Postgraduate Program in Biosciences Applied to Health (PPGB), UNIFAL, Alfenas, MG, Brazil; Laboratory of Neuroscience, Neuromodulation and Study of Pain (LANNED), UNIFAL-MG, Alfenas, MG, Brazil.
Graduation in Physiotherapy at the Motricity Sciences Institute, UNIFAL, Alfenas, MG, Brazil; Laboratory of Neuroscience, Neuromodulation and Study of Pain (LANNED), UNIFAL-MG, Alfenas, MG, Brazil.
Behav Brain Res. 2023 Oct 2;454:114633. doi: 10.1016/j.bbr.2023.114633. Epub 2023 Aug 18.
This study investigates the effects of repetitive pinprick stimulation on preterm offspring and its impact on nociceptive responses and inflammatory hypersensitivity in adulthood.
The objective is to shed light on the potential long-term consequences of neonatal pain and prematurity on sensory processing.
Term and preterm rats were subjected to repetitive pinprick (PP) stimulation or control (CC) during the neonatal period. Adult rats received CFA injection to induce inflammatory hypersensitivity, and mechanical hypersensitivity was measured. Gender differences in inflammatory hypersensitivity were also examined. Maternal behavior, litter weight, and offspring growth were monitored to assess any potential influences of the stimulation on these parameters.
In preterm rats, the PP stimulation did not affect baseline thresholds to mechanical stimuli, but increased mechanical hypersensitivity after CFA injection in adult rats. Females exhibited greater inflammatory hypersensitivity compared to males. Maternal behavior, litter weight, and offspring growth were not influenced by the stimulation. PP stimulation during the neonatal period led to changes in nociceptive responses in adulthood, potentially altering sensory processing.
PP stimulation in preterm rats during the neonatal period resulted in changes in nociceptive responses in adulthood, leading to increased inflammatory hypersensitivity. The study emphasizes how early development can significantly impact sensory processing and further highlights the potential long-term consequences of prematurity and neonatal pain on this processing.
本研究旨在探讨重复性刺痛刺激对早产儿的影响,及其对成年后痛觉反应和炎症性过敏的影响。
旨在阐明新生儿疼痛和早产对感觉处理的潜在长期后果。
足月和早产大鼠在新生儿期接受重复性刺痛(PP)刺激或对照(CC)。成年大鼠接受 CFA 注射以诱导炎症性过敏反应,并测量机械性过敏反应。还检查了炎症性过敏反应的性别差异。监测母体行为、窝重和后代生长,以评估刺激对这些参数的潜在影响。
在早产大鼠中,PP 刺激不会影响机械刺激的基线阈值,但会增加成年大鼠 CFA 注射后的机械过敏反应。与雄性相比,雌性表现出更大的炎症性过敏反应。母体行为、窝重和后代生长不受刺激影响。新生儿期的 PP 刺激导致成年期痛觉反应发生变化,可能改变感觉处理。
新生儿期对早产大鼠进行的 PP 刺激导致成年期痛觉反应发生变化,导致炎症性过敏反应增加。该研究强调了早期发育如何显著影响感觉处理,并进一步强调了早产和新生儿疼痛对这种处理的潜在长期后果。