Fujii E, Mellon S H
Department of Obstetrics, Gynecology, and Reproductive Sciences, Center for Reproductive Sciences, University of California, San Francisco, California 94143, USA.
Endocrinology. 2001 May;142(5):1770-7. doi: 10.1210/endo.142.5.8153.
Uterine contractions at parturition depend upon a variety of factors, including gamma-aminobutyric acid (GABA)-ergic stimulation. A new subunit of the GABA(A) receptor, pi, has recently been identified as being particularly abundant in the rat uterus. Reduced derivatives of progesterone, such as the 3alpha,5alpha-reduced derivative termed allopregnanolone, modulate GABA(A) receptor activity and neuronal inhibition by modulating the frequency and duration of GABA(A) channel opening. This modulation depends on the specific subunit composition of the GABA(A) receptor. In particular, assembly of recombinant pi and delta GABA(A) receptor subunits into a functional GABA(A) receptor have been reported to reduce sensitivity to allopregnanolone. As allopregnanolone works through the GABA(A) receptor to reduce uterine contraction, we hypothesized that incorporation of the pi-subunit into this receptor in the uterus might change the sensitivity of the GABA(A) receptor to allopregnanolone and modulate parturition. We therefore determined the expression of GABA(A) receptor subunit messenger RNAs (mRNAs) in rat uteri from various gestational ages and determined the physiological properties of the receptors. GABA(A) pi-subunit mRNA abundance was constant throughout gestation, but decreased at the onset of labor. Other GABA(A) subunits fluctuated differently during pregnancy: GABA(A) alpha(1)-subunit mRNA expression increased, whereas alpha(2)- and delta-subunit mRNA expression decreased during pregnancy, and beta(3)-subunit mRNA only appeared on postpartum day 1. We determined how allopregnanolone affected the binding of muscimol, a ligand for the GABA(A) receptor, to rat uterine GABA(A) receptors throughout pregnancy. Allopregnanolone caused the greatest increase in muscimol binding to uterine GABA(A) receptors at 19.5 days gestation and the least increase during labor, a time when pi and alpha(1) receptor subunit mRNA concentrations were low, and delta and alpha(2) receptor subunit mRNA concentrations were high. Thus, the subunit composition of the GABA(A) receptor differs in rat uteri throughout gestation. These changes may also affect the sensitivity of the GABA(A) receptor to allopregnanolone and thus contribute to the regulation of parturition.
分娩时子宫收缩取决于多种因素,包括γ-氨基丁酸(GABA)能刺激。最近发现GABA(A)受体的一个新亚基π在大鼠子宫中特别丰富。孕酮的还原衍生物,如被称为别孕烯醇酮的3α,5α-还原衍生物,通过调节GABA(A)通道开放的频率和持续时间来调节GABA(A)受体活性和神经元抑制。这种调节取决于GABA(A)受体的特定亚基组成。特别是,据报道,重组的π和δGABA(A)受体亚基组装成功能性GABA(A)受体会降低对别孕烯醇酮的敏感性。由于别孕烯醇酮通过GABA(A)受体发挥作用以减少子宫收缩,我们推测子宫中该受体中π亚基的掺入可能会改变GABA(A)受体对别孕烯醇酮的敏感性并调节分娩。因此,我们测定了不同妊娠阶段大鼠子宫中GABA(A)受体亚基信使核糖核酸(mRNA)的表达,并测定了受体的生理特性。GABA(A)π亚基mRNA丰度在整个妊娠期保持恒定,但在分娩开始时下降。其他GABA(A)亚基在孕期波动不同:GABA(A)α(1)亚基mRNA表达增加,而α(2)和δ亚基mRNA表达在孕期下降,β(3)亚基mRNA仅在产后第1天出现。我们测定了别孕烯醇酮在整个孕期如何影响GABA(A)受体配体蝇蕈醇与大鼠子宫GABA(A)受体的结合。别孕烯醇酮在妊娠19.5天时导致蝇蕈醇与子宫GABA(A)受体结合增加最多,而在分娩期间增加最少,此时π和α(1)受体亚基mRNA浓度较低,而δ和α(2)受体亚基mRNA浓度较高。因此,GABA(A)受体的亚基组成在大鼠子宫的整个妊娠期有所不同。这些变化也可能影响GABA(A)受体对别孕烯醇酮的敏感性,从而有助于分娩的调节。