巴氯芬对吗啡诱导的多囊卵巢大鼠背海马氧化应激的保护作用

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摘要

背景和目的:研究表明,多囊卵巢(PCO)可能被吗啡诱导,CA1可能被PCO相关的氧化应激损伤,但可以受到强效GABAB受体激动剂的保护。因此,本研究旨在研究巴氯芬对吗啡治疗的卵巢囊肿大鼠背侧海马(DH)氧化应激的保护作用。材料与方法:选用雌性Wistar大鼠66只,随机分为对照组和实验组。对照组接受生理盐水(1 ml/kg,腹膜内[腹膜内],每天一次)。在吗啡(5mg/kg,i.p.)之前,实验组用吗啡(5mgg/kg,i.p..)、单独的巴氯芬(10-30mg/kg,i.p。一组在下丘脑腹内侧接受一次吗啡(0.4µg/只),最后一组在恢复后接受吗啡(5 mg/kg,腹腔注射)。然后制备血液和海马体样本。此外,还评估了DH中氧化应激因子(GPX、MDA、SOD和CAT)的水平以及雌激素和糖皮质激素受体的强度。卵巢和子宫也进行了生物测定。结果:与对照组相比,吗啡治疗组无论注射方法如何,卵泡发育都很罕见,相反,厚壁卵泡囊肿非常多。然而,在单独接受巴氯芬或巴氯芬与吗啡联合治疗的组中,囊肿数量减少,成熟卵泡数量显著增加。氧化剂在吗啡治疗组的DH中显示出高水平,这与DH中的低雌激素受体有关。然而,巴氯芬预处理改善了这些条件。此外,DH中的糖皮质激素受体在不同组中没有显示出显著差异,并且在吗啡接受组和其他组中都没有观察到CA1区的坏死。子宫在任何一组中都没有显示出显著的变化。结论:预防性使用巴氯芬可预防吗啡副作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protective Effect of Baclofen against Oxidative Stress in Dorsal Hippocampus of Rats with Morphine-Induced Ovarian Polycystic
Background and Objectives: Studies have shown that polycystic ovary (PCO) may be induced by morphine and CA1 may be damaged by PCO-related oxidative stress but can be protected by a potent GABAB receptor agonist. Therefore, this study aimed to investigate the protective effect of baclofen against oxidative stress in the dorsal hippocampus (DH) of morphine-treated rats with ovarian cysts. Materials and Methods:  In total, 66 female Wistar rats were selected and randomly divided into control and experimental groups. The control group received saline (1 ml/kg, intraperitoneally [i.p.], once a day). Experimental groups were treated with morphine (5 mg/kg, i.p.), baclofen alone (10-30 mg/kg, i.p.), and baclofen (10, 20, 30 mg/kg, i.p.) before morphine (5 mg/kg, i.p.), once daily. One group received morphine (0.4 µg/rat) once in the ventromedial hypothalamus, and the last ovariectomized group was administered morphine (5 mg/kg, i.p.) after recovery. Then blood and hippocampus samples were prepared. Moreover, the levels of oxidative stress factors (GPX, MDA, SOD, and CAT), and the intensity of estrogen and glucocorticoid receptors in DH were evaluated. Ovaries and the uterus were also examined biometrically. Results: In the morphine-treated groups, regardless of the injection method, the development of follicles was rare, compared to the control group, instead, thick-walled follicular cysts were abundant. However, in the groups that received baclofen alone or baclofen together with morphine, the number of cysts decreased and the number of mature follicles increased significantly. Oxidative agents showed high levels in the DH of the morphine-treated group, which correlated with low estrogen receptors in DH. However, baclofen pretreatment improved these conditions. Besides, glucocorticoid receptors in DH did not show significant differences in different groups, and necrosis in the CA1 area was not observed either in the morphine-receiving group or in the other groups. The uterus did not show significant changes in any group. Conclusion: Prophylactic use of baclofen can protect against morphine side effects.
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