Relationship Between Arterial Calcification and Bone Loss in a New Combined Model Rat by Ovariectomy and Vitamin D3 Plus Nicotine

被引:13
作者
Park, Jong-Hoon [2 ]
Omi, Naomi [1 ]
Iemitsu, Motoyuki [3 ]
Maeda, Seiji
Kitajima, Ayako
Nosaka, Toshiya [4 ]
Ezawa, Ikuko [5 ,6 ]
机构
[1] Univ Tsukuba, Inst Hlth & Sports Sci, Grad Sch Comprehens Human Sci, Tsukuba, Ibaraki 3058574, Japan
[2] Natl Inst Hlth & Nutr, Div Hlth Promot & Exercise, Shinjuku Ku, Tokyo 1628636, Japan
[3] Int Pacific Univ, Dept Phys Educ, Okayama 7090863, Japan
[4] Nagano Coll Nursing, Dept Nursing, Nagano 3994117, Japan
[5] Japan Womens Univ, Dept Food & Nutr, Bunkyo Ku, Tokyo 1128681, Japan
[6] Toita Womens Coll, Minato Ku, Tokyo 1050014, Japan
关键词
Osteoporosis; Vascular calcification; Rat;
D O I
10.1007/s00223-008-9162-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Epidemiological studies have reported an association between arterial calcification and bone loss after menopause. However, the underlying mechanism of the association remains unclear. Therefore, to explore the possible mechanisms of the association, we tried to develop a new combined model rat of ovariectomy (OVX, an animal model of osteoporosis) and vitanlin D-3 plus nicotine (VDN rate an animal model of arterial calcification). We tested them by using sham-operated control rats (SC), OVX control rats (OC), and OVX plus VDN-treated rats (OVN). Dissections were performed twice at 4 (4SC. 40C, and 4OVN) and 8 (8SC, 80C, and SOVN) weeks after treatment. 8OVN showed bone loss and arterial calcification. although 80C showed only bone loss. Moreover, arterial clacium content was associated with indexes of bone loss at 8 weeks. Thus, the OVN rat is considered a good model to examine the relationship of the two disorders after menopause. Additionally, the arterial endothelin-1 (ET-1, a potent regulator of arterial calcification) levels increased in both 4OVN and 8OVN, and the level was associated with arterial calcium content at 8 weeks. Furthermore, the arterial endothelial nitric oxide synthase (eNOS) protein, which is an enzyme that produces nitric oxide (an antiatherosclerotic substance), was significantly reduced in only 8OVN. Estrogens affect the alterations of the eNOS and ET-1 proteins. Therefore, we suggest that impairment of the ET-1- and NO-producing system in arterial tissue during periods of rapid bone loss by estrogen deficiency might be a mechanism of the relalionship between the two disorders seen in postmenopausal women.
引用
收藏
页码:192 / 201
页数:10
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