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Tx2-6 toxin of the Phoneutria nigriventer spider potentiates rat erectile function

机译:Phoneutria nigriventer蜘蛛的Tx2-6毒素增强大鼠勃起功能

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摘要

The venom of the spider Phoneutria nigriventer contains several toxins that have bioactivity in mammals and insects. Accidents involving humans are characterized by various symptoms including penile erection. Here we investigated the action of Tx2-6, a toxin purified from the P. nigriventer spider venom that causes priapism in rats and mice. Erectile function was evaluated through changes in intracavernosal pressure/mean arterial pressure ratio (ICP/MAP) during electrical stimulation of the major pelvic ganglion (MPG) of normotensive and deoxycorticosterone-acetate (DOCA)-salt hypertensive rats. Nitric oxide (NO) release was detected in cavernosum slices with fluorescent dye (DAF-FM) and confocal microscopy. The effect of Tx2-6 was also characterized after intracavernosal injection of a non-selective nitric oxide synthase (NOS) inhibitor, l-NAME. Subcutaneous or intravenous injection of Tx2-6 potentiated the elevation of ICP/MAP induced by ganglionic stimulation. l-NAME inhibited penile erection and treatment with Tx2-6 was unable to reverse this inhibition. Tx2-6 treatment induced a significant increase of NO release in cavernosum tissue. Attenuated erectile function of DOCA-salt hypertensive rats was fully restored after toxin injection. Tx2-6 enhanced erectile function in normotensive and DOCA-salt hypertensive rats, via the NO pathway. Our studies suggest that Tx2-6 could be important for development of new pharmacological agents for treatment of erectile dysfunction.
机译:蜘蛛Phoneutria nigriventer的毒液包含几种毒素,这些毒素在哺乳动物和昆虫中具有生物活性。涉及人类的事故的特征是包括阴茎勃起在内的各种症状。在这里,我们研究了Tx2-6的作用,Tx2-6是从黑腹果蝇蜘蛛毒液中纯化的毒素,可在大鼠和小鼠中引起阴茎异常勃勃。通过电刺激正常血压和醋酸脱氧皮质酮(DOCA)-盐高血压大鼠的主要骨盆神经节(MPG)期间的海绵体内压力/平均动脉压比(ICP / MAP)评估勃起功能。使用荧光染料(DAF-FM)和共聚焦显微镜在海绵体切片中检测到一氧化氮(NO)释放。在腔内注射非选择性一氧化氮合酶(NOS)抑制剂l-NAME后,还表征了Tx2-6的作用。皮下或静脉内注射Tx2-6可增强神经节刺激引起的ICP / MAP升高。 l-NAME抑制了阴茎勃起,用Tx2-6治疗无法逆转这种抑制作用。 Tx2-6处理诱导海绵体组织中NO的释放显着增加。注射毒素后,DOCA-盐高血压大鼠的勃起功能减弱。 Tx2-6通过NO途径增强了正常血压和DOCA-盐高血压大鼠的勃起功能。我们的研究表明,Tx2-6对于开发治疗勃起功能障碍的新药物可能很重要。

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