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A Study on Experimental Testicular Disorder II. Recovery from Testicular Dysfunction Produced by Experimental Internal Irradiation of 32P with Special Reference to Histopathological Study on Spermatopoietic Function of the Testicle

机译:实验性睾丸疾病II的研究。实验性内照射32P引起的睾丸功能障碍的恢复,特别是对睾丸生精功能的病理组织学研究

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摘要

1) Mice weighing between 100 and 200 grams were emplo y ed for this study. Histopapathological study on spermatopoietic function of seminiferous tubule of the testicle removed surgically from I-Group receiving internal irradiation of 32P in a dosis of 250 pc, II-Group with 300 p c, III-Group with 350 pc, IV-Group with 400 pc, and V-Group with 450 p c, 2) Various repairing drugs were administered subcutaneously starting from 24 hour aft e r the irradiation to each group every other day for 3-4 weeks and then recovery of spermatopoietic function was classified histopathologically. 3) A week after internal irradia t ion of 32Pi n a dosis of 250 pc to I-Group, disarrangement, diminution and disappearance of seminiferous tubular epithelium, apperance of giant cells, and slight disturbance of spermatopoietic function were observed. Gonagen forte, Havita, and ATP appeared to improve spermatopoietic function. Synahorin and Mercazole seemed to be less effective than the above substances. 4) Three weeks after internal irradiatio n of 32Pi n a dosis of 300 pc to II-Group, slight changes in seminiferous tubule were spermatozoon disappeared was observed. Marked improvement of spermatopoietic function was observed by administration of Anteron, Luteogen, and Chondron every other day and the less marked improvement was obtained by Royal Jelly. 5) Th r ee weeks after internal irradiation of 82P in a dosis of 350 pc to III-Group, the changes were rather slight but affected site was wider than that in II-Group. The method of administration of was the same as II-Group. The most remarkable improvement of spermatopoietic function was obtained by Parotin, Atropin, yolk, and Nicodermin and Syncorta, Tioctan, Fatogen, and Zyscal produced less marked improvement. 6) Three weekes after internal irradiation of 82P in a do s i s of 400 pc to IV-Group, the changes were slight and regeneration of seminiferous tubule was observed. The marked improvement was obtained by Synahorin, Enarmon, and Orotonsan. PVL and Gonagen forte less markedly improved the function. 7) Two weeks after internal irradiation of 82P in a dosis of 450 pc to V-Group, duct lumen was filled with spermatozoid and there were only few spermatozoon. Spermiocyte was in karyokinesis and giant cells appeared in few duct lumen. Moriamin-S resulted in remarkable improvement of spermatopoietic function. 8) Three weeks after internal irradiation of 32P in a dosis of 600 tic, all phases from disturbance to regeneration were found in seminiferous tubule. 9) In conclusion Parotin, yolk, Atropin, Moriamin-S , Anteron, Luteogen, Orotonsan, and Chondron improved of spermatopoietic function markedly.
机译:1)这项研究使用了体重在100到200克之间的小鼠。手术从I组接受32P内照射的睾丸生精小管的精子造血功能的组织病理学研究,其中I组接受250 pc剂量,II组具有300 pc,III组具有350 pc,IV组具有400 pc,和450组的V-Group,2)从照射后24小时开始每隔一天皮下施用各种修复药物,持续3-4周,然后在组织病理学上分类精子生成功能。 3)在对I-基团进行250μg的内照射后一周,观察到生精小管上皮的排列紊乱,缩小和消失,巨细胞的出现以及精子造血功能的轻微紊乱。 Gonagen forte,Havita和ATP似乎可以改善精子生成功能。 Synahorin和Mercazole似乎不如上述物质有效。 4)对II组进行32Pn剂量的内照射300周后三周,观察到生精小管的细微变化,精子消失。每隔一天给予Anteron,Luteogen和Chondron可观察到精子生成功能的显着改善,而Royal Jelly则可观察到较不明显的改善。 5)在对III组进行350 pc剂量的82P内照射后三周,变化很小,但受累部位比II组宽。的给药方法与II-Group相同。 Parotin,Atropin,蛋黄和Nicodermin和Syncorta,Tioctan,Fatogen和Zyscal产生的精子功能最显着改善。 6)在对IV组进行400 pc剂量的82P内照射后三周,变化很小,观察到生精小管的再生。 Synahorin,Enarmon和Orotonsan获得了显着的改进。 PVL和Gonagen forte不太明显地改善了功能。 7)在以450 pc的剂量向V-Group进行82P内部照射后两周,导管腔内充满了精子,并且精子很少。精子细胞在核运动中,巨细胞出现在很少的管腔中。 Moriamin-S显着改善了精子生成功能。 8)在剂量为600 tic的32 P内部照射后3周,在生精小管中发现了从扰动到再生的所有阶段。 9)结论帕罗汀,蛋黄,阿托普汀,Morimin-S,Anteron,黄体生成素,Orotonsan和Chondron可以显着改善精子生成功能。

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    山本 武;

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  • 年度 1961
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  • 原文格式 PDF
  • 正文语种 ja
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