In vivo tests demonstrate acute antinociceptive activity of cinnamaldehyde in male mice, suggesting involvement of opioid receptors.
-adrenergic contribution. Docking simulations showed favorable interactions of CA with κ- and δ-opioid receptors, NMDA, AMPA, and TRPV1, supporting a multimodal mechanism. CA displays acute antinociceptive activity, and the findings suggest the involvement of central pathways, including opioid and adrenergic systems.
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Rêgo et al. (2026) studied this question.
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