URINARY CREATINE PROFILES AFTER ADMINISTRATION OF CELL-SPECIFIC TESTICULAR TOXICANTS TO THE RAT

被引:20
作者
MOORE, NP [1 ]
CREASY, DM [1 ]
GRAY, TJB [1 ]
TIMBRELL, JA [1 ]
机构
[1] BRITISH IND BIOL RES ASSOC,SURREY SM5 4DS,ENGLAND
关键词
METHOXYACETIC ACID; DI-NORMAL-PENTYL PHTHALATE; 1,3-DINITROBENZENE; ETHANE-1,2-DIMETHANE SULFONATE; TESTIS; CREATINE; CREATINURIA;
D O I
10.1007/BF02035135
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Cell-specific testicular toxicants have been used to examine the distribution of creatine within the rat testis, and to examine the potential use of creatinuria as a non-invasive indicator of testicular damage. Groups of rats were administered single doses of various toxicants: a germ cell toxicant (methoxyacetic acid, MAA), one of two Sertoli cell toxicants (di-n-pentyl phthalate, DPP or 1,3-dinitrobenzene, 1,3-DNB), or a Leydig cell toxicant (ethane- 1,2-dimethane sulphonate, EDS). Urinary creatine and creatinine levels were monitored in 24 h periods over the following 48 h, after which time the testes were removed, weighed and, after processing, sections were examined by light microscopy. All four treatments resulted in reductions in relative testis weight (RTW) and produced morphological changes similar to those which have been previously reported. In addition, MAA, DPP and 1,3-DNB all caused significant elevations in urinary creatine excretion and the urinary creatine: creatinine ratio (Cr/Crn) within 24 h. EDS had no such effect. We conclude that creatine is associated with the cells of the seminiferous epithelium, and that elevated urinary excretion of creatine may serve as a non-invasive marker for damage to these cells in vivo.
引用
收藏
页码:435 / 442
页数:8
相关论文
共 45 条
[31]   THE ROLE OF METABOLISM IN 2-METHOXYETHANOL-INDUCED TESTICULAR TOXICITY [J].
MOSS, EJ ;
THOMAS, LV ;
COOK, MW ;
WALTERS, DG ;
FOSTER, PMD ;
CREASY, DM ;
GRAY, TJB .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1985, 79 (03) :480-489
[32]   THE EFFECT OF MONO-(2-ETHYLHEXYL) PHTHALATE AND OTHER PHTHALATE-ESTERS ON LACTATE PRODUCTION BY SERTOLI CELLS-INVITRO [J].
MOSS, EJ ;
COOK, MW ;
THOMAS, LV ;
GRAY, TJB .
TOXICOLOGY LETTERS, 1988, 40 (01) :77-84
[33]  
MOSS EJ, 1987, HUM TOXICOL, V6, P425
[34]  
NICHOLSON JK, 1989, MOL PHARMACOL, V36, P398
[35]  
PARIZEK J, 1956, NATURE, V177, P1036
[36]   URINARY CREATINE AS A POSSIBLE MARKER FOR TESTICULAR DAMAGE - STUDIES WITH THE TESTICULAR TOXIC COMPOUND 2-METHOXYETHANOL [J].
RAWCLIFFE, L ;
CREASY, D ;
TIMBRELL, JA .
REPRODUCTIVE TOXICOLOGY, 1989, 3 (04) :269-274
[37]   CHANGES IN TESTICULAR AND SERUM HORMONE CONCENTRATIONS IN THE MALE-RAT FOLLOWING TREATMENT WITH META-DINITROBENZENE [J].
REHNBERG, GL ;
LINDER, RE ;
GOLDMAN, JM ;
HEIN, JF ;
MCELROY, WK ;
COOPER, RL .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1988, 95 (02) :255-264
[38]   ETHANE DIMETHANE SULFONATE (EDS) SPECIFICALLY INHIBITS LH STIMULATED STEROIDOGENESIS IN LEYDIG-CELLS ISOLATED FROM MATURE RATS BUT NOT IN CELLS FROM IMMATURE RATS [J].
ROMMERTS, FFG ;
GROOTENHUIS, AJ ;
HOOGERBRUGGE, JW ;
VANDERMOLEN, HJ .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1985, 42 (02) :105-111
[39]   HEPATIC-EFFECTS OF PHTHALATE-ESTERS [J].
SETH, PK .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1982, 45 (NOV) :27-34
[40]  
SIEDEL J, 1984, CLIN CHEM, V30, P968