Departamento de Fisiología, Laboratorio de Nucleótidos, Centro de Envejecimiento y Regeneración CARE, Facultad de Ciencias Biológicas, P. Universidad Católica de Chile, Santiago, Chile.
Neuroscience. 2012 Feb 17;203:216-29. doi: 10.1016/j.neuroscience.2011.11.067. Epub 2011 Dec 9.
The rat vas deferens has scattered sensory afferens plus a dense network of sympathetic motor efferens; these fibers are not known to interact functionally. We ascertained whether sensory fibers modulate the release of sympathetic transmitters through the release of calcitonin gene-related peptide (CGRP) and reciprocally assessed whether sympathetic transmitters modulate the overflow of ir-CGRP from sensory fibers. The tissue overflow of electrically evoked sympathetic co-transmitters (ATP/metabolites, noradrenaline (NA), and immunoreactive neuropeptide tyrosine (ir-NPY)) and the motor responses elicited were quantified following either exogenous CGRP or capsaicin application to elicit peptide release. Conversely, the outflow of ir-CGRP was examined in the presence of sympathetic transmitters. Exogenous CGRP reduced in a concentration-dependent manner the electrically evoked outflow of ATP/metabolites, NA, and ir-NPY with EC(50) values of 1.3, 0.18, and 1.9 nM, respectively. CGRP also reduced the basal NA overflow. The CGRP-evoked modulation was blocked by CGRP8-37 or H-89. Release of endogenous CGRP by capsaicin significantly reduced the basal overflow of NA, ir-NPY, and the electrically evoked sympathetic transmitter release. ADP, 2-methylthioadenosine-5'-O-diphosphate (2-MeSADP), or UTP decreased the electrically evoked ir-CGRP overflow, whereas clonidine, α,β-methyleneadenosine 5'-triphosphate (α,β-mATP), or adenosine (ADO) were inactive. CGRP acting postjunctionally also reduced the motor responses elicited by exogenous NA, ATP, or electrically evoked contractions. We conclude that CGRP exerts a presynaptic modulator role on sympathetic nerve endings and reciprocally ATP or related nucleotides influence the release of ir-CGRP from sensory fibers, highlighting a dynamic sympatho-sensory control between sensory fibers and sympathetic nerve ending. Postjunctional CGRP receptors further contribute to reduce the tissue sympathetic motor tone implying a pre and postjunctional role of CGRP as a sympathetic tone modulator.
大鼠输精管散布有感觉传入纤维和密集的交感运动传出纤维网络;目前尚不清楚这些纤维在功能上相互作用。我们确定感觉纤维是否通过释放降钙素基因相关肽 (CGRP) 来调节交感神经递质的释放,并反过来评估交感神经递质是否调节感觉纤维中 ir-CGRP 的溢出。电刺激诱发的交感神经共递质 (ATP/代谢物、去甲肾上腺素 (NA) 和免疫反应性神经肽酪氨酸 (ir-NPY)) 的组织溢出以及运动反应在给予外源性 CGRP 或辣椒素以引发肽释放后进行定量。相反,在存在交感神经递质的情况下检查 ir-CGRP 的流出。外源性 CGRP 以浓度依赖性方式降低电刺激诱发的 ATP/代谢物、NA 和 ir-NPY 的流出,EC50 值分别为 1.3、0.18 和 1.9 nM。CGRP 还降低了基础 NA 溢出。CGRP8-37 或 H-89 阻断了 CGRP 诱发的调制。辣椒素释放内源性 CGRP 显著降低了基础 NA、ir-NPY 和电刺激诱发的交感神经递质释放。ADP、2-甲基硫腺苷 5'-二磷酸 (2-MeSADP) 或 UTP 降低电刺激的 ir-CGRP 溢出,而可乐定、α,β-亚甲基腺苷 5'-三磷酸 (α,β-mATP) 或腺苷 (ADO) 则没有作用。CGRP 在后突触也降低了外源性 NA、ATP 或电刺激收缩引起的运动反应。我们得出结论,CGRP 对交感神经末梢发挥突触前调制器作用,相反,ATP 或相关核苷酸影响感觉纤维中 ir-CGRP 的释放,突出了感觉纤维和交感神经末梢之间动态的交感感觉控制。后突触 CGRP 受体进一步有助于降低组织交感运动张力,暗示 CGRP 作为交感神经张力调节剂具有前突触和后突触作用。