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Abstract I)ISCUSSION SUMMARY AND CO.NCLUSION The present study was conducted to study the effect of . estradiol benzoate injection postnatally on the development of the testis in albino rats. Also, this study tried to enlighten the possible mechanisms by which estrogen can affect the process of spermatogenesis. In this study, 75 male rats at the lSI day of life were used. These rates were divided into three groups: Group A: 25 male rats were injected sUbcutaneouslywith a single dose of estradiol benzoate (E2B) 0.5 mg/5 gm B.W(low dose). Group B: 25 male rats were injected subcutaneously with a single dose ofE2B 1 mg/5gm B.W (high dose). Group C: 25 male rats were injected SUbcutaneouslywith a single dose of normal saline (control group). 5 rats of each groups were killed at postnatal days 10, 22, 33, 45 and 60. The abdomen was opened and locati•on of the testes lI\~~v{\ 50 . detected. Then the testes were removed and preserved in Bouin’ s solution, then stained by (Hx & E) and examined by light microscope, DISCUSSION It was found that the testes of estrogenized rats remained intraabdominally (while normally the testes reach the scrotum at day 22 old rats) and the size of the testes were smaller than normal. The seminiferous tubules showed dilated lumena and impairment of spermatogenesis with no sperm production until adult age. The rete testis showed dilatation and anastomosing of their channels, and there is impairment of spermatogenesis.These changes in spermatogenesis were present at all parts of the testis (caudal and cranial parts) of those treated with high dose E2B. On the other hand, those treated with low dose of E2B, the cranial part of the testis showed permanent impairment of spermatogenesis typical to those treated with high dose while the caudal part showed less influence and seemed more or less normal i.e., no dilatation of the lumen, no sloughs, no inflammatory cells and the series of cells were present till primary spermatocytes only.No spermatids or sperms were observed. This was due to their existence further from rete testis. As the testicular descent in rat occurred after birth normally and the human testicular descent occurred before birth, the results. of this study are typical to that of human pregnant female exposed to estrogen during pregnancy .. In conclusion, our study can support the idea that estrogen exposure to pregnant mothers leads to abnormalities in the male feti reproductive system in the form of cryptorchidism and impairment of spermatogenesis. So we advise to avoid exposure of female to. estrogen during pregnancy. - - -4\ 97 ibIo It was found that the testes of estrogenized rats remained intraabdominally (while normally the testes reach the scrotum at day 22 old rats) and the size of the testes were smaller than normal. . The seminiferous tubules showed dilated lum~Ina and impairment of spermatogenesis with no sperm production until adult age. The rete testis showed dilatation and anastomosing of their channels, and there is iITlP~irment.?f spermatogenesis. These changes in spermatogenesis were present at all parts of the testis (caudal and cranial parts) of those treated with high dose E2B. On the other hand, those treated with low dose of E2B, the cranial part of the testis showed permanent impairment of spermatogenesis typical to those treated with high dose while the caudal part showed less influence and seemed more or less normal i.e., no dilatation of the lumen, no sloughs, no inflammatory cells and the series of cells were present till primary spermatocytes only.No spermatids or sperms were observed. This was due to their existence further from rete testis. As the testicular descent in rat occurred after birth normally and the human testicular descent occurred before birth, the results of this study are typical to that of human pregnant female exposed to estrogen during pregnancy . .- ~I--n, . conclu.=s’.io%n.,- our study can support the idea that estro.gen exposure to pregnant mothers leads to abnormalities in the male feti reproductive system in the· form of cryptorchidism and impairment of spermatogenesis. So we advise to avoid exposure of female to estrogen during pregnancy. - |