Laboratorio de Biología Celular y Molecular Aplicada, Instituto de Ciencias Veterinarias del Litoral, Universidad Nacional del Litoral, Consejo Nacional de Investigaciones Científicas y Técnicas, R. P. Kreder 2805, CP3080, Esperanza, Santa Fe, Argentina; and Facultad de Ciencias Veterinarias del Litoral, Universidad Nacional del Litoral, R. P. Kreder 2805, CP3080, Esperanza, Santa Fe, Argentina.
Laboratorio de Biología Celular y Molecular Aplicada, Instituto de Ciencias Veterinarias del Litoral, Universidad Nacional del Litoral, Consejo Nacional de Investigaciones Científicas y Técnicas, R. P. Kreder 2805, CP3080, Esperanza, Santa Fe, Argentina.
Reprod Fertil Dev. 2020 May;32(8):748-762. doi: 10.1071/RD19232.
Cattle undergo numerous environmental and management stressors that reduce fertility and affect ovulation. The extracellular matrix of the follicle wall can be altered by matrix metalloproteinases (MMPs), the activities of which are regulated by interleukins and tissue-specific inhibitors of metalloproteinases (TIMPs), especially during ovulation. The aims of the present study were to: (1) evaluate changes in the hormone milieu, the localisation and activity of MMP2 and MMP9 and the localisation of MMP14, TIMP1 and TIMP2 in response to adrenocorticotrophic hormone (ACTH) during the preovulatory period in cows; and (2) determine the direct effects of ACTH on the mRNA expression of MMP2 and MMP9 in the cultured follicle wall of bovine ovaries obtained from an abattoir. 100IU ACTH was administered during pro-oestrus every 12h until ovariectomy, which was performed before ovulation. Cortisol concentrations in the plasma and follicular fluid (FF) of preovulatory follicles were higher in ACTH-treated than control cows. Progesterone presented subluteal concentrations in plasma of ACTH-treated cows (P<0.05). MMP2 immunostaining and activity in ovaries were higher in ACTH-treated than control cows (P<0.05), whereas MMP9 immunostaining was similar between the two groups. However, unlike in control cows, MMP9 activity was absent in the FF of ACTH-treated cows. These results suggest that the administration of ACTH during the preovulatory period in cows could cause changes that culminate in modifications in the content and activation of MMPs and TIMPs in the ovary, which could interfere with the ovulation process.
牛经历了许多环境和管理压力,这些压力会降低其生育能力并影响排卵。卵泡壁的细胞外基质可以被基质金属蛋白酶(MMPs)改变,其活性受白细胞介素和组织特异性金属蛋白酶抑制剂(TIMPs)调节,尤其是在排卵期间。本研究的目的是:(1)评估在促性腺激素释放激素(GnRH)刺激排卵前周期中,牛卵泡壁中 MMP2 和 MMP9 的定位和活性以及 MMP14、TIMP1 和 TIMP2 的定位的变化;(2)确定促肾上腺皮质激素(ACTH)对从屠宰场获得的牛卵巢培养卵泡壁中 MMP2 和 MMP9 mRNA 表达的直接影响。在发情前期,每 12 小时给 100IU 的 ACTH 处理,直到发情前进行卵巢切除术。与对照组相比,ACTH 处理的牛发情前卵泡液(FF)中的皮质醇浓度更高。与对照组相比,ACTH 处理的牛血浆中孕酮呈亚黄体浓度(P<0.05)。与对照组相比,ACTH 处理的牛卵巢中 MMP2 免疫染色和活性更高(P<0.05),而两组之间 MMP9 免疫染色相似。然而,与对照组不同的是,ACTH 处理的牛的 FF 中缺乏 MMP9 活性。这些结果表明,在牛发情前周期中给予 ACTH 可能会导致导致 MMPs 和 TIMPs 在卵巢中的含量和激活发生变化,从而干扰排卵过程。