Open access · CC-BY
via OpenAlex
Mucuna pruriens (Velvet bean) Rescues Motor, Olfactory, Mitochondrial and Synaptic Impairment in PINK1B9 Drosophila melanogaster Genetic Model of Parkinson’s Disease
Simone Poddighe, Francescaelena De Rose, Roberto Marotta, Roberta Ruffilli, Maura Fanti, Pietro Paolo Secci, Maria Cristina Mostallino, Maria Dolores Setzu, Maria Antonietta Zuncheddu, Ignazio Collu, Paolo Solla, Francesco Marrosu, Sanjay Kasture, Elio Acquas, Anna Maria Liscia
PLoS ONE · 2014 · ▲ 58 citations
Abstract
The fruit fly Drosophila melanogaster (Dm) mutant for PTEN-induced putative kinase 1 (PINK1B9) gene is a powerful tool to investigate physiopathology of Parkinson's disease (PD). Using PINK1B9 mutant Dm we sought to explore the effects of Mucuna pruriens methanolic extract (Mpe), a L-Dopa-containing herbal remedy of PD. The effects of Mpe on PINK1B9 mutants, supplied with standard diet to larvae and adults, were assayed on 3-6 (I), 10-15 (II) and 20-25 (III) days old flies. Mpe 0.1% significantly extended lifespan of PINK1B9 and fully rescued olfactory response to 1-hexanol and improved climbing behavior of PINK1B9 of all ages; in contrast, L-Dopa (0.01%, percentage at which it is present in Mpe 0.1%) ameliorated climbing of only PINK1B9 flies of age step II. Transmission electron microscopy analysis of antennal lobes and thoracic ganglia of PINK1B9 revealed that Mpe restored to wild type (WT) levels both T-bars and damaged mitochondria. Western blot analysis of whole brain showed that Mpe, but not L-Dopa on its own, restored bruchpilot (BRP) and tyrosine hydroxylase (TH) expression to age-matched WT control levels. These results highlight multiple sites of action of Mpe, suggesting that its effects cannot only depend upon its L-Dopa content and support the clinical observation of Mpe as an effective medication with intrinsic ability of delaying the onset of chronic L-Dopa-induced long-term motor complications. Overall, this study strengthens the relevance of using PINK1B9 Dm as a translational model to study the properties of Mucuna pruriens for PD treatment.
◌ CITATION ONLY
Full text is not openly licensed for redistribution here. Read it at the source:
Provenance
- Source
- OpenAlex
- DOI
- 10.1371/journal.pone.0110802
- Canonical
- link ↗
- Fetched
- 2026-07-06 MST
Cite this
APA
Poddighe, S., Rose, F.D., Marotta, R., Ruffilli, R., Fanti, M., Secci, P.P., Mostallino, M.C., Setzu, M.D., Zuncheddu, M.A., Collu, I., Solla, P., Marrosu, F., Kasture, S., Acquas, E., & Liscia, A.M. (2014). Mucuna pruriens (Velvet bean) Rescues Motor, Olfactory, Mitochondrial and Synaptic Impairment in PINK1B9 Drosophila melanogaster Genetic Model of Parkinson’s Disease. <em>PLoS ONE</em>. https://doi.org/10.1371/journal.pone.0110802
Vancouver
Poddighe S, Rose FD, Marotta R, Ruffilli R, Fanti M, Secci PP, et al. Mucuna pruriens (Velvet bean) Rescues Motor, Olfactory, Mitochondrial and Synaptic Impairment in PINK1B9 Drosophila melanogaster Genetic Model of Parkinson’s Disease. PLoS ONE. 2014. doi:10.1371/journal.pone.0110802.
BibTeX
@article{simone2014Mucuna,
title = {Mucuna pruriens (Velvet bean) Rescues Motor, Olfactory, Mitochondrial and Synaptic Impairment in PINK1B9 Drosophila melanogaster Genetic Model of Parkinson’s Disease},
author = {Simone Poddighe and Francescaelena De Rose and Roberto Marotta and Roberta Ruffilli and Maura Fanti and Pietro Paolo Secci and Maria Cristina Mostallino and Maria Dolores Setzu and Maria Antonietta Zuncheddu and Ignazio Collu and Paolo Solla and Francesco Marrosu and Sanjay Kasture and Elio Acquas and Anna Maria Liscia},
journal = {PLoS ONE},
year = {2014},
doi = {10.1371/journal.pone.0110802},
}
Research neighborhood
References, citing works, and semantically nearest findings. Click a node to open it.
Related findings
G3 Genes Genomes Genetics 2018
Open access · CC-BY
Shortened Lifespan and Other Age-Related Defects in Bang Sensitive Mutants of <i>Drosophila melanogaster</i>
Genome biology 2013
Open access · CC-BY
DNA methylation of distal regulatory sites characterizes dysregulation of cancer genes
Aging and Disease 2016
Open access · CC-BY
Mitochondrial Dysfunction in Alzheimer’s Disease and the Rationale for Bioenergetics Based Therapies
Acta Neuropathologica 2021
Open access · CC-BY
Mitochondrial bioenergetic deficits in C9orf72 amyotrophic lateral sclerosis motor neurons cause dysfunctional axonal homeostasis
Autophagy 2024
Open access · CC-BY
Poly-GP accumulation due to C9orf72 loss of function induces motor neuron apoptosis through autophagy and mitophagy defects
PLoS ONE 2012
Open access · CC-BY