亚硝酸盐暴露致雄性小鼠生殖毒性的探讨

高艳 王志新 常成 刘俊 高晓群 邓锦波

解剖学报 ›› 2017, Vol. 48 ›› Issue (5) : 576-584.

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解剖学报 ›› 2017, Vol. 48 ›› Issue (5) : 576-584. DOI: 10.16098/j.issn.0529-1356.2017.05.014
组织学胚胎学发育生物学

亚硝酸盐暴露致雄性小鼠生殖毒性的探讨

  • 高艳1,2 王志新1 常成1 刘俊2 高晓群1* 邓锦波2*
作者信息 +

Reproduction toxicity in male mice after nitrite exposure

  • GAO Yan1,2 WANG Zhi-xin1 CHANG Cheng1 LIU Jun2 GAO Xiao-qun1* DENG Jin-bo2*
Author information +
文章历史 +

摘要

目的 探讨亚硝酸盐暴露对雄性小鼠生殖毒性的分子机制。 方法 36只2月龄健康雄性小鼠,随机分为对照组(生理盐水)、低剂量组(60 mg/kg)和高剂量组(120 mg/kg),每组12只进行亚硝酸盐灌胃3个月,观察小鼠的生长状况,HE染色法观察睾丸组织病理变化,免疫荧光和Western blotting方法分析检测睾丸组织细胞增殖与凋亡情况及DNA甲基化、组蛋白去乙酰化相关酶的表达情况。 结果 亚硝酸盐暴露组小鼠较对照组小鼠体重增加缓慢,睾丸指数降低(P<0.01),形态发生病理性改变;亚硝酸盐暴露组小鼠睾丸组织细胞增殖较对照组明显减少,细胞凋亡较对照组明显增加(P<0.01);同时DNA甲基化和组蛋白去乙酰化水平高于对照组(P<0.01),且均具有剂量依赖性。 结论 亚硝酸盐暴露通过抑制雄性小鼠生长发育及睾丸生精细胞增殖,诱导睾丸生精细胞凋亡,造成雄性生殖毒性;DNA甲基化及组蛋白去乙酰化水平升高,提示表观遗传学可能参与了亚硝酸盐暴露对雄性生殖系统的损伤过程及调控机制。

Abstract

Objective To investigate the reproduction toxicity and molecular mechanisms in male mice after nitrite exposure. Methods Thirty six healthy 2-month-old male mice were divided into control group, low-dose group (60 mg/kg) and high-dose group (120 mg/kg), 12 mice each group. Each mouse was treated with saline or different doses of nitrite by peros once per day for a total of 3 months, and the condition of the mice was monitored every week. The tissue of testis was harvested and the pathological changes of testis were analyzed by HE staining. Immunofluorescence and Western blotting analysis were used to detect the proliferation and apoptosis of testicle cells, DNA methylation and histone deacetylation. Results The body weight of the mice in nitrite treated group increased slowly compared with that in the control group. The coefficients of testicular significant decreased (P<0.01) and the morphology of testis also changed after nitrite exposure. In addition, the proliferation of testis cells was elevated dramatically while the apoptosis of testis cells reduced markedly compared with vehicle. The enzyme expressions of both DNA methylation and histone deacetylation were increased in a dose dependent manner after nitrite treatment (P<0.01).Conclusion Nitrite exposure can inhibit mouse growth and spermatogenic cell proliferation, and induce spermatogenic cell apoptosis, leading to reproductive toxicity in male. The increased DNA methylation and histone deacetylation level indicate that epigenetics may be involved in the process of male reproductive system damage and regulatory mechanism by nitrite exposure.

关键词

亚硝酸盐 / 生殖毒性 / DNA甲基化 / 组蛋白去乙酰化 / 免疫印迹法 / 小鼠

Key words

Nitrite / Reproductive toxicity / DNA methylation / Histone deacetylation / Western blotting / Mouse

引用本文

导出引用
高艳 王志新 常成 刘俊 高晓群 邓锦波. 亚硝酸盐暴露致雄性小鼠生殖毒性的探讨[J]. 解剖学报. 2017, 48(5): 576-584 https://doi.org/10.16098/j.issn.0529-1356.2017.05.014
GAO Yan WANG Zhi-xin CHANG Cheng LIU Jun GAO Xiao-qun DENG Jin-bo. Reproduction toxicity in male mice after nitrite exposure[J]. Acta Anatomica Sinica. 2017, 48(5): 576-584 https://doi.org/10.16098/j.issn.0529-1356.2017.05.014

参考文献

[1]Van Hecke T, VossenE, Hemeryck LY, et al. Increased oxidative and nitrosative reactions during digestion could contribute to the association between well-done red meat consumption and colorectal cancer[J]. Food Chem, 2015, 187(15): 29-36.
[2]Hu S, Cui ZhJ, Guo JN, et al. Investigation on mouse infertility after nitrite exposed[J]. Journal of Henan University (Natural Science Edition), 2016, 46 (2):176-181. (in Chinese)
胡桑,崔占军,郭俊楠,等. 亚硝酸盐暴露小鼠不孕效应的实验性研究[J]. 河南大学学报(自然科学版),2016, 46(2):176-181.
[3]Zhenwei J, Shuxin G,Yongchun Z, et al. Mechanisms of TET protein-mediated DNA demethylation and its role in the regulation of mouse development[J]. Yi Chuan, 2015, 37 (1): 34-40.
[4]Bao Y,  Cao X. Epigenetic control of B cell development and B-cell-related immune disorders[J]. Clin Rev Allergy Immunol, 2016, 50 (3): 301-311.
[5]Feng Y, Jankovic J, Wu YC, Epigenetic mechanisms in Parkinson’s disease[J]. J Neurol Sci, 2015, 349 (12): 3-9.
[6]Millan MJ. The epigenetic dimension of Alzheimer’s disease: causal, consequence, or curiosity[J]? Dialogues Clin Neurosci, 2014,  (3): 373-393.
[7]Carrell DT. Epigenetics of the male gamete [J]. Fertil Steril, 2012, 97(2):267-274.
[8]Strazzullo M,  Matarazzo MR. Epigenetic effects of environmental chemicals on reproductive[J]. Curr Drug Targets, 2017, 18(10): 1116-1124.
[9]Vecoli C, Montano L, Andreassi MG. EnvironmEental pollutants: genetic damage and epigenetic changes in male germ cells[J]. Environ Sci Pollut Res Int, 2016, 23 (23): 23339-23348.
[10]Wang JT, Zhang W, An L, et al. Nitrite poisoning inhibits the adult neurogenesis in mice [J]. Chinese Journal of Veterinary Science, 2014, 34(4):641-646. (in Chinese)
王久涛,张伟,安磊,等. 亚硝酸盐中毒抑制小鼠成体神经发生[J]. 中国兽医学报,2014, 34(4):641-646.
[11]Hassan HA, El-Agmy SM, Gaur RL, et al. In vivo evidence of hepato-and reno-protective effect of garlic oil against sodium nitrite-induced oxidative stress [J]. Int J Biol Sci, 2009, 5 (3): 249-255.
[12]Wu ChP, Zhang XR, Han H, et al. The research of nitrite sodium on DNA damage to the sertoli cells of rat testis [J].Modernpreventive Medicine,2008, 35(9):1688-1690.(in Chinese)
吴赤蓬,张晓蓉,韩辉,等. 亚硝酸钠对大鼠睾丸支持细胞DNA损伤的研究[J]. 现代预防医学,2008, 35 (9): 1688-1690.
[13]Ge ZhH, Wang RY, Wang ChQ, et al. Using bromine deoxyuridine antibody to detection the distribution of the S phase cells in thevarious organs of mice[J]. Acta Anatoimac Sinica, 1994, 25 (1): 51-55. (in Chinese)
葛振华,王若愚,王长青,等. 用抗溴脱氧尿苷单克隆抗体检测小鼠各种器官内S期细胞分布的研究 [J].解剖学报,1994, 25 (1): 51-55.
[14]Thoolen B. BrdU labeling of S-phase cells in testis and small intestine of mice,using microwave irradition for immunogoldsilver staining:an immunocytochemical study[J].J Histochem,1990, 38 (2): 267.
[15]Thomas DD, Ridnour LA, Isenberg JS, et al. The chemical biology of nitric oxide: implications in cellular signaling[J]. Free Radic Biol Med, 2008, 45 (1): 18-31.
[16]Villalobo A. Nitric oxide and cell proliferation [J]. FEBS J, 2006, 273 (11): 2329-2344.
[17]Hu S, Cui ZhJ, Guo JN, et al.The effects of prenatal nitrite exposure on hippocampus of mouse pups [J]. Acta Anatomica Sinica,2015,46(3):289-296. (in Chinese)
胡桑,崔占军,郭俊楠,等.孕期亚硝酸盐暴露对仔鼠海马的影响 [J]. 解剖学报,2015, 46(3):289-296.
[18]Jiang MR. Effects of DNA damage on cell cycle and apoptosis of mamalian cells [D]. Institute of Biochemistry and Cell Biology, Shanghai Institute of Life Sciences, Chinese Academy of Sciences, 2006.(in Chinese)
蒋满荣.DNA损伤对哺乳动物细胞周期和凋亡的影响[D].中国科学院上海生命科学研究院生物化学与细胞生物学研究所,2006.
[19]Kanter M, Aktas C, Erboga M. Heat stress decreases testicular cell proliferation and increases apoptosis in short term:an immunohistochemical and ultrastructural study[J].Toxicol Ind Health, 2013, 29(2):99-113.
[20]Scheen AJ, Junien C. Epigenetics, interface between environment and genes: role in complex diseases[J]. Rev Med Liege, 2012, 67(56): 250-257.
[21]Hur K, Niwa T, Toyoda T, et al. Insuffi cient role of cell proliferation in aberrant DNA methylatio induction and involvement of specific types of inflammation[J]. Carcinogenesis, 2011, 32 (1): 35-41.
[22]Yang Y, Ye Y, Lin X, et al. Inhibition of pirfenidone on TGF-beta 2 induced proliferation, migration and epithlialmesenchymal transition of human lens epithelial cells line SRA01/04[J]. PLoS One, 2013, 8 (2): e56837.
[23]Assam EO, Phillip K, Zalcberg JR, et al. Precipitous release of methyl-CpG binding protein 2 and histone deacetylase 1 from the methylated human multidrug resistance gene (MDR1) on activation[J]. Mol Cell Biol, 2002, 22(6):1844-1857. 
[24]Barros SP, Offenbacher S. Epigenetics: connecting environment and genotype to phenotype and disease[J]. J Dent Res, 2009, 88(5): 400-408.
[25]Prokhortchouk A, Hendrieh B, Jorgensen H, et al. The peatenin partner kaiso is a DNA methylation dependent transeriptional repressor[J]. Genes Dev,2001,15(13): 13-18.
[26]Grewal SI, Moazed D. Heterochromatin and epigenetic control of gene expression [J].Science, 2003, 301 (5634): 798-802.
[27]Wang ZhG, Wu JX. DNA methyltransferase classification, functions and research progress[J]. Hereditas, 2009, 31 (9):903-912. (in Chinese)
王志刚,吴建新. DNA甲基转移酶分类、功能及其研究进展[J]. 遗传, 2009, 31 (9): 903-912.
[28]Suzuki MM, Adrian B. DNA methylation landscapes: provocative insights from epigenomics[J]. Nat Rev Genet, 2008, (6): 465-476.
[29]Molaro A, Hodges E, Fang F, et al. Sperm methylation profiles reveal features of epigenetic inheritance and evolution in primates[J]. Cell, 2011,146 (6):1029-1041.
[30]Yang B, Xia XY, Huang YF, et al. Epigenetics research progress of sperm[J], National Journal of Andrology, 2007, (12): 1125-1129. (in  Chinese)
杨滨,夏欣一,黄宇烽,等.精子的表观遗传学研究进展[J].中华男科学杂志,2007, 13(12):1125-1129.

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高等学校博士学科点专项科研基金

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