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首页> 外文期刊>Neural regeneration research >Interleukin-18 levels in the hippocampus and behavior of adult rat offspring exposed to prenatal restraint stress during early and late pregnancy
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Interleukin-18 levels in the hippocampus and behavior of adult rat offspring exposed to prenatal restraint stress during early and late pregnancy

机译:白细胞介素-18在早期和晚期怀孕期间暴露于产前约束压力的成人大鼠后代的海马蛋白蛋白-18水平

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Exposure to maternal stress during prenatal life is associated with an increased risk of neuropsychiatric disorders, such as depression and anxiety, in offspring. It has also been increasingly observed that prenatal stress alters the phenotype of offspring via immunological mechanisms and that immunological dysfunction, such as elevated interleukin-18 levels, has been reported in cultures of microglia. Prenatal restraint stress (PRS) in rats permits direct experimental investigation of the link between prenatal stress and adverse outcomes. However, the majority of studies have focused on the consequences of PRS delivered in the second half of pregnancy, while the effects of early prenatal stress have rarely been examined. Therefore, pregnant rats were subjected to PRS during early/middle and late gestation (days 8–14 and 15–21, respectively). PRS comprised restraint in a round plastic transparent cylinder under bright light (6500 lx) three times per day for 45 minutes. Differences in interleukin-18 expression in the hippocampus and in behavior were compared between offspring rats and control rats on postnatal day 75. We found that adult male offspring exposed to PRS during their late prenatal periods had higher levels of anxiety-related behavior and depression than control rats, and both male and female offspring exhibited higher levels of depression-related behavior, impaired recognition memory and diminished exploration of novel objects. Moreover, an elevated level of interleukin-18 was observed in the dorsal and ventral hippocampus of male and female early- and late-PRS offspring rats. The results indicate that PRS can cause anxiety and depression-related behaviors in adult offspring and affect the expression of interleukin-18 in the hippocampus. Thus, behavior and the molecular biology of the brain are affected by the timing of PRS exposure and the sex of the offspring. All experiments were approved by the Animal Experimentation Ethics Committee at Kunming Medical University, China (approval No. KMMU2019074) in January 2019.
机译:产前生活期间暴露于产前生命中的母体胁迫与后代抑郁和焦虑,例如抑郁和焦虑的风险增加。还越来越多地观察到产前胁迫通过免疫机制改变后代的表型,并且在微胶质细胞的培养中报道了在微胶质细胞的培养上报道了免疫功能障碍,例如升高的白细胞介素-18水平。大鼠的产前抑制应力(PRS)允许直接实验调查产前压力和不良结果之间的联系。然而,大多数研究都集中在怀孕后半部分递送的PRS的后果,而早期产前胁迫的影响很少被检查。因此,在早期/中期妊娠(分别为8-14和15-21天)期间对孕大鼠进行PRS。 PRS在圆形塑料透明圆柱体下约束在明亮的灯光(6500 LX)下每天三次,45分钟。在产后第75天的后代大鼠和对照大鼠之间比较了海马和对照大鼠的白细胞介素-18表达的差异。我们发现在其晚期产前期间暴露于PRS的成年男性后代具有更高水平的焦虑相关行为和抑郁症。对照大鼠,男性和女性后代均表现出更高水平的抑郁相关行为,受损的识别记忆和微小的新物体探索。此外,在雄性和女性早期和晚期后代大鼠的背部和腹侧海马中观察到白细胞介素-18的升高水平。结果表明,PRS可能导致成人后代焦虑和抑郁相关行为,影响海马中白细胞介素-18的表达。因此,大脑的行为和分子生物学受到预曝光和后代性行为的影响。 2019年1月,昆明医科大学动物实验伦理委员会批准了所有实验均批准,昆明医科大学(批准号KMMU2019074)。

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