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Opposing actions of 5HT1A and 5HT2-like serotonin receptors on modulations of the electric signal waveform in the electric fish Brachyhypopomus pinnicaudatus

机译:5HT1A和5HT2样血清素受体对电鱼Brachyhypopomus pinnicaudatus中电信号波形的调制的反作用

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摘要

Serotonin (5-HT) is an indirect modulator of the electric organ discharge (EOD) in the weakly electric gymnotiform fish, Brachyhypopomus pinnicaudatus. Injections of 5-HT enhance EOD waveform “masculinity”, increasing both waveform amplitude and the duration of the second phase. This study investigated the pharmacological identity of 5-HT receptors that regulate the electric waveform and their effects on EOD amplitude and duration. We present evidence that two sets of serotonin receptors modulate the EOD in opposite directions. We found that the 5HT1AR agonist 8-OH-DPAT diminishes EOD duration and amplitude while the 5HT1AR antagonist WAY100635 increases these parameters. In contrast, the 5HT2R agonist α-Me-5-HT increases EOD amplitude but not duration, yet 5-HT-induced increases in EOD duration can be inhibited by blocking 5HT2A/2C-like receptors with ketanserin. These results show that 5-HT exerts bi-directional control of EOD modulations in B. pinnicaudatus via action at receptors similar to mammalian 5HT1A and 5HT2 receptors. The discordant amplitude and duration response suggests separate mechanisms for modulating these waveform parameters.
机译:5-羟色胺(5-HT)是弱电裸gym形鱼类Brachyhypopomus pinnicaudatus中电器官放电(EOD)的间接调节剂。注入5-HT会增强EOD波形的“男性气质”,同时增加波形幅度和第二阶段的持续时间。这项研究调查了5-HT受体的药理学特征,该受体调节电波形及其对EOD幅度和持续时间的影响。我们提供的证据表明,两组血清素受体在相反方向上调节EOD。我们发现5HT1AR激动剂8-OH-DPAT减少了EOD持续时间和振幅,而5HT1AR拮抗剂WAY100635增加了这些参数。相反,5HT2R激动剂α-Me-5-HT增加EOD幅度,但不增加持续时间,然而,通过用酮色林阻断5HT2A / 2C样受体可以抑制5HT诱导的EOD持续时间的增加。这些结果表明,5-HT通过对类似于哺乳动物5HT1A和5HT2受体的受体起作用,在松果双歧杆菌中对EOD调节进行双向控制。不一致的幅度和持续时间响应建议了用于调制这些波形参数的单独机制。

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