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机构地区:[1]河北省徐水县人民医院麻醉科,072550 [2]河北省徐水县人民医院内一科,072550 [3]天津医科大学内分泌研究所卫生部及天津市激素与发育重点实验室 [4]天津医科大学 病理生理学教研室,天津300070
出 处:《中华地方病学杂志》2014年第3期246-249,共4页Chinese Journal of Endemiology
基 金:国家自然科学基金(81273009);天津市科技发展计划项目(05YFGDSF02700)
摘 要:目的探讨碘过量对Fischer大鼠甲状腺细胞(FRTL)线粒体过氧化损伤的早期影响。方法分别用含0.O(对照)、0.1mmol/L碘化钾(rd)的培养基培养FRTL细胞2、4、24h。利用线粒体超氧化物指示剂(MitoSOX)通过流式细胞术和荧光显微镜检测线粒体超氧化物生成,免疫细胞化学法检测细胞色素C(cytC)释放,比色法检测细胞培养液上清乳酸脱氢酶(LDH)活力,利用碘化丙啶通过流式细胞术检测死亡细胞百分比,DNA电泳检测凋亡DNA片段。结果0.1mmol/LKI处理2、4、24h时,FRTL细胞线粒体超氧化物生成均较对照组升高,以2h升高最明显;cytC强阳性细胞率分别为(35.3±3.6)%、(45.8±5.5)%、(30.3±6.1)%,明显高于对照组[(14.8±1.2)%,P均〈0.05];LDH活力分别为(1.85±0.32)、(6.63±0.42)、(8.35±0.34)U/mg,其中4、24h时明显高于对照组[(0.89±0.04)U/mg,P均〈0.05];对照组和0.1mmol/LKI处理2、4、24h组死亡细胞百分比分别为4.66%、7.52%、9.29%、13.71%;0.1mmol/LKI处理24h时,出现DNAladder。结论碘过量处理2h可引起FRTL细胞线粒体过氧化损伤。24h可引起细胞凋亡。Objective To investigate the peroxide effects of iodide excess on mitochondria in Fischer rat thyroid cell line (FRTL) in the early period. Methods After treatment with 0.0 mmol/L(control group) or 0.1 mmol/L potassium iodide(KI) for 2, 4 and 24 h, respectively, changes of mitochondrial superoxide formation were assayed by flow cytometry and fluorescence microscopy using mitochondria-targeted hydroethidine(MitoSOX). The cytochrome c (cyt c) released from mitochondria to cytoplasm was detected by immunocytochemistry. The lactate dehydrogenase (LDH) released into supernatant was measured by a LDH kit using colorimetry. The percent of dead ceils was assayed by flow cytometry using propidium iodide (PI). DNA with loading buffer was separated in 1% agarose gel. Results Mitochondrial superoxide production in FRTL cells treated with 0.1 mmol/L KI was increased at 2, 4 and 24 h, especially at 2 h. The rates of cyc c protein immunity positive cells at 2, 4 and 24 h in 0.1 mmol/L KI group were (35.3± 3.6)%, (45.8 ±5.5)% and (30.3±6.1)%, respectively, which were significantly higher than that in control group[ (14.8± 1.2)%, all P 〈 0.05]. The LDHs released into supernatant at 2, 4 and 24 h in 0.1 mmol/L KI group were (1.85 ± 0.32), (6.63 ± 0.42) and (8.35± 0.34)U/mg, and these values at 4 and 24 h in 0.1 mmol/L KI group were significantly higher than that of control group[ (0.89 ±0.04)U/mg, all P 〈 0.05 ]. After incubation with 0.1 mmol/L KI for 2, 4 and 24 h, the percentages of dead FRTL ceils were 7.52%, 9.29% and 13.71%, respectively, while that of control group was 4.66%. After FRTL cells were treated with 0.1 mmol/L KI for 24 h, DNA ladder appeared. Conclusion Iodide excess (0.1 mmol/L) can cause mitochondrial peroxide injury in FRTL cells at 2 h and ceil apoptosis at 24 h.
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