논문 및 학회지

대한생식의학회지   제23권 제1호 2010년

생식보조시술시 단백질원으로서 인간난포액의 적합성 및 효율성에 관한 연구;I. 인간난포액이 생쥐난포란의 체외성숙에 미치는 효과

한나여성의원 시험관아기센터;한나여성의원 시험관아기센터;한나여성의원 시험관아기센터;한나여성의원 시험관아기센터;한나여성의원 시험관아기센터;건국대학교 동물자원연구센터;

지희준;김동훈;김지연;구정진;장상식;정길생;,

Studies on the Suitability and Efficiency of Human Follicular Fluid as Protein Supplement in Assisted Reproductive Technology(ART);I. Effect of Human Follicular Fluid on Meiotic Maturation of Mouse Follicular Oocytes In Vitro

Chi, H.J.;Kim, D.H.;Kim, J.Y.;Koo, J.J.;Chang, S.S.;Chung, K.S.;

IVF Center, Hanna Women's Clinic;IVF Center, Hanna Women's Clinic;IVF Center, Hanna Women's Clinic;IVF Center, Hanna Women's Clinic;IVF Center, Hanna Women's Clinic;Animal Resources Research Center, Kon-Kuk University;

For evaluating the suitability of human follicular fluid(HFF) as protein supplement in ART, this preliminary study was performed to examine the maturation promoting activity of HFF on mouse follicular oocytes in vitro. Mouse follicular oocytes were collected from ovaries of 21-28 day old ICR mice by puncturing the antral follicles with fine needle at 48 hours after PMSG injection. The oocytes were rinsed and cultured in modified Whittingham's $T_6$ medium containing purines or dbcAMP to maintain meiotic arrest, and different concentrations of HFF were added into the culture medium to examine the effect of HFF on releasing the oocytes from the suppressive influence of the meiotic inhibitors. As a control for HFF, the maturation promoting activity of human fetal cord serum(HFCS) was investigated and compared with the activity of HFF. While HFF was separated, by molecular weight(M.W), into high M.W. fraction(M.W>30,000) and low M.W. fraction(M.W<30,000) and the effects of the fractions on meiotic resumption were investigated in the presence of the meiotic inhibitors. Also hormone analysis was performed to compare the content of hormones in HFF with that in HFCS. Same concentrations of HFF and HFCS induced similar germinal vesicle break down(GVBD) rates of the oocytes meiotic arrested by purines(4mM hypoxanthine+0.75mM adenosine), but the extrusion rate of 1st polar body(PB) of the oocytes cultured in HFF(65.0%, P<0.05) was significantly higher than that(51.6%) in HFCS. While, in the presence of 200 M dbcAMP, the maturation promoting activity of HFF (GVBD: 70.5%, $p<10^{-6}$; 1st PB extrusion: 67.1%, $p<10^{-3}$) was significantly greater than that of HFCS(GVBD: 35.2%; 1st PB extrusion: 41.1%). The oocytes cultured in the fraction of HFF containing high M.W. components showed higher meiotic maturation rates than the oocytes cultured in the low M.W. fraction of HFF. Gonadotropins and $E_2$ were known to improve the completion of maturation changes, and the levels of these hormones were higher in HFF than in HFCS. Therefore, HFF was more effective than HFCS to use for promoting meiotic resumption of mouse oocytes in vitro.

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