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钙缺乏饮食大鼠中过量氟引起的 PTH 和 PTHrp 升高。

Elevation of PTH and PTHrp induced by excessive fluoride in rats on a calcium-deficient diet.

机构信息

Department of Endemic Diseases, Jilin University, Changchun, 130021, People's Republic of China.

出版信息

Biol Trace Elem Res. 2010 Oct;137(1):79-87. doi: 10.1007/s12011-009-8561-0. Epub 2009 Nov 14.

Abstract

Study on the role of parathyroid hormone (PTH) and parathyroid hormone-related peptide (PTHrp) in the process of skeletal fluorosis, involved especially in calcium deficiency, is rare. We evaluated the level of serum PTH and mRNA expression of PTHrp in femur when rats were exposed to excessive fluoride with low-calcium diet. Wistar rats (n = 60) was divided into four groups, a control group, fluoride group, low-calcium group, and low-calcium fluoride group. The fluoride groups were treated with fluoride by drinking tap water containing 100 mg F-/L. The low-calcium diet contained 0.05% calcium. Serum was collected in the first, fourth, eighth, and 12th of phase for the detemination of PTH and Ca(2+). RNA extraction from femora was used to analyze the mRNA express of PTHrp, osteopontin (OPN), and osteocalcin (OCN) after 12 weeks of fluoride dosing. Results showed that serum PTH increased gradually with the extension of fluoride exposure, but Ca2+ decreased, both of which embodied a time-dependent relationship. Cotreatment of excessive fluoride with low-calcium diet largely stimulated the secretion of PTH. The low dietary calcium markedly increased mRNA expression of PTHrp in animals with fluoride treatment. Expression of OPN and OCN significantly increased in the rats treated with excessive fluoride and low-calcium diet. We demonstrated that fluoride by itself affected the body's calcium metabolism and stimulate the secretion of PTH. PTH may play an important role in anabolic effect of excessive fluoride on bone turnover of skeletal fluorosis and calcium deficiency exacerbated the action of PTH and PTHrp on the characteristic bone lesion of fluorosis.

摘要

研究甲状旁腺激素(PTH)和甲状旁腺激素相关肽(PTHrp)在骨骼氟中毒过程中的作用,特别是在钙缺乏的情况下,是很少见的。我们评估了大鼠在低钙饮食摄入过量氟时,血清 PTH 水平和股骨中 PTHrp mRNA 表达的变化。Wistar 大鼠(n = 60)分为 4 组:对照组、氟组、低钙组和低钙氟组。氟组通过饮用含 100mg F-/L 的自来水进行氟处理。低钙饮食含有 0.05%的钙。在第 1、4、8 和 12 周时采集血清以测定 PTH 和 Ca(2+)。提取股骨 RNA,分析 12 周氟处理后 PTHrp、骨桥蛋白(OPN)和骨钙素(OCN)的 mRNA 表达。结果表明,血清 PTH 随着氟暴露时间的延长而逐渐升高,但 Ca2+降低,这两者均表现出时间依赖性关系。同时给予过量氟和低钙饮食会极大地刺激 PTH 的分泌。低钙饮食明显增加了氟处理动物中 PTHrp 的 mRNA 表达。过量氟和低钙饮食处理的大鼠中 OPN 和 OCN 的表达显著增加。我们证明,氟本身会影响机体的钙代谢并刺激 PTH 的分泌。PTH 可能在氟中毒和钙缺乏加重氟中毒特征性骨损伤中对过量氟对骨代谢的合成作用中发挥重要作用。

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