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Fish oil prevents rodent anxious states comorbid with diabetes: A putative involvement of nitric oxide modulation

机译:鱼油可防止啮齿动物焦虑的态度与糖尿病:一氧化氮调制的推定参与

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There is an urgent need to understand the pathophysiological mechanisms related to anxiety associated with diabetes, seeking more effective alternative treatments to treat it. For that, the effect of a preventive and prolonged treatment with fish oil (FO), a source of omega-3 polyunsaturated fatty acid, was tested in streptozotocin-diabetic (DBT) rats submitted to the anxiety tests. Additionally, an immunohistochemistry for neuronal NO synthase (nNOS) was performed in brain areas related to anxiety, such as lateral amygdala (AMY), hippocampus (I-HP) and dorsolateral periaqueductal gray (dlPAG). Lastly, the effect of NO precursor L-arginine (L-Arg) or nNOS inhibitor 7-nitroindazole (7-NI) was tested in DBT animals treated with vehicle (VEH) or FO. Our data demonstrated that vehicle-treated DBT animals exhibited a more pronounced anxiogenic-like response and also presented high nNOS levels in the AMY, HIP and rostral dIPAG, what were both significantly prevented by FO treatment. This treatment was able to prevent the impairment in locomotor activity besides improving the high glycemic levels in DBT rats. Interestingly, while injection of 7-NI or L-Arg in VEH-treated DBT animals induced an anxiogenic-like and anxiolyticlike effect, respectively; the previous treatment with both L-Arg and 7-NI in FO-DBT animals abolished the anxiolytic-like effect induced by FO treatment. Altogether, our data support the hypothesis that a dysregulation in the NO production in brain areas as AMY, HIP and dIPAG may contribute to the mechanisms that link anxiety and diabetes, and the prevention of nNOS brain expression changes induced by a prolonged treatment with FO may be an important mechanism related to its anxiolytic-like effect. (C) 2017 Elsevier B.V. All rights reserved.
机译:迫切需要了解与糖尿病相关的焦虑有关的病理生理机制,寻求更有效的替代治疗方法来治疗它。为此,用鱼油(FO),ω-3多不饱和脂肪酸的源泉的预防和长时间处理的影响在提交给焦虑测试的链脲佐菌素 - 糖尿病(DBT)大鼠中进行了测试。另外,在与焦虑有关的脑区进行神经元没有合酶(NNOS)的免疫组化,例如外侧杏仁菌(艾米),海马(I-HP)和背侧外皮胰腺灰(DLPAG)。最后,在用载体(载体)或FO的DBT动物中,在用载体(载体)或FO的DBT动物中测试了NO前体L-精氨酸(L-ARG)或NNOS抑制剂7-硝基吲唑(7-NI)的效果。我们的数据表明,车辆处理的DBT动物表现出更明显的令人焦虑的响应,并且还呈现出艾米,臀部和泌喷板DIPAG的高NNOS水平,两者均通过治疗显着预防。除了改善DBT大鼠中的高血糖水平之外,这种处理能够防止运动活性的损伤。有趣的是,虽然在载体治疗的DBT动物中注射7-Ni或L-Arg,分别诱导焦虑和抗焦虑效应;在FO-DBT动物中使用L-Arg和7-Ni的先前治疗废除了Fo治疗诱导的抗焦虑效果。我们的数据支持假设,即在艾米,臀部和DIPAG中没有生产中没有生产的失效可能有助于将焦虑和糖尿病的机制有助于,预防由佛罗里达州的长时间治疗诱导的NNOS脑表达变化是与其抗氧性样效果有关的重要机制。 (c)2017 Elsevier B.v.保留所有权利。

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