Acute adverse effects of the indenopyridine CDB-4022 on the ultrastructure of Sertoli cells, spermatocytes, and spermiatids in rat testes: Comparison to the known Sertoli cell toxicant di-n-pentylphthalate DPP

被引:27
作者
Hild, Sheri Ann
Reel, Jerry R.
Dykstra, Michael J.
Mann, Peter C.
Marshall, Gary R.
机构
[1] BIOQUAL Inc, Rockville, MD 20850 USA
[2] N Carolina State Univ, Coll Vet Med, Lab Adv Elect & Light Opt Methods, Raleigh, NC USA
[3] Labs Inc, Herndon, VA USA
[4] Univ Pittsburgh, Sch Med, Dept Med, Pittsburgh, PA USA
来源
JOURNAL OF ANDROLOGY | 2007年 / 28卷 / 04期
关键词
antifertility; morphology; ultrastructure; seminiferous; epithelium; germ cells;
D O I
10.2164/jandrol.106.002295
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
Acute effects of CDB-4022 on testicular ultrastructure were determined. Rats were treated orally with vehicle or a maximally effective single dose of CDB-4022 or Di-n-pentlphthalate (DPP). Preserved testes were processed for transmission electron microscopy. Sertoli and germ cells,of vehicle-treated rats demonstrated normal morphological characteristics. Disruption of Sertoli cell ultrastructure was apparent in CDB-4022-treated rats by 3 hours. A decrease in the presence of nucleoli, an increase in the amount and diameter of swollen smooth endoplasmic reticulum, and decreases in cytoplasmic ground substance were observed. The severity of these degenerative effects increased at 6 and 12 hours: Vacuoles were apparent; increased cellular debris, swollen mitochondria, and phagocytic structures were observed; and membranes became more disorganized. Similar ultrastructural changes were observed in the Sertoli cells of DPP-treated rats. By 3 hours, spermatocytes and spermatids were adversely affected by CDB-4M treatment with swelling of the nuclear envelope. The Step 8 spermatids were especially noteworthy; chromatin was more diffuse and rarefied, the nuclear envelopes were incomplete or broken, and the position of the spermatid nucleus within the cell and relative to Sertoli cell cytoplasm was unusual. Fusion of spermatids to form giant cells was observed by 12 hours. CDB-4022 acts acutely on Sertoli cells to induce marked cellular rarefaction and degeneration, but not necrosis. A rapid and direct effect of CDB-4022 on spermatocytes and spermatids Was observed. the antispermatogenic activity of CDB-4022 appears to be a consequence of direct effects on Sertoli and germ cells.
引用
收藏
页码:621 / 629
页数:9
相关论文
共 18 条
[1]  
BOEKELHEIDE K, 2005, SERTOLI CELL BIOL, P345
[2]   THE MORPHOGENESIS OF TESTICULAR DEGENERATION INDUCED IN RATS BY ORALLY-ADMINISTERED 2,5-HEXANEDIONE [J].
CHAPIN, RE ;
MORGAN, KT ;
BUS, JS .
EXPERIMENTAL AND MOLECULAR PATHOLOGY, 1983, 38 (02) :149-169
[3]   AF-2364 [1-(2,4-dichlorobenzyl)-1H-indazole-3-carbohydrazide] is a potential male contraceptive: a review of recent data [J].
Cheng, CY ;
Mruk, D ;
Silvestrini, B ;
Bonanomi, M ;
Wong, CH ;
Siu, MKY ;
Lee, NPY ;
Lui, WY ;
Mo, MY .
CONTRACEPTION, 2005, 72 (04) :251-261
[4]   THE ULTRASTRUCTURAL EFFECTS OF DI-N-PENTYL PHTHALATE ON THE TESTIS OF THE MATURE RAT [J].
CREASY, DM ;
BEECH, LM ;
GRAY, TJB ;
BUTLER, WH .
EXPERIMENTAL AND MOLECULAR PATHOLOGY, 1987, 46 (03) :357-371
[5]   THE MORPHOLOGICAL DEVELOPMENT OF DI-N-PENTYL PHTHALATE INDUCED TESTICULAR ATROPHY IN THE RAT [J].
CREASY, DM ;
FOSTER, JR ;
FOSTER, PMD .
JOURNAL OF PATHOLOGY, 1983, 139 (03) :309-321
[6]   Suggested Standard Operating Procedures (SOPs) for the preparation of electron microscopy samples for toxicology/pathology studies in a GLP environment [J].
Dykstra, MJ ;
Mann, PC ;
Elwell, MR ;
Ching, SV .
TOXICOLOGIC PATHOLOGY, 2002, 30 (06) :735-743
[7]   Lactate inhibits germ cell apoptosis in the human testis [J].
Erkkilä, K ;
Aito, H ;
Aalto, K ;
Pentikäinen, V ;
Dunkel, L .
MOLECULAR HUMAN REPRODUCTION, 2002, 8 (02) :109-117
[8]  
HAUSLER A, 1979, ARCH TOXICOL S, V2, P387
[9]   The ability of a gonadotropin-releasing hormone antagonist, acyline, to prevent irreversible infertility induced by the indenopyridine, CDB-4022, in adult male rats: The role of testosterone [J].
Hild, SA ;
Attardi, BJ ;
Reel, JR .
BIOLOGY OF REPRODUCTION, 2004, 71 (01) :348-358
[10]  
Hild SA, 2001, BIOL REPROD, V65, P165, DOI 10.1095/biolreprod65.1.165