Project/Area Number |
13671649
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Urology
|
Research Institution | KYOTO UNIVERSITY |
Principal Investigator |
YAMAMOTO Shingo School of Medicine, Kyoto University, Associated professor, 医学研究科, 講師 (80322741)
|
Co-Investigator(Kenkyū-buntansha) |
NISHIYAMA Hiroyuki School of Medicine, Kyoto University, Assisstaat professor, 医学研究科, 助手 (20324642)
OGAWA Osamu School of Medicine, Kyoto University, Professor, 医学研究科, 教授 (90260611)
諸井 誠二 京都大学, 医学研究科, 助手 (50314191)
|
Project Period (FY) |
2001 – 2002
|
Project Status |
Completed (Fiscal Year 2002)
|
Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2002: ¥1,700,000 (Direct Cost: ¥1,700,000)
Fiscal Year 2001: ¥1,800,000 (Direct Cost: ¥1,800,000)
|
Keywords | Male infertility / Environmental factors / Genetic susceptibility / 遺伝子多型 / 酸化ストレス / 遺伝的要因 / 男性生殖機能障害 |
Research Abstract |
Male reproductive function is impaired by various environmental factors such as smoking, heat stress, endocrine-disrupting chemicals and oxidative stresses. There are inter-individual variability of xenobiotic metabolism, and genetic polymorphisms modulate susceptibility to male infertility associated with environmental factors. Polymorphisms of glutathione S-transferase (GST) M1/T1, key enzymes in the extrahepatic metabolism of xenobiotics, have been shown to influence susceptibility to male infertility associated with xenobiotics including smoking. First, the association between smoking and GSTTI/M1 polymorphisms were investigated in 194 infertile Japanese men. Of the 145 patients with non-obstructive male infertility, 85(58.6%) men had GSTM1 null genotype. Control population and infertile patients with normal spermatogenesis had GSTM1 null genotype in 52.2% and 55.1%. In contrast, the frequencies of GSTT1(+) is not significantly different between non-obstructive male infertility and
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control. Of non-obstructive male infertility, patients with varicocele had higher frequency of GSTM1 null genotype than control. These preliminary results suggest that the GSTM1 null genotype may be associated with individual susceptibility to male infertility associated with varicocele. Secondly, to investigate the effect of oxidative stress and heat stress on male infertility, we examined experimentally induced cryptorchid testes in thioredoxin transgenic mice, which have cytoprotective effects against various types of oxidative stresses. Unilateral cryptorchidism was surgically induced both in TRX transgenic (TRX-tg) and wild type adult mice, and testicular damage was evaluated by measuring testis weight and analyzing tcsticular histology. Weight reduction of cryptorchid testis was significantly decreased in TRX-tg mice, compared with those in wild type mice. Moreover, testicular histology and TUNEL staining demonstrated that apoptotic changes were delayed by 4 days in TRX-tg mice compared with those in WT mice. These results suggest that oxidative stress is associated with male infertility and polymorphisms of oxidative stress-related genes may be associated with individual susceptibility to male infertility induced by environmental factors Less
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