Differences in the ultrastructure of neurons in the spinal ganglion and dorsal rootlet between rats treated with cisplatin only versus co‐administration with a sphingosine 1‐phosphate receptor 2 agonist in attenuating neuropathy and allodynia

Author:

Chayaburakul Kanokporn1ORCID,Ong Wei Yi2,Herr Deron R.3,Kobutree Phetnarin1,Chantra Kraisri4

Affiliation:

1. Anatomy Unit, Faculty of Science Rangsit University Meung, Pathum Tani Thailand

2. Department of Anatomy, Yong Loo Lin School of Medicine National University Health System, National University of Singapore Singapore Singapore

3. Department of Pharmacology, Yong Loo Lin School of Medicine National University Health System, National University of Singapore Singapore Singapore

4. Department of Neurosurgery, Faculty of Medicine, King Chulalongkorn Memorial Hospital Chulalongkorn University Bangkok Thailand

Abstract

AbstractBackground and AimsCisplatin is a chemotherapeutic agent for many types of cancer. The neurotoxicity of cisplatin includes neuropathy and allodynia. We aimed to study structural changes by using CYM54‐78, attenuating cisplatin‐induced neuropathy and blocking the pathogenesis in neurons, and promoting axonal regeneration.MethodsTEM (transmission electron microscopy) was used to distinguish ultrastructural changes in dorsal root ganglion (DRG) and dorsal rootlets (DR) between rats treated with cisplatin alone and rats co‐treated with cisplatin and sphingosine ‐1‐phosphate receptor2 (S1P2) agonist, CYM‐5478.ResultsIn DRG of rats treated with cisplatin alone, TEM micrographs showed necrosis and apoptotic cells. Neuronal cytoplasm showed numerous vacuole (stage C) and swelling (stage B➔C) mitochondrial degeneration. Neurons in DRG from cisplatin+CYM‐5478 group showed a higher percentage of healthy mitochondria (from 5.3% to 75.6%) than those treated with cisplatin alone. DR of cisplatin only group showed abnormal axoplasm, axolemma, and focal detached myelin sheaths, especially in Aδ (fast pain) and Aβ (touch) fibers, and revealed collateral branches that sprouted from Aβ fibers, which is characteristic of allodynia. Moreover, vasoconstriction was observed in DRG and DR. Rats in cisplatin+CYM‐5478 group showed not only fewer abnormal structures than those in cisplatin only group, but also showed Bands of Büngner and onion bulb‐like structures, which are characteristic of nerve regeneration.InterpretationTogether with our previous study, showed that CYM‐5478 attenuated neuropathy and allodynia in a rat model of cisplatin‐induced neuropathy, these results suggest S1P2 agonists as a potential approach the for treatment of cancer due to the reduction of side effects of cisplatin.

Publisher

Wiley

Subject

Neurology (clinical),General Neuroscience

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