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肝脏病变与口服避孕药类固醇

Liver lesions and oral contraceptive steroids.

作者信息

Barrows G H, Christopherson W M, Drill V A

出版信息

J Toxicol Environ Health. 1977 Sep;3(1-2):219-30. doi: 10.1080/15287397709529561.

DOI:10.1080/15287397709529561
PMID:926189
Abstract

Two strains of mice, CF-LP and Swiss-Webster random-bred, were evaluated for liver neoplasia after administration of oral contraceptive steroids. No increased incidence of hepatocellular tumors was found beyond the variation expected by chance. The overall tumor incidence in treated and untreated groups was identical. No significant increase in tumor size was observed in the treated animals. Liver weights progressively increased in several of the treated groups. In both treated and untreated animals hepatocellular neoplasia was usually accompanied by intracytoplasmic inclusions similar to those observed in human liver tumors. Vascular lesions were observed in some of the animals receiving large doses of contraceptive steroids. While these may be the result of local toxicity, their similarity to lesions observed in benign liver tumors warrants further investigation. No evidence was found to suggest that contraceptive steroids act as initiators of liver neoplasia.

摘要

对两种品系的小鼠,即CF-LP和瑞士韦伯斯特随机繁殖小鼠,在给予口服避孕类固醇后进行了肝肿瘤形成评估。未发现肝细胞肿瘤的发生率有超出偶然预期变异的增加。治疗组和未治疗组的总体肿瘤发生率相同。在接受治疗的动物中未观察到肿瘤大小有显著增加。几个治疗组的肝脏重量逐渐增加。在治疗和未治疗的动物中,肝细胞肿瘤通常伴有与人类肝脏肿瘤中观察到的相似的胞质内包涵体。在一些接受大剂量避孕类固醇的动物中观察到血管病变。虽然这些可能是局部毒性的结果,但它们与良性肝肿瘤中观察到的病变相似性值得进一步研究。没有发现证据表明避孕类固醇是肝肿瘤形成的启动剂。

相似文献

1
Liver lesions and oral contraceptive steroids.肝脏病变与口服避孕药类固醇
J Toxicol Environ Health. 1977 Sep;3(1-2):219-30. doi: 10.1080/15287397709529561.
2
[Primary liver cancer following prolonged use of contraceptive drugs].长期使用避孕药后发生的原发性肝癌
Orv Hetil. 1977 Feb 6;118(6):334-6.
3
NTP Toxicology and Carcinogenesis Studies of Coumarin (CAS No. 91-64-5) in F344/N Rats and B6C3F1 Mice (Gavage Studies).香豆素(CAS编号91-64-5)在F344/N大鼠和B6C3F1小鼠中的NTP毒理学和致癌性研究(灌胃研究)
Natl Toxicol Program Tech Rep Ser. 1993 Sep;422:1-340.
4
NTP Toxicology and Carcinogenesis Studies of Oxazepam (CAS No. 604-75-1) in Swiss-Webster and B6C3F1 Mice (Feed Studies).奥沙西泮(化学物质登记号:604-75-1)对瑞士韦伯斯特小鼠和B6C3F1小鼠的NTP毒理学与致癌性研究(饲料喂养研究)
Natl Toxicol Program Tech Rep Ser. 1993 Aug;443:1-321.
5
Hepatic adenomas and focal nodular hyperplasia of the liver in young women on oral contraceptives: case reports.口服避孕药的年轻女性肝脏的肝腺瘤和局灶性结节性增生:病例报告
J Nucl Med. 1977 Mar;18(3):263-6.
6
NTP Toxicology and Carcinogenesis Studies of C.I. Direct Blue 218 (CAS No. 28407-37-6) in F344/N Rats and B6C3F1 Mice (Feed Studies).F344/N大鼠和B6C3F1小鼠中C.I. 直接蓝218(化学物质登录号28407-37-6)的NTP毒理学和致癌性研究(饲料喂养研究)
Natl Toxicol Program Tech Rep Ser. 1994 Feb;430:1-280.
7
Oral contraceptive steroids as promoters or complete carcinogens for liver in female Sprague-Dawley rats.口服避孕甾体激素作为雌性斯普拉格-道利大鼠肝脏的促癌剂或完全致癌物。
Environ Health Perspect. 1983 Apr;50:109-12. doi: 10.1289/ehp.8350109.
8
[Drug-induced liver damage following use of the oral contraceptive Femigen].使用口服避孕药 Femigen 后出现的药物性肝损伤
Patol Pol. 1974 Jan-Mar;25(1):101-6.
9
[Rupture of hepatic adenoma and oral contraceptives].[肝腺瘤破裂与口服避孕药]
Prensa Med Mex. 1978 Jan-Feb;43(1-2):35-6.
10
[Infecundin and benign liver adenoma].[不育素与良性肝腺瘤]
Orv Hetil. 1980 Jan 13;121(2):71-6.

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