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Investigation of the neuroprotective effects of a novel synthetic compound via the mitochondrial pathway.
- Source :
-
Molecular medicine reports [Mol Med Rep] 2017 Aug; Vol. 16 (2), pp. 1133-1138. Date of Electronic Publication: 2017 Jun 09. - Publication Year :
- 2017
-
Abstract
- The present study aimed to investigate the neuroprotective effect of a novel synthetic compound (5zou) on differentiated PC12 cells against 6‑hydroxydopamine (6‑OHDA) and L‑glutamic acid (L‑Glu) neurotoxin‑induced cell injury and the potential mechanisms involved. 5zou is a 2, 2‑disubstituted 1,2‑dihydropyridine. PC12 cells were treated with 6‑OHDA and L‑Glu to establish neurotoxic cell models. MTT assay, DCFH‑DA staining, Fluo‑4‑AM staining, JC‑1 staining and western blotting were used to determine the changes in cell viability, intracellular reactive oxygen species concentration, Ca2+ influx, mitochondrial membrane potential and the protein expressions of B‑cell lymphoma‑2 (Bcl‑2) and B‑cell lymphoma‑extra large (Bcl‑xL). Morphological analysis demonstrated the effect of 5zous on neuritogenesis and differentiation in PC12 cells. The results suggested that 5zou rescued the cell viability, intracellular ROS level, Ca2+ influx, mitochondrial membrane potential, and expression of Bcl‑2 and Bcl‑xL, which were altered by 6‑OHDA and L‑Glu. The study confirmed that 5zou has neuroprotective effects on neurotoxin‑induced differentiated PC12 cells injury, potentially via the mitochondrial apoptosis pathway.
- Subjects :
- Animals
Calcium metabolism
Cell Differentiation drug effects
Cell Nucleus Shape drug effects
Cell Survival drug effects
Glutamic Acid
Membrane Potential, Mitochondrial drug effects
Mitochondria drug effects
Neuroprotective Agents chemistry
Neurotoxins toxicity
Oxidopamine
PC12 Cells
Rats
Reactive Oxygen Species metabolism
bcl-X Protein metabolism
Mitochondria metabolism
Neuroprotective Agents pharmacology
Signal Transduction drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1791-3004
- Volume :
- 16
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Molecular medicine reports
- Publication Type :
- Academic Journal
- Accession number :
- 28627694
- Full Text :
- https://doi.org/10.3892/mmr.2017.6745