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成年大鼠经口暴露于甲基叔丁基醚后睾丸的组织学和组织形态计量学变化

Histologic and histomorphometric changes of testis following oral exposure to methyl tertiary-butyl ether in adult rat.

作者信息

Gholami S, Ansari-Lari M, Khalili L

机构信息

Department of Basic Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, Iran;

Department of Food Hygiene and Public Health, School of Veterinary Medicine, Shiraz University, Shiraz, Iran;

出版信息

Iran J Vet Res. 2015 Summer;16(3):288-92.

PMID:27175191
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4782700/
Abstract

Methyl tertiary-butyl ether (MTBE) is used to reduce carbon monoxide and ozone in urban air and to boost fuel octane. There is a lack of knowledge in the literature about the histomorphometric changes of the testis following exposure to MTBE. Therefore, this experimental study was performed to determine the effect of oral exposure to MTBE on histologic and histomorphometric changes of testis in adult rat. A total of 25 adult male Sprague-Dawley rats were randomly divided into five equal experimental groups: control, almond oil and three treatment groups which received 400, 800 and 1600 mg/kg/day MTBE in almond oil by gavages for 30 consecutive days. Histomorphometric analysis showed no significant difference in absolute and relative testis weight, connective tissue thickness, germinal epithelium height, tunica albuginea thickness and Sertoli cell numbers between experimental groups (P>0.05). However, trend analysis showed that the seminiferous tubule diameter increased and interstitial cell numbers as well as spermatocyte and spermatid cell numbers decreased significantly in MTBE treated groups (P<0.05). It may be concluded that MTBE could exert adverse effects on spermatogenic cells in adult rat. Whether the observed changes in the present study are due to the direct effect of MTBE via passing blood-testis barrier or its indirect effect through another mechanism should be elucidated in future studies.

摘要

甲基叔丁基醚(MTBE)用于减少城市空气中的一氧化碳和臭氧,并提高燃料辛烷值。文献中缺乏关于暴露于MTBE后睾丸组织形态计量学变化的知识。因此,进行本实验研究以确定经口暴露于MTBE对成年大鼠睾丸组织学和组织形态计量学变化的影响。总共25只成年雄性Sprague-Dawley大鼠被随机分为五个相等的实验组:对照组、杏仁油组和三个处理组,三个处理组连续30天通过灌胃给予含400、800和1600 mg/kg/天MTBE的杏仁油。组织形态计量学分析显示,实验组之间的绝对和相对睾丸重量、结缔组织厚度、生精上皮高度、白膜厚度和支持细胞数量无显著差异(P>0.05)。然而,趋势分析表明,MTBE处理组的曲细精管直径增加,间质细胞数量以及精母细胞和精子细胞数量显著减少(P<0.05)。可以得出结论,MTBE可能对成年大鼠的生精细胞产生不利影响。本研究中观察到的变化是由于MTBE通过血睾屏障的直接作用还是通过另一种机制的间接作用,应在未来的研究中阐明。

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本文引用的文献

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Toxicity of methyl tertiary-butyl ether (MTBE) following exposure of Wistar Rats for 13 weeks or one year via drinking water.经饮用水染毒 13 周或 1 年的 Wistar 大鼠的甲基叔丁基醚(MTBE)毒性。
J Appl Toxicol. 2012 Sep;32(9):687-706. doi: 10.1002/jat.1674. Epub 2011 Mar 24.
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Cytotoxicity and oxidative stress study in cultured rat Sertoli cells with methyl tert-butyl ether (MTBE) exposure.甲基叔丁基醚(MTBE)暴露对培养的大鼠支持细胞的细胞毒性和氧化应激研究。
Reprod Toxicol. 2009 Apr;27(2):170-6. doi: 10.1016/j.reprotox.2008.12.004. Epub 2008 Dec 30.
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Effect of oral methyl-t-butyl ether (MTBE) on the male mouse reproductive tract and oxidative stress in liver.口服甲基叔丁基醚(MTBE)对雄性小鼠生殖道及肝脏氧化应激的影响。
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The effects of methyl tert-butyl ether (MTBE) on the male rat reproductive system.甲基叔丁基醚(MTBE)对雄性大鼠生殖系统的影响。
Food Chem Toxicol. 2008 Jul;46(7):2402-8. doi: 10.1016/j.fct.2008.03.024. Epub 2008 Apr 3.
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Methyl tert-butyl ether (MTBE)-induced cytotoxicity and oxidative stress in isolated rat spermatogenic cells.甲基叔丁基醚(MTBE)对离体大鼠生精细胞的细胞毒性和氧化应激作用。
J Appl Toxicol. 2007 Jan-Feb;27(1):10-7. doi: 10.1002/jat.1178.
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Absence of acute testicular toxicity of methyl-tert butyl ether and breakdown products in mice.
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Subchronic studies in Sprague-Dawley rats to investigate mechanisms of MTBE-induced Leydig cell cancer.在斯普拉格-道利大鼠中进行的亚慢性研究,以探究甲基叔丁基醚诱导睾丸间质细胞瘤的机制。
Toxicol Sci. 2003 Mar;72(1):31-42. doi: 10.1093/toxsci/kfg011.
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Alterations in endocrine responses in male Sprague-Dawley rats following oral administration of methyl tert-butyl ether.雄性斯普拉格-道利大鼠口服甲基叔丁基醚后内分泌反应的变化。
Toxicol Sci. 2000 Mar;54(1):168-76. doi: 10.1093/toxsci/54.1.168.
9
Oncogenicity studies of inhaled methyl tertiary-butyl ether (MTBE) in CD-1 mice and F-344 rats.吸入甲基叔丁基醚(MTBE)对CD-1小鼠和F-344大鼠的致癌性研究。
J Appl Toxicol. 1997 May;17 Suppl 1:S45-55. doi: 10.1002/(sici)1099-1263(199705)17:1+<s45::aid-jat410>3.3.co;2-b.
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J Appl Toxicol. 1997 May;17 Suppl 1:S1-2. doi: 10.1002/(sici)1099-1263(199705)17:1+<s1::aid-jat404>3.3.co;2-8.