An inhibitor of voltage-gated calcium channels
SKF 96365 hydrochloride is an inhibitor of store-operated calcium entry (SOCE). Also, it inhibits transient receptor potential cation channels (TRPCs) and voltage-gated sodium current [1] [2] [3].
Store-operated calcium entry (SOCE) increases cytosolic Ca2+ and induces the entry of extracellular calcium. TRPC channels are divided into store-operated and receptor-operated channels and play a critical role in brain development [1] [2].
SKF 96365 hydrochloride is a SOCE inhibitor. In MPP+ stressed PC12 cells, SKF-96365 (10, 50 μM) significantly prevented nuclear damage, decreased LDH release, increased cell viability and inhibited apoptosis. Also, SKF-96365 inhibited Homer1-mediated endoplasmic reticulum (ER) Ca2+ release and intracellular calcium overload induced by MPP+ injury [1]. In rat ventricular myocytes, SKF-96365 inhibited INa in a frequency-dependent and use-dependent way [3]. In Madin Darby canine kidney (MDCK) cells, SKF 96365 (25-100 μM) induced a robust [Ca2+]i transient in a dose-dependent way [4].
In rats, SKF-96365 significantly inhibited persistent spontaneous nociception induced by melittin and reduced hypersensitivity to both mechanical and thermal stimuli. These results suggested that SKF-96365-sensitive TRPC channels were involved in the processing of melittin-induced hypersensitivity and inflammatory pain [2].
参考文献:
[1].? Chen T, Zhu J, Zhang C, et al. Protective effects of SKF-96365, a non-specific inhibitor of SOCE, against MPP+-induced cytotoxicity in PC12 cells: potential role of Homer1. PLoS One, 2013, 8(1): e55601.
[2].? Ding J, Zhang JR, Wang Y, et al. Effects of a non-selective TRPC channel blocker, SKF-96365, on melittin-induced spontaneous persistent nociception and inflammatory pain hypersensitivity. Neurosci Bull, 2012, 28(2): 173-181.
[3].? Chen KH, Liu H, Yang L, et al. SKF-96365 strongly inhibits voltage-gated sodium current in rat ventricular myocytes. Pflugers Arch, 2015, 467(6): 1227-1236.
[4].? Jan CR, Ho CM, Wu SN, et al. Multiple effects of 1-[beta-[3-(4-methoxyphenyl)propoxy]-4-methoxyphenethyl]-1H-imidazole hydrochloride (SKF 96365) on Ca2+ signaling in MDCK cells: depletion of thapsigargin-sensitive Ca2+ store followed by capacitative Ca2+ entry, activation of a direct Ca2+ entry, and inhibition of thapsigargin-induced capacitative Ca2+ entry. Naunyn Schmiedebergs Arch Pharmacol, 1999, 359(2): 92-101.
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Animal experiment: |
Mice: Five to six-week-old female athymic BALB/c mice are inoculated into the right oxter with HCT116 cells. When the diameter of the subcutaneous tumor reaches approximately 0.5 cm, animals are randomLy assigned to the vehicle, SKF-96365 alone, HCQ alone or SKF-96365+HCQ. SKF-96365 is applied (20 mg/kg) and HCQ is applied (60 mg/kg) daily for 14 successive days by i.p. injection. Tumor sizes and volume are determined. Eight mice are included in each group. Mice are sacrificed 24 h after the last treatment. The tumors are weighed and processed for western blot analysis or paraffin embedding[2]. |
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参考文献: [1]. Liu H, et al. SKF-96365 blocks human ether-à-go-go-related gene potassium channels stably expressed in HEK 293 cells. Pharmacological Research. Pharmacol Res, 2016 Feb, 104:61-9. |
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