1965
DOI: 10.1016/0024-3205(65)90147-5
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Serotonin — bradykinin potentiation on the pain receptors in man

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Cited by 101 publications
(21 citation statements)
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“…Furthermore, animal studies have shown increased pain sensitivity with pharmacological and neural lesion depletion of brain serotonin (29)(30)(31). Serotonin is suggested as a peripheral mediator in the pain-producing action of bradykinin and potassium on vascular systems (36). Peripheral serotonergic mechanisms have also been implicated in the induction of pain (35).…”
Section: Nrem Sleep Disturbance and Symptomsmentioning
confidence: 99%
“…Furthermore, animal studies have shown increased pain sensitivity with pharmacological and neural lesion depletion of brain serotonin (29)(30)(31). Serotonin is suggested as a peripheral mediator in the pain-producing action of bradykinin and potassium on vascular systems (36). Peripheral serotonergic mechanisms have also been implicated in the induction of pain (35).…”
Section: Nrem Sleep Disturbance and Symptomsmentioning
confidence: 99%
“…Activation of nociceptors causes immediate, overt pain whereas sensitization of nociceptors is responsible for the development of inflammatory hyperalgesia. Bradykinin was established as a pain mediator because it produced immediate, overt pain in man (Armstrong et al, 1957;Sicuteri et al, 1965;Ferreira, 1972;Whalley et al, 1987). This immediate effect of bradykinin has been the subject of numerous behavioural and electro-physiological studies (Dray et al, 1988;Lang et al, 1990;Handwerker & Reeh, 1991) and appears to result from the activation of the high threshold nociceptors associated with C fibres.…”
Section: Introductionmentioning
confidence: 99%
“…It is still uncertain, however, the extent to which other inflammatory mediators found in tissue exudates may contribute to the sensitization of peripheral sensory receptor mechanisms. Keele & Armstrong (1964) demonstrated that 5-hydroxytryptamine (5-HT) has the ability to cause pain when applied to a blister base, and 5-HT was later shown to lower thresholds for chemically-induced pain in man (Sicuteri et al, 1965) and to enhance pseudoaffective responses to bradykinin in animals (Nakano & Taira, 1976). Sensory nerve endings associated with small myelinated and non-myelinated axons have been found to be activated and sensitized by 5-HT in ' Author for correspondence.…”
Section: Introductionmentioning
confidence: 99%