Garcinia morella extract confers dopaminergic neuroprotection by mitigating mitochondrial dysfunctions and inflammation in mouse model of Parkinson's disease.
Ankumoni DuttaBanashree Chetia PhukanRubina RoyMuhammed Khairujjaman MazumderRajib PaulAmarendranath ChoudhuryDiwakar KumarPallab BhattacharyaJoyobrato NathSanjeev KumarAnupom BorahPublished in: Metabolic brain disease (2022)
Dopaminergic neuroprotection is the main interest in designing novel therapeutics against Parkinson's disease (PD). In the process of dopaminergic degeneration, mitochondrial dysfunctions and inflammation are significant. While the existing drugs provide symptomatic relief against PD, a therapy conferring total neuroprotection by targeting multiple degenerative pathways is still lacking. Garcinia morella is a common constituent of Ayurvedic medication and has been used for the treatment of inflammatory disorders. The present study investigates whether administration of G. morella fruit extract (GME) in MPTP mouse model of PD protects against dopaminergic neurodegeneration, including the underlying pathophysiologies, and reverses the motor behavioural abnormalities. Administration of GME prevented the loss of dopaminergic cell bodies in the substantia nigra and its terminals in the corpus striatum of PD mice. Subsequently, reversal of parkinsonian behavioural abnormalities, viz. akinesia, catalepsy, and rearing, was observed along with the recovery of striatal dopamine and its metabolites in the experimental model. Furthermore, reduced activity of the mitochondrial complex II in the nigrostriatal pathway of brain of the mice was restored after the administration of GME. Also, MPTP-induced enhanced activation of Glial fibrillary acidic protein (GFAP) and neuronal nitric oxide synthase (nNOS) in the nigrostriatal pathway, which are the markers of inflammatory stress, were found to be ameliorated on GME treatment. Thus, our study presented a novel mode of dopaminergic neuroprotection by G. morella in PD by targeting the mitochondrial dysfunctions and neuroinflammation, which are considered to be intricately associated with the loss of dopaminergic neurons.
Keyphrases
- oxidative stress
- cerebral ischemia
- mouse model
- diabetic rats
- nitric oxide synthase
- brain injury
- nitric oxide
- subarachnoid hemorrhage
- ms ms
- single cell
- traumatic brain injury
- emergency department
- small molecule
- stem cells
- spinal cord
- metabolic syndrome
- mesenchymal stem cells
- white matter
- inflammatory response
- endothelial cells
- high glucose
- lps induced
- binding protein