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1.
Graefes Arch Clin Exp Ophthalmol ; 252(3): 433-9, 2014 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-24390400

RESUMEN

BACKGROUND: To evaluate the effect of intracameral lidocaine anesthesia on macular thickness and macular ganglion cell-inner plexiform layer (GC-IPL) thickness following uneventful phacoemusification in healthy subjects. METHODS: This is a prospective, randomized and double- masked study. One hundred eyes of 74 consecutive patients were randomized to receive intracameral preservative-free lidocaine 1 % (intracameral lidocaine group) or intracameral injection of balanced salt solution (sham injection group) at the time of the phacoemulsification surgery. Preoperative and postoperative macular thickness analyses with spectral domain optical coherence tomography (SD-ODT) were performed and the results between the two groups were compared. RESULTS: Postoperatively, both the central foveal thickness (CFT) and the thickness of perifoveal macula were significantly improved in both groups (p < 0.001). There was no statistically significant difference between CFT and the inner and outer macular zone thicknesses of the two groups at any follow-up time. In both groups, GC-IPL thickness was significantly increased at the first week and first month visits (p < 0.001). There was no statistically significant difference between GC-IPL thickness measurements of the two groups at any follow-up time. CONCLUSION: The current study demonstrated that supplementary intracameral lidocaine 1 % did not cause more macular thickening than the intracameral sham injection during a follow-up period of 3 months. The present study also showed a tendency for a transient increase in high definition SD-OCT-based GC-IPL thickness measurements within a few months following cataract surgery under both intracameral lidocaine anesthesia and intracameral sham injection.


Asunto(s)
Anestesia Local/métodos , Anestésicos Locales/administración & dosificación , Lidocaína/administración & dosificación , Mácula Lútea/anatomía & histología , Facoemulsificación , Células Bipolares de la Retina/citología , Células Ganglionares de la Retina/citología , Anciano , Anciano de 80 o más Años , Cámara Anterior/efectos de los fármacos , Método Doble Ciego , Femenino , Humanos , Inyecciones Intraoculares , Implantación de Lentes Intraoculares , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Tomografía de Coherencia Óptica , Agudeza Visual/fisiología
2.
PLoS One ; 7(8): e43074, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-22900092

RESUMEN

Saffron, an extract from Crocus sativus, has been largely used in traditional medicine for its antiapoptotic and anticarcinogenic properties. In this work, we investigate the effects of safranal, a component of saffron stigmas, in attenuating retinal degeneration in the P23H rat model of autosomal dominant retinitis pigmentosa. We demonstrate that administration of safranal to homozygous P23H line-3 rats preserves both photoreceptor morphology and number. Electroretinographic recordings showed higher a- and b-wave amplitudes under both photopic and scotopic conditions in safranal-treated versus non-treated animals. Furthermore, the capillary network in safranal-treated animals was preserved, unlike that found in untreated animals. Our findings indicate that dietary supplementation with safranal slows photoreceptor cell degeneration and ameliorates the loss of retinal function and vascular network disruption in P23H rats. This work also suggests that safranal could be potentially useful to retard retinal degeneration in patients with retinitis pigmentosa.


Asunto(s)
Crocus/química , Ciclohexenos/farmacología , Fármacos Neuroprotectores/farmacología , Retina/efectos de los fármacos , Degeneración Retiniana/tratamiento farmacológico , Terpenos/farmacología , Animales , Comunicación Celular/efectos de los fármacos , Ciclohexenos/administración & dosificación , Modelos Animales de Enfermedad , Fármacos Neuroprotectores/administración & dosificación , Células Fotorreceptoras/citología , Células Fotorreceptoras/efectos de los fármacos , Ratas , Retina/patología , Células Bipolares de la Retina/citología , Células Bipolares de la Retina/efectos de los fármacos , Degeneración Retiniana/fisiopatología , Células Horizontales de la Retina/citología , Células Horizontales de la Retina/efectos de los fármacos , Retinitis Pigmentosa/tratamiento farmacológico , Retinitis Pigmentosa/fisiopatología , Transmisión Sináptica/efectos de los fármacos , Terpenos/administración & dosificación
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