PKCζ-Mitogen-activated protein kinase signaling mediates crotalphine-Induced antinociception

Translated title
A sinalização da proteína quinase ativada por PKCζ-mitógeno medeia a antinocicepção induzida por crotalfina

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Article
Language
English
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Open access
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CC BY
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Abstract
Crotalphine (CRP) is a structural analogue to a peptide that was first identified in the crude venom from the South American rattlesnake Crotalus durissus terrificus. This peptide induces a potent and long-lasting antinociceptive effect that is mediated by the activation of peripheral opioid receptors. The opioid receptor activation regulates a variety of intracellular signaling, including the mitogen-activated protein kinase (MAPK) pathway. Using primary cultures of sensory neurons, it was demonstrated that crotalphine increases the level of activated ERK1/2 and JNK-MAPKs and this increase is dependent on the activation of protein kinase Cζ (PKCζ). However, whether PKCζ-MAPK signaling is critical for crotalphine-induced antinociception is unknown. Here, we biochemically demonstrated that the systemic crotalphine activates ERK1/2 and JNK and decreases the phosphorylation of p38 in the lumbar spinal cord. The in vivo pharmacological inhibition of spinal ERK1/2 and JNK, but not of p38, blocks the antinociceptive effect of crotalphine. Of interest, the administration of a PKCζ pseudosubstrate (PKCζ inhibitor) prevents crotalphine-induced ERK activation in the spinal cord, followed by the abolishment of crotalphine-induced analgesia. Together, our results demonstrate that the PKCζ-ERK signaling pathway is involved in crotalphine-induced analgesia. Our study opens a perspective for the PKCζ-MAPK axis as a target for pain control.
Reference
Freitas BG, Hösch NG, Pereira LM, Barbosa TC, Picolo G, Cury Y, et al. PKCζ-Mitogen-activated protein kinase signaling mediates crotalphine-Induced antinociception. Toxins. 2021 Dec; 13(12):912. doi:10.3390/toxins13120912.
Link to cite this reference
https://repositorio.butantan.gov.br/handle/butantan/4083
URL
https://doi.org/10.3390/toxins13120912
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Issue Date
2021


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