Pizzo Fabiola, Caloni Francesca, Schreiber Nicole B, Schutz Luis F, Totty Morgan L, Albonico Marco, Spicer Leon J
Department of Health, Animal Science and Food Safety, Università degli Studi di Milano, Via Celoria, 10 20133 Milan, Italy.
Department of Animal Science, Oklahoma State University, Stillwater, OK 74078, USA.
Ecotoxicol Environ Saf. 2015 Mar;113:314-20. doi: 10.1016/j.ecoenv.2014.12.009. Epub 2014 Dec 18.
Domoic acid (DA) is a potent neurotoxin produced by alga Pseudo-nitzschia spp. and has been associated with reproductive disorders in mammals. The aim of this study was to investigate if DA can affect the reproductive system via direct action on ovarian function. Bovine granulosa and theca cells were used as in vitro models for evaluating DA effects on ovarian cell proliferation and steroid production. In small-follicle granulosa cells (SMGC), cell proliferation and estradiol (E2) production was not affected (P>0.05) while progesterone (P4) production was inhibited (P<0.05) by DA at all doses tested. In large-follicle granulosa cells (LGGC), DA had no effect (P>0.05) on cell proliferation or P4 production while E2 production was stimulated by 1 and 5 µg/ml DA (P<0.05). DA (1 µg/ml) attenuated (P<0.05) insulin-like growth factor 1 (IGF-1)-induced P4 production by large-follicle theca cells (LGTC), but did not affect androstenedione (A4) production or proliferation of LGTC. In glutamate-free medium, DA inhibited (P<0.05) SMGC E2 production and this inhibition was similar to inhibition of E2 by trans-(±)-1-amino-1,3-cyclopentanedicarboxylic acid monohydrate (ACPD; a selective metabotropic glutamate receptor subtype agonist) while kainic acid (KA; an ionotropic glutamate receptor subtype agonist) had no effect (P>0.10) on E2 production. Collectively, these results show for the first time that DA has direct effects on ovarian GC and TC steroidogenesis. Because DA inhibited E2 and P4 production, DA has the potential to be an endocrine disruptor.
软骨藻酸(DA)是一种由拟菱形藻属藻类产生的强效神经毒素,与哺乳动物的生殖紊乱有关。本研究的目的是调查DA是否能通过直接作用于卵巢功能来影响生殖系统。牛颗粒细胞和卵泡膜细胞被用作体外模型,以评估DA对卵巢细胞增殖和类固醇生成的影响。在小卵泡颗粒细胞(SMGC)中,所有测试剂量的DA均未影响细胞增殖和雌二醇(E2)生成(P>0.05),而孕酮(P4)生成受到抑制(P<0.05)。在大卵泡颗粒细胞(LGGC)中,DA对细胞增殖或P4生成无影响(P>0.05),而1和5μg/ml的DA刺激了E2生成(P<0.05)。DA(1μg/ml)减弱了(P<0.05)胰岛素样生长因子1(IGF-1)诱导的大卵泡膜细胞(LGTC)P4生成,但不影响LGTC的雄烯二酮(A4)生成或增殖。在无谷氨酸的培养基中,DA抑制了(P<0.05)SMGC的E2生成,这种抑制与反式 -(±)-1-氨基-1,3-环戊烷二羧酸一水合物(ACPD;一种选择性代谢型谷氨酸受体亚型激动剂)对E2的抑制相似,而 kainic 酸(KA;一种离子型谷氨酸受体亚型激动剂)对E2生成无影响(P>0.10)。总体而言,这些结果首次表明DA对卵巢颗粒细胞和卵泡膜细胞的类固醇生成有直接影响。由于DA抑制了E2和P4生成,它有可能成为一种内分泌干扰物。