Electrical stimulation enhances mitochondrial trafficking as a neuroprotective mechanism against chemotherapy-induced peripheral neuropathy.

iScience

Center for Biomedical Engineering and Science, Department of Mechanical Engineering and Engineering Science, University of North Carolina at Charlotte, Charlotte, NC 28223, USA.

Published: March 2024

AI Article Synopsis

  • Electrical stimulation (ESTIM) effectively alleviates pain from peripheral nerve damage but its neuroprotective mechanisms are unclear.
  • The study showed that ESTIM improves mitochondrial trafficking, which helps protect nerves from damage caused by chemotherapy, particularly from drugs like paclitaxel and oxaliplatin.
  • Findings indicate that ESTIM boosts the regeneration of peripheral nerves by enhancing mitochondrial movement, offering a potential solution for chemotherapy-induced peripheral neuropathies (CIPN).

Article Abstract

Electrical stimulation (ESTIM) has shown to be an effective symptomatic treatment to treat pain associated with peripheral nerve damage. However, the neuroprotective mechanism of ESTIM on peripheral neuropathies is still unknown. In this study, we identified that ESTIM has the ability to enhance mitochondrial trafficking as a neuroprotective mechanism against chemotherapy-induced peripheral neuropathies (CIPNs). CIPN is a debilitating and painful sequalae of anti-cancer chemotherapy treatment which results in degeneration of peripheral nerves. Mitochondrial dynamics were analyzed within axons in response to two different antineoplastic mechanisms by chemotherapy drug treatments paclitaxel and oxaliplatin . Mitochondrial trafficking response to chemotherapy drug treatment was observed to decrease in conjunction with degeneration of distal axons. Using low-frequency ESTIM, we observed enhanced mitochondrial trafficking to be a neuroprotective mechanism against CIPN. This study confirms ESTIM enhances regeneration of peripheral nerves by increased mitochondrial trafficking.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10875116PMC
http://dx.doi.org/10.1016/j.isci.2024.109052DOI Listing

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