首页> 外文期刊>British Journal of Pharmacology >Dual coupling of heterologously-expressed rat P2Y_6 nucleotide receptors to N-type Ca~2+ and M-type K~+ currents in rat sympathetic neurones
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Dual coupling of heterologously-expressed rat P2Y_6 nucleotide receptors to N-type Ca~2+ and M-type K~+ currents in rat sympathetic neurones

机译:大鼠交感神经元中异源表达的大鼠P2Y_6核苷酸受体与N型Ca〜2 +和M型K〜+电流的双重偶联

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1. The P2Y_6 receptor is a uridine nucleotide-specific G protein-linked receptor previouslyreported to stimulate the phosphoinositide (PI) pathway. We have investigated its effect in neurones, by micro-injecting its cRNA into dissociated rat sympathetic neurones and recording respnses of N- type Ca~+ (I_Ca(N)) and M-type K~+ (I_k(M)) currents. 2. In P2Y_6 cRNA-injected neurones, UDP or UTP produced a voltage-dependent inhibition of I_Ca(N)) by ~ 53/100 in whole-cell (disrupted-patch) mode and by ~ 73/100 in perforated-patch mode; no Inhibition occurred in control cells.
机译:1. P2Y_6受体是尿苷核苷酸特异性的G蛋白连接受体,先前已报道其可刺激磷酸肌醇(PI)途径。我们已经通过将其cRNA微注射到解离的大鼠交感神经元中并记录N型Ca〜+(I_Ca(N))和M型K〜+(I_k(M))电流的响应,研究了其在神经元中的作用。 2.在注射了P2Y_6 cRNA的神经元中,UDP或UTP在全细胞(打断贴片)模式下对I_Ca(N))的电压依赖性抑制作用约为53/100,而在穿孔打孔模式下则约为73/100 ;在对照细胞中没有抑制作用发生。

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