Wenzel B, Elsner N, Heinrich R
Department of Neurobiology, Institute of Zoology and Anthropology, Georg-August-University, Berliner Strasse 28, 37073 Goettingen, Germany.
J Neurophysiol. 2002 Feb;87(2):876-88. doi: 10.1152/jn.00312.2001.
The species-specific sound production of acoustically communicating grasshoppers can be stimulated by pressure injection of both nicotinic and muscarinic agonists into the central body complex and a small neuropil situated posterior and dorsal to it. To determine the role of muscarinic acetylcholine receptors (mAChRs) in the control of acoustic communication behavior and to identify the second-messenger pathways affected by mAChR-activation, muscarinic agonists and membrane-permeable drugs known to interfere with specific mechanisms of intracellular signaling pathways were pressure injected to identical sites in male grasshopper brains. Repeated injections of small volumes of muscarine elicited stridulation of increasing duration associated with decreased latencies. This suggested an accumulation of excitation over time that is consistent with the suggested role of mAChRs in controlling courtship behavior: to provide increasing arousal leading to higher intensity of stridulation and finally initiating a mating attempt. At sites in the brain where muscarine stimulation was effective, stridulation could be evoked by forskolin, an activator of adenylate cyclase (AC); 8-Br-cAMP-activating protein kinase A (PKA); and 3-isobuty-1-methylxanthine, leading to the accumulation of endogenously generated cAMP through inhibition of phosphodiesterases. This suggested that mAChRs mediate excitation by stimulating the AC/cAMP/PKA pathway. In addition, muscarine-stimulated stridulation was inhibited by 2'-5'-dideoxyadenonsine and SQ 22536, two inhibitors of AC; H-89 and Rp-cAMPS, two inhibitors of PKA; and by U-73122 and neomycin, two agents that inhibit phospholipase C (PLC) by independent mechanisms. Because the inhibition of AC, PKA, or PLC by various individually applied substances entirely suppressed muscarine-evoked stridulation in a number of experiments, activation of both pathways, AC/cAMP/PKA and PLC/IP(3)/diacylglycerine, appeared to be necessary to mediate the excitatory effects of mAChRs. With these studies on an intact "behaving" grasshopper preparation, we present physiological relevance for mAChR-evoked excitation mediated by sequential activation of the AC- and PLC-initiated signaling pathways that has been reported in earlier in vitro studies.
通过向中枢复合体以及位于其后方和背侧的一个小神经纤维网中压力注射烟碱样和毒蕈碱样激动剂,可以刺激通过声音进行交流的蚱蜢产生物种特异性的发声。为了确定毒蕈碱型乙酰胆碱受体(mAChRs)在控制声学通讯行为中的作用,并识别受mAChR激活影响的第二信使途径,将毒蕈碱样激动剂和已知会干扰细胞内信号通路特定机制的膜通透性药物压力注射到雄性蚱蜢大脑中的相同部位。重复小剂量注射毒蕈碱会引发持续时间增加且潜伏期缩短的摩擦发声。这表明兴奋随时间积累,这与mAChRs在控制求偶行为中的作用相一致:提供逐渐增加的唤醒,导致更高强度的摩擦发声,最终引发交配尝试。在大脑中对毒蕈碱刺激有效的部位,腺苷酸环化酶(AC)的激活剂福斯高林、激活蛋白激酶A(PKA)的8-溴-cAMP以及3-异丁基-1-甲基黄嘌呤可诱发摩擦发声,通过抑制磷酸二酯酶导致内源性产生的cAMP积累。这表明mAChRs通过刺激AC/cAMP/PKA途径介导兴奋。此外,毒蕈碱刺激的摩擦发声受到AC的两种抑制剂2'-5'-二脱氧腺苷和SQ 22536、PKA的两种抑制剂H-89和Rp-cAMPS以及通过独立机制抑制磷脂酶C(PLC)的两种药物U-73122和新霉素的抑制。因为在许多实验中,各种单独应用的物质对AC、PKA或PLC的抑制完全抑制了毒蕈碱诱发的摩擦发声,AC/cAMP/PKA和PLC/IP(3)/二酰甘油这两条途径的激活似乎对于介导mAChRs的兴奋作用是必要的。通过对完整的“有行为”蚱蜢制剂的这些研究,我们展示了早期体外研究中报道的由AC和PLC启动的信号通路的顺序激活介导的mAChR诱发兴奋的生理相关性。