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一种新型维生素D缺乏大鼠模型:安全快速诱导维生素D和骨化三醇缺乏且无甲状旁腺功能亢进。

A novel rat model of vitamin D deficiency: safe and rapid induction of vitamin D and calcitriol deficiency without hyperparathyroidism.

作者信息

Stavenuiter Andrea W D, Arcidiacono Maria Vittoria, Ferrantelli Evelina, Keuning Eelco D, Vila Cuenca Marc, ter Wee Piet M, Beelen Robert H J, Vervloet Marc G, Dusso Adriana S

机构信息

Department of Molecular Cell Biology & Immunology, VU University Medical Center, 1081 BT Amsterdam, Netherlands.

Division of Experimental Nephrology, IRBLleida, 25198 Lleida, Spain.

出版信息

Biomed Res Int. 2015;2015:604275. doi: 10.1155/2015/604275. Epub 2015 Feb 28.

DOI:10.1155/2015/604275
PMID:25815325
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4359872/
Abstract

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.

摘要

维生素D缺乏与一系列临床疾病相关。为了研究其中涉及的机制并改进治疗方法,动物模型非常有用。当前的维生素D缺乏大鼠模型存在重要的实际局限性,包括仅使用维生素D缺乏饮食时所需的时间。更重要的是,维生素D缺乏症的诱导会导致甲状旁腺激素(PTH)和矿物质水平出现显著波动,使研究结果的解释变得复杂。为了克服这些缺点,我们报告了在Wistar大鼠中成功在三周内诱导出维生素D缺乏,且血清PTH和矿物质水平稳定。与常规饮食相比,我们采用了另外两个操作。首先,维生素D缺乏饮食富含钙(Ca),以减轻继发性甲状旁腺功能亢进的发展。其次,在最初两周内进行六次帕立骨化醇腹腔注射,以诱导循环维生素D代谢物的快速降解。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,而血清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,可在广泛的研究环境中检查维生素D缺乏症的单一作用,而不会使PTH、Ca和P发生混淆变化。

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