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1
SELECTIVE DESTRUCTION IN TESTIS INDUCED BY 7,12-DIMETHYLBENZ [a] ANTHRACENE.7,12-二甲基苯[a]蒽诱导的睾丸选择性破坏。
J Exp Med. 1963 Jul 1;118(1):27-40. doi: 10.1084/jem.118.1.27.
2
Cell-specific metabolic activation of 7,12-dimethylbenz[a]anthracene in rat testis.大鼠睾丸中7,12-二甲基苯并[a]蒽的细胞特异性代谢激活
Chem Biol Interact. 1989;72(1-2):65-78. doi: 10.1016/0009-2797(89)90018-5.
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AROMATIC-INDUCED PREVENTION OF FETAL TOXICITY OF 7,12-DIMETHYLBENZ(ALPHA)ANTHRACENE.芳香族化合物诱导预防7,12 - 二甲基苯并(α)蒽的胎儿毒性
J Exp Med. 1964 Jan 1;119(6):943-54. doi: 10.1084/jem.119.6.943.
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Murine oocyte destruction following intraovarian treatment with 3-methylcholanthrene or 7,12-dimethylbenz(a)anthracene: protection by alpha-naphthoflavone.用3-甲基胆蒽或7,12-二甲基苯并(a)蒽进行卵巢内治疗后小鼠卵母细胞的破坏:α-萘黄酮的保护作用。
Teratog Carcinog Mutagen. 1985;5(6):463-72. doi: 10.1002/tcm.1770050609.
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Oocyte destruction by polycyclic aromatic hydrocarbons is not linked to the inducibility of ovarian aryl hydrocarbon (benzo(a)pyrene) hydroxylase activity in (DBA/2N X C57BL/6N) F1 X DBA/2N backcross mice.多环芳烃对卵母细胞的破坏与(DBA/2N×C57BL/6N)F1×DBA/2N回交小鼠卵巢芳烃(苯并(a)芘)羟化酶活性的诱导性无关。
Pediatr Pharmacol (New York). 1982;2(1):11-21.
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Evidence for a free-radical-dependent metabolism of 7,12-dimethylbenz(a)anthracene in rat testis.大鼠睾丸中7,12-二甲基苯并(a)蒽自由基依赖性代谢的证据。
Toxicol Appl Pharmacol. 1987 Jan;87(1):141-54. doi: 10.1016/0041-008x(87)90092-5.
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Benzo(e)pyrene-induced alterations in the binding of benzo(a)pyrene and 7,12-dimethylbenz(a)anthracene to DNA in Sencar mouse epidermis.苯并(e)芘诱导的苯并(a)芘和7,12-二甲基苯并(a)蒽与Sencar小鼠表皮中DNA结合的改变。
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Correlation between formation of a specific hydrocarbon-deoxyribonucleoside adduct and tumor-initiating activity of 7,12-dimethylbenz(a)anthracene and its 9- and 10-monofluoroderivatives in mice.小鼠体内特定烃 - 脱氧核糖核苷加合物的形成与7,12 - 二甲基苯并(a)蒽及其9 - 和10 - 单氟衍生物的肿瘤起始活性之间的相关性。
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Tumor-initiating activity of 4-fluoro-7,12-dimethylbenz[a]anthracene and 1,2,3,4-tetrahydro-7,12-dimethylbenz[a]anthracene in female SENCAR mice.4-氟-7,12-二甲基苯并[a]蒽和1,2,3,4-四氢-7,12-二甲基苯并[a]蒽在雌性SENCAR小鼠中的肿瘤起始活性。
Carcinogenesis. 1982;3(6):651-5. doi: 10.1093/carcin/3.6.651.

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Increased sensitivity to testicular toxicity of transplacental benzo[a]pyrene exposure in male glutamate cysteine ligase modifier subunit knockout (Gclm-/-) mice.雄性谷氨酸胱氨酸连接酶修饰亚单位敲除(Gclm-/-)小鼠中转胎盘苯并[a]芘暴露致睾丸毒性的敏感性增加。
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2
AROMATIC-INDUCED PREVENTION OF FETAL TOXICITY OF 7,12-DIMETHYLBENZ(ALPHA)ANTHRACENE.芳香族化合物诱导预防7,12 - 二甲基苯并(α)蒽的胎儿毒性
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3
CANCER AND THE ADRENAL.癌症与肾上腺
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The effect of 7,12-dimethylbenz(a)anthracene on the incorporation of thymidine-H3 into deoxyribonucleic acid in normal and regenerating liver.7,12-二甲基苯并(a)蒽对正常及再生肝脏中胸腺嘧啶核苷-H3掺入脱氧核糖核酸的影响。
Experientia. 1965 Aug 15;21(8):473-4. doi: 10.1007/BF02150830.
5
Hundred day leukemia: preferential induction in rat by pulse-doses of 7,8,12-trimethylbenz(a)anthracene.百日白血病:7,8,12-三甲基苯并(a)蒽脉冲剂量在大鼠中优先诱导产生
J Exp Med. 1970 Feb;131(2):321-30. doi: 10.1084/jem.131.2.321.
6
Effect of styrene administration on rat testis.苯乙烯给药对大鼠睾丸的影响。
Arch Toxicol. 1989;63(1):43-6. doi: 10.1007/BF00334633.
7
Testicular effects of di-n-butyl phthalate (DBP): biochemical and histopathological alterations.邻苯二甲酸二丁酯(DBP)对睾丸的影响:生化及组织病理学改变
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Autoradiographic study of DNA synthesis and the cell cycle in spermatogonia and spermatocytes of mouse testis using tritiated thymidine.利用氚标记胸腺嘧啶核苷对小鼠睾丸精原细胞和精母细胞中DNA合成及细胞周期的放射自显影研究。
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7,12-二甲基苯[a]蒽诱导的睾丸选择性破坏。

SELECTIVE DESTRUCTION IN TESTIS INDUCED BY 7,12-DIMETHYLBENZ [a] ANTHRACENE.

机构信息

Ben May Laboratory for Cancer Research, The University of Chicago, Chicago.

出版信息

J Exp Med. 1963 Jul 1;118(1):27-40. doi: 10.1084/jem.118.1.27.

DOI:10.1084/jem.118.1.27
PMID:19867232
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2137575/
Abstract

After a single feeding or intravenous injection of 7,12-dimethylbenz[a]anthracene, the testis of rat was severely and selectively damaged, whereas the ovary of sisters was spared from injury. After many weeks, complete recovery of the testis ensued. The destructive effect of 7,12-DMBA on testis was not shared by other powerful carcinogenic hydrocarbons; 3-methylcholanthrene; benzo[a]pyrene; 2-acetaminophenanthrene. The primary sites of destruction inflicted by 7,12-DMBA on testis were spermatogonia and resting spermatocytes, the only cells in testis which synthesize deoxyribose nucleic acid. No other cells in the germinal epithelium are damaged by 7,12-DMBA. The severe atrophy of testis that ensues after some weeks is secondary to destruction of precursors in the seminiferous cell line. Moreover, interstitial cells of testis are not destroyed by the hydrocarbon. Estimation of malic dehydrogenase is a simple and useful quantitative measure of damage and subsequent repair in testis. Following administration of 7,12-DMBA, the level of MDH had an inverse relationship to weight of the testis.

摘要

单次经口或静脉注射 7,12-二甲基苯并蒽后,大鼠的睾丸受到严重且选择性的损伤,而其姊妹的卵巢则免受损伤。数周后,睾丸完全恢复。7,12-DMBA 对睾丸的破坏作用并不为其他强效致癌烃;3-甲基胆蒽;苯并[a]芘;2-乙酰氨基菲所共有。7,12-DMBA 对睾丸造成的主要破坏部位是精原细胞和休止期精母细胞,这是睾丸中唯一合成脱氧核糖核酸的细胞。生殖上皮中的其他细胞不受 7,12-DMBA 损害。数周后发生的严重睾丸萎缩是生精细胞系中前体细胞破坏的继发结果。此外,间质细胞不受该烃类破坏。苹果酸脱氢酶的测定是睾丸损伤和随后修复的一种简单而有用的定量测量方法。给予 7,12-DMBA 后,MDH 的水平与睾丸重量呈反比关系。