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Abstract

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(denervation)µîÀÌ °í·ÁµÇ°í ÀÖ´Ù.
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ÀÎ Æò°¡°¡ ÇÊ¿äÇѵ¥ °íȯÁ¶Á÷ÀÇ Á¤·®Àû ¹Ì¼¼ÃøÁ¤¹ý(quantitative micrometry)°ú DNA À¯¼¼
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ÀÌ¿¡ ÀúÀÚ´Â ¹é¼­¸¦ ÀÌ¿ëÇØ Ã´¼ö¼Õ»ó ÈÄ ½Ã°£ÀÇ °æ°ú¿¡ µû¸¥ ¹é¼­ÀÇ Ã¼Áß º¯È­¾ç»ó°ú ÀÌ
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ÅëÇØ ¼¼Á¤°ü´Ü ¼º¼÷µÈ Á¤ÀÚ¼¼Æ÷¿Í Sertoli ¼¼Æ÷¼ö¸¦ ºñ±³ÇÏ¿´À¸¸ç ÀÌ¿Í ÇÔ²² DNA À¯¼¼Æ÷°Ë
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#ÃÊ·Ï#
Male infertility occurs after spinal cord injury (SCI). However, little is known about
the effect of SCI on male reproductive function. We evaluated objective assessment of
spermatogenesis of spinal cord injured rats by quantitative micrometry and DNA flow
cytometry analysis at various time intervals. SCI was produce(B in 30 rats by 710
spinal cord transection. Controls received similar surgery without transaction. From 10
randomly selected seminiferous tubules per subject the mean number of mature
spermatids, Sertoli cells, tubular diameter and tubular wall thickness were determined in
both groups. The percentage of haploid, diploid and tetraploid cells were determined of
each subject by DNA (low cytometry, Two way analysis of variance (ANOVA) was
performed. In the SCI rats the mean number of spermatid per tubule was significantly
lower (p=0.01) than that of controls. The mean number of Sertoli cells per tubule was
not different from that of controls. Mean of spermatid to Sertoli cell ratio per
seminiferous tubule in SCI rats was significantly lower than in controls (p=0.048). No
significant differences of tubulr wall thickness, diameter and percentage of haploid cells
were noted between both groups.
These results suggest that the effect of SCI on spermatogenesis is associated with
inadequacy of spermatid formation and maturation delay of spermatid.

Å°¿öµå

Spermatogenesis; Spinal cord injury; Micrometry; flow cytometry;

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