Department of Human Physiology and Pathophysiology, School of Medicine, Collegium Medicum, University of Warmia and Mazury in Olsztyn, Warszawska 30, 10-082 Olsztyn, Poland.
Department of Animal Anatomy, Faculty of Veterinary Medicine, University of Warmia and Mazury in Olsztyn, Oczapowskiego 13, 10-719 Olsztyn, Poland.
Int J Mol Sci. 2021 Dec 13;22(24):13399. doi: 10.3390/ijms222413399.
Although guanethidine (GUA) was used in the past as a drug to suppress hyperactivity of the sympathetic nerve fibers, there are no available data concerning the possible action of this substance on the sensory component of the peripheral nervous system supplying the urinary bladder. Thus, the present study was aimed at disclosing the influence of intravesically instilled GUA on the distribution, relative frequency, and chemical coding of dorsal root ganglion neurons associated with the porcine urinary bladder. The investigated sensory neurons were visualized with a retrograde tracing method using Fast Blue (FB), while their chemical profile was disclosed with single-labeling immunohistochemistry using antibodies against substance P (SP), calcitonin gene-related peptide (CGRP), pituitary adenylate cyclase activating polypeptide (PACAP), galanin (GAL), neuronal nitric oxide synthase (nNOS), somatostatin (SOM), and calbindin (CB). After GUA treatment, a slight decrease in the number of FB neurons containing SP was observed when compared with untreated animals (34.6 ± 6.5% vs. 45.6 ± 1.3%), while the number of retrogradely traced cells immunolabeled for GAL, nNOS, and CB distinctly increased (12.3 ± 1.0% vs. 7.4 ± 0.6%, 11.9 ± 0.6% vs. 5.4 ± 0.5% and 8.6 ± 0.5% vs. 2.7 ± 0.4%, respectively). However, administration of GUA did not change the number of FB neurons containing CGRP, PACAP, or SOM. The present study provides evidence that GUA significantly modifies the sensory innervation of the porcine urinary bladder wall and thus may be considered a potential tool for studying the plasticity of this subdivision of the bladder innervation.
虽然胍乙啶(GUA)过去曾被用作抑制交感神经纤维过度活跃的药物,但关于这种物质对供应膀胱的周围感觉神经成分可能产生的作用,尚无可用数据。因此,本研究旨在揭示膀胱内注入的 GUA 对与猪膀胱相关的背根神经节神经元的分布、相对频率和化学编码的影响。使用逆行示踪法(Fast Blue,FB)显示研究中的感觉神经元,并用单标记免疫组织化学法(针对物质 P(SP)、降钙素基因相关肽(CGRP)、垂体腺苷酸环化酶激活肽(PACAP)、甘丙肽(GAL)、神经元型一氧化氮合酶(nNOS)、生长抑素(SOM)和钙结合蛋白(CB)的抗体)揭示其化学特征。与未处理动物相比,GUA 处理后,含有 SP 的 FB 神经元数量略有减少(34.6 ± 6.5% vs. 45.6 ± 1.3%),而被逆行追踪并免疫标记为 GAL、nNOS 和 CB 的细胞数量明显增加(12.3 ± 1.0% vs. 7.4 ± 0.6%、11.9 ± 0.6% vs. 5.4 ± 0.5%和 8.6 ± 0.5% vs. 2.7 ± 0.4%)。然而,GUA 的给药并未改变含有 CGRP、PACAP 或 SOM 的 FB 神经元的数量。本研究提供了证据表明,GUA 可显著改变猪膀胱壁的感觉神经支配,因此可被视为研究膀胱神经支配这一分支可塑性的潜在工具。