Aminoglycoside block of P2X2 receptors heterologously expressed in Xenopus laevis oocytes

Purinergic Signalling

Jürgen Rettinger²  Ralf Hausmann¹  Eva-Verena Bongartz² 

[1] RWTH Aachen University$$;Max Planck Institute of Biophysics$$

关键词: Open pore block;   

DOI  :  10.1007/s11302-010-9204-9

学科分类：分子生物学，细胞生物学和基因

来源: Springer

【 摘 要 】

Aminoglycosides are polycationic antibiotics that have been shown to block a variety of cation channels. The inhibitory effect of externally applied aminoglycosides on P2X2 receptor currents was examined after heterologous expression in Xenopus laevis oocytes using the two-electrode voltage-clamp technique. All of the aminoglycosides tested inhibited the ATP-evoked responses with potencies ranging from 71 μM to 2 mM (IC₅₀ values). The ranked order of potency was streptomycin > gentamicin > neomycin > paromomycin > kanamycin. The inhibition of P2X receptor currents was independent of the ATP concentration used for the activation, which is compatible with a noncompetitive mechanism. The inhibition was voltage-dependent and was reduced at more positive membrane potentials. To examine whether the current block was dependent on the receptor conformation, the aminoglycoside effect on a non-desensitizing P2X2-X1 receptor chimera was analyzed. The results from these measurements suggest that inhibition is caused by an open pore block that locks the P2X receptor chimera in an open nonconducting state from which the agonist dissociation is slow. We also demonstrate that the P2X2-X1 chimera can serve as a tool to directly test whether an antagonist acts competitively or not.

【 授权许可】

Unknown