Nakasone Ruka, Ashina Mariko, Kido Takumi, Miyauchi Harunori, Saito Masafumi, Inoue Shigeaki, Shinohara Masakazu, Nozu Kandai, Fujioka Kazumichi
Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan.
Department of Pediatric Surgery, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan.
J Clin Med. 2021 Dec 13;10(24):5823. doi: 10.3390/jcm10245823.
Neonatal sepsis is characterized by systemic bacterial invasion followed by a massive inflammatory response. At present, no therapeutic strategy has been found that significantly reduces the mortality of neonatal sepsis. We aimed to investigate the protective role of an initial low-dose septic challenge for the prevention of subsequent lethal sepsis in a mouse model. A stock cecal slurry (CS) solution was prepared from adult ceca. The LD83 (1.5 mg CS/g) was used for all animals. An initial challenge of normal saline (NS) or 0.5 mg CS/g (non-lethal dose) was administered at four days of age, then 1.5 mg CS/g was administered intraperitoneally at seven days of age (72 h post-initial challenge), and survival was monitored. Initial exposure to NS ( = 10) resulted in 90% mortality following exposure to the LD83 CS dose in contrast to an initial exposure to CS ( = 16), which significantly decreased mortality to 6% ( 0.0001), reduced blood bacterial counts, attenuated inflammatory responses, and suppressed lipid mediators. Initial exposure to a non-lethal CS dose prior to exposure to a lethal CS dose significantly reduces sepsis mortality, a protective effect that might be mediated by modulating abnormal systemic inflammatory responses.
新生儿败血症的特征是全身性细菌入侵,随后是大规模炎症反应。目前,尚未找到能显著降低新生儿败血症死亡率的治疗策略。我们旨在研究在小鼠模型中,初次低剂量脓毒症激发对预防随后致命性败血症的保护作用。用成年盲肠制备储备盲肠灌洗液(CS)溶液。所有动物均使用LD83(1.5毫克CS/克)。在4日龄时给予初次生理盐水(NS)或0.5毫克CS/克(非致死剂量)激发,然后在7日龄(初次激发后72小时)腹腔注射1.5毫克CS/克,并监测存活率。初次暴露于NS(n = 10)的小鼠在暴露于LD83 CS剂量后死亡率为90%,而初次暴露于CS(n = 16)的小鼠死亡率显著降至6%(P < 0.0001),血液细菌计数减少,炎症反应减弱,脂质介质受到抑制。在暴露于致死性CS剂量之前,初次暴露于非致死性CS剂量可显著降低败血症死亡率,这种保护作用可能是通过调节异常的全身炎症反应介导的。