Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2023 Jan 9:16:1084493.
doi: 10.3389/fnins.2022.1084493. eCollection 2022.

Small molecules to perform big roles: The search for Parkinson's and Huntington's disease therapeutics

Affiliations
Review

Small molecules to perform big roles: The search for Parkinson's and Huntington's disease therapeutics

Rodrigo Pérez-Arancibia et al. Front Neurosci. .

Abstract

Neurological motor disorders (NMDs) such as Parkinson's disease and Huntington's disease are characterized by the accumulation and aggregation of misfolded proteins that trigger cell death of specific neuronal populations in the central nervous system. Differential neuronal loss initiates the impaired motor control and cognitive function in the affected patients. Although major advances have been carried out to understand the molecular basis of these diseases, to date there are no treatments that can prevent, cure, or significantly delay the progression of the disease. In this context, strategies such as gene editing, cellular therapy, among others, have gained attention as they effectively reduce the load of toxic protein aggregates in different models of neurodegeneration. Nevertheless, these strategies are expensive and difficult to deliver into the patients' nervous system. Thus, small molecules and natural products that reduce protein aggregation levels are highly sought after. Numerous drug discovery efforts have analyzed large libraries of synthetic compounds for the treatment of different NMDs, with a few candidates reaching clinical trials. Moreover, the recognition of new druggable targets for NMDs has allowed the discovery of new small molecules that have demonstrated their efficacy in pre-clinical studies. It is also important to recognize the contribution of natural products to the discovery of new candidates that can prevent or cure NMDs. Additionally, the repurposing of drugs for the treatment of NMDs has gained huge attention as they have already been through clinical trials confirming their safety in humans, which can accelerate the development of new treatment. In this review, we will focus on the new advances in the discovery of small molecules for the treatment of Parkinson's and Huntington's disease. We will begin by discussing the available pharmacological treatments to modulate the progression of neurodegeneration and to alleviate the motor symptoms in these diseases. Then, we will analyze those small molecules that have reached or are currently under clinical trials, including natural products and repurposed drugs.

Keywords: Huntington's disease; Parkinson's disease; drug repurposing; natural products; pharmacological therapy; small molecules.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Targets of small molecules in neurodegenerative motor disorders. Synthetic small molecules (A), small molecules from natural sources (B) or Repurposing FDA-approved drugs (C) used to alleviate clinical symptoms of Parkinson's disease (blue box) or Huntington's disease (orange box). These molecules participate in modified specific cellular pathways related to alleviating or delaying the neurodegenerative process, as protein aggregation, inflammatory response (inflammosome), cellular differentiation, G protein coupled receptor, calcium channel activity or reactive oxygen species (ROS) production.

Similar articles

Cited by

References

    1. Achenbach J., Saft C. (2021). Another perspective on Huntington's disease: disease burden in family members and pre-manifest HD when compared to genotype-negative participants from ENROLL-HD. Brain Sci. 11, 1621. 10.3390/brainsci11121621 - DOI - PMC - PubMed
    1. Aldewachi H., Al-Zidan R. N., Conner M. T., Salman M. M. (2021). High-throughput screening platforms in the discovery of novel drugs for neurodegenerative diseases. Bioengineering 8, 30. 10.3390/bioengineering8020030 - DOI - PMC - PubMed
    1. Ammal Kaidery N., Tarannum S., Thomas B. (2013). Epigenetic landscape of Parkinson's disease: emerging role in disease mechanisms and therapeutic modalities. Neurotherapeutics 10, 698–708. 10.1007/s13311-013-0211-8 - DOI - PMC - PubMed
    1. Apostol B. L., Illes K., Pallos J., Bodai L., Wu J., Strand A., et al. . (2006). Mutant huntingtin alters MAPK signaling pathways in PC12 and striatal cells: ERK1/2 protects against mutant huntingtin-associated toxicity. Hum. Mol. Genet. 15, 273–285. 10.1093/hmg/ddi443 - DOI - PubMed
    1. Arbo B. D., André-Miral C., Nasre-Nasser R. G., Schimith L. E., Santos M. G., Costa-Silva D., et al. . (2020). Resveratrol derivatives as potential treatments for Alzheimer's and Parkinson's disease. Front. Aging Neurosci. 12, 103. 10.3389/fnagi.2020.00103 - DOI - PMC - PubMed

LinkOut - more resources