首页> 外文期刊>Toxicon: An International Journal Devoted to the Exchange of Knowledge on the Poisons Derived from Animals, Plants and Microorganisms >Pharmacological characterization of the presynaptic activity of Tityus serrulatus venom in the rat anococcygeus muscle
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Pharmacological characterization of the presynaptic activity of Tityus serrulatus venom in the rat anococcygeus muscle

机译:鼠尾草Tityus serrulatus毒液突触前活性的药理学表征

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摘要

Scorpion venoms are known to cause peripheral nerve stimulation with enhanced autonomic responses. This study, therefore, examined the effects of Tityus serrulatus venom (TSV) on adrenergic, cholinergic and nitrergic nerve fibers using the rat anococcygeus muscle. The contractile effects of TSV (1 mug/ml) and electrical field stimulation were markedly reduced by phentolamine (5 muM), prazosin (0.1 muM), guanethidine (30 muM) and tetrodotoxin (TTX, l muM), whereas imipramine (3 muM) enhanced these responses. The responses to tyramine (10 muM) were partially reduced by guanethidine and completely blocked by phentolamine, prazosin and imipramine. Atropine (1 muM) fully prevented carbachol (CCh, 30 muM)-induced contractions without affecting those mediated by TSV. Neostigmine significantly potentiated TSV-and ACh-evoked contractions, whereas hexamethonium had no effect. The relaxant responses induced by EFS and TSV (3 mug/ml) were completely blocked by L-NAME (100 muM), ODQ (1 muM) or TTX (1 muM). Addition of L-arginine (1 mM) reversed the effect of L-NAME. Thus, the motor and inhibitory responses of TSV in the rat anococcygeus muscle are mediated by prejunctional mechanisms dependent on Na+ channel activation, causing the stimulation of NA and NO release from adrenergic and nitrergic nerve fibers, respectively.
机译:已知蝎毒会引起周围神经刺激,并增强自主神经反应。因此,本研究使用大鼠无囊球菌肌肉检查了马齿ity肉毒液(TSV)对肾上腺素能,胆碱能和硝酸能神经纤维的作用。苯妥拉明(5μM),哌唑嗪(0.1μM),胍乙啶(30μM)和河豚毒素(TTX,1μM)显着降低了TSV(1杯/毫升)和电场刺激的收缩作用,而丙咪嗪(3μM) )增强了这些响应。胍乙啶对酪胺(10μM)的反应部分降低,而苯妥拉明,哌唑嗪和丙咪嗪则完全阻断了对酪胺的反应。阿托品(1μM)完全阻止了卡巴胆碱(CCh,30μM)引起的收缩,而不会影响TSV介导的收缩。新斯的明可显着增强TSV和ACh引起的收缩,而六甲铵则无作用。由EFS和TSV(3杯/毫升)诱导的松弛反应被L-NAME(100μM),ODQ(1μM)或TTX(1μM)完全阻断。加入L-精氨酸(1 mM)可以逆转L-NAME的作用。因此,TSV在大鼠无球藻肌肉中的运动和抑制反应是由依赖于Na +通道激活的结节机制介导的,分别刺激了肾上腺素能和硝化神经纤维释放NA和NO。

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