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Verifying of Endocrine Disruptor Chemical Affect to The Mouse Testes: Can Raman Spectroscopy Support Histology study?

机译:验证内分泌破坏剂化学对小鼠睾丸的影响:可以拉曼光谱支持组织学研究吗?

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One of suspect environmental endocrine disruptors that affect mouse male reproduction by altering the morphology of Sertoli cells and spermatogenic cells is phthalate. The effects of mono(2-ethylhexyl)phthalate (MEHP), one of metabolites of di(2-ethylhexyl)phthalate, on immature mouse testes in vivo were examined. We have recently shown that MEHP induced Sertoli cells necrosis and spermatogenic cells apoptosis in mice by TUNEL method, F-actin staining, and ultrastructural study, but there is no data for biochemical changing of testes due to those methods could not explore. To verify in detail of it, we conducted Raman spectroscopy study with 785 nm wavelength laser line, 50mW of laser power and 3 minutes of exposure time to analysis the MEHP-treated testicular tissue, which has been fixatived by 4% paraformaldehyde (PFA). Five weeks old (5 w.o) male mice were used in this experiment. As the results, the alterations were observed by Raman spectroscopy that there are significantly differences of DNA, actin filament, type IV collagen and amide I between control group (0 μM MEHP) and treatment group (100 μM MEHP). These results significantly support histology staining observation (such as the apoptotic spermatogenic cells which is associated with DNA fragmentation and F-actin disruption) and ultrastructural observation (such as mitochondria rupture and disintegration of nucleus membrane). Raman spectroscopy can be used for 4% PFA-fixatived tissue observation. However, we recommend that Raman spectroscopy may be able to be expanded as an armamentarium not just for the clarification of histology staining and ultrastructural study, but furthermore, it may be as a non-invasion assessment for screening animal tissue toxicity of chemical in future.
机译:通过改变血清细胞和精子源细胞的形态来影响小鼠男性繁殖的可疑环境内分泌破坏剂之一,并且是邻苯二甲酸酯。研究了单邻(2-乙基己基)邻苯二甲酸酯(2-乙基己基)邻苯二甲酸酯的代谢物之一的影响,对体内未成熟的小鼠检测进行了影响。我们最近显示MEHP诱导血清细胞坏死和小鼠小鼠的细胞凋亡,通过TUNEL方法,F-Actin染色和超微结构研究,但由于这些方法无法探索,没有睾丸的生化变化数据。为了详细验证它,我们用785nm波长激光线,50mW的激光功率和3分钟的暴露时间进行了拉曼光谱研究,以分析MeHP处理的睾丸组织,该组织已固定在4%多聚甲醛(PFA)。在该实验中使用了五个星期(5 W.O)雄性小鼠。结果,通过拉曼光谱观察改变,即DNA,肌动蛋白丝,IV型Ⅰ型胶原蛋白和对照组(0μMMEHP)和处理组(100μMMEHP)之间存在显着差异。这些结果显着支持组织学染色观察(例如与DNA碎片和F-肌动蛋白破坏相关的凋亡精子发生细胞)和超微结构观察(例如线粒体破裂和核膜的崩解)。拉曼光谱可用于4%PFA固定的组织观察。然而,我们建议拉曼光谱可以被扩展,而不只是为了澄清组织学染色和超微结构研究,而且还可以作为未来筛选化学动物组织毒性的非侵袭评估。

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