Szilágyi A, Benz R, Rossmanith W G
Department of Obstetrics and Gynecology, University of Ulm, Donau, Germany.
Gynecol Endocrinol. 1992 Dec;6(4):293-300. doi: 10.3109/09513599209024994.
Gonadotropin releasing hormone (GnRH) has been proposed to play a role in the regulation of human chorionic gonadotropin (hCG) release from the human placenta. To test this assumption, we utilized an in vitro perifusion system, together with cultures of placental explants, to investigate short- and long-term effects of GnRH and its respective antagonist on the hCG secretion from the early human placenta. Tissue slices of human placenta (100 mg), obtained from first-trimester terminations of pregnancies, were continuously perifused and the effluent collected in fractions of 2-20 min. After initial perifusion periods of 30-40 min, either GnRH, a GnRH antagonist (SB-75; Asta Pharma, Frankfurt, Germany) or both compounds at equimolar concentrations were added to the perifusion medium at final concentration of 10(-4)-10(-8) mol/l). Administration was effected either continuously or intermittently in 10-min pulses. Further, 50-mg pieces of placental tissue explants were cultured in tissue culture plates for up to 6 days. During the perifusions, hCG (determined by enzymeimmunoassay) was found to be released spontaneously in a pulsatile fashion. Pulse amplitudes and frequencies of this episodic hCG secretion were increased in response to GnRH, but not affected by GnRH antagonist. Also, GnRH stimulated the hCG secretion during cultures of placental explants. When pharmacological doses of GnRH (10(-4) mol/l) were utilized, this stimulatory effect of GnRH was no longer evident, while perifusion with medium containing GnRH antagonist at identical concentrations stimulated the hCG secretion, indicating an intrinsic agonistic activity of the antagonist.(ABSTRACT TRUNCATED AT 250 WORDS)
促性腺激素释放激素(GnRH)被认为在调节人胎盘释放人绒毛膜促性腺激素(hCG)中发挥作用。为了验证这一假设,我们利用体外灌流系统以及胎盘外植体培养,来研究GnRH及其相应拮抗剂对早期人胎盘hCG分泌的短期和长期影响。从妊娠早期终止妊娠获取的人胎盘组织切片(100毫克),进行连续灌流,并将流出液以2 - 20分钟的间隔收集。在最初30 - 40分钟的灌流期后,将GnRH、一种GnRH拮抗剂(SB - 75;德国法兰克福的阿斯塔制药公司)或两种等摩尔浓度的化合物添加到灌流培养基中,终浓度为10(-4)-10(-8)摩尔/升。给药方式为连续给药或以10分钟脉冲的方式间歇给药。此外,将50毫克的胎盘组织外植体在组织培养板中培养长达6天。在灌流过程中,发现hCG(通过酶免疫测定法测定)以脉冲方式自发释放。这种间歇性hCG分泌的脉冲幅度和频率因GnRH而增加,但不受GnRH拮抗剂影响。同样,GnRH在胎盘外植体培养过程中刺激hCG分泌。当使用药理剂量的GnRH(10(-4)摩尔/升)时,GnRH的这种刺激作用不再明显,而用含有相同浓度GnRH拮抗剂的培养基灌流则刺激hCG分泌,表明该拮抗剂具有内在激动活性。(摘要截短至250字)