Chavatte-Palmer P, Duchamp G, Palmer E, Ousey J C, Rossdale P D, Lombès M
Institut National Agronomique Paris-Grignon, Department des Sciences Animales, 16 rue Claude Bernard, 75231 Paris cedex 05, France.
J Reprod Fertil Suppl. 2000(56):661-72.
Progesterone, oestrogen and glucocorticoid receptor concentrations in the uterus and mammary glands of pregnant mares during mid- to late gestation (from day 150 of gestation to term) were measured by binding assays to investigate the hormonal mechanisms involved in pregnancy maintenance and lactation. Uterine progesterone receptor concentrations did not increase significantly with increasing gestational age (from 67.8 +/- 13.7 to 126.1 +/- 48.7fmol mg(-1) protein), whereas oestrogen receptor concentrations were significantly higher in pregnant mares (271.7 +/- 28.9 fmol mg(-1) protein) than in non-pregnant control mares (54.9 +/- 8.1 fmol mg(-1) protein; P < 0.05). There was no correlation between progesterone and oestrogen receptor concentrations, and plasma progesterone and oestrone sulphate concentrations, respectively. In contrast, mammary gland progesterone and oestrogen receptor concentrations decreased significantly with gestational age (from 139.7 +/- 34.6 to 66.7 +/- 22.0 fmol mg(-1) protein and 225.2 +/- 13.3 to 87.6 +/- 14.4 fmol mg(-1) protein, respectively; P < 0.05). The dissociation constant (Kd value) of 16alpha-ethyl-21-hydroxy-19-nor-4-pregnene-3,20-dione (ORG2058) for progesterone receptors was 22 nmol l(-1). 5alpha-pregnane-3,20-dione (5alpha-DHP) had a high affinity for progesterone receptors, which was similar to that of progesterone, whereas other equine progestagens and 11-[4-(dimethylamino)phenyl]-17-hydroxy-17(1-propynyl)estra-4,9-diene-3-one (RU486) did not bind to progesterone receptors. Oestradiol bound the oestrogen receptors with a Kd value of 0.9 nmol l(-1), which was 10 times more potent than that of 3-hydroxy-1,3,5(10),7-oestratetraen-17-one (equilin). The concentration of glucocorticoid receptors (Kd value = 1.3 nmol l(-1)) was constant between the tissues and reproductive stages. In the present study, striking differences were observed between progesterone receptor expression in the uterus and the mammary glands during pregnancy, probably due to tissue-specific variations in 5alpha-DHP activity. This finding indicates that 5alpha-DHP has an important physiological role in equine gestation.
通过结合测定法测量了妊娠中期至晚期(从妊娠第150天至足月)怀孕母马子宫和乳腺中孕酮、雌激素和糖皮质激素受体的浓度,以研究参与维持妊娠和泌乳的激素机制。子宫孕酮受体浓度并未随着胎龄增加而显著升高(从67.8±13.7增至126.1±48.7fmol mg⁻¹蛋白质),而怀孕母马的雌激素受体浓度(271.7±28.9 fmol mg⁻¹蛋白质)显著高于未怀孕的对照母马(54.9±8.1 fmol mg⁻¹蛋白质;P<0.05)。孕酮与雌激素受体浓度之间以及血浆孕酮与硫酸雌酮浓度之间均无相关性。相比之下,乳腺中孕酮和雌激素受体浓度随胎龄显著降低(分别从139.7±34.6降至66.7±22.0 fmol mg⁻¹蛋白质以及从225.2±13.3降至87.6±14.4 fmol mg⁻¹蛋白质;P<0.05)。16α-乙基-21-羟基-19-去甲-4-孕烯-3,20-二酮(ORG-2058)对孕酮受体的解离常数(Kd值)为22 nmol l⁻¹。5α-孕烷-3,20-二酮(5α-DHP)对孕酮受体具有高亲和力,与孕酮相似,而其他马属孕激素和11-[4-(二甲氨基)苯基]-17-羟基-17-(1-丙炔基)雌-4,9-二烯-3-酮(RU486)不与孕酮受体结合。雌二醇以0.9 nmol l⁻¹的Kd值与雌激素受体结合,其效力是3-羟基-1,3,5(10),7-雌四烯-17-酮(马萘雌酮)的10倍。糖皮质激素受体浓度(Kd值 = 1.3 nmol l⁻¹)在不同组织和生殖阶段保持恒定。在本研究中,观察到妊娠期间子宫和乳腺中孕酮受体表达存在显著差异,这可能是由于5α-DHP活性的组织特异性变化所致。这一发现表明5α-DHP在马属动物妊娠中具有重要的生理作用。