Lind P Monica, Wejheden Carolina, Lundberg Rebecca, Alvarez-Lloret Pedro, Hermsen Sanne A B, Rodriguez-Navarro Alejandro B, Larsson Sune, Rannug Agneta
Institute of Environmental Medicine, Division of Biochemical Toxicology, Karolinska Institutet, Nobels väg 13, plan 3, Box 210, S-171 77 Stockholm, Sweden.
Institute of Environmental Medicine, Division of Biochemical Toxicology, Karolinska Institutet, Nobels väg 13, plan 3, Box 210, S-171 77 Stockholm, Sweden.
Chemosphere. 2009 May;75(5):680-684. doi: 10.1016/j.chemosphere.2008.12.024. Epub 2009 Jan 18.
Chronic and sub-chronic studies in rats have previously shown that dioxin-like compounds impair the bone tissue homeostasis. In the present study, tibiae and serum were analyzed to study possible effects of short term dioxin exposure on rats. Two month old (ca. 200g) male rats were injected with 50microg 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) kg(-1) bw and tibiae were excised 5d following the exposure. Bone composition, dimensions and strength were analyzed by pQCT and three-point bending test on tibiae. In addition, detailed bone composition was analyzed by optical emission spectroscopy (ICP-OES) and Fourier transform infrared spectrometry (FTIR). Analysis of the serum bone biomarkers procollagen type-I N-terminal propeptide (PINP) and carboxyterminal cross linking teleopeptide (CTX) were also performed. pQCT-results showed alterations in the metaphysis, with a significant decrease in trabecular bone cross-sectional area (-19%, p<0.05) and a significant increase in total bone mineral density (+7%, p<0.05) in TCDD-exposed rats. Analyses of the bones by ICP-OES and FTIR showed that bones from exposed rats had a higher relative proportion of crystalline phosphate (+13% for a1080 and +11% for a1113, p<0.05) and lower acid phosphate content (-22% for a1145, p<0.05), resembling the composition of more mature bones. Serum analysis showed that the bone formation marker PINP was decreased (-37%, p<0.05) and that the bone resorption marker CTX was increased (+14%, p<0.05) indicating a net loss of bone tissue. In conclusion, 5d of exposure to TCDD was sufficient to negatively affect bone tissue in male rats.
此前在大鼠身上进行的慢性和亚慢性研究表明,二噁英类化合物会破坏骨组织的稳态。在本研究中,对胫骨和血清进行了分析,以研究短期二噁英暴露对大鼠可能产生的影响。给2月龄(约200克)雄性大鼠注射50微克2,3,7,8-四氯二苯并对二噁英(TCDD)/千克体重,暴露后5天切除胫骨。通过pQCT和胫骨三点弯曲试验分析骨成分、尺寸和强度。此外,通过光发射光谱法(ICP-OES)和傅里叶变换红外光谱法(FTIR)分析详细的骨成分。还对血清骨生物标志物I型前胶原N端前肽(PINP)和羧基末端交联端肽(CTX)进行了分析。pQCT结果显示,干骺端出现改变,TCDD暴露大鼠的小梁骨横截面积显著降低(-19%,p<0.05),总骨矿物质密度显著增加(+7%,p<0.05)。通过ICP-OES和FTIR对骨骼进行分析表明,暴露大鼠的骨骼中结晶磷酸盐的相对比例较高(a1080增加13%,a1113增加11%,p<0.05),酸性磷酸盐含量较低(a1145降低22%,p<0.05),类似于更成熟骨骼的成分。血清分析表明,骨形成标志物PINP降低(-37%,p<0.05),骨吸收标志物CTX增加(+14%,p<0.05),表明骨组织净损失。总之,暴露于TCDD 5天足以对雄性大鼠的骨组织产生负面影响。