4.7 Article

Fast green FCF prevents postoperative cognitive dysfunction via the downregulation of the P2X4 receptor in mice

Journal

INTERNATIONAL IMMUNOPHARMACOLOGY
Volume 121, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.intimp.2023.110462

Keywords

Fast green FCF; Postoperative cognitive dysfunction; Neuroinflammation; NF-& kappa;B

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Postoperative cognitive dysfunction (POCD) refers to a decline in cognitive function in aged patients after surgery, with unclear pathological mechanisms. The overexpression of the P2X4 receptor in the central nervous system (CNS) has been associated with the onset of POCD. This study explored the potential of the food dye FGF to prevent POCD by down-regulating the CNS P2X4 receptor. The results showed that FGF significantly attenuated cognitive impairments, decreased P2X4 receptor expression, and inhibited neuroinflammation, suggesting that FGF may be a potential treatment for POCD.
Postoperative cognitive dysfunction (POCD) is a decline in cognitive function affecting the mental health of aged patients after surgery. The pathological mechanisms underlying POCD have not yet been clarified. The overexpression of the P2X4 receptor in the central nervous system (CNS) was reported to be associated with the onset of POCD. Fast green FCF (FGF), a widely used food dye, could decrease the expression of the P2X4 receptor in the CNS. This study aimed to explore whether FGF could prevent POCD via the down-regulation of CNS P2X4 receptor. Exploratory laparotomy under the anesthesia of fentanyl and droperidol was carried to establish an animal model of POCD in 10-12-months-olds mice. FGF significantly attenuated cognitive impairments and down-regulated the expression of the P2X4 receptor induced by surgery in mice. Moreover, the blockade of CNS P2X4 receptor by intrahippocampal injection of 5-BDBD induced cognitive-enhancing effects on POCD mice. In addition, the effects of FGF were abolished by ivermectin, which is a positive allosteric modulator of the P2X4 receptor. FGF also inhibited M1 polarization of microglia cells, decreased the phosphorylation of nuclear factor?B (NF-?B), and reduced the production of pro-inflammatory cytokines. These results suggested that FGF produced anti-POCD cognitive-enhancing effects via down-regulation of the P2X4 receptor-associated neuroinflammation, providing a support that FGF might be a potential treatment for POCD.

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