Cilastatin as a Potential Anti-Inflammatory and Neuroprotective Treatment in the Management of Glaucoma.
Miguel A Martínez-LópezSara Rubio-CasadoDiego San FelipeBeatriz Martín-SánchezJose A Fernández-AlbarralElena Salobrar-GarciaJosé A MatamorosJosé M RamírezRosa de de HozJuan J SalazarEva M MarcoAna I RamírezAlberto LazaroMeritxell López-GallardoPublished in: International journal of molecular sciences (2024)
Glaucoma is a neurodegenerative disease that causes blindness. In this study, we aimed to evaluate the protective role of cilastatin (CIL), generally used in the treatment of nephropathologies associated with inflammation, in an experimental mouse model based on unilateral (left) laser-induced ocular hypertension (OHT). Male Swiss mice were administered CIL daily (300 mg/kg, i.p.) two days before OHT surgery until sacrifice 3 or 7 days later. Intraocular Pressure (IOP), as well as retinal ganglion cell (RGC) survival, was registered, and the inflammatory responses of macroglial and microglial cells were studied via immunohistochemical techniques. Results from OHT eyes were compared to normotensive contralateral (CONTRA) and naïve control eyes considering nine retinal areas and all retinal layers. OHT successfully increased IOP values in OHT eyes but not in CONTRA eyes; CIL did not affect IOP values. Surgery induced a higher loss of RGCs in OHT eyes than in CONTRA eyes, while CIL attenuated this loss. Similarly, surgery increased macroglial and microglial activation in OHT eyes and to a lesser extent in CONTRA eyes; CIL prevented both macroglial and microglial activation in OHT and CONTRA eyes. Therefore, CIL arises as a potential effective strategy to reduce OHT-associated damage in the retina of experimental mice.
Keyphrases
- diabetic rats
- optical coherence tomography
- oxidative stress
- optic nerve
- diabetic retinopathy
- induced apoptosis
- cataract surgery
- minimally invasive
- inflammatory response
- lipopolysaccharide induced
- blood pressure
- insulin resistance
- cell proliferation
- stem cells
- risk assessment
- mesenchymal stem cells
- high fat diet induced
- acute coronary syndrome
- spinal cord injury
- blood brain barrier
- metabolic syndrome
- atrial fibrillation
- combination therapy
- endoplasmic reticulum stress
- skeletal muscle
- high glucose
- drug induced
- endothelial cells