2024
DOI: 10.1016/j.bja.2024.01.005
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Enhancing spinal cord stimulation-induced pain inhibition by augmenting endogenous adenosine signalling after nerve injury in rats

Xiang Cui,
Jing Liu,
Ankit Uniyal
et al.
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Cited by 5 publications
(2 citation statements)
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“…IL-10 is secreted by T and B cells, monocytes, macrophages, and epithelial cells [62]. Studies have demonstrated that acute administration of IL-10 can inhibit the onset of spinally mediated pain enhancement in various animal models, including peripheral neuritis, spinal cord excitotoxic injury, and peripheral nerve injury [63][64][65]. Conversely, blocking spinal IL-10 has been shown to prevent and even reverse established neuropathic pain behaviors [63][64][65].…”
Section: Interleukin-10 (Il-10)mentioning
confidence: 99%
See 1 more Smart Citation
“…IL-10 is secreted by T and B cells, monocytes, macrophages, and epithelial cells [62]. Studies have demonstrated that acute administration of IL-10 can inhibit the onset of spinally mediated pain enhancement in various animal models, including peripheral neuritis, spinal cord excitotoxic injury, and peripheral nerve injury [63][64][65]. Conversely, blocking spinal IL-10 has been shown to prevent and even reverse established neuropathic pain behaviors [63][64][65].…”
Section: Interleukin-10 (Il-10)mentioning
confidence: 99%
“…Studies have demonstrated that acute administration of IL-10 can inhibit the onset of spinally mediated pain enhancement in various animal models, including peripheral neuritis, spinal cord excitotoxic injury, and peripheral nerve injury [63][64][65]. Conversely, blocking spinal IL-10 has been shown to prevent and even reverse established neuropathic pain behaviors [63][64][65]. IL-10 has the potential to interfere with neutrophil function, which plays an essential role in moderating systemic inflammation [62].…”
Section: Interleukin-10 (Il-10)mentioning
confidence: 99%