A Proline Derivative-Enriched Fraction from Sideroxylon obtusifolium Protects the Hippocampus from Intracerebroventricular Pilocarpine-Induced Injury Associated with Status Epilepticus in Mice.
Pedro Everson Alexandre de AquinoJéssica Rabelo BezerraTyciane de Souza NascimentoJuliete TavaresI Rosal LustosaAdriano José Maia Chaves FilhoMelina MottinDanielle Silveira MacêdoGeanne Matos de AndradeKelly Rose Tavares NevesGiuseppe BiaginiEdilberto Rocha SilveiraGlauce Socorro de Barros VianaPublished in: International journal of molecular sciences (2020)
The N-methyl-(2S,4R)-trans-4-hydroxy-l-proline-enriched fraction (NMP) from Sideroxylon obtusifolium was evaluated as a neuroprotective agent in the intracerebroventricular (icv) pilocarpine (Pilo) model. To this aim, male mice were subdivided into sham (SO, vehicle), Pilo (300 µg/1 µL icv, followed by the vehicle per os, po) and NMP-treated groups (Pilo 300 µg/1 µL icv, followed by 100 or 200 mg/kg po). The treatments started one day after the Pilo injection and continued for 15 days. The effects of NMP were assessed by characterizing the preservation of cognitive function in both the Y-maze and object recognition tests. The hippocampal cell viability was evaluated by Nissl staining. Additional markers of damage were studied-the glial fibrillary acidic protein (GFAP) and the ionized calcium-binding adaptor molecule 1 (Iba-1) expression using, respectively, immunofluorescence and western blot analyses. We also performed molecular docking experiments revealing that NMP binds to the γ-aminobutyric acid (GABA) transporter 1 (GAT1). GAT1 expression in the hippocampus was also characterized. Pilo induced cognitive deficits, cell damage, increased GFAP, Iba-1, and GAT1 expression in the hippocampus. These alterations were prevented, especially by the higher NMP dose. These data highlight NMP as a promising candidate for the protection of the hippocampus, as shown by the icv Pilo model.
Keyphrases
- cerebral ischemia
- poor prognosis
- molecular docking
- binding protein
- high glucose
- diabetic rats
- cognitive impairment
- oxidative stress
- prefrontal cortex
- subarachnoid hemorrhage
- molecular dynamics simulations
- brain injury
- working memory
- blood brain barrier
- drug induced
- metabolic syndrome
- type diabetes
- endothelial cells
- bone marrow
- ultrasound guided
- dna binding
- spinal cord
- double blind
- water soluble