Rodríguez Villanueva Javier, de la Villa Pedro, Herrero-Vanrell Rocío, Bravo-Osuna Irene, Guzmán-Navarro Manuel
Unidad Docente de Farmacia y Tecnología Farmacéutica, Departamento de Ciencias Biomédicas, Facultad de Farmacia, Universidad de Alcalá, Ctra. de Madrid-Barcelona A-2, Km. 33,600, 28871 Alcalá de Henares, Spain.
Departamento de Biología de Sistemas, Facultad de Medicina, Universidad de Alcalá, Ctra. de Madrid-Barcelona A-2, Km. 33,600, 28871 Alcalá de Henares, Spain.
Pharmaceutics. 2024 Mar 15;16(3):406. doi: 10.3390/pharmaceutics16030406.
Excitotoxicity has been linked to the pathogenesis of several serious degenerative ocular diseases. Long-term overactivation of the NMDA receptor by glutamate in retinal ganglion cells (RGCs) results in degeneration, apoptosis and loss of function leading to blindness. NMDA receptor antagonists have been proposed as a pharmacological blockage of glutamate excitotoxicity. However, an inhibition of the pathway activated by glutamate receptors has intolerable side effects. An interesting pharmacological alternative would be the use of antiapoptotic compounds as RGCs' neuroprotective active substances. Several mechanisms have been proposed to explain neuroprotection, including anti-inflammatory and scavenging activities. Here, the role of dexamethasone in neuroprotection was studied. For this purpose, original controlled release systems composed of microparticles containing dexamethasone with or without vitamin E and human serum albumin (HSA) were designed. The particles were prepared by the solid-in-oil-in-water (S/O/W) emulsion-evaporation technique. After properly characterization of the particles, they were intravitreally injected into an rat model of acute ocular excitotoxicity injury. The functionality of the retina was determined by electroretinography and RGCs were counted after cell immunohistochemistry. These microparticulate systems showed the ability to maintain normal electroretinal activity and promoted significant protection of RGCs. Through this proof of concept, we demonstrated that dexamethasone could be a useful anti-inflammatory agent to avoid the progression of degenerative ocular diseases. Furthermore, when administered in controlled release systems that provide low concentrations during prolonged periods of time, not only can the patient's comfort be increased but the cytotoxicity of the drugs can also be avoided.
兴奋性毒性与几种严重的退行性眼病的发病机制有关。视网膜神经节细胞(RGCs)中谷氨酸对NMDA受体的长期过度激活会导致细胞退化、凋亡和功能丧失,进而导致失明。NMDA受体拮抗剂已被提议作为对谷氨酸兴奋性毒性的药理学阻断剂。然而,抑制谷氨酸受体激活的途径会产生难以忍受的副作用。一种有趣的药理学替代方法是使用抗凋亡化合物作为RGCs的神经保护活性物质。已经提出了几种机制来解释神经保护作用,包括抗炎和清除活性。在此,研究了地塞米松在神经保护中的作用。为此,设计了由含有地塞米松以及有或没有维生素E和人血清白蛋白(HSA)的微粒组成的新型控释系统。通过水包油包固体(S/O/W)乳液蒸发技术制备微粒。在对微粒进行适当表征后,将其玻璃体内注射到急性眼兴奋性毒性损伤的大鼠模型中。通过视网膜电图测定视网膜的功能,并在细胞免疫组织化学后对RGCs进行计数。这些微粒系统显示出维持正常视网膜电图活性的能力,并对RGCs具有显著的保护作用。通过这个概念验证,我们证明了地塞米松可能是一种有用的抗炎剂,可避免退行性眼病的进展。此外,当以控释系统给药时,在较长时间内提供低浓度药物,不仅可以提高患者的舒适度,还可以避免药物的细胞毒性。