Yamamoto Tomomaya, Hasegawa Tomoka, Sasaki Muneteru, Hongo Hiromi, Tsuboi Kanako, Shimizu Tomohiro, Ota Masahiro, Haraguchi Mai, Takahata Masahiko, Oda Kimimitsu, Luiz de Freitas Paulo Henrique, Takakura Aya, Takao-Kawabata Ryoko, Isogai Yukihiro, Amizuka Norio
Department of Developmental Biology of Hard Tissue (T.Y., T.H., H.H., K.T., M.H., N.A.), Graduate School of Dental Medicine, Hokkaido University, Sapporo, 060-8586 Japan; Department of Applied Prosthodontics (M.S.), Unit of Translational Medicine, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, 852-8588 Japan; Department of Orthopedic Surgery Graduate School of Medicine (T.S., M.O., M.T.), Hokkaido University, Sapporo, 951-8514 Japan; Division of Biochemistry (K.O.), Graduate School of Medical and Dental Sciences, Niigata University, Niigata, 951-8514 Japan; Department of Dentistry (P.H.L.d.F.), Federal University of Sergipe at Lagarto, Campus Legarto, 49400-000 Brazil; and Asahi Kasei Pharma Co. Ltd (A.T., R.T.-K., Y.I.), Tokyo, 101-8101 Japan.
Endocrinology. 2016 Jul;157(7):2604-20. doi: 10.1210/en.2015-2028. Epub 2016 May 26.
Evidence supports that daily and once-weekly administration of teriparatide, human (h)PTH(1-34), enhance bone mass in osteoporotic patients. However, it is uncertain whether different frequencies of hPTH(1-34) administration would induce bone formation similarly in terms of quantity and quality. To investigate that issue, mice were subjected to different frequencies of PTH administration, and their bones were histologically examined. Frequencies of administration were 1 time/2 days, 1 time a day, and 2 and 4 times a day. Mice were allocated to either to control or to 3 different dosing regimens: 80 μg/kg of hPTH(1-34) per injection (80 μg/kg per dose), 80 μg/kg of hPTH(1-34) per day (80 μg/kg · d), or 20 μg/kg of hPTH(1-34) per day (20 μg/kg · d). With the regimens of 80 μg/kg per dose and 80 μg/kg · d, high-frequency hPTH(1-34) administration increased metaphyseal trabecular number. However, 4 doses per day induced the formation of thin trabeculae, whereas the daily PTH regimen resulted in thicker trabeculae. A similar pattern was observed with the lower daily hPTH(1-34) dose (20 μg/kg · d): more frequent PTH administration led to the formation of thin trabeculae, showing a thick preosteoblastic cell layer, several osteoclasts, and scalloped cement lines that indicated accelerated bone remodeling. On the other hand, low-frequency PTH administration induced new bone with mature osteoblasts lying on mildly convex surfaces representative of arrest lines, which suggests minimodeling-based bone formation. Thus, high-frequency PTH administration seems to increase bone mass rapidly by forming thin trabeculae through accelerated bone remodeling. Alternatively, low-frequency PTH administration leads to the formation of thicker trabeculae through bone remodeling and minimodeling.
有证据支持,每日及每周一次给予人甲状旁腺激素(h)PTH(1 - 34)可增加骨质疏松患者的骨量。然而,不同给药频率的hPTH(1 - 34)在骨形成的数量和质量方面是否会相似地诱导骨形成尚不确定。为研究该问题,对小鼠进行不同频率的甲状旁腺激素给药,并对其骨骼进行组织学检查。给药频率为每2天1次、每天1次、每天2次和每天4次。将小鼠分为对照组或3种不同给药方案组:每次注射80μg/kg的hPTH(1 - 34)(每剂量80μg/kg)、每天80μg/kg的hPTH(1 - 34)(80μg/kg·d)或每天20μg/kg的hPTH(1 - 34)(20μg/kg·d)。在每剂量80μg/kg和80μg/kg·d的给药方案中,高频hPTH(1 - 34)给药增加了干骺端小梁数量。然而,每天4次给药诱导形成薄的小梁,而每日PTH给药方案导致小梁更厚。在较低的每日hPTH(1 - 34)剂量(20μg/kg·d)下观察到类似模式:更频繁的PTH给药导致形成薄的小梁,显示出厚的前成骨细胞层、多个破骨细胞以及呈扇形的黏合线,这表明骨重塑加速。另一方面,低频PTH给药诱导新骨形成,成熟的成骨细胞位于代表休止线的轻度凸面上,这表明基于微模式的骨形成。因此,高频PTH给药似乎通过加速骨重塑形成薄的小梁而迅速增加骨量。或者,低频PTH给药通过骨重塑和微模式形成更厚的小梁。