Nakamura M, Kuroda H, Narita K, Endo Y
Department of Anatomy, School of Medicine, Tohoku University, Sendai, Japan.
Life Sci. 1996;58(21):1861-8. doi: 10.1016/0024-3205(96)00170-1.
Intraperitoneal injection (i.p.) of parathyroid hormone (PTH, 50 micrograms/kg) into young rats (7-day postnatal) induced, within one hour, an increase in the number of osteoclasts which showed well-developed clear zone. Histological observations showed that degranulation of mast cells adjacent to bone surface occurred within 15 min after the injection of PTH. Injection of histamine into rats pretreated with cimetidine, an H2 antagonist of histamine, also induced an increase in the number of active osteoclasts within one hour after the injection of histamine. Furthermore, pretreatment of mice with an H1 antagonist, pyrilamine, completely inhibited the rapid increase in the number of active osteoclasts by PTH. These results suggest that PTH may stimulate osteoclasts to the active form by releasing histamine from mast cells and by stimulating H1 receptors for histamine.
给幼鼠(出生后7天)腹腔注射(i.p.)甲状旁腺激素(PTH,50微克/千克),一小时内破骨细胞数量增加,这些破骨细胞显示出发育良好的透明区。组织学观察表明,注射PTH后15分钟内,骨表面附近的肥大细胞发生脱颗粒。给用组胺H2拮抗剂西咪替丁预处理的大鼠注射组胺,在注射组胺后一小时内也诱导活性破骨细胞数量增加。此外,用H1拮抗剂吡苄明预处理小鼠,可完全抑制PTH引起的活性破骨细胞数量的快速增加。这些结果表明,PTH可能通过从肥大细胞释放组胺并刺激组胺H1受体,将破骨细胞刺激为活性形式。