Mita Atsuki, Yoshida Misaki, Nagayama Toshiki
Division of Biology, Graduate School of Science and Engineering, Yamagata University, 990-8560 Yamagata, Japan.
Department of Biology, Faculty of Science, Yamagata University, 990-8560 Yamagata, Japan.
J Exp Biol. 2014 Dec 15;217(Pt 24):4423-31. doi: 10.1242/jeb.110551. Epub 2014 Dec 1.
The modulatory effects of nitric oxide (NO) and cAMP on the rhythmic beating activity of the swimmeret motor neurones in the crayfish were examined. Swimmerets are paired appendages located on the ventral side of each abdominal segment that show rhythmic beating activity during forward swimming, postural righting behaviour and egg ventilation in gravid females. In isolated abdominal nerve cord preparations, swimmeret motor neurones are usually silent or show a continuous low-frequency spiking activity. Application of carbachol, a cholinergic agonist, elicited rhythmic bursts of motor neurone spikes. The co-application of L-arginine, the substrate for NO synthesis with carbachol increased the burst frequency of the motor neurones. The co-application of the NO donor SNAP with carbachol also increased the burst frequency of the motor neurones. By contrast, co-application of a NOS inhibitor, L-NAME, with carbachol decreased beating frequency of the motor neurones. These results indicate that NO may act as a neuromodulator to facilitate swimmeret beating activity. The facilitatory effect of L-arginine was cancelled by co-application of the soluble guanylate cyclase (sGC) inhibitor ODQ suggesting that NO acts by activating sGC to promote the production of cGMP. Application of L-arginine alone or membrane-permeable cGMP analogue 8-Br-cGMP alone did not elicit rhythmic activity of motor neurones, but co-application of 8-Br-cGMP with carbachol increased bursting frequency of the motor neurones. Furthermore, application of the membrane-permeable cAMP analogue CPT-cAMP alone produced rhythmic bursting of swimmeret motor neurones, and the bursting frequency elicited by CPT-cAMP was increased by co-application with L-arginine. Co-application of the adenylate cyclase inhibitor SQ22536 ceased rhythmic bursts of motor neurone spikes elicited by carbachol. These results suggest that a cAMP system enables the rhythmic bursts of motor neurone spikes and that a NO-cGMP signaling pathway increases cAMP activity to facilitate swimmeret beating.
研究了一氧化氮(NO)和环磷酸腺苷(cAMP)对小龙虾游泳足运动神经元节律性搏动活动的调节作用。游泳足是位于每个腹节腹侧的成对附肢,在向前游泳、姿势矫正行为以及怀孕雌虾的卵通气过程中表现出节律性搏动活动。在离体腹神经索标本中,游泳足运动神经元通常处于静息状态或呈现持续的低频放电活动。应用胆碱能激动剂卡巴胆碱可引发运动神经元动作电位的节律性爆发。将L-精氨酸(NO合成的底物)与卡巴胆碱共同应用可增加运动神经元的爆发频率。将NO供体硝普钠(SNAP)与卡巴胆碱共同应用也可增加运动神经元的爆发频率。相比之下,将一氧化氮合酶(NOS)抑制剂L-硝基精氨酸甲酯(L-NAME)与卡巴胆碱共同应用可降低运动神经元的搏动频率。这些结果表明,NO可能作为一种神经调节剂促进游泳足的搏动活动。L-精氨酸的促进作用可被可溶性鸟苷酸环化酶(sGC)抑制剂ODQ共同应用所抵消,这表明NO通过激活sGC来促进环磷酸鸟苷(cGMP)的产生。单独应用L-精氨酸或膜通透性cGMP类似物8-溴-cGMP均未引发运动神经元的节律性活动,但将8-溴-cGMP与卡巴胆碱共同应用可增加运动神经元的爆发频率。此外,单独应用膜通透性cAMP类似物环磷腺苷(CPT-cAMP)可产生游泳足运动神经元的节律性爆发,并且与L-精氨酸共同应用可增加CPT-cAMP引发的爆发频率。腺苷酸环化酶抑制剂SQ22536共同应用可终止卡巴胆碱引发的运动神经元动作电位的节律性爆发。这些结果表明,cAMP系统可使运动神经元动作电位产生节律性爆发,并且NO-cGMP信号通路可增加cAMP活性以促进游泳足的搏动。