratos , Ratos Wistar , Receptores de N-Metil-D-Aspartato/antagonistas & inibidores , Receptores de N-Metil-D-Aspartato/fisiologia , Reflexo/efeitos dos fármacos , Reflexo/fisiologia , Doenças da Bexiga Urinária/induzido quimicamente , Doenças da Bexiga Urinária/tratamento farmacológico , Micção/fisiologia
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