Butkevich Irina P, Mikhailenko Viktor A, Vershinina Elena A, Aloisi Anna Maria
Department of Ontogenesis of the Nervous System, I.P. Pavlov Institute of Physiology, Russian Academy of Sciences, St. Petersburg 199034, Russia.
Department of Normal Physiology, St. Petersburg State Pediatric Medical University, St. Petersburg 194100, Russia.
Chin J Physiol. 2016 Aug 31;59(4):225-31. doi: 10.4077/CJP.2016.BAE412.
Neonatal pain and stress induce long-term changes in pain sensitivity. Therefore their interrelation is a topical subject of clinical and basic research. The present study investigated the effects of inflammatory peripheral pain and stress of maternal deprivation (MD)-isolation in 1-2- and 7-8-day-old Wistar rats (P1,2 and P7,8 respectively, ages comparable to preterm and full-term human babies) on basal pain and pain sensitivity in conditions of inflammatory pain (formalin test) during adolescence. The neonatal impacts were: pain (formalin injection, FOR in the paw), stress (a short 60-min MD), or pain+stress combination (FOR+MD), and appropriate controls. We found that stress of short-term maternal deprivation-isolation and inflammatory pain on P1,2 and P7,8 significantly increased the vulnerability of the nociceptive system to inflammatory pain. Maternal deprivation-isolation on P1,2 as compared with a similar impact on P7,8 had a greater effect on pain sensitivity of the adolescent rats, but the influence of early pain was independent of the injury age. Only adolescent rats with an early combination of pain and maternal deprivation-isolation showed hypoalgesia in the hot plate (HP) test. However licking duration (reflecting pain sensitivity) in these rats did not exceed licking duration in animals exposed only to maternal deprivation-isolation or pain. This study adds new data to the growing body of work demonstrating that early noxious impacts have long-term consequences for the functional activity of the nociceptive system. Our new findings may help to understand the impact of pain and maternal separation in the neonatal intensive care unit.
新生儿疼痛和应激会导致疼痛敏感性的长期变化。因此,它们之间的相互关系是临床和基础研究的热门课题。本研究调查了炎症性外周疼痛以及母体剥夺(MD)应激——隔离1至2日龄和7至8日龄的Wistar大鼠(分别为P1,2和P7,8,其年龄与早产和足月人类婴儿相当)——对青春期炎症性疼痛(福尔马林试验)条件下基础疼痛和疼痛敏感性的影响。新生儿受到的影响包括:疼痛(爪部注射福尔马林,FOR)、应激(60分钟的短期MD)或疼痛 + 应激组合(FOR + MD),以及相应的对照。我们发现,P1,2和P7,8的短期母体剥夺——隔离应激和炎症性疼痛显著增加了伤害感受系统对炎症性疼痛的易感性。与P7,8受到的类似影响相比,P1,2的母体剥夺——隔离对青春期大鼠的疼痛敏感性影响更大,但早期疼痛的影响与损伤年龄无关。只有早期经历疼痛和母体剥夺——隔离组合的青春期大鼠在热板(HP)试验中表现出痛觉减退。然而,这些大鼠的舔舐持续时间(反映疼痛敏感性)并未超过仅经历母体剥夺——隔离或疼痛的动物的舔舐持续时间。这项研究为越来越多的研究工作增添了新数据,表明早期有害影响对伤害感受系统的功能活动具有长期影响。我们的新发现可能有助于理解新生儿重症监护病房中疼痛和母婴分离的影响。