Prado Armando Pérez de, Pérez-Martínez Claudia, Regueiro-Purriños Marta, Cuellas-Ramón Carlos, López-Benito María, Gonzalo-Orden José Manuel, Estévez-Loureiro Rodrigo, Cortina-Rivero Ana Isabel, Viñuela-Baragaño David, R Altonaga José, Tellez Armando, Fernández-Vázquez Felipe
Fundación Investigación Sanitaria de León, Hospital Universitario de León-Instituto de Biomedicina (IBIOMED), Universidad de León, 24071 León, Spain.
Alizée Pathology LLC., Thurmont, MD 21788, USA.
Animals (Basel). 2020 Aug 19;10(9):1446. doi: 10.3390/ani10091446.
New-generation catheters-based renal denervation (RDN) is under investigation for the treatment of uncontrolled hypertension (HTN). We assessed the feasibility of a large animal model of HTN to accommodate the human RDN devices. Ten minipigs were instrumented to measure blood pressure (BP) in an awake-state. HTN was induced with subcutaneous 11-deoxycorticosterone (DOCA, 100 mg/kg) implants. Five months after, the surviving animals underwent RDN with the Symplicity system. Norepinephrine (NE) renal gradients were determined before and 1 month after RDN. Renal arteries were processed for histological (hematoxylin-eosin, Movat pentachrome) and immunohistochemical (S100, tyrosine-hydroxylase) analyses. BP significantly rose after DOCA implants. Six animals died prematurely, mainly from infectious causes. The surviving animals showed stable BP levels after 5 months. One month after RDN, nerve damage was showed in three animals, with impedance drop >10%, NE gradient drop and reduction in BP. The fourth animal showed no nerve damage, impedance drop <10%, NE gradient increase and no change in BP. In conclusion, the minipig model of DOCA-induced HTN is feasible, showing durable effects. High mortality should be addressed in next iterations of this model. RDN may partially offset the DOCA-induced HTN. Impedance drop and NE renal gradient could be markers of RDN success.
新一代基于导管的肾去神经支配术(RDN)正在接受治疗难治性高血压(HTN)的研究。我们评估了一种大型高血压动物模型以适配人类RDN设备的可行性。对10只小型猪进行仪器植入以在清醒状态下测量血压(BP)。通过皮下植入11-脱氧皮质酮(DOCA,100 mg/kg)诱导高血压。五个月后,存活的动物接受了使用Symplicity系统的RDN。在RDN术前和术后1个月测定去甲肾上腺素(NE)肾梯度。对肾动脉进行组织学(苏木精-伊红染色、Movat五色染色)和免疫组织化学(S100、酪氨酸羟化酶)分析。DOCA植入后BP显著升高。6只动物过早死亡,主要死于感染原因。存活的动物在5个月后BP水平稳定。RDN术后1个月,3只动物显示神经损伤,阻抗下降>10%,NE梯度下降且BP降低。第四只动物未显示神经损伤,阻抗下降<10%,NE梯度增加且BP无变化。总之,DOCA诱导的高血压小型猪模型是可行的,显示出持久的效果。在该模型的后续迭代中应解决高死亡率问题。RDN可能部分抵消DOCA诱导的高血压。阻抗下降和NE肾梯度可能是RDN成功的标志物。