Kraisoon A, Redmer D A, Bass C S, Navanukraw C, Dorsam S T, Valkov V, Reyaz A, Grazul-Bilska A T
Department of Animal Science, Faculty of Agriculture, Khon Kaen University, Khon Kaen, Thailand.
Department of Animal Sciences, North Dakota State University, Fargo, ND, USA.
Domest Anim Endocrinol. 2018 Jan;62:16-23. doi: 10.1016/j.domaniend.2017.08.002. Epub 2017 Aug 12.
The corpus luteum (CL) is an ovarian structure which is critical for the maintenance of reproductive cyclicity and pregnancy support. Diet and/or diet components may affect some luteal functions. FSH is widely used to induce multiple follicle development and superovulation. We hypothesized that FSH would affect luteal function in ewes fed different nutritional planes. Therefore, the aim of this study was to determine if FSH-treatment affects (1) ovulation rate; (2) CL weight; (3) cell proliferation; (4) vascularity; (5) expression of endothelial nitric oxide (eNOS) and soluble guanylate cyclase (sGC) proteins; and (6) luteal and serum progesterone (P4) concentration in control (C), overfed (O), and underfed (U) ewes at the early- and mid-luteal phases. In addition, data generated from this study were compared to data obtained from nonsuperovulated sheep and described by Bass et al. Ewes were categorized by weight and randomly assigned into nutrition groups: C (2.14 Mcal/kg; n = 11), O (2xC; n = 12), and U (0.6xC; n = 11). Nutritional treatment was initiated 60 d prior to day 0 of the estrous cycle. Ewes were injected with FSH on day 13-15 of the first estrous cycle, and blood samples and ovaries were collected at early- and mid-luteal phases of the second estrous cycle. The number of CL/ewe was determined, and CL was dissected and weighed. CL was fixed for evaluation of expression of Ki67 (a proliferating cell marker), CD31 (an endothelial cell marker), and eNOS and sGC proteins using immunohistochemistry and image analysis. From day 0 until tissue collection, C maintained, O gained, and U lost body weight. The CL number was greater (P < 0.03) in C and O than U. Weights of CL, cell proliferation, vascularity, and eNOS but not sGC expression were greater (P < 0.001), and serum, but not luteal tissue, P4 concentrations tended to be greater (P = 0.09) at the early- than mid-luteal phase. Comparisons of CL measurements demonstrated greater (P < 0.01) cell proliferation and serum P4 concentration, but less vascularity at the early and mid-luteal phases, and less CL weight at the mid-luteal phase in superovulated than nonsuperovulated ewes; however, concentration of P4 in luteal tissues was similar in both groups. Thus, in superovulated ewes, luteal cell proliferation and vascularity, expression of eNOS, and serum P4 concentration depend on the stage of luteal development, but not diet. Comparison to control ewes demonstrated several differences and some similarities in luteal functions after FSH-induced superovulation.
黄体(CL)是一种卵巢结构,对维持生殖周期性和支持妊娠至关重要。饮食和/或饮食成分可能会影响某些黄体功能。促卵泡素(FSH)被广泛用于诱导多个卵泡发育和超数排卵。我们假设FSH会影响处于不同营养水平的母羊的黄体功能。因此,本研究的目的是确定FSH处理是否会影响(1)排卵率;(2)黄体重量;(3)细胞增殖;(4)血管生成;(5)内皮型一氧化氮合酶(eNOS)和可溶性鸟苷酸环化酶(sGC)蛋白的表达;以及(6)在黄体早期和中期,对照(C)、过度饲喂(O)和营养不足(U)的母羊的黄体和血清孕酮(P4)浓度。此外,将本研究产生的数据与未进行超数排卵的绵羊的数据进行比较,并由巴斯等人进行了描述。根据体重对母羊进行分类,并随机分为营养组:C(2.14兆卡/千克;n = 11)、O(2xC;n = 12)和U(0.6xC;n = 11)。在发情周期第0天前60天开始营养处理。在第一个发情周期的第13 - 15天给母羊注射FSH,并在第二个发情周期的黄体早期和中期采集血样和卵巢。确定每只母羊的黄体数量,解剖并称重黄体。使用免疫组织化学和图像分析对黄体进行固定,以评估增殖细胞核抗原Ki67(一种增殖细胞标记物)、CD31(一种内皮细胞标记物)以及eNOS和sGC蛋白的表达。从第0天到组织采集期间,C组母羊体重维持不变,O组母羊体重增加,U组母羊体重减轻。C组和O组的黄体数量比U组多(P < 0.03)。黄体重量、细胞增殖、血管生成和eNOS的表达,但不包括sGC的表达,在黄体早期比中期更高(P < 0.001),血清P4浓度(但不是黄体组织中的P4浓度)在黄体早期也倾向于更高(P = 0.09)。黄体测量结果的比较表明,与未进行超数排卵的母羊相比,超数排卵的母羊在黄体早期和中期细胞增殖和血清P4浓度更高(P < 0.01),但血管生成较少,在黄体中期黄体重量较轻;然而,两组黄体组织中的P4浓度相似。因此,在超数排卵的母羊中,黄体细胞增殖和血管生成、eNOS的表达以及血清P4浓度取决于黄体发育阶段,而不是饮食。与对照母羊的比较表明,FSH诱导超数排卵后,黄体功能存在一些差异和一些相似之处。