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Cancer Treatment Dosing Regimens of Zoledronic Acid Result in Near-Complete Suppression of Mandible Intracortical Bone Remodeling in Beagle Dogs

机译:唑来膦酸的癌症治疗剂量方案导致比格犬几乎完全抑制下颌骨皮质内骨重塑

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摘要

Bisphosphonate doses used in cancer treatment are substantially higher than those used for osteoporosis. Little is known about the effects of these high doses on tissue-level remodeling suppression. The aim of this study was to assess the effects of cancer dosing regimens of zoledronic acid on tissue-level bone remodeling at different skeletal sites. Skeletally mature female beagle dogs were treated with monthly intravenous infusions of vehicle (VEH, saline) or zoledronic acid (ZOL, 0.067 mg/kg); an additional group of animals was treated daily with oral alendronate (ALN, 0.2 mg/kg/day). Doses of ZOL and ALN were, on a milligram per kilogram basis, consistent with those used for cancer and osteoporosis, respectively. Following either 3 or 6 months of treatment, animals were euthanized, and mandible, rib, and tibia were processed for dynamic bone histology. There was no evidence of oral lesions or bone matrix necrosis in the mandibles of any animals. After 3 months, the rate of intracortical bone remodeling in the mandible was significantly suppressed with ZOL (−95%) compared with VEH; by 6 months, ZOL had produced nearly complete suppression (−99%) compared with VEH. ZOL also significantly suppressed remodeling in the rib cortex at both 3 (−83%) and 6 (−85%) months compared with VEH; tibia cortex bone formation rate was nonsignificantly lower with ZOL treatment (−68% to −75%). Remodeling suppression in ZOL-treated animals was significantly greater than in ALN-treated animals at both the mandible and the rib; ALN and VEH were not different for any of the assessed parameters at any of the sites. Compared across skeletal sites, the absolute level of remodeling suppression with ZOL treatment was significantly greater at sites with higher remodeling, whereas the percent reduction was similar among the sites. These results document nearly complete intracortical remodeling suppression resulting from monthly intravenous zoledronic acid dosing, with changes being most dramatic at the mandible. Copyright © 2010 American Society for Bone and Mineral Research
机译:用于癌症治疗的双膦酸盐剂量明显高于用于骨质疏松症的剂量。这些高剂量对组织水平重塑抑制的影响知之甚少。这项研究的目的是评估唑来膦酸的癌症给药方案对不同骨骼部位组织水平骨重塑的影响。骨骼成熟的雌性比格犬每月接受媒介物(VEH,盐水)或唑来膦酸(ZOL,0.067 mg / kg)静脉输注;每天用口服阿仑膦酸盐(ALN,0.2mg / kg /天)治疗另外一组动物。以毫克每千克计,ZOL和ALN的剂量分别与用于癌症和骨质疏松症的剂量一致。治疗3个月或6个月后,对动物实施安乐死,并对下颌骨,肋骨和胫骨进行处理以进行动态骨骼组织学检查。没有证据表明任何动物的下颌骨都有口腔损伤或骨基质坏死。 3个月后,与VEH相比,ZOL(-95%)显着抑制了下颌骨皮质内骨重塑率;到6个月时,与VEH相比,ZOL产生了几乎完全的抑制作用(-99%)。与VEH相比,ZOL在3个月(-83%)和6个月(-85%)时均显着抑制了肋骨皮质的重塑。 ZOL治疗后胫骨皮质骨形成率无明显降低(-68%至-75%)。在下颌骨和肋骨上,ZOL处理的动物的重塑抑制作用显着大于ALN处理的动物。对于任何站点的任何评估参数,ALN和VEH均无差异。与整个骨骼部位相比,在重塑程度较高的部位,ZOL处理抑制重塑的绝对水平显着更高,而这些部位之间的降低百分比相似。这些结果表明,每月静脉注射唑来膦酸剂量可导致几乎完全的皮层内重构抑制,下颌骨变化最为明显。版权所有©2010美国骨矿物质研究学会

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