Reserpine

50-55-5

C33H40N2O9

DMSO : 7 mg/mL (11.50 mM; Need ultrasonic)

Membrane Transporter/Ion Channel; Autophagy

Reserpine is an inhibitor of the vesicular monoamine transporter 2 (VMAT2). IC50 & Target: VMAT2^[1] In Vitro: Reserpine is an inhibitor of the vesicular monoamine transporter 2 (VMAT2). Reserpine displays a significant effect on the density of dopamine D1 receptors (F_{2, 12}=8.81, p<0.01) in the rat striatum. The affinity (Kd) for the dopamine D1 and D2 receptors during withdrawal from acute and chronic administration of reserpine is not change^[1]. IC₅₀ values of 43.9 and 54.9 uM are obtained after 1 day of treatment with Reserpine in JB6 P+ and HepG2-C8 cells, respectively. Reserpine induces luciferase activity in a dose-dependent manner at concentrations ranging from 5 to 50 uM, and no significant induction is observed at concentrations lower than 5 uM. Results demonstrate that Reserpine (2.5 to 10 uM) also increases the protein expression of Nrf2, HO-1, and NQO1. Reserpine at concentrations of 2.5 to 10 uM decreases the mRNA expression of DNMT1, DNMT3a, and DNMT3b in a concentration-dependent manner in JB6 P+ cells after 7 days of treatment. Reserpine at 10 uM generates a significant difference for DNMT3a expression (p<0.05)^[2]. In Vivo: Withdrawal (48 h) from chronic (14-day) but not acute Reserpine administration in a dose of 0.2 mg/kg i.p. produces a significant reduction of the immobility time (F_{2, 18}=3.68, p<0.05), but increases the climbing time (F_{2, 18}=4.48, p<0.02), and does not change the swimming time (F_{2, 18}=1.78; NS) in the forced swim test (FST) in rats^[1]. Reserpine at a dose of 5 mg/kg body weight produces significant increase in the urinary excretion profile of vanillylmandelic acid (VMA) compare to control animals. The amount of 5-hydroxyindoleacetic acid (5-HIAA) excreted in animals treated with Reserpine is found to be more than in the control. Dose dependent hypotension is observed with Reserpine. Reserpine at doses of 0.5, 1, 5, 10 and 15 ug/kg produce significant (p<0.01) reduction in blood pressure compare to control^[3].