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Neuromedin U potentiates ADP- and epinephrine-induced human platelet activation.

Thrombosis research (2017-10-28)
C Grippi, B Izzi, F Gianfagna, F Noro, E Falcinelli, A Di Pardo, E Amico, M B Donati, G de Gaetano, L Iacoviello, M F Hoylaerts, C Cerletti
ZUSAMMENFASSUNG

Neuromedin U (NmU) is a pleiotropic hypothalamic neuropeptide involved in the gut-brain axis. It acts via both a Gαq/11-coupled receptor (NMUR1) and a Gαi-coupled receptor (NMUR2) in different cell types. Expression of both receptors was reported in platelets, but their significance for NmU signaling remains elusive. We studied the potential effects of NmU on human platelet activation. In platelet-rich plasma (PRP), NmU alone (up to 10μM) did not induce any measurable aggregation, but at nanomolar concentrations, it potentiated platelet aggregation by low (mean 0.47μM) ADP concentrations (from 25.9±3.6% to 74.8±2.7% maximal aggregation for ADP vs. ADP+NmU, 100nM, mean±SEM, n=13), accompanied by platelet P-selectin expression and intracellular calcium mobilization. Accordingly, platelet preincubation with NmU for 2min sensitized platelets for subsequent activation by ADP. When P2Y

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Adenosin-5′-diphosphat Natriumsalz, bacterial, ≥95% (HPLC)
Supelco
Serotonin, analytical standard