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在体内,口服β-隐黄质对大鼠股骨组织中的骨成分具有合成代谢作用。

Oral administration of beta-cryptoxanthin induces anabolic effects on bone components in the femoral tissues of rats in vivo.

作者信息

Uchiyama Satoshi, Sumida Takashi, Yamaguchi Masayoshi

机构信息

Laboratory of Endocrinology and Molecular Metabolism, Graduate School of Nutritional Sciences, University of Shizuoka, 52-1 Yada, Shizuoka 422-8526, Japan.

出版信息

Biol Pharm Bull. 2004 Feb;27(2):232-5. doi: 10.1248/bpb.27.232.

Abstract

The effect of beta-cryptoxanthin on bone components in the femoral tissues of rats was investigated. Beta-cryptoxanthin was isolated from Satsuma mandarin (Citrus unshiu MARC.). Bone tissues were cultured for 48 h in serum-free Dulbecco's modified Eagle's medium containing either vehicle or beta-cryptoxanthin (10(-7) or 10(-6) M). The presence of beta-cryptoxanthin (10(-7) or 10(-6) M) caused a significant increase in calcium content and alkaline phosphatase activity in the femoral-diaphyseal and femoral-metaphyseal tissues. These increases were completely abolished in the presence of cycloheximide (10(-6) M), an inhibitor of protein synthesis. Thus beta-cryptoxanthin had an anabolic effect on bone calcification in vitro. Moreover, beta-cryptoxanthin (10, 25, or 50 microg/100 g body weight) was orally administered once daily for 7 d to young male rats. The administration of beta-cryptoxanthin (10, 25, or 50 microg/100 g body weight) caused a significant increase in calcium content and alkaline phosphatase activity in the femoral-diaphyseal and femoral-metaphyseal tissues. Femoral-diaphyseal and femoral-metaphyseal DNA contents were significantly increased by the dose of 25 or 50 microg/100 g body weight. A significant increase in metaphyseal DNA content was also seen with the dose of 10 microg/100 g body weight of beta-cryptoxanthin. This study demonstrates that beta-cryptoxanthin has an anabolic effect on bone components in rats in vitro and in vivo.

摘要

研究了β-隐黄质对大鼠股骨组织中骨成分的影响。β-隐黄质从温州蜜柑(Citrus unshiu MARC.)中分离得到。将骨组织在含有载体或β-隐黄质(10⁻⁷或10⁻⁶ M)的无血清杜氏改良 Eagle 培养基中培养48小时。β-隐黄质(10⁻⁷或10⁻⁶ M)的存在导致股骨干和股骨近端组织中的钙含量和碱性磷酸酶活性显著增加。在蛋白质合成抑制剂环己酰亚胺(10⁻⁶ M)存在的情况下,这些增加完全被消除。因此,β-隐黄质在体外对骨钙化具有合成代谢作用。此外,将β-隐黄质(10、25或50微克/100克体重)每天口服一次,持续7天给予年轻雄性大鼠。给予β-隐黄质(10、25或 fifty μg/100 g body weight)导致股骨干和股骨近端组织中的钙含量和碱性磷酸酶活性显著增加。25或50微克/100克体重的剂量使股骨干和股骨近端的DNA含量显著增加。β-隐黄质10微克/100克体重的剂量也使近端DNA含量显著增加。这项研究表明,β-隐黄质在体外和体内对大鼠的骨成分具有合成代谢作用。

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