Crotalphine Attenuates Pain and Neuroinflammation Induced by Experimental Autoimmune Encephalomyelitis in Mice

Multiple sclerosis (MS) is a demyelinating disease of inflammatory and autoimmune origin, which induces sensory and progressive motor impairments, including pain. Cells of the immune system actively participate in the pathogenesis and progression of MS by inducing neuroinflammation, tissue damage, a...

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Autores principales: Aline C. Giardini, Bianca G. Evangelista, Morena B. Sant’Anna, Barbara B. Martins, Carmen L. P. Lancellotti, Adriano P. Ciena, Marucia Chacur, Rosana L. Pagano, Orlando G. Ribeiro, Vanessa O. Zambelli, Gisele Picolo
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spelling oai:doaj.org-article:f282483231014517b60503237b3b4e992021-11-25T19:09:11ZCrotalphine Attenuates Pain and Neuroinflammation Induced by Experimental Autoimmune Encephalomyelitis in Mice10.3390/toxins131108272072-6651https://doaj.org/article/f282483231014517b60503237b3b4e992021-11-01T00:00:00Zhttps://www.mdpi.com/2072-6651/13/11/827https://doaj.org/toc/2072-6651Multiple sclerosis (MS) is a demyelinating disease of inflammatory and autoimmune origin, which induces sensory and progressive motor impairments, including pain. Cells of the immune system actively participate in the pathogenesis and progression of MS by inducing neuroinflammation, tissue damage, and demyelination. Crotalphine (CRO), a structural analogue to a peptide firstly identified in <i>Crotalus durissus terrificus</i> snake venom, induces analgesia by endogenous opioid release and type 2 cannabinoid receptor (CB2) activation. Since CB2 activation downregulates neuroinflammation and ameliorates symptoms in mice models of MS, it was presently investigated whether CRO has a beneficial effect in the experimental autoimmune encephalomyelitis (EAE). CRO was administered on the 5th day after immunization, in a single dose, or five doses starting at the peak of disease. CRO partially reverted EAE-induced mechanical hyperalgesia and decreased the severity of the clinical signs. In addition, CRO decreases the inflammatory infiltrate and glial cells activation followed by TNF-α and IL-17 downregulation in the spinal cord. Peripherally, CRO recovers the EAE-induced impairment in myelin thickness in the sciatic nerve. Therefore, CRO interferes with central and peripheral neuroinflammation, opening perspectives to MS control.Aline C. GiardiniBianca G. EvangelistaMorena B. Sant’AnnaBarbara B. MartinsCarmen L. P. LancellottiAdriano P. CienaMarucia ChacurRosana L. PaganoOrlando G. RibeiroVanessa O. ZambelliGisele PicoloMDPI AGarticleneurodegenerative diseaseneurodegenerationinflammationIL-17glial cellsMedicineRENToxins, Vol 13, Iss 827, p 827 (2021)
institution DOAJ
collection DOAJ
language EN
topic neurodegenerative disease
neurodegeneration
inflammation
IL-17
glial cells
Medicine
R
spellingShingle neurodegenerative disease
neurodegeneration
inflammation
IL-17
glial cells
Medicine
R
Aline C. Giardini
Bianca G. Evangelista
Morena B. Sant’Anna
Barbara B. Martins
Carmen L. P. Lancellotti
Adriano P. Ciena
Marucia Chacur
Rosana L. Pagano
Orlando G. Ribeiro
Vanessa O. Zambelli
Gisele Picolo
Crotalphine Attenuates Pain and Neuroinflammation Induced by Experimental Autoimmune Encephalomyelitis in Mice
description Multiple sclerosis (MS) is a demyelinating disease of inflammatory and autoimmune origin, which induces sensory and progressive motor impairments, including pain. Cells of the immune system actively participate in the pathogenesis and progression of MS by inducing neuroinflammation, tissue damage, and demyelination. Crotalphine (CRO), a structural analogue to a peptide firstly identified in <i>Crotalus durissus terrificus</i> snake venom, induces analgesia by endogenous opioid release and type 2 cannabinoid receptor (CB2) activation. Since CB2 activation downregulates neuroinflammation and ameliorates symptoms in mice models of MS, it was presently investigated whether CRO has a beneficial effect in the experimental autoimmune encephalomyelitis (EAE). CRO was administered on the 5th day after immunization, in a single dose, or five doses starting at the peak of disease. CRO partially reverted EAE-induced mechanical hyperalgesia and decreased the severity of the clinical signs. In addition, CRO decreases the inflammatory infiltrate and glial cells activation followed by TNF-α and IL-17 downregulation in the spinal cord. Peripherally, CRO recovers the EAE-induced impairment in myelin thickness in the sciatic nerve. Therefore, CRO interferes with central and peripheral neuroinflammation, opening perspectives to MS control.
format article
author Aline C. Giardini
Bianca G. Evangelista
Morena B. Sant’Anna
Barbara B. Martins
Carmen L. P. Lancellotti
Adriano P. Ciena
Marucia Chacur
Rosana L. Pagano
Orlando G. Ribeiro
Vanessa O. Zambelli
Gisele Picolo
author_facet Aline C. Giardini
Bianca G. Evangelista
Morena B. Sant’Anna
Barbara B. Martins
Carmen L. P. Lancellotti
Adriano P. Ciena
Marucia Chacur
Rosana L. Pagano
Orlando G. Ribeiro
Vanessa O. Zambelli
Gisele Picolo
author_sort Aline C. Giardini
title Crotalphine Attenuates Pain and Neuroinflammation Induced by Experimental Autoimmune Encephalomyelitis in Mice
title_short Crotalphine Attenuates Pain and Neuroinflammation Induced by Experimental Autoimmune Encephalomyelitis in Mice
title_full Crotalphine Attenuates Pain and Neuroinflammation Induced by Experimental Autoimmune Encephalomyelitis in Mice
title_fullStr Crotalphine Attenuates Pain and Neuroinflammation Induced by Experimental Autoimmune Encephalomyelitis in Mice
title_full_unstemmed Crotalphine Attenuates Pain and Neuroinflammation Induced by Experimental Autoimmune Encephalomyelitis in Mice
title_sort crotalphine attenuates pain and neuroinflammation induced by experimental autoimmune encephalomyelitis in mice
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/f282483231014517b60503237b3b4e99
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