Neuroprotective Effect of Sterculia setigera Leaves Hydroethanolic Extract.
Yendubé T KantatiMagloire K KodjoBenjamin LefrancMagali Basille-DugaySébastien HupinValentina CalabreseJérôme LeprinceMessanvi GbeassorDavid VaudryPublished in: Journal of molecular neuroscience : MN (2024)
Plants are a valuable source of information for pharmacological research and new drug discovery. The present study aimed to evaluate the neuroprotective potential of the leaves of the medicinal plant Sterculia setigera. In vitro, the effect of Sterculia setigera leaves dry hydroethanolic extract (SSE) was tested on cultured cerebellar granule neurons (CGN) survival when exposed to hydrogen peroxide (H 2 O 2 ) or 6-hydroxydopamine (6-OHDA), using the viability probe fluorescein diacetate (FDA), a lactate dehydrogenase (LDH) activity assay, an immunocytochemical staining against Gap 43, and the quantification of the expression of genes involved in apoptosis, necrosis, or oxidative stress. In vivo, the effect of intraperitoneal (ip) injection of SSE was assessed on the developing brain of 8-day-old Wistar rats exposed to ethanol neurotoxicity by measuring caspase-3 activity on cerebellum homogenates, the expression of some genes in tissue extracts, the thickness of cerebellar cortical layers and motor coordination. In vitro, SSE protected CGN against H 2 O 2 and 6-OHDA-induced cell death at a dose of 10 µg/mL, inhibited the expression of genes Casp3 and Bad, and upregulated the expression of Cat and Gpx7. In vivo, SSE significantly blocked the deleterious effect of ethanol by reducing the activity of caspase-3, inhibiting the expression of Bax and Tp53, preventing the reduction of the thickness of the internal granule cell layer of the cerebellar cortex, and restoring motor functions. Sterculia setigera exerts neuroactive functions as claimed by traditional medicine and should be a good candidate for the development of a neuroprotective treatment against neurodegenerative diseases.
Keyphrases
- poor prognosis
- cell death
- oxidative stress
- hydrogen peroxide
- binding protein
- genome wide
- optical coherence tomography
- nitric oxide
- cell cycle arrest
- dna damage
- healthcare
- cerebral ischemia
- multiple sclerosis
- long non coding rna
- stem cells
- transcription factor
- gene expression
- diabetic rats
- high throughput
- ischemia reperfusion injury
- functional connectivity
- dna methylation
- endothelial cells
- spinal cord
- subarachnoid hemorrhage
- endoplasmic reticulum stress
- pi k akt
- anti inflammatory
- spinal cord injury
- brain injury
- single molecule
- cell therapy
- living cells
- heat shock protein
- bioinformatics analysis
- stress induced
- flow cytometry