2017
DOI: 10.1016/j.procbio.2016.08.025
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Host–guest inclusion complexation of β-cyclodextrin and hecogenin acetate to enhance anti-hyperalgesic effect in an animal model of musculoskeletal pain

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Cited by 16 publications
(11 citation statements)
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“…However, the HA/β-CD complex was superior in producing an analgesic profile using lower nominal doses of the active principle (HA). In addition, the interaction of the HA with opioid receptors and a decrease in SP levels in the lumbar spinal cord were verified, which indicate participation of this substance in the descending inhibitory pain pathway [33,85].…”
Section: Discussion Of Unusual Topics In Fibromyalgiamentioning
confidence: 83%
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“…However, the HA/β-CD complex was superior in producing an analgesic profile using lower nominal doses of the active principle (HA). In addition, the interaction of the HA with opioid receptors and a decrease in SP levels in the lumbar spinal cord were verified, which indicate participation of this substance in the descending inhibitory pain pathway [33,85].…”
Section: Discussion Of Unusual Topics In Fibromyalgiamentioning
confidence: 83%
“…Quintans et al [33] evaluated the effect of hecogenin acetate (HA), an acetylated steroidal saponin, complexed with β-CD in a chronic noninflammatory widespread pain model. Hecogenin is already used in the pharmaceutical industry to synthesize some oral contraceptive agents.…”
Section: Discussion Of Unusual Topics In Fibromyalgiamentioning
confidence: 99%
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“…As the authors established, the functionalization of silicone-based materials with ACNSs are promising potential platforms for the prevention of biofilm-associated infections caused by E. coli. The role of cyclodextrines (CD) as inclusion complexes was evaluated for fibromialgy treatment by complexation with a steroidal acetylated-sapogenin, hecogenin acetate (HA) [13]. The aim was to improve the anti-hyperalgesic effect of HA in a non-inflammatory animal model of musculoskeletal pain (considered to be a suitable animal model for FM), evaluating its effectiveness by examining its effect on substance P (SP) in the spinal cord, and its influence on the opioid system.…”
mentioning
confidence: 99%