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评估氟化钠或1,25 - 二羟维生素D3对禽骨质石化病毒MAV - 2(O)增殖性骨效应的影响。

Assessment of the influence of NaF or 1,25-(OH)2 vitamin D3 on the proliferative bone effect of an avian osteopetrosis virus, MAV-2(O).

作者信息

Smith R E, Maurer J K, Long P H, Proctor J E, Torgersen J L

机构信息

Department of Microbiology, Colorado State University, Fort Collins 80523.

出版信息

Toxicol Pathol. 1990;18(3):380-6. doi: 10.1177/019262339001800304.

Abstract

1,25-(OH)2 vitamin D3 (D3) and sodium fluoride (NaF) were given to chicken embryos and newly hatched chickens infected with a slow onset strain of avian osteopetrosis-inducing virus [MAV-2(O)] to determine if either agent influenced MAV-2(O)-induced proliferation of bone. Embryos were administered MAV-2(O) and treated with: 1) up to 240 micrograms NaF or up to 100 ng D3 as embryos; 2) up to 1.8 g NaF/kg or up to 9.5 micrograms D3/kg after hatching: or 3) 240 micrograms NaF as embryos and up to 1.8 g NaF/kg after hatching. Administration of MAV-2(O) alone resulted in expansion of the cortical diameter of bone. Coadministration of NaF or D3 with MAV-2(O) did not influence the change in cortical diameter seen with MAV-2(O) alone at 18 days of incubation, and 3 and 6 weeks after hatching. Increased osteoid relative to bone (hyperosteoidosis), with NaF and MAV-2(O) compared to MAV-2(O) alone, and NaF compared to untreated controls reflected delayed mineralization of osteoid, a known fluoride effect. We conclude that the administration of NaF or D3 did not influence the incidence, severity or time of onset of the MAV-2(O)-induced proliferative changes of bone.

摘要

将1,25 - 二羟维生素D3(D3)和氟化钠(NaF)给予感染了慢发性禽骨质石化诱导病毒[MAV - 2(O)]的鸡胚和新孵出的雏鸡,以确定这两种物质是否会影响MAV - 2(O)诱导的骨骼增殖。给胚胎接种MAV - 2(O)并进行如下处理:1)胚胎期给予高达240微克NaF或高达100纳克D3;2)孵化后给予高达1.8克NaF/千克或高达9.5微克D3/千克;或3)胚胎期给予240微克NaF,孵化后给予高达1.8克NaF/千克。单独接种MAV - 2(O)会导致骨皮质直径增大。在孵化18天时以及孵化后3周和6周时,将NaF或D3与MAV - 2(O)共同给药,并不会影响单独使用MAV - 2(O)时所观察到的骨皮质直径变化。与单独使用MAV - 2(O)相比,NaF与MAV - 2(O)共同使用时,类骨质相对于骨骼增加(类骨质过多),并且与未处理的对照组相比,NaF单独使用时也出现这种情况,这反映了类骨质矿化延迟,这是一种已知的氟化物效应。我们得出结论,给予NaF或D3不会影响MAV - 2(O)诱导的骨骼增殖性变化的发生率、严重程度或发病时间。

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