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首页> 外文期刊>Journal of toxicology and environmental health, Part A >Effects of BmKNJX11, a bioactive polypeptide purified from Buthus martensi Karsch, on sodium channels in rat dorsal root ganglion neurons.
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Effects of BmKNJX11, a bioactive polypeptide purified from Buthus martensi Karsch, on sodium channels in rat dorsal root ganglion neurons.

机译:BmKNJX11是从马氏蟾蜍(Buthus martensi Karsch)纯化的生物活性多肽,对大鼠背根神经节神经元的钠通道的影响。

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摘要

A long-chain polypeptide BmKNJX11 was purified from the venom of Asian scorpion Buthus martensi Karsch (BmK) by a combination of gel filtration, ion-exchange chromatography, and reverse-phase high-performance liquid chromatography. The molecular mass was found to be 7036.85 Da by electrospray ionization mass spectrometry. The first 15 N-terminal amino acid sequence of BmKNJX11 was determined to be GRDAY IADSE NCTYT by Edman degradation. With whole cell recording, BmKNJX11 inhibited tetrodotoxin-sensitive voltage-gated sodium channels (TTX-S VGSC) in freshly isolated rat dorsal root ganglion (DRG) neurons in a concentration- and voltage-dependent manner. At a concentration of 40 mug/ml BmKNJX11 lowered the activation threshold and produced negative shifting of TTX-S sodium current (I(Na)) activation curve. In addition, BmKNJX11 induced shifting of the steady-state inactivation curve to the left, delayed the recovery of TTX-S I(Na) from inactivation, and also reduced the fraction of available sodium channels. These results suggested that BmKNJX11 might exert effects on VGSC by binding to a specific site. Considering that TTX-S VGSC expressed in DRG neurons play a critical role in nociceptive transmission, the interaction of BmKNJX11 with TTX-S VGSC might lead to a change in excitability of nociceptive afferent fibers, which may be involved in the observed peripheral pain expression.
机译:通过凝胶过滤,离子交换色谱和反相高效液相色谱相结合,从亚洲蝎子Buthus martensi Karsch(BmK)的毒液中纯化出长链多肽BmKNJX11。通过电喷雾电离质谱法发现分子量为7036.85Da。通过埃德曼降解确定BmKNJX11的前15个N末端氨基酸序列为GRDAY IADSE NCTYT。通过全细胞记录,BmKNJX11以浓度和电压依赖性方式抑制了新鲜分离的大鼠背根神经节(DRG)神经元中河豚毒素敏感性电压门控钠通道(TTX-S VGSC)。在40杯/毫升的浓度下,BmKNJX11降低了激活阈值,并产生了TTX-S钠电流(I(Na))激活曲线的负向偏移。此外,BmKNJX11诱导稳态灭活曲线向左移动,延迟了灭活过程中TTX-S I(Na)的恢复,并减少了可用钠通道的比例。这些结果表明,BmKNJX11可能通过与特定位点结合而对VGSC产生影响。考虑到DRG神经元中表达的TTX-S VGSC在伤害感受传递中起关键作用,BmKNJX11与TTX-S VGSC的相互作用可能导致伤害感受传入纤维的兴奋性发生变化,这可能与观察到的周围疼痛表达有关。

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