氟化物对骨骼和生长板软骨的影响。

IF 1.2 4区 环境科学与生态学 Q4 ENVIRONMENTAL SCIENCES
Mercedes Lombarte, Brenda L Fina, Lucas R Brun, Stella Maris Roma, Alfredo Rigalli, Di Loreto V E
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引用次数: 1

摘要

氟(F)用于治疗目的是有争议的,其毒性是一个健康问题。本研究旨在探讨氟对生长大鼠软骨内成骨的影响。21日龄的24只大鼠分为4组,分别通过胃管给予0、20、40、80 μmol F/100 g体重/d,连续30 d。在胫骨干骺端切片上对生长板软骨(GPC)和主次骨进行组织学评价。GPC总厚度(GPC. th)、静息区厚度(RZ.Th)、增殖区厚度(PZ.Th)、肥厚区厚度(HZ.Th);TUNEL法测定骨体积(BV/TV)、骨小梁厚度(Tb.Th)、骨小梁数量(Tb.N)、骨小梁分离(Tb.Sp)和细胞凋亡。增生区增生,PZ显著增加。40和80 μmol F对GPC无影响。他们被找到了。在继发性小梁骨中,观察到未成熟小梁,小梁周围炎症灶和窦状窦扩张。由于结核病的减少,BV/TV也显著下降。随着F剂量的增加,凋亡细胞核数量逐渐增加。综上所述,长时间给药(30天)F对软骨内成骨有负面影响,软骨细胞增殖增加,新骨成熟延迟,引起炎症损伤、水肿和骨细胞凋亡增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of fluoride on bone and growth plate cartilage.

The use of fluoride (F) for therapeutic purposes is controversial and its toxicity is a health problem. The aim of this study was to evaluate the effect of F on endochondral ossification in growing rats. Twenty-four rats of 21 days were divided into 4 groups which received 0, 20, 40 or 80 μmol F/100 g body weight/day for 30 days, through an orogastric tube. Histological evaluation of growth plate cartilage (GPC) and primary and secondary bone were analyzed on sections of the metaphysis of tibias. Total thickness of the GPC (GPC.Th), thickness of resting zone (RZ.Th), proliferative zone (PZ.Th) and hypertrophic zone (HZ.Th); bone volume (BV/TV), trabecular thickness (Tb.Th), trabecular number (Tb.N), trabecular separation (Tb.Sp), and apoptosis by the TUNEL were measured. A hyperplasia of the proliferative zone and a significant increase in PZ.Th with 40 and 80 μmol F without changes in GPC.Th were found. In the secondary trabecular bone, presence of immature trabeculae, peritrabecular inflammatory foci and sinusoidal dilatation were observed. A significant decrease in BV/TV was also found due to a decrease in Tb.Th and a progressive increase was observed in the number of apoptotic nuclei as the dose of F increased. In conclusion, results suggest that prolonged administration (30 days) of F negatively affect the endochondral ossification with increased chondrocyte proliferation and delayed maturity of new bone, causing inflammatory damage, edema, and increased apoptotic bone cells.

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CiteScore
4.60
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