Dietary soy protein reverses obesity-induced liver steatosis and alters fecal microbial composition independent of isoflavone level.

IF 4 2区 农林科学 Q2 NUTRITION & DIETETICS Frontiers in Nutrition Pub Date : 2024-10-28 eCollection Date: 2024-01-01 DOI:10.3389/fnut.2024.1487859
Reza Hakkak, Soheila Korourian, Wei Li, Beverly Spray, Nathan C Twaddle, Christopher E Randolph, Elisabet Børsheim, Michael S Robeson Ii
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Abstract

Introduction: Metabolic dysfunction-associated steatotic liver disease (MASLD) is a major public health concern that is exacerbated by the obesity pandemic. Dietary interventions have the potential to alleviate obesity-associated MASLD through variable mechanisms, including optimizing the gut microbiota. Previously, we reported that soy protein concentrate (SPC) with low or high levels of isoflavone (LIF or HIF) protected young obese Zucker rats from developing liver steatosis. The current study was designed to test whether SPC-LIF and SPC-HIF diets would reverse liver steatosis and alter fecal microbial composition in adult obese Zucker rats with existing steatosis.

Methods: Six-week-old male obese Zucker rats (n = 26) were fed a casein control diet (CAS) for 8 weeks and 7 rats were randomly selected and sacrificed to confirm liver steatosis. The remaining rats were randomly assigned to receive CAS, SPC-LIF, or SPC-HIF diet (n = 6-7/group) for an additional 10 weeks.

Results: Compared to CAS diet, feeding SPC-LIF and SPC-HIF diets resulted in significantly lower liver weight, liver steatosis score, and liver microvesicular score (p < 0.05), but did not lead to difference in body weight, liver macrovesicular score, serum ALT, or serum AST. Isoflavone levels (e.g., LIF vs. HIF) did not affect any of these measurements except in the SPC-HIF group, which had an additional decrease in liver weight (p < 0.05) compared to the SPC-LIF group. The SPC-HIF group also had significantly higher levels of the aglycone forms of daidzein, genistein, and equol as well as the total levels of daidzein, genistein, and equol compared to SPC-LIF or CAS diet fed rats (p < 0.05). The distribution of microbial communities based on measures of beta diversity of both SPC-LIF and SPC-HIF groups were significantly different to that of the CAS group (p ≤ 0.005). Alpha-diversity did not differ between any of the groups.

Conclusion: Taken together, dietary soy protein can reverse liver steatosis in adult Zucker rats, and the reversal of steatosis is accompanied by alterations in gut microbial composition.

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膳食大豆蛋白可逆转肥胖引起的肝脏脂肪变性,并改变粪便微生物组成,而与异黄酮水平无关。
简介代谢功能障碍相关性脂肪性肝病(MASLD)是一个主要的公共卫生问题,肥胖症的流行加剧了这一问题。膳食干预措施有可能通过各种机制缓解肥胖相关性脂肪肝,包括优化肠道微生物群。此前,我们曾报道过含有低或高水平异黄酮(LIF或HIF)的浓缩大豆蛋白(SPC)可保护年轻肥胖扎克大鼠免于发生肝脏脂肪变性。目前的研究旨在测试 SPC-LIF 和 SPC-HIF 饮食是否会逆转肝脏脂肪变性,并改变已有脂肪变性的成年肥胖 Zucker 大鼠的粪便微生物组成:给六周大的雄性肥胖 Zucker 大鼠(n = 26)喂食酪蛋白控制饮食(CAS)8 周,随机选择 7 只大鼠并将其处死以确认肝脏脂肪变性。剩下的大鼠被随机分配接受 CAS、SPC-LIF 或 SPC-HIF 饮食(n = 6-7/组),持续 10 周:与 CAS 日粮相比,饲喂 SPC-LIF 和 SPC-HIF 日粮可显著降低肝脏重量、肝脏脂肪变性评分和肝脏微泡评分(p < 0.05),但体重、肝脏大泡评分、血清谷丙转氨酶和血清谷草转氨酶没有差异。异黄酮水平(如 LIF 与 HIF)对上述测量结果均无影响,但 SPC-HIF 组除外,与 SPC-LIF 组相比,SPC-HIF 组的肝脏重量进一步减轻(p < 0.05)。与 SPC-LIF 或 CAS 膳食喂养的大鼠相比,SPC-HIF 组的双歧因子、染料木素和赤藓醇的苷元形式以及双歧因子、染料木素和赤藓醇的总含量也明显更高(p < 0.05)。根据贝塔多样性的测量结果,SPC-LIF 组和 SPC-HIF 组的微生物群落分布与 CAS 组有显著差异(p ≤ 0.005)。各组之间的α-多样性没有差异:综上所述,膳食大豆蛋白可以逆转成年 Zucker 大鼠的肝脏脂肪变性,而且脂肪变性的逆转伴随着肠道微生物组成的改变。
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来源期刊
Frontiers in Nutrition
Frontiers in Nutrition Agricultural and Biological Sciences-Food Science
CiteScore
5.20
自引率
8.00%
发文量
2891
审稿时长
12 weeks
期刊介绍: No subject pertains more to human life than nutrition. The aim of Frontiers in Nutrition is to integrate major scientific disciplines in this vast field in order to address the most relevant and pertinent questions and developments. Our ambition is to create an integrated podium based on original research, clinical trials, and contemporary reviews to build a reputable knowledge forum in the domains of human health, dietary behaviors, agronomy & 21st century food science. Through the recognized open-access Frontiers platform we welcome manuscripts to our dedicated sections relating to different areas in the field of nutrition with a focus on human health. Specialty sections in Frontiers in Nutrition include, for example, Clinical Nutrition, Nutrition & Sustainable Diets, Nutrition and Food Science Technology, Nutrition Methodology, Sport & Exercise Nutrition, Food Chemistry, and Nutritional Immunology. Based on the publication of rigorous scientific research, we thrive to achieve a visible impact on the global nutrition agenda addressing the grand challenges of our time, including obesity, malnutrition, hunger, food waste, sustainability and consumer health.
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