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...
Guardado en:
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
MDPI AG
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/f282483231014517b60503237b3b4e99 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:f282483231014517b60503237b3b4e99 |
---|---|
record_format |
dspace |
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 |
work_keys_str_mv |
AT alinecgiardini crotalphineattenuatespainandneuroinflammationinducedbyexperimentalautoimmuneencephalomyelitisinmice AT biancagevangelista crotalphineattenuatespainandneuroinflammationinducedbyexperimentalautoimmuneencephalomyelitisinmice AT morenabsantanna crotalphineattenuatespainandneuroinflammationinducedbyexperimentalautoimmuneencephalomyelitisinmice AT barbarabmartins crotalphineattenuatespainandneuroinflammationinducedbyexperimentalautoimmuneencephalomyelitisinmice AT carmenlplancellotti crotalphineattenuatespainandneuroinflammationinducedbyexperimentalautoimmuneencephalomyelitisinmice AT adrianopciena crotalphineattenuatespainandneuroinflammationinducedbyexperimentalautoimmuneencephalomyelitisinmice AT maruciachacur crotalphineattenuatespainandneuroinflammationinducedbyexperimentalautoimmuneencephalomyelitisinmice AT rosanalpagano crotalphineattenuatespainandneuroinflammationinducedbyexperimentalautoimmuneencephalomyelitisinmice AT orlandogribeiro crotalphineattenuatespainandneuroinflammationinducedbyexperimentalautoimmuneencephalomyelitisinmice AT vanessaozambelli crotalphineattenuatespainandneuroinflammationinducedbyexperimentalautoimmuneencephalomyelitisinmice AT giselepicolo crotalphineattenuatespainandneuroinflammationinducedbyexperimentalautoimmuneencephalomyelitisinmice |
_version_ |
1718410254218166272 |