Differential cortical aspartate uptake across the oestrous cycle is associated with changes in gut microbiota in Wistar-Kyoto rats

IF 2.5 4区 医学 Q3 NEUROSCIENCES Neuroscience Letters Pub Date : 2025-01-31 DOI:10.1016/j.neulet.2024.138096
Jahangir Sajjad , Jennifer Morael , Thieza G. Melo , Tara Foley , Amy Murphy , James Keane , Jelena Popov , Catherine Stanton , Timothy G. Dinan , Gerard Clarke , John F. Cryan , James M. Collins , Siobhain M. O’Mahony
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Abstract

Pain and psychological stress are intricately linked, with sex differences evident in disorders associated with both systems. Glutamatergic signalling in the central nervous system is influenced by gonadal hormones via the hypothalamic–pituitary–adrenal axis and is central in pain research. Emerging evidence supports an important role for the gut microbiota in influencing pain signalling. Here, the functional activity of excitatory amino acid transporters (EAATs) in the anterior cingulate cortex (ACC) and lumbosacral spinal cord of male and female Wistar-Kyoto rats, an animal model of comorbid visceral hypersensitivity and enhanced stress responsivity, was investigated across the oestrous cycle. Correlations between the gut microbiota and changes in the functional activity of the central glutamatergic system were also investigated.
EAAT function in the lumbosacral spinal cord was similar between males and females across the oestrous cycle. EAAT function was higher in the ACC of dioestrus females compared to proestrus and oestrus females. In males, aspartate uptake in the ACC positively correlated with Bacteroides, while aspartate uptake in the spinal cord positively correlated with the relative abundance of Lachnospiraceae NK4A136. Positive associations with aspartate uptake in the spinal cord were also observed for Alistipes and Bifidobacterium during oestrus, and Eubacterium coprostanoligenes during proestrus. Clostridium sensu stricto1 was negatively associated with aspartate uptake in the ACC in males and dioestrus females.
These data indicate that glutamate metabolism in the ACC is oestrous stage-dependent and that short-chain fatty acid-producing bacteria are positively correlated with aspartate uptake in males and during specific oestrous stages in females.

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Wistar-Kyoto大鼠发情周期中皮层天冬氨酸摄取的差异与肠道微生物群的变化有关。
疼痛和心理压力有着错综复杂的联系,在与这两个系统相关的疾病中,性别差异很明显。中枢神经系统中的谷氨酸能信号通过下丘脑-垂体-肾上腺轴受性腺激素的影响,在疼痛研究中处于中心地位。新出现的证据支持肠道微生物群在影响疼痛信号传导中的重要作用。本研究以Wistar-Kyoto大鼠为动物模型,研究了雄性和雌性Wistar-Kyoto大鼠在整个发情周期内,前扣带皮层(ACC)和腰骶脊髓兴奋性氨基酸转运蛋白(EAATs)的功能活性。肠道微生物群与中枢谷氨酸系统功能活性变化之间的相关性也被研究。EAAT在腰骶脊髓中的功能在整个发情周期中在男性和女性之间是相似的。发情期雌鼠ACC的EAAT功能高于发情期雌鼠和发情期雌鼠。在雄性中,ACC中的天冬氨酸摄取与拟杆菌类正相关,而脊髓中的天冬氨酸摄取与毛缕科NK4A136的相对丰度正相关。在发情期间,阿利斯特和双歧杆菌以及共前列腺寡真杆菌也观察到脊髓与天冬氨酸摄取呈正相关。窄感梭状芽胞杆菌1与雄性和雌雌期雌性ACC中的天冬氨酸摄取呈负相关。这些数据表明,ACC中的谷氨酸代谢依赖于发情期,短链脂肪酸产生细菌与雄性和雌性特定发情期的天冬氨酸摄取呈正相关。
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来源期刊
Neuroscience Letters
Neuroscience Letters 医学-神经科学
CiteScore
5.20
自引率
0.00%
发文量
408
审稿时长
50 days
期刊介绍: Neuroscience Letters is devoted to the rapid publication of short, high-quality papers of interest to the broad community of neuroscientists. Only papers which will make a significant addition to the literature in the field will be published. Papers in all areas of neuroscience - molecular, cellular, developmental, systems, behavioral and cognitive, as well as computational - will be considered for publication. Submission of laboratory investigations that shed light on disease mechanisms is encouraged. Special Issues, edited by Guest Editors to cover new and rapidly-moving areas, will include invited mini-reviews. Occasional mini-reviews in especially timely areas will be considered for publication, without invitation, outside of Special Issues; these un-solicited mini-reviews can be submitted without invitation but must be of very high quality. Clinical studies will also be published if they provide new information about organization or actions of the nervous system, or provide new insights into the neurobiology of disease. NSL does not publish case reports.
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