Quinic acid protects against the development of Huntington's disease in Caenorhabditis elegans model.

BMC Complement Med Ther

Department of Pharmaceutical Biology, Faculty of Pharmacy and Biotechnology, German University in Cairo, New Cairo, 11835, Egypt.

Published: October 2024

AI Article Synopsis

  • - Quinic acid (QA), found in common foods like tea and coffee, shows antioxidant and neuroprotective effects, particularly towards oxidative stress related to aging disorders, such as Huntington's disease (HD).
  • - In experiments with C. elegans worms, QA improved survival under oxidative stress and activated the SKN-1 pathway, which is key for antioxidant response and protection.
  • - The study suggests QA could be a promising natural compound for reducing harmful protein aggregates associated with HD, indicating its potential role in combating neurodegenerative diseases.

Article Abstract

Background: Quinic acid (QA), a cyclitol and cyclohexanecarboxylic acid, is a natural product that is present and can be isolated from edible herbals like tea, coffee and several fruits and vegetables. It was previously reported that QA exerted antioxidant and neuroprotective activity against dementia. However, it was not tested for its neuroprotective potential against Huntington's disease (HD). Since aging related disorders are greatly linked to oxidative stress conditions, we focused on testing the oxidative stress resistant activity and protective effect of QA against the development of HD by using the multicellular Caenorhabditis elegans (C. elegans) worm model.

Methods: Firstly, QA was tested for its oxidative stress resistant properties. In survival assay, wild type and mutant skn-1 and daf-16 worms were exposed to oxidative stress conditions by using HO. Activation of SKN-1 pathway and expression of its downstream genes gcs-1 and gst-4 were also tested. Secondly, the effect of QA was evaluated on HD by testing its ability to decrease the formation of polyQ150 aggregates. Furthermore, its effect on the accumulation of polyglutamine (polyQ35 and polyQ40 aggregates) was tested.

Results: Here we report that QA could improve the survival of C. elegans after exposure to oxidative stress caused by HO while also exerting antioxidant effects through the activation of SKN-1/Nrf2 pathway. Moreover, QA could be a potential candidate to protect against HD due to its effects on decreasing the formation of polyQ150, polyQ35 and polyQ40 aggregates.

Conclusions: This study highlights the importance of QA as a natural compound in defending against oxidative stress and the development of neurodegenerative diseases like HD.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11514749PMC
http://dx.doi.org/10.1186/s12906-024-04670-4DOI Listing

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