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- W2015391771 abstract "The neuropeptide bradykinin (BK) sensitizes nociceptor activation following its release in response to inflammatory injury. Thereafter, the bioactivity of bradykinin is controlled by the enzymatic activities of circulating peptidases. One such enzyme, the metalloendopeptidase EC3.4.24.15 (EP24.15), is co-expressed with bradykinin receptors in primary afferent neurons. In this study, using approaches encompassing pharmacology, biochemistry, cell biology, and behavioral animal models, we identified a crucial role for EP24.15 and the closely related EP24.16 in modulating bradykinin-mediated hyperalgesia. Pharmacological analyses indicated that EP24.15 and EP24.16 inhibition significantly enhances bradykinin type-2 receptor activation by bradykinin in primary trigeminal ganglia cultures. In addition, bradykinin-induced sensitization of TRPV1 activation was increased in the presence of the EP24.15/16 inhibitor JA-2. Furthermore, behavioral analyses illustrated a significant dose–response relationship between JA-2 and bradykinin-mediated thermal hyperalgesia. These results indicate an important physiological role for the metallopeptidases EP24.15 and EP24.16 in regulating bradykinin-mediated sensitization of primary afferent nociceptors. Metalloendopeptidases EP24.15 and EP24.16 regulate inflammatory sensitization of primary afferent nociceptors by mediating bradykinin type-2 receptor activation by bradykinin." @default.
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- W2015391771 date "2011-07-01" @default.
- W2015391771 modified "2023-10-15" @default.
- W2015391771 title "Metallopeptidase inhibition potentiates bradykinin-induced hyperalgesia" @default.
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- W2015391771 doi "https://doi.org/10.1016/j.pain.2011.02.044" @default.
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