Smith Nicholas A, Germundson Danielle L, Combs Colin K, Vendsel Lane P, Nagamoto-Combs Kumi
Department of Pathology, University of North Dakota School of Medicine and Health Sciences, Grand Forks, ND, United States.
Department of Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, ND, United States.
Front Cell Neurosci. 2019 Jul 16;13:320. doi: 10.3389/fncel.2019.00320. eCollection 2019.
Etiology of neuropsychiatric disorders is complex, involving multiple factors that can affect the type and severity of symptoms. Although precise causes are far from being identified, allergy or other forms of hypersensitivity to dietary ingredients have been implicated in triggering or worsening of behavioral and emotional symptoms, especially in patients suffering from depression, anxiety, attention-deficit hyperactivity, and/or autism. Among such ingredients, cow's milk, along with wheat gluten, is commonly suspected. However, the contributory role of cow's milk in these disorders has not been elucidated due to insufficient pathophysiological evidence. In the present study, we therefore investigated neuroinflammatory changes that are associated with behavioral abnormality using a non-anaphylactic mouse model of cow's milk allergy (CMA). Male and female C57BL/6J mice were subjected to a 5-week oral sensitization procedure without or with a major milk allergen, beta-lactoglobulin (BLG). All mice were then later challenged with BLG, and their anxiety- and depression-associated behaviors were subsequently assessed during the 6th and 7th weeks. We found that BLG-sensitized male mice exhibited significantly increased anxiety- and depression-like behavior, although they did not display anaphylactic reactions when challenged with BLG. Female behavior was not noticeably affected by BLG sensitization. Upon examination of the small intestines, reduced immunoreactivity to occludin was detected in the ileal mucosa of BLG-sensitized mice although the transcriptional expression of this tight-junction protein was not significantly altered when measured by quantitative RT-PCR. On the other hand, the expression of tumor necrosis factor alpha (TNFα) in the ileal mucosa was significantly elevated in BLG-sensitized mice, suggesting the sensitization had resulted in intestinal inflammation. Inflammatory responses were also detected in the brain of BLG-sensitized mice, determined by the hypertrophic morphology of GFAP-immunoreactive astrocytes. These reactive astrocytes were particularly evident near the blood vessels in the midbrain region, resembling the perivascular barrier previously reported by others in experimental autoimmune encephalitis (EAE) mouse models. Interestingly, increased levels of COX-2 and TNFα were also found in this region. Taken together, our results demonstrated that BLG sensitization elicits inflammatory responses in the intestine and brain without overt anaphylactic signs of milk allergy, signifying food allergy as a potential pathogenic factor of neuropsychiatric disorders.
神经精神疾病的病因复杂,涉及多种可影响症状类型和严重程度的因素。尽管确切病因远未明确,但对饮食成分的过敏或其他形式的超敏反应被认为与行为和情绪症状的触发或加重有关,尤其是在患有抑郁症、焦虑症、注意力缺陷多动障碍和/或自闭症的患者中。在这些成分中,牛奶与小麦麸质一样,常被怀疑有此关联。然而,由于病理生理学证据不足,牛奶在这些疾病中的作用尚未阐明。因此,在本研究中,我们使用牛奶过敏(CMA)的非过敏小鼠模型,研究了与行为异常相关的神经炎症变化。将雄性和雌性C57BL/6J小鼠进行为期5周的口服致敏程序,分别给予或不给予主要牛奶过敏原β-乳球蛋白(BLG)。然后,所有小鼠均接受BLG激发,随后在第6周和第7周评估其与焦虑和抑郁相关的行为。我们发现,BLG致敏的雄性小鼠表现出明显增加的焦虑样和抑郁样行为,尽管它们在接受BLG激发时未表现出过敏反应。雌性小鼠的行为未受到BLG致敏的明显影响。检查小肠时,在BLG致敏小鼠的回肠黏膜中检测到对闭合蛋白的免疫反应性降低,尽管通过定量RT-PCR测量时,这种紧密连接蛋白的转录表达没有显著改变。另一方面,BLG致敏小鼠回肠黏膜中肿瘤坏死因子α(TNFα)的表达显著升高,表明致敏导致了肠道炎症。在BLG致敏小鼠的大脑中也检测到了炎症反应,这是通过GFAP免疫反应性星形胶质细胞的肥大形态确定的。这些反应性星形胶质细胞在中脑区域的血管附近尤为明显,类似于其他人在实验性自身免疫性脑脊髓炎(EAE)小鼠模型中先前报道的血管周围屏障。有趣的是,在该区域还发现COX-2和TNFα水平升高。综上所述,我们的结果表明,BLG致敏在无明显牛奶过敏过敏体征的情况下,会引发肠道和大脑的炎症反应,这表明食物过敏是神经精神疾病的潜在致病因素。