2014
DOI: 10.1016/j.neulet.2014.02.022
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Resveratrol attenuates morphine antinociceptive tolerance via SIRT1 regulation in the rat spinal cord

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Cited by 27 publications
(15 citation statements)
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“…Conversely, the HDAC inhibitor SAHA enhanced these responses [39] (Table 1). The intrathecal injection of resveratrol suppressed the established morphine analgesic tolerance, reversed the morphine-induced decrease in spinal Sirt1, and attenuated the morphine-induced increase in spinal histone H3 acetylation [40]. Interestingly, baicalin, a flavonoid compound isolated from Huang Qin, ameliorated SNL-induced neuropathic pain by suppressing HDAC1 expression and preventing histone-H3 acetylation in the spinal cord dorsal horn [41] (Table 1).…”
Section: Histone Modification In Chronic Painmentioning
confidence: 99%
“…Conversely, the HDAC inhibitor SAHA enhanced these responses [39] (Table 1). The intrathecal injection of resveratrol suppressed the established morphine analgesic tolerance, reversed the morphine-induced decrease in spinal Sirt1, and attenuated the morphine-induced increase in spinal histone H3 acetylation [40]. Interestingly, baicalin, a flavonoid compound isolated from Huang Qin, ameliorated SNL-induced neuropathic pain by suppressing HDAC1 expression and preventing histone-H3 acetylation in the spinal cord dorsal horn [41] (Table 1).…”
Section: Histone Modification In Chronic Painmentioning
confidence: 99%
“…Recently, SIRT1 was demonstrated to regulate algesthesia. Upregulation of the expression of SIRT1 in the spinal dorsal horn reversed chronic morphine antinociceptive tolerance (41). Increased spinal SIRT1 expression attenuated mechanical allodynia and thermal hyperalgesia in a chronic constriction injury model (42,43), and SIRT1 has also been observed to be crucial in inflammatory diseases, including obesity, type 2 diabetes mellitus, and atherosclerosis (44,45).…”
Section: Discussionmentioning
confidence: 98%
“…Interestingly, another lab found that intrathecal application of resveratrol attenuated morphine tolerance (MT) developed in rats after twice daily i.p. for six days [174]. They further found that Sirt 1 expression at mRNA and protein levels in the spinal cord of MT rats was significantly downregulated.…”
Section: Introductionmentioning
confidence: 99%
“…Different from studies reported by He and co-workers who applied steady amounts of morphine for 7 days to produce MT and found that Sirt1 was involved [174], Liang et al treated mice with increasing amount of morphine for 4 days and were able to detect mechanical and thermal hypersensitivity in addition to MT [181]. They treated these animals with HAT inhibitor (curcumin) and HDACi (SAHA) in the presence of morphine treatment.…”
Section: Introductionmentioning
confidence: 99%