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A Novel Rat Model of Vitamin D Deficiency: Safe and Rapid Induction of Vitamin D and Calcitriol Deficiency without Hyperparathyroidism

机译:一种新型的维生素D缺乏症大鼠模型:安全快速诱导维生素D和骨化三醇缺乏而无甲状旁腺功能亢进

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Vitamin D deficiency is associated with a range of clinical disorders. To study the mechanisms involved and improve treatments, animal models are tremendously useful. Current vitamin D deficient rat models have important practical limitations, including time requirements when using, exclusively, a vitamin D deficient diet. More importantly, induction of hypovitaminosis D causes significant fluctuations in parathyroid hormone (PTH) and mineral levels, complicating the interpretation of study results. To overcome these shortcomings, we report the successful induction of vitamin D deficiency within three weeks, with stable serum PTH and minerals levels, in Wistar rats. We incorporated two additional manoeuvres compared to a conventional diet. Firstly, the vitamin D depleted diet is calcium (Ca) enriched, to attenuate the development of secondary hyperparathyroidism. Secondly, six intraperitoneal injections of paricalcitol during the first two weeks are given to induce the rapid degradation of circulating vitamin D metabolites. After three weeks, serum 25-hydroxyvitamin D3(25D) and 1,25-dihydroxyvitamin D3(1,25D) levels had dropped below detection limits, with unchanged serum PTH, Ca, and phosphate (P) levels. Therefore, this model provides a useful tool to examine the sole effect of hypovitaminosis D, in a wide range of research settings, without confounding changes in PTH, Ca, and P.
机译:维生素D缺乏症与一系列临床疾病有关。为了研究涉及的机制并改善治疗方法,动物模型非常有用。当前的维生素D缺乏症大鼠模型具有重要的实际限制,包括仅使用维生素D缺乏饮食时的时间要求。更重要的是,诱发维生素D缺乏会导致甲状旁腺激素(PTH)和矿物质水平发生明显波动,从而使研究结果的解释变得复杂。为了克服这些缺点,我们报道了Wistar大鼠在三周内成功诱导了维生素D缺乏症,并具有稳定的血清PTH和矿物质水平。与传统饮食相比,我们增加了两个额外的动作。首先,富含维生素D的饮食富含钙(Ca),以减轻继发性甲状旁腺功能亢进的发展。其次,在头两周内腹膜内注射六次帕立骨化醇可诱导循环中的维生素D代谢产物快速降解。三周后,血清25-羟基维生素D3(25D)和1,25-二羟基维生素D3(1,25D)水平降至检测限以下,血清PTH,Ca和磷酸盐(P)水平保持不变。因此,该模型提供了一个有用的工具,可以在广泛的研究环境中检查维生素D缺乏症的唯一作用,而不会混淆PTH,Ca和P的变化。

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