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Hexamethonium Bromide

CAS No. : 55-97-0

MCE 国际站：Hexamethonium Bromide

产品活性：Hexamethonium Bromide 是一种非选择性的神经节烟碱受体 (nAChR) 拮抗剂，具有竞争性和非竞争性活性。Hexamethonium Bromide 具有降压作用。在自发性高血压动物模型中，Hexamethonium Bromide 能降低其交感神经活动和血压。

研究领域：Membrane Transporter/Ion Channel | Neuronal Signaling | Apoptosis

作用靶点：nAChR | Apoptosis

In Vitro: Hexamethonium Bromide (100 µM; 60 minutes) abolishes epibatidine-induced depolarisations of smooth muscle cells.
The α3β4α5 receptors have greater sensitivity to Hexamethonium Bromide than the other potential ganglionic models, α3β4, α3β2, and α3β2α5.

In Vivo: Hexamethonium Bromide (0.2-25 mg/kg; i.v.) significantly reduces the renal sympathetic nerve activity (RSNA), mean arterial pressure (MAP) and heart rate (HR) in the Wistar rats and the spontaneously hypertensive rats (SHRs).
Hexamethonium Bromide (0.2-1.0 mg/kg; i.v.) treatments show no significant differences in the RSNA, MAP or HR between Wistar rats and SHRs.
Hexamethonium Bromide (5.0-25 mg/kg; i.v.) results in a greater reduction in the RSNA and MAP in SHRs compared with Wistar rats.

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