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口服呋喃丹对大鼠雄性生殖系统的影响。

Effect of oral administration of carbofuran on male reproductive system of rat.

作者信息

Pant N, Prasad A K, Srivastava S C, Shankar R, Srivastava S P

机构信息

Industrial Toxicology Research Centre, MG Marg, Lucknow, India.

出版信息

Hum Exp Toxicol. 1995 Nov;14(11):889-94. doi: 10.1177/096032719501401106.

Abstract
  1. Carbofuran was administered orally to adult male rats at dose levels of 0.1, 0.2, 0.4 or 0.8 mg kg-1 body weight, 5 d wk-1 for 60 days. A dose dependent decrease was observed in body weight of rats treated with 0.2-0.8 mg carbofuran kg-1 body weight. 2. A significant decrease in the weight of epididymides, seminal vesicles, ventral prostate and coagulating glands was observed at various test doses of carbofuran except at the lowest dose. 3. Decreased sperm motility, reduced epididymal sperm count along with increased morphological abnormalities in head, neck and tail regions of spermatozoa were observed in rats exposed to 0.2, 0.4, or 0.8 mg carbofuran kg-1 body weight. 4. In addition, significant alterations were observed in the activities of marker testicular enzymes viz. sorbitol dehydrogenase (SDH), glucose-6-P-dehydrogenase (G6PDH) (decreased), lactate dehydrogenase (LDH) and gamma-glutamyl transpeptidase (gamma-GT) (increased) depending on dose. 5. Histologically, the results indicated the toxicity of carbofuran on testes depending on dose. The changes predominantly consisted of moderate oedema, congestion, damage to Sertoli cells and germ cells, along with the accumulation of cellular debris and presence of giant cells in the lumen of a few seminiferous tubules which showed disturbed spermatogenesis with the higher doses of carbofuran. 6. These observations determined a no effect level dose of 0.1 mg kg-1 body weight of carbofuran on the biochemical and morphological indices studied for male reproductive toxicity assessment in the rat model. The results of the present study provide first hand information on the reproductive toxicity of carbofuran in male rats.
摘要
  1. 将呋喃丹以0.1、0.2、0.4或0.8毫克/千克体重的剂量水平口服给予成年雄性大鼠,每周5天,持续60天。在用0.2 - 0.8毫克呋喃丹/千克体重处理的大鼠中观察到体重呈剂量依赖性下降。2. 除最低剂量外,在呋喃丹的各种测试剂量下,附睾、精囊、腹侧前列腺和凝固腺的重量均显著下降。3. 在暴露于0.2、0.4或0.8毫克呋喃丹/千克体重的大鼠中,观察到精子活力下降、附睾精子计数减少以及精子头部、颈部和尾部区域的形态异常增加。4. 此外,根据剂量不同,在睾丸标记酶即山梨醇脱氢酶(SDH)、葡萄糖-6-磷酸脱氢酶(G6PDH)(降低)、乳酸脱氢酶(LDH)和γ-谷氨酰转肽酶(γ-GT)(升高)的活性方面观察到显著变化。5. 组织学结果表明,呋喃丹对睾丸的毒性取决于剂量。这些变化主要包括中度水肿、充血、支持细胞和生殖细胞受损,以及细胞碎片的积累和一些生精小管管腔内巨细胞的存在,在高剂量呋喃丹作用下,生精过程受到干扰。6. 这些观察结果确定了在大鼠模型中用于雄性生殖毒性评估的所研究生化和形态学指标方面,呋喃丹的无效应剂量水平为0.1毫克/千克体重。本研究结果提供了关于呋喃丹对雄性大鼠生殖毒性的第一手信息。

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