Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, USA.
Department of Obstetrics and Gynecology, Duke University Medical Center, USA.
Neurotoxicol Teratol. 2019 Jul-Aug;74:106808. doi: 10.1016/j.ntt.2019.05.001. Epub 2019 May 16.
Studies of intergenerational effects of parental chemical exposure have principally focused on maternal exposure, particularly for studies of adverse neurobehavioral consequences on the offspring. Maternal nicotine exposure has long been known to cause adverse neurobehavioral effects on the offspring. However, paternal toxicant exposure has also been found to cause neurobehavioral toxicity in their offspring. Recent work suggests that paternal nicotine exposure can have epigenetic effects, although it remains unclear whether such changes lead to neurobehavioral effects. In the current study, we investigated the effects of paternal nicotine exposure on neurobehavioral development of their offspring. Male Sprague-Dawley rats were exposed to 0 or 2 mg/kg/day nicotine (sc) for 56 consecutive days with two consecutive 2ML4 osmotic minipumps. Following treatment, these males were mated with drug-naïve female rats. Offspring of both sexes were tested in a behavioral battery to assess locomotion, emotional function and cognition. Paternal nicotine exposure did not impact offspring viability, health or growth. However, behavioral function of the offspring was significantly altered by paternal nicotine exposure. Male offspring with paternal nicotine exposure exhibited locomotor hyperactivity in the Figure-8 apparatus when tested during adolescence. When retested in adulthood and regardless of sex, offspring of the nicotine exposed father showed significantly reduced habituation of locomotor activity over the course of the session. Compared to controls, female offspring of nicotine-exposed fathers showed significantly reduced response latency in the radial arm maze test. In addition to locomotor hyperactivity, the offspring of nicotine-exposed fathers also showed significantly diminished habituation in the novel object recognition test. These results indicate that chronic paternal nicotine exposure can impact the behavior of offspring, producing locomotor hyperactivity and impaired habituation.
研究父母化学暴露的代际效应主要集中在母体暴露上,特别是在研究母体暴露对后代的不良神经行为后果方面。长期以来,母体尼古丁暴露已被证明会对后代产生不良的神经行为影响。然而,也有研究发现,父体毒物暴露也会导致其后代出现神经行为毒性。最近的研究表明,父体尼古丁暴露会产生表观遗传效应,尽管尚不清楚这些变化是否会导致神经行为效应。在本研究中,我们调查了父体尼古丁暴露对其后代神经行为发育的影响。雄性 Sprague-Dawley 大鼠连续 56 天每天接受 0 或 2mg/kg 尼古丁(sc)暴露,使用两个连续的 2ML4 渗透压微型泵。治疗结束后,这些雄性大鼠与未经药物处理的雌性大鼠交配。雄性和雌性后代均进行行为学测试,以评估运动、情绪和认知功能。父体尼古丁暴露不会影响后代的活力、健康或生长。然而,父体尼古丁暴露会显著改变后代的行为功能。暴露于父体尼古丁的雄性后代在青春期时在 8 字形装置中表现出运动过度活跃。当在成年期重新测试时,无论性别如何,暴露于尼古丁的父体的后代在整个测试过程中运动活动的习惯化明显减少。与对照组相比,暴露于尼古丁的父体的雌性后代在放射臂迷宫测试中表现出明显缩短的反应潜伏期。除了运动过度活跃外,暴露于尼古丁的父体的后代在新奇物体识别测试中也表现出明显减少的习惯化。这些结果表明,慢性父体尼古丁暴露会影响后代的行为,导致运动过度活跃和习惯化受损。