Rane S G, Gerlach P H, Wyse G A
J Neurobiol. 1984 May;15(3):207-20. doi: 10.1002/neu.480150304.
Both octopamine and proctolin potentiate nerve-evoked skeletal muscle contractions in the horseshoe crab, Limulus. The threshold concentration for octopamine was 10(-9) to 10(-8)M, while for proctolin it was 3 X 10(-9)M. Norepinephrine and dopamine produced effects similar to octopamine but at higher thresholds; tyramine and serotonin were ineffective. Octopamine caused significant increases in amplitudes of excitatory postsynaptic potentials (epsps) of muscle fibers, but had little effect on muscle fiber input resistance or membrane potential. Also, octopamine did not affect depolarization of muscle fibers and subsequent contraction due to the direct action of exogenously applied glutamate. These results suggest that octopamine potentiates nerve-evoked contractions primarily by facilitating release of neuromuscular transmitter. At concentrations above 10(-7)M, however, octopamine sometimes caused muscle spikes in response to motoneuron stimulation, a finding that suggests that octopamine may also have some postsynaptic action. Proctolin potentiated the muscle contractions evoked by glutamate but had little effect on glutamate-evoked muscle fiber depolarization, muscle fiber input resistance, or membrane potential. Thus, proctolin appears to act directly on skeletal muscle to enhance contractility. The proctolin-induced potentiations of contraction were sometimes accompanied by modest increases in epsp amplitude, so that unlike lobster skeletal and Limulus cardiac neuromuscular preparations, proctolin may have a secondary direct synaptic effect. Both octopamine and proctolin have been found in Limulus cardiac ganglion. This potential access to the hemolymph and the relatively low threshold concentrations needed for physiological action suggest that octopamine and proctolin could function as hormonal modulators of neuromuscular function in Limulus.
章鱼胺和促肠肌肽均可增强鲎(Limulus)中神经诱发的骨骼肌收缩。章鱼胺的阈浓度为10⁻⁹至10⁻⁸M,而促肠肌肽的阈浓度为3×10⁻⁹M。去甲肾上腺素和多巴胺产生的作用与章鱼胺相似,但阈浓度更高;酪胺和5-羟色胺则无作用。章鱼胺可使肌肉纤维兴奋性突触后电位(epsps)的幅度显著增加,但对肌肉纤维的输入电阻或膜电位影响很小。此外,章鱼胺不影响外源性施加谷氨酸直接作用引起的肌肉纤维去极化及随后的收缩。这些结果表明,章鱼胺主要通过促进神经肌肉递质的释放来增强神经诱发的收缩。然而,在浓度高于10⁻⁷M时,章鱼胺有时会在运动神经元刺激下引起肌肉锋电位,这一发现表明章鱼胺可能也有一些突触后作用。促肠肌肽增强了谷氨酸诱发的肌肉收缩,但对谷氨酸诱发的肌肉纤维去极化、肌肉纤维输入电阻或膜电位影响很小。因此,促肠肌肽似乎直接作用于骨骼肌以增强收缩性。促肠肌肽诱导的收缩增强有时伴随着epsp幅度的适度增加,所以与龙虾骨骼肌和鲎心脏神经肌肉标本不同,促肠肌肽可能有次要的直接突触作用。在鲎心脏神经节中已发现章鱼胺和促肠肌肽。这种对血淋巴的潜在接触以及生理作用所需的相对较低阈浓度表明,章鱼胺和促肠肌肽可能作为鲎神经肌肉功能的激素调节剂发挥作用。