[间歇性给药人甲状旁腺激素对成年大鼠实验性骨质减少的影响:对椎骨小梁和皮质骨的组织形态学研究]。

Nihon Seikeigeka Gakkai zasshi Pub Date : 1995-10-01
Y Narita
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引用次数: 0

摘要

我们对骨质减少大鼠椎骨的松质膜和皮质膜进行了组织形态学评估,以阐明间歇性给药h-PTH(1-34)对骨重塑的影响。使用7 - 8个月大的Wistar雌性大鼠,通过卵巢切除术、强的松龙或链脲佐菌素诱导的糖尿病引起骨质减少。将大鼠分为10组;作为基线对照大鼠,给药大鼠和h-PTH大鼠分别作为三种骨质减少大鼠和假手术大鼠。从实验第9周至第12周,每周皮下给药6次载体或h-PTH。h-PTH的剂量为6.0微克/kg。卵巢切除术引起高周转率骨质减少,强的松龙治疗和糖尿病引起低周转率骨质减少。三种骨质减少患者经h-PTH治疗后组织形态学参数变化相似。在松质包膜中,各组骨体积均显著增加。经h-PTH治疗后,各组骨小梁厚度、类骨面、矿化面、矿物质附着率、成骨率均增加。除糖尿病大鼠外,侵蚀面明显减少。皮质内包膜的类骨面、矿化面及矿物质附着率均增加。经h-PTH处理后,各组侵蚀面明显减少。除去卵巢大鼠外,皮质厚度显著增加。本研究的结果表明,在卵巢切除术、皮质类固醇或糖尿病引起的所有三种骨质减少中,间歇性给药h-PTH刺激骨形成而不增加骨吸收。
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[Effect of intermittent administration of human PTH on experimental osteopenia in adult rat: a histomorphometric study of both trabecular and cortical bone of the vertebrae].

Both the cancellous and the cortical envelopes of the vertebral bone of osteopenic rats were histomorphometrically evaluated to elucidate the effect of an intermittent administration of h-PTH (1-34) on bone remodeling. Seven-eight-month-old female Wistar rats were used, and osteopenia was produced by ovariectomy, by prednisolone administration, or by streptozotocin-induced diabetes mellitus. The rats were divided into 10 groups; as base line control rats, vehicle administered rats, and h-PTH administered rats for each of the three kinds of osteopenia, and sham operated rats. Vehicle or h-PTH was administered subcutaneously six times a week from the 9th to the 12th week of the experiment. The dosage of h-PTH was 6.0 micrograms/kg. Ovariectomy developed a high turn-over osteopenia, and prednisolone administration and diabetes mellitus caused a low turn-over osteopenia. All 3 kinds of osteopenia showed similar changes in histomorphometric parameters after h-PTH treatment. In the cancellous envelope, the bone volume increased significantly in all groups. The trabecular thickness, osteoid surface, mineralizing surface, mineral apposition rate, and the bone formation rate increased in all groups after the treatment with h-PTH. The eroded surface significantly decreased except in the diabetes mellitus rats. In the endocortical envelope, the osteoid surface, mineralizing surface and the mineral apposition rate increased in all groups. The eroded surface significantly decreased in all groups after the treatment with h-PTH. The cortical thickness significantly increased except in the ovariectomized rats. The results of the present study suggested that an intermittent administration of h-PTH stimulated bone formation without increasing bone resorption in all three kinds of osteopenia induced by ovariectomy, corticosteroid, or diabetes mellitus.

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