Structural Changes in the Medial Prefrontal Cortex and Anterior Cingulate Cortex of Dehydroepiandrosterone-Induced Wistar Rat Model of Polycystic Ovarian Syndrome.

IF 1 Q4 NEUROSCIENCES Basic and Clinical Neuroscience Pub Date : 2022-09-01 DOI:10.32598/bcn.2022.2985.1
Enya Joseph Igbo, Ukwenya Okoliko, Imam Aminu, Aisha Kopada, Samson Olorunnado, Oluwole B Akinola
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Abstract

Introduction: Polycystic ovary syndrome (PCOS) is a complex endocrine disorder in women that is associated with an increased risk of infertility. This study aims to evaluate the neurobehavioral and neurochemical changes along with the associated changes in the medial prefrontal cortex (mPFC) and anterior cingulate cortex (ACC) of the dehydroepiandrosterone (DHEA)-induced PCOS model rats.

Methods: A total of 12 female juvenile Wistar rats (30 to 50 g) about 22 to 44 days old were divided into 2 groups. The control group received sesame oil while the PCOS group received sesame oil plus DHEA. All treatment was done via daily subcutaneous injection for 21 days.

Results: Subcutaneous DHEA-induced PCOS significantly depleted the line crossing and rearing frequency in the open field, along with the percentage of the time in the white box, line crossing, rearing, and peeping frequency in the black and white box, and the percentage of alternation in the Y-maze. PCOS significantly increased the immobility time, freezing period, and the percentage of time in the dark area in the forced swim test, open field test, and black and white box, respectively. The level of luteinizing hormone, follicle-stimulating hormone, malondialdehyde (MDA), reactive oxygen species (ROS), and interleukin-6 (IL-6) increased significantly, while norepinephrine depleted significantly with an obvious decrease in the brain-derived neurotrophic factor level in the PCOS model rats. PCOS rats exhibited cystic follicles in the ovaries and necrotic or degenerative like features in the hippocampal pyramidal cells.

Conclusion: DHEA-induced PCOS results in anxiety and depressive behavior with structural alteration in rats, possibly through the elevation of MDA, ROS, and IL-6 levels, which also attributes to impaired emotional and executive functions in the mPFC and ACC.

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脱氢表雄酮诱导的多囊卵巢综合征Wistar大鼠模型的额前内侧皮质和前角皮质结构变化。
引言:多囊卵巢综合征(PCOS)是一种复杂的女性内分泌紊乱,与不孕风险增加有关。本研究旨在评估脱氢表雄酮(DHEA)诱导的PCOS模型大鼠的神经行为和神经化学变化,以及内侧前额叶皮层(mPFC)和前扣带皮层(ACC)的相关变化。方法:将12只22~44日龄雌性Wistar幼鼠(30~50g)分为2组。对照组给予芝麻油,PCOS组给予芝油加DHEA。所有治疗均通过每日皮下注射进行,持续21天。结果:皮下DHEA诱导的PCOS显著降低了露地杂交和饲养频率,降低了在白盒中的时间百分比、杂交、饲养和在黑白盒中的窥视频率,以及在Y迷宫中的交替百分比。PCOS在强迫游泳试验、开放场地试验和黑白箱试验中分别显著增加了静止时间、冷冻期和黑暗区域的时间百分比。PCOS模型大鼠的促黄体生成素、卵泡刺激素、丙二醛(MDA)、活性氧(ROS)和白细胞介素-6(IL-6)水平显著升高,而去甲肾上腺素水平显著降低,脑源性神经营养因子水平明显下降。多囊卵巢综合征大鼠卵巢出现囊性卵泡,海马锥体细胞出现坏死或变性样特征。结论:DHEA诱导的PCOS可导致大鼠的焦虑和抑郁行为,并伴有结构改变,可能是通过升高MDA、ROS和IL-6水平,这也归因于mPFC和ACC的情绪和执行功能受损。
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来源期刊
CiteScore
2.60
自引率
0.00%
发文量
64
审稿时长
4 weeks
期刊介绍: BCN is an international multidisciplinary journal that publishes editorials, original full-length research articles, short communications, reviews, methodological papers, commentaries, perspectives and “news and reports” in the broad fields of developmental, molecular, cellular, system, computational, behavioral, cognitive, and clinical neuroscience. No area in the neural related sciences is excluded from consideration, although priority is given to studies that provide applied insights into the functioning of the nervous system. BCN aims to advance our understanding of organization and function of the nervous system in health and disease, thereby improving the diagnosis and treatment of neural-related disorders. Manuscripts submitted to BCN should describe novel results generated by experiments that were guided by clearly defined aims or hypotheses. BCN aims to provide serious ties in interdisciplinary communication, accessibility to a broad readership inside Iran and the region and also in all other international academic sites, effective peer review process, and independence from all possible non-scientific interests. BCN also tries to empower national, regional and international collaborative networks in the field of neuroscience in Iran, Middle East, Central Asia and North Africa and to be the voice of the Iranian and regional neuroscience community in the world of neuroscientists. In this way, the journal encourages submission of editorials, review papers, commentaries, methodological notes and perspectives that address this scope.
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