Polyphenolic grape stalk and coffee extracts attenuate spinal cord injury‑induced neuropathic pain development in ICR‑CD1 female mice

Autoři	BAGÓ MAS Anna KORIMOVÁ Andrea DEULOFEU FIGUERAS Meritxell VERDÚ Enrico FIOL Núria SVOBODOVÁ Viktorie DUBOVÝ Petr BOADAS-VAELLO Pere
Rok publikování	2022
Druh	Článek v odborném periodiku
Časopis / Zdroj	Scientific Reports
Fakulta / Pracoviště MU	Lékařská fakulta
Citace
www	https://www.webofscience.com/wos/woscc/full-record/WOS:000849436000038
Doi	http://dx.doi.org/10.1038/s41598-022-19109-4
Klíčová slova	GALLIC ACID; CHLOROGENIC ACID; INFLAMMATORY RESPONSES; CENTRAL SENSITIZATION; DORSAL-HORN; CATHEPSIN-S; EXPRESSION; MICROGLIA; FRACTALKINE; PREVALENCE
Popis	More than half of spinal cord injury (SCI) patients develop central neuropathic pain (CNP), which is largely refractory to current treatments. Considering the preclinical evidence showing that polyphenolic compounds may exert antinociceptive effects, the present work aimed to study preventive effects on SCI-induced CNP development by repeated administration of two vegetal polyphenolic extracts: grape stalk extract (GSE) and coffee extract (CE). Thermal hyperalgesia and mechanical allodynia were evaluated at 7, 14 and 21 days postinjury. Then, gliosis, ERK phosphorylation and the expression of CCL2 and CX3CL1 chemokines and their receptors, CCR2 and CX3CR1, were analyzed in the spinal cord. Gliosis and CX3CL1/CX3CR1 expression were also analyzed in the anterior cingulate cortex (ACC) and periaqueductal gray matter (PAG) since they are supraspinal structures involved in pain perception and modulation. GSE and CE treatments modulated pain behaviors accompanied by reduced gliosis in the spinal cord and both treatments modulated neuronglia crosstalk-related biomolecules expression. Moreover, both extracts attenuated astrogliosis in the ACC and PAG as well as microgliosis in the ACC with an increased M2 subpopulation of microglial cells in the PAG. Finally, GSE and CE prevented CX3CL1/CX3CR1 upregulation in the PAG, and modulated their expression in ACC. These findings suggest that repeated administrations of either GSE or CE after SCI may be suitable pharmacologic strategies to attenuate SCI-induced CNP development by means of spinal and supraspinal neuroinflammation modulation.