Hisada Chie, Kajimoto Kyoko, Tsugane Hiroko, Mitsuo Iinuma, Azuma Kagaku, Kubo Kin-Ya
Departments of Pediatric Dentistry, Asahi University School of Dentistry, Gifu, Japan.
Department of Anatomy, School of Medicine, University of Occupational and Environmental Health, Kitakyusyu, Japan.
J Prosthodont Res. 2023 Oct 13;67(4):588-594. doi: 10.2186/jpr.JPR_D_22_00255. Epub 2023 Feb 14.
Prenatal stress affects the hippocampal structure and function in pups. Maternal chewing ameliorates hippocampus-dependent cognitive impairments induced by prenatal stress. In this study, we investigated hippocampal microglia-mediated neuroinflammation in pups of dams exposed to prenatal stress with or without chewing during gestation.
Pregnant mice were randomly assigned to control, stress, and stress/chewing groups. Stress and stress/chewing animals were subjected to restraint stress for 45 min three times daily from gestation day 12 to parturition, and were given a wooden stick to chew during the stress period. Four-month-old male pups were intraperitoneally administered with lipopolysaccharide (LPS). Serum corticosterone levels were determined 24 h after administration. The expression levels of hippocampal inflammatory cytokines were measured, and the microglia were analyzed morphologically.
Prenatal stress increased serum corticosterone levels, induced hippocampal microglia priming, and facilitated the release of interleukin-1β and tumor necrosis factor-α in the offspring. LPS treatment significantly increased the effects of prenatal stress on serum corticosterone levels, hippocampal microglial activation, and hippocampal neuroinflammation. Maternal chewing significantly inhibited the increase in serum corticosterone levels, suppressed microglial overactivation, and normalized inflammatory cytokine levels under basal prenatal stress conditions as well as after LPS administration.
Our findings indicate that maternal chewing can alleviate the increase in corticosterone levels and inhibit hippocampal microglia-mediated neuroinflammation induced by LPS administration and prenatal stress in adult offspring.
产前应激会影响幼崽的海马结构和功能。母体咀嚼可改善产前应激诱导的海马依赖性认知障碍。在本研究中,我们调查了孕期暴露于产前应激且有或无咀嚼行为的母鼠所产幼崽海马中由小胶质细胞介导的神经炎症。
将怀孕小鼠随机分为对照组、应激组和应激/咀嚼组。从妊娠第12天至分娩,应激组和应激/咀嚼组动物每天接受3次45分钟的束缚应激,并在应激期间给予一根木棍供其咀嚼。对4月龄雄性幼崽腹腔注射脂多糖(LPS)。给药24小时后测定血清皮质酮水平。检测海马炎性细胞因子的表达水平,并对小胶质细胞进行形态学分析。
产前应激会增加血清皮质酮水平,诱导海马小胶质细胞预激活,并促进后代白细胞介素-1β和肿瘤坏死因子-α的释放。LPS处理显著增强了产前应激对血清皮质酮水平、海马小胶质细胞激活和海马神经炎症的影响。在基础产前应激条件下以及LPS给药后,母体咀嚼显著抑制了血清皮质酮水平的升高,抑制了小胶质细胞的过度激活,并使炎性细胞因子水平恢复正常。
我们的研究结果表明,母体咀嚼可减轻皮质酮水平的升高,并抑制成年后代中由LPS给药和产前应激诱导的海马小胶质细胞介导的神经炎症。