服用维生素 D3 和高脂饮食对实验性多囊卵巢综合征氧化应激和炎症的影响

Q2 Medicine Medicine and Pharmacy Reports Pub Date : 2024-10-01 Epub Date: 2024-10-30 DOI:10.15386/mpr-2798
Talida Vulcan, Tudor Sergiu Suciu, Lavinia Manuela Lenghel, Vlad Alexandru Toma, Nicoleta Decea, Remus Moldovan, Daniela-Rodica Mitrea, Ioana Baldea, Gabriela Adriana Filip
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引用次数: 0

摘要

背景:多囊卵巢综合征(PCOS)通常与肥胖有关,缺乏维生素D3可能会加重肥胖:44只体重180-200克、10周大的雌性Wistar大鼠被随机分为2组(n=22),分别接受芝麻油(I组)或芝麻油中的戊酸雌二醇(5毫克)(II组)的单剂量肌肉注射。4 周后,根据超声波检查结果,II 组大鼠出现卵巢内囊肿。接下来,每组一半大鼠接受标准饮食(SD),另一半大鼠接受高脂肪饮食,连续灌胃 17 周,分为以下几组:对照组(SD)、高脂饮食组(HFD)、多囊卵巢综合症组(PCOS+SD)和多囊卵巢综合症+高脂饮食组(PCOS+HFD)。然后,所有大鼠连续 5 周口服维生素 D3,剂量为 500 UI/kg/天。通过评估卵巢和卵巢周围组织中丙二醛的水平来评估脂质过氧化,并通过NFkB、pNFkB、NRF2和SOD1的表达来量化卵巢中的炎症。收集所有组的卵巢进行组织病理学分析。在整个实验过程中采集血液样本以评估基础胰岛素、甘油三酯和总胆固醇水平:结果:两组多囊卵巢综合征患者的卵巢中丙二醛含量均显著增加(P0.05)。高密度脂蛋白胆固醇膳食诱发卵巢炎症,从组织学角度和通过 COX2 表达的增加可以得到证明(p结论:多囊卵巢综合征与卵巢组织和血液中的氧化应激和炎症以及胰岛素、总胆固醇和甘油三酯水平的升高有关,口服维生素 D3 可部分缓解这些症状。
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The impact of vitamin D3 administration and of high fat diet on oxidative stress and inflammation in experimentally induced polycystic ovary syndrome.

Background: Polycystic ovary syndrome (PCOS) is commonly associated with obesity and may be exacerbated by the lack of vitamin D3.

Aim: The study aimed to investigate the effects of vitamin D3 administration in female rats with PCOS and prolonged high fat diet (HFD).

Methods: Forty-four female Wistar rats, 180-200 g, 10 weeks old, were randomly allocated into 2 groups (n=22) that received a single dose intramuscular injection of: sesame oil (group I), or estradiol valerate (5 mg) in sesame oil (group II). After 4 weeks, intraovarian cysts developed in group II, as evidenced by ultrasonography. In the next step, half of rats from each group received standard diet (SD) and the other half high fat diet, through oral gavage, for 17 weeks, the following groups being obtained: Control (SD), HFD, PCOS (PCOS+SD) and PCOS+HFD. Next, all the rats received, for 5 weeks, 500 UI/kg/day vitamin D3, through oral gavage. Lipid peroxidation was assessed through malondialdehyde level in the ovary and periovarian tissue and the inflammation was quantified in ovary by NFkB, pNFkB, NRF2 and SOD1 expressions. Ovaries from all groups were collected for histopathological analysis. Blood samples were taken to evaluate the basal insulin, triglycerides and total cholesterol levels throughout the experiment.

Results: Both groups with PCOS recorded significant increases of malondialdehyde in ovaries (p<0.001) and in periovarian tissue, especially in PCOS+HFD (p<0.05), even after vitamin D3 administration. PCOS+HFD group treated with vitamin D3 showed a high degree of inflammation in ovarian histopathology but with decreased pNFkB expression (p<0.01) while PCOS group recorded an increased SOD1 expression (p<0.05). Additionally, vitamin D3 treatment attenuated the insulin level (p<0.001) in PCOS and in HFD groups and the total cholesterol level in PCOS+HFD group, but triglycerides recordings were without statistical significance (p>0.05). HFD induced inflammation in ovaries, evidenced histologically and through increases of COX2 expressions (p<0.05) without significant influences on oxidative stress and on cholesterol levels.

Conclusions: Polycystic ovary syndrome is associated with oxidative stress and inflammation in the ovary tissue and in blood with increased levels of insulin, total cholesterol and triglycerides that might be partially mitigated by vitamin D3 oral administration.

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Medicine and Pharmacy Reports
Medicine and Pharmacy Reports Medicine-Medicine (all)
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