Protective Effect of a Mitochondria-Targeted Peptide against the Development of Chemotherapy-Induced Peripheral Neuropathy in Mice.
Satoshi ToyamaNaohito ShimoyamaHazel H SzetoPeter W SchillerMegumi ShimoyamaPublished in: ACS chemical neuroscience (2018)
Several chemotherapeutic agents used for cancer treatment induce dose-limiting peripheral neuropathy that compromises patients' quality of life and limits cancer treatment. Recently, mitochondrial dysfunction has been shown to be involved in the mechanism of chemotherapy-induced peripheral neuropathy. SS-20 is a mitochondria-targeted peptide that promotes mitochondrial respiration and restores mitochondrial bioenergetics. In the present study, we examined the protective effect of SS-20 against the development of chemotherapy-induced peripheral neuropathy utilizing a murine model of peripheral neuropathy induced by oxaliplatin, a first-line chemotherapy agent for colon cancer. Weekly administrations of oxaliplatin induced peripheral neuropathy as demonstrated by the development of neuropathic pain and loss of intraepidermal nerve fibers in the hind paw. Continuous administration of SS-20 protected against the development of oxaliplatin-induced neuropathic pain and mitigated the loss of intraepidermal nerve fibers to normal levels. Our findings suggest that SS-20 may be a drug candidate for the prevention of chemotherapy-induced peripheral neuropathy.
Keyphrases
- chemotherapy induced
- neuropathic pain
- spinal cord
- spinal cord injury
- end stage renal disease
- oxidative stress
- emergency department
- high glucose
- chronic kidney disease
- newly diagnosed
- cell death
- type diabetes
- drug delivery
- skeletal muscle
- peritoneal dialysis
- prognostic factors
- patient reported outcomes
- insulin resistance
- squamous cell carcinoma
- radiation therapy
- locally advanced