EFFECTS OF MEGADOSES OF PYRIDOXINE ON SPERMATOGENESIS AND MALE REPRODUCTIVE-ORGANS IN RATS

被引:21
作者
MORI, K [1 ]
KAIDO, M [1 ]
FUJISHIRO, K [1 ]
INOUE, N [1 ]
KOIDE, O [1 ]
机构
[1] UNIV OCCUPAT & ENVIRONM HLTH,SCH MED,DEPT PATHOL & SURG PATHOL,KITAKYUSHU,FUKUOKA 807,JAPAN
关键词
PYRIDOXINE; VITAMIN-B; TESTIS; REPRODUCTIVE SYSTEM; SPERMATOGENESIS; RAT;
D O I
10.1007/BF01974015
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Although it has been indicated that many neurotoxicants also cause reproductive toxicity, the reproductive toxicity of megadoses of pyridoxine, which is a neurotoxicant, has not been studied. In this paper, we studied the effects of megadoses of pyridoxine on male reproductive organs. Pyridoxine hydrochloride, 125 mg/kg, 250 mg/kg, 500 mg/kg or 1000 mg/kg, daily, was intraperitoneally injected into Wistar male rats 5 days a week for 2 or 6 weeks, and its effects on the male reproductive organs were investigated. After 2 weeks of administration, absolute weights of the testis in the 500 and 1000 mg/kg epididymis in all the exposed groups and prostate gland in the 1000 mg/kg group decreased, and mature spermatid counts in the testis decreased in the 1000 mg/kg group. After 6 weeks administration, the absolute and relative weights of the testis, epididymis, prostate gland and seminal vesicle decreased in the 500 mg/kg and 1000 mg/kg groups, and mature spermatid counts in the testis and sperm counts in the epididymis decreased in these groups. Among the marker enzymes of the testicular cells, LDH-X activity decreased, and beta-glucuronidase activity, cytochrome P-450 content and cytochrome b5 content increased in the 1000 mg/kg group. Plasma testosterone concentration did not significantly alter in all the exposed groups. From these results, it was concluded that megadoses of pyridoxine affected the spermatogenesis and decreased reproductive organ weights in the rat.
引用
收藏
页码:198 / 203
页数:6
相关论文
共 41 条
[1]  
ABRAHAM G E, 1980, Infertility, V3, P155
[2]  
Amann R P, 1982, Fundam Appl Toxicol, V2, P13, DOI 10.1016/S0272-0590(82)80059-6
[3]   SUCCESSFUL TREATMENT OF HOMOCYSTINURIA WITH PYRIDOXINE [J].
BARBER, GW ;
SPAETH, GL .
JOURNAL OF PEDIATRICS, 1969, 75 (03) :463-&
[4]  
CAKE MH, 1978, J BIOL CHEM, V253, P4886
[5]   TREATMENT OF HOMOCYSTINURIA WITH PYRIDOXINE - A PRELIMINARY STUDY [J].
CARSON, NAJ ;
CARRE, IJ .
ARCHIVES OF DISEASE IN CHILDHOOD, 1969, 44 (235) :387-&
[6]   THE INTERACTION OF SERTOLI AND LEYDIG-CELLS IN THE TESTICULAR TOXICITY OF TRI-ORTHO-CRESYL PHOSPHATE [J].
CHAPIN, RE ;
PHELPS, JL ;
SOMKUTI, SG ;
HEINDEL, JJ ;
BURKA, LT .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1990, 104 (03) :483-495
[7]   PYRIDOXAL-PHOSPHATE INDUCED ALTERATIONS IN GLUCOCORTICOID RECEPTOR CONFORMATION [J].
CIDLOWSKI, JA ;
THANASSI, JW .
BIOCHEMISTRY, 1979, 18 (11) :2378-2384
[8]   SAFETY OF PYRIDOXINE - A REVIEW OF HUMAN AND ANIMAL STUDIES [J].
COHEN, M ;
BENDICH, A .
TOXICOLOGY LETTERS, 1986, 34 (2-3) :129-139
[9]   HIGH PYRIDOXINE DIET IN RAT - POSSIBLE IMPLICATIONS FOR MEGAVITAMIN THERAPY [J].
COHEN, PA ;
SCHNEIDM.K ;
GINSBERG.F ;
STURMAN, JA ;
KNITTLE, J ;
GAULL, GE .
JOURNAL OF NUTRITION, 1973, 103 (01) :143-151
[10]  
COX SH, 1962, P SOC EXP BIOL MED, V109, P242, DOI 10.3181/00379727-109-27166