Aleurone supplementation enhances the metabolic benefits of training in Standardbred mares: impacts on glucose-insulin dynamics and gut microbiome composition.

IF 3.2 3区 医学 Q2 PHYSIOLOGY
Frontiers in Physiology Pub Date : 2025-04-10 eCollection Date: 2025-01-01 DOI:10.3389/fphys.2025.1565005
Berit Boshuizen, Lorie De Maré, Maarten Oosterlinck, Filip Van Immerseel, Venessa Eeckhaut, Constance De Meeus, Lindsey Devisscher, Carmen Vidal Moreno de Vega, Maarten Willems, Jean Eduardo De Oliveira, Guilherme Hosotani, Yannick Gansemans, Tim Meese, Filip Van Nieuwerburgh, Dieter Deforce, Katrien Vanderperren, Elisabeth-Lidwien Verdegaal, Cathérine Delesalle
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引用次数: 0

Abstract

Introduction: Aleurone, derived from the bran layer of grains like wheat and barley, has demonstrated positive effects on energy metabolism in pigs, mice, and untrained horses, influencing glucose-insulin dynamics and gut microbiome composition. Training itself enhances insulin sensitivity in horses, similar to the improvements in performance capacity observed in human athletes. This study aimed to investigate whether aleurone supplementation provides additional benefits to training by modulating insulin metabolism and gut microbiota in Standardbred mares.

Methods: Sixteen Standardbred mares (aged 3-5 years) participated in a cross-over study with two 8-week training periods separated by 8 weeks of detraining. Each horse received either 200 g/day aleurone supplementation or a control diet. Insulin metabolism was evaluated using oral (OGTT) and intravenous (FSIGTT) glucose tolerance tests, measuring parameters such as Maximumglucose, AUCglucose, Maximuminsulin, AUCinsulin, Time to peakinsulin (OGTT), Acute Insulin Response to Glucose (AIRg), glucose effectiveness (Sg), and disposition index (DI) (FSIGTT). Fecal samples underwent metagenomic analysis to assess alpha and beta diversity and microbial composition.

Results: Training alone: Training significantly improved OGTT parameters by decreasing Maximuminsulin (P = 0.005) and AUCinsulin (P = 0.001), while increasing Time to peakinsulin (P = 0.03), indicating enhanced insulin sensitivity. FSIGTT results also showed a decrease in logAIRg (P = 0.044). Training with Aleurone: Aleurone supplementation further reduced FSIGTT AIRg (P = 0.030), logAIRg (P = 0.021) while increasing glucose effectiveness (Sg; P = 0.031). These findings suggest aleurone improves insulin sensitivity, glucose disposal, and fasting glucose regulation beyond training. Microbiome analysis revealed training decreased Pseudomonas, associated with dysbiosis, while aleurone reduced inflammation-associated Desulfovibrio. Beta diversity metrics showed no significant changes.

Conclusion: Aleurone supplementation enhances training-induced improvements in glucose metabolism and fecal microbiota composition, which could offer potential benefits for equine athletes by optimizing metabolic flexibility. It also supports improvements in glucose and insulin dynamics, particularly by further enhancing insulin sensitivity and glucose-mediated disposal. Future studies should investigate the mechanisms of aleurone at the muscle and gut level and explore its potential applications for metabolic disorders such as Equine Metabolic Syndrome.

淀粉粉补充提高了标准种马训练的代谢益处:对葡萄糖-胰岛素动力学和肠道微生物组组成的影响。
从小麦和大麦等谷物的麸皮层中提取的糊粉已被证明对猪、小鼠和未经训练的马的能量代谢有积极影响,影响葡萄糖-胰岛素动力学和肠道微生物组组成。训练本身增强了马的胰岛素敏感性,类似于在人类运动员身上观察到的表现能力的提高。本研究旨在研究是否通过调节标准种马的胰岛素代谢和肠道微生物群来补充淀粉粉对训练有额外的好处。方法:16匹标准种母马(3-5岁)进行交叉研究,两期训练8周,中间间隔8周去训练。每匹马分别补充200 g/d糊粉素或对照饲料。采用口服(OGTT)和静脉(FSIGTT)葡萄糖耐量试验评估胰岛素代谢,测量参数如最大葡萄糖、auc葡萄糖、最大胰岛素、auc胰岛素、胰岛素峰值时间(OGTT)、急性胰岛素对葡萄糖反应(AIRg)、葡萄糖有效性(Sg)和处置指数(DI) (FSIGTT)。对粪便样本进行宏基因组分析以评估α和β多样性和微生物组成。结果:单纯训练:通过降低Maximuminsulin (P = 0.005)和AUCinsulin (P = 0.001),增加胰岛素到达峰值时间(P = 0.03),显著改善OGTT参数,表明胰岛素敏感性增强。FSIGTT结果也显示logAIRg下降(P = 0.044)。用糊粉酮训练:补充糊粉酮进一步降低了FSIGTT AIRg (P = 0.030), logAIRg (P = 0.021),同时增加了葡萄糖有效性(Sg;P = 0.031)。这些发现表明糊粉可以改善胰岛素敏感性、葡萄糖处理和训练之外的空腹葡萄糖调节。微生物组分析显示,训练减少了与生态失调相关的假单胞菌,而糊粉蛋白减少了与炎症相关的脱硫弧菌。Beta多样性指标没有显著变化。结论:补充糊粉酮可以增强训练诱导的葡萄糖代谢和粪便微生物群组成的改善,这可能通过优化代谢灵活性为马运动员提供潜在的益处。它还支持改善葡萄糖和胰岛素动力学,特别是通过进一步增强胰岛素敏感性和葡萄糖介导的处置。今后的研究应进一步探讨糊粉在肌肉和肠道水平的作用机制,并探索其在代谢性疾病如马代谢综合征中的潜在应用。
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来源期刊
CiteScore
6.50
自引率
5.00%
发文量
2608
审稿时长
14 weeks
期刊介绍: Frontiers in Physiology is a leading journal in its field, publishing rigorously peer-reviewed research on the physiology of living systems, from the subcellular and molecular domains to the intact organism, and its interaction with the environment. Field Chief Editor George E. Billman at the Ohio State University Columbus is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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