Calmangafodipir Reduces Sensory Alterations and Prevents Intraepidermal Nerve Fibers Loss in a Mouse Model of Oxaliplatin Induced Peripheral Neurotoxicity

Oxaliplatin (OHP) is an antineoplastic compound able to induce peripheral neurotoxicity. Oxidative stress has been suggested to be a key factor in the development of OHP-related peripheral neurotoxicity. Mangafodipir, a contrast agent possessing mitochondrial superoxide dismutase (MnSOD)-mimetic act...

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Main Authors: Annalisa Canta (Author), Alessia Chiorazzi (Author), Eleonora Pozzi (Author), Giulia Fumagalli (Author), Laura Monza (Author), Cristina Meregalli (Author), Valentina A. Carozzi (Author), Virginia Rodriguez-Menendez (Author), Norberto Oggioni (Author), Jacques Näsström (Author), Paola Marmiroli (Author), Guido Cavaletti (Author)
Format: Book
Published: MDPI AG, 2020-07-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Annalisa Canta  |e author 
700 1 0 |a Alessia Chiorazzi  |e author 
700 1 0 |a Eleonora Pozzi  |e author 
700 1 0 |a Giulia Fumagalli  |e author 
700 1 0 |a Laura Monza  |e author 
700 1 0 |a Cristina Meregalli  |e author 
700 1 0 |a Valentina A. Carozzi  |e author 
700 1 0 |a Virginia Rodriguez-Menendez  |e author 
700 1 0 |a Norberto Oggioni  |e author 
700 1 0 |a Jacques Näsström  |e author 
700 1 0 |a Paola Marmiroli  |e author 
700 1 0 |a Guido Cavaletti  |e author 
245 0 0 |a Calmangafodipir Reduces Sensory Alterations and Prevents Intraepidermal Nerve Fibers Loss in a Mouse Model of Oxaliplatin Induced Peripheral Neurotoxicity 
260 |b MDPI AG,   |c 2020-07-01T00:00:00Z. 
500 |a 10.3390/antiox9070594 
500 |a 2076-3921 
520 |a Oxaliplatin (OHP) is an antineoplastic compound able to induce peripheral neurotoxicity. Oxidative stress has been suggested to be a key factor in the development of OHP-related peripheral neurotoxicity. Mangafodipir, a contrast agent possessing mitochondrial superoxide dismutase (MnSOD)-mimetic activity, has been tested as a cytoprotector in chemotherapy-induced peripheral neurotoxicity (CIPN). Calmangafodipir (PledOx<sup>®</sup>) has even better therapeutic activity. We investigated a BALB/c mouse model of OHP-related CIPN and the effects of the pre-treatment of calmangafodipir (2.5, 5, or 10 mg/kg intravenously) on sensory perception, and we performed a pathological study on skin biopsies to assess intraepidermal nerve fiber (IENF) density. At the end of the treatments, OHP alone or in pre-treatment with calmangafodipir 2.5 and 10 mg/kg, induced mechanical allodynia and cold thermal hyperalgesia, but calmangafodipir 5 mg/kg prevented these effects. Accordingly, OHP alone or in pre-treatment with calmangafodipir 2.5 and 10 mg/kg, induced a significant reduction in IENF density, but calmangafodipir 5 mg/kg prevented this reduction. These results confirm a protective effect of calmangafodipir against OHP-induced small fiber neuropathy. Interestingly, these results are in agreement with previous observations suggesting a U-shaped effect of calmangafodipir, with the 10 mg/kg dose less effective than the lower doses. 
546 |a EN 
690 |a calmangafodipir 
690 |a oxaliplatin 
690 |a IENF density 
690 |a cold hyperalgesia 
690 |a mechanical allodynia 
690 |a neurotoxicity 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Antioxidants, Vol 9, Iss 7, p 594 (2020) 
787 0 |n https://www.mdpi.com/2076-3921/9/7/594 
787 0 |n https://doaj.org/toc/2076-3921 
856 4 1 |u https://doaj.org/article/6ea08a32b15b46a1ba40a13deca1175c  |z Connect to this object online.