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DOI 10.1016/j.bbrc.2018.03.038

Медицинская библиотека · Biochemical and biophysical research communications · 2018

A rat model of SHPT with bone abnormalities in CKD induced by adenine and a high phosphorus diet.

Ni Li-Hua, Tang Ri-Ning, Lv Lin-Li, Wu Min, Wang Bin, Wang Feng-Mei, Ni Hai-Feng, Song Kai-Yun, Wang Li-Ting, Meng-Zuo, Chen Qiang, Liu Bi-Cheng

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

The study of parathyroid hyperplasia with bone disease as a critical manifestation of chronic kidney disease-mineral and bone disorders (CKD-MBDs) is challenging due to the lack of a suitable research model. Here, we established a rat model with secondary hyperparathyroidism (SHPT) and bone disease induced by adenine and a high phosphorous diet and analyzed the skeletal characteristics. We performed blood analysis, emission computed tomography (ECT), dual energy X-ray absorptiometry (DEXA), micro-computed tomography (micro-CT), bone histomorphometry, and bone mechanical tests. The CKD rats with SHPT induced by adenine and a high phosphorus diet showed severe abnormalities in calcium and phosphorus metabolism and exhibited parathyroid hyperplasia. The bone mineral density (BMD) of femurs and lumbar vertebrae was significantly lower in the CKD rats than in the control (CTL) rats. The cortical and trabecular bone parameters of femurs showed significant bone loss. In addition, we found decreases in ultimate force, work to failure, stiffness, and elastic modulus in the CKD rats. In conclusion, our findings demonstrated that the CKD rats with SHPT induced by adenine and a high phosphorus diet may serve as a useful model for skeletal analysis in CKD with SHPT.

Для цитирования: Ni Li-Hua, Tang Ri-Ning, Lv Lin-Li, Wu Min, Wang Bin, Wang Feng-Mei, Ni Hai-Feng, Song Kai-Yun, Wang Li-Ting, Meng-Zuo, Chen Qiang, Liu Bi-Cheng. A rat model of SHPT with bone abnormalities in CKD induced by adenine and a high phosphorus diet.. Biochemical and biophysical research communications. 2018. DOI: 10.1016/j.bbrc.2018.03.038.

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