Laboratory Medicine Department, Faculty of Applied Medical Sciences, Umm Al-Qura University, Al Abdeyah, PO Box 7607, Mecca, Kingdom of Saudi Arabia.
Department of Clinical Pathology, Faculty of Veterinary Medicine, Mansoura University, Mansoura, Egypt.
Histochem Cell Biol. 2021 Jun;155(6):655-668. doi: 10.1007/s00418-021-01975-0. Epub 2021 Feb 27.
This study measured the sequelae of cholecalciferol (VD) therapy on ovarian functions in adult VD-replete rats (n = 48). The animals were distributed into the control and VD groups following estrous cycle synchronisation. The VD group received VD injections for 4 weeks (600 IU/Kg; 3 times/week). Vaginal cytology and cycle durations were recorded throughout the study. Serum VD (25-OH VD), Ca, gonadotrophins (FSH & LH) and sex steroids (E2 & progesterone) were measured following euthanasia. Follicles and corpora lutea were counted in ovarian tissue sections. VD receptor, binding protein, Ca-sensing receptor and retinoid X receptor-α genes and proteins were measured by quantitative RT-PCR and immunohistochemistry. Serum VD, LH, E2 and progesterone levels were significantly higher, whereas FSH declined, in the VD group than controls. VD therapy was also associated with markedly higher rates alongside shorter durations of estrous cycles than controls. While serum Ca levels were equal between the study groups, they correlated directly with serum 25-OH VD. The numbers of small and medium size ovarian follicles were equal in both study groups, whereas large follicles and corpora lutea counts were significantly higher in the VD group. The mRNAs and proteins of targeted molecules also increased substantially in the VD group than controls. In conclusion, treating VD-sufficient female rats with supraphysiological VD supplements was not associated with hypercalcaemia, and could contribute to ovarian functions by regulating the hypothalamic-pituitary-ovarian hormones and ovarian VD-related molecules. However, further studies are still needed to illustrate the clinical significance of VD in female reproduction.
本研究旨在测量胆钙化醇(VD)治疗对成年 VD 充足大鼠卵巢功能的后遗症(n=48)。动物在发情周期同步后分为对照组和 VD 组。VD 组接受 VD 注射治疗 4 周(600 IU/Kg;每周 3 次)。整个研究过程中记录阴道细胞学和周期持续时间。安乐死后测量血清 VD(25-OH VD)、Ca、促性腺激素(FSH 和 LH)和性激素(E2 和孕酮)。卵巢组织切片中计数卵泡和黄体。通过定量 RT-PCR 和免疫组织化学测量 VD 受体、结合蛋白、Ca 敏感受体和视黄酸 X 受体-α基因和蛋白。与对照组相比,VD 组血清 VD、LH、E2 和孕酮水平显著升高,而 FSH 下降。VD 治疗还与发情周期明显缩短和频率增加有关。尽管两组血清 Ca 水平相等,但与血清 25-OH VD 直接相关。两组研究中小和中卵泡数量相等,而 VD 组大卵泡和黄体计数明显增加。VD 组目标分子的 mRNAs 和蛋白也明显高于对照组。总之,用超生理剂量的 VD 补充剂治疗 VD 充足的雌性大鼠不会导致高钙血症,并且可以通过调节下丘脑-垂体-卵巢激素和卵巢 VD 相关分子来促进卵巢功能。然而,仍需要进一步的研究来阐明 VD 在女性生殖中的临床意义。