Wei sheng yan jiu = Journal of hygiene research · 2010
[Reproductive toxicity of male rats exposed to two isomers of bromopropanes].
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Huang Fen, Xin Qianqian, Wang Hua, Zhang Wanjun, Wang Hailan, Song Xiangrong, Ye Dongqing
Аннотация
OBJECTIVE: To study the reproductive toxicity of male rats exposed to 1-bromopropane and 2-bromopropane and to explore the toxic mechanism of two isomers.
METHODS: 18 SPF SD male rats were randomly divided into 3 groups of 6 each, respectively. The groups were exposed to corn oil, 1-BP (1 g/kg) and 2-BP (1 g/ kg) for 7 days by intraperitoneally injection. Trait of reproductive organs, sperm characteristics, testicular histological and apoptotic findings and the lipid peroxidation in the testicular and epididymal tissue were determined.
RESULTS: Results showed that treatment with bromopropanes induced reduction in sperm concentration and increments in abnormalities of sperm injuries to sperm quality. In addition, 1-BP increased GR activity (7. 42 +/- 2.98 vs. 4.25 +/- 1.18, P < 0.05) in testis, and SOD activity (91.87 +/- 3.93 vs. 80.59 +/- 9.92, P < 0.05) and MDA level (0.49 -/+ 0.20 vs. 0.39 +/- 0.08, P < 0.05) in epididymis. 2-BP decreased the GSH lever (6.35 +/- 1.86 vs. 10.89 +/- 3.69, P < 0.05) and increased the MDA level (0.42 +/- 0.07 vs. 0.24 +/- 0. 11, P < 0.05; 0.48 +/- 0.08 vs. 0.39 +/- 0.08, P < 0.05) in epididymis and testis, decreased GST ( 53.21 +/- 9.60 vs. 61.98 +/- 10.41, P < 0.05) and GR activity (2.48 +/- 1.21 vs. 7.75 +/- 8.56, P < 0.05) in epididymis. There were no histopathological changes in treatment with 1-BP rats, except that retained and elongated spermatids near basement membrane at the spermatogenesis cycle were found. Whereas, treatment with 2-BP induced vacuolation, degeneration and necrosis in seminiferous tubules. Paralleling with testicular lesion, treatment with 2-BP increased the total apoptotic cells per tubule, the percentage of apoptotic cells and apoptotic index significantly, comparing with control (17.72 +/- 4.59 vs. 5.92 +/- 1.05, P < 0.05; 0.34 +/- 0.14 vs. 0.10 +/- 0.02, P < 0.05; 6.64 +/- 3.40 vs. 0.59 +/- 0.20, P < 0.01). As compring with 1-BP group, exposed to 2-BP increased the percentages of TUNEL-positive tubules and apoptotic cellindex (0.34 +/- 0. 14 vs. 0.12 +/- 0. 03, P < 0.05; 6.64 +/- 3.40 vs. 0.76 +/- 0.21, P < 0.01). In addition, 2-BP group increased the proportion of apoptotic germ cells and the number of active caspase-3-positive cells per tubule, compared with 1-BP and control (P < 0.01, P < 0.01; P < 0.01, P < 0.01).
CONCLUSION: This study indicates that bromopropanes can cause reproductive disorder in male rats, the rats treatment with 2-BP had more toxicity than that with 1-BP, and it might have different toxic mechanism between two isomers.
METHODS: 18 SPF SD male rats were randomly divided into 3 groups of 6 each, respectively. The groups were exposed to corn oil, 1-BP (1 g/kg) and 2-BP (1 g/ kg) for 7 days by intraperitoneally injection. Trait of reproductive organs, sperm characteristics, testicular histological and apoptotic findings and the lipid peroxidation in the testicular and epididymal tissue were determined.
RESULTS: Results showed that treatment with bromopropanes induced reduction in sperm concentration and increments in abnormalities of sperm injuries to sperm quality. In addition, 1-BP increased GR activity (7. 42 +/- 2.98 vs. 4.25 +/- 1.18, P < 0.05) in testis, and SOD activity (91.87 +/- 3.93 vs. 80.59 +/- 9.92, P < 0.05) and MDA level (0.49 -/+ 0.20 vs. 0.39 +/- 0.08, P < 0.05) in epididymis. 2-BP decreased the GSH lever (6.35 +/- 1.86 vs. 10.89 +/- 3.69, P < 0.05) and increased the MDA level (0.42 +/- 0.07 vs. 0.24 +/- 0. 11, P < 0.05; 0.48 +/- 0.08 vs. 0.39 +/- 0.08, P < 0.05) in epididymis and testis, decreased GST ( 53.21 +/- 9.60 vs. 61.98 +/- 10.41, P < 0.05) and GR activity (2.48 +/- 1.21 vs. 7.75 +/- 8.56, P < 0.05) in epididymis. There were no histopathological changes in treatment with 1-BP rats, except that retained and elongated spermatids near basement membrane at the spermatogenesis cycle were found. Whereas, treatment with 2-BP induced vacuolation, degeneration and necrosis in seminiferous tubules. Paralleling with testicular lesion, treatment with 2-BP increased the total apoptotic cells per tubule, the percentage of apoptotic cells and apoptotic index significantly, comparing with control (17.72 +/- 4.59 vs. 5.92 +/- 1.05, P < 0.05; 0.34 +/- 0.14 vs. 0.10 +/- 0.02, P < 0.05; 6.64 +/- 3.40 vs. 0.59 +/- 0.20, P < 0.01). As compring with 1-BP group, exposed to 2-BP increased the percentages of TUNEL-positive tubules and apoptotic cellindex (0.34 +/- 0. 14 vs. 0.12 +/- 0. 03, P < 0.05; 6.64 +/- 3.40 vs. 0.76 +/- 0.21, P < 0.01). In addition, 2-BP group increased the proportion of apoptotic germ cells and the number of active caspase-3-positive cells per tubule, compared with 1-BP and control (P < 0.01, P < 0.01; P < 0.01, P < 0.01).
CONCLUSION: This study indicates that bromopropanes can cause reproductive disorder in male rats, the rats treatment with 2-BP had more toxicity than that with 1-BP, and it might have different toxic mechanism between two isomers.