Hsu Chien-Ning, Hou Chih-Yao, Chang-Chien Guo-Ping, Lin Sufan, Yang Hung-Wei, Tain You-Lin
Department of Pharmacy, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 833, Taiwan.
School of Pharmacy, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Biomedicines. 2020 Dec 4;8(12):567. doi: 10.3390/biomedicines8120567.
The gut microbiota plays a critical role in kidney disease and hypertension; however, whether maternal chronic kidney disease (CKD)-induced offspring hypertension is associated with alterations of the microbiota and microbial metabolites remains elusive. Using rat as an animal model, we conducted a maternal adenine-induced CKD model to examine whether adult male offspring develop hypertension and kidney disease. As resveratrol has antioxidant and prebiotic properties, we also aimed to elucidate whether its use in pregnancy and lactation can benefit hypertension programmed by maternal CKD via mediation of the gut microbiota and oxidative stress. Female Sprague-Dawley rats received regular chow (C) or chow supplemented with 0.5% adenine (CKD) from 3 weeks before pregnancy until lactation. One group of the adenine-induced CKD pregnant rats received resveratrol (R; 50 mg/L) in drinking water during gestation and lactation. Male offspring were divided into three groups: C, CKD, and CKD+R. The microbial metabolites analyzed were short chain fatty acids (SCFAs) in feces and trimethylamine (TMA)/trimethylamine N-oxide (TMAO) in plasma. We found perinatal resveratrol therapy protected against maternal CKD-induced hypertension in adult male offspring. The overall microbial compositions and diversity of bacterial community in the three groups were different. Resveratrol therapy increased α-diversity, decreased the to ratio, and increased the abundance of the genera and . Perinatal resveratrol therapy increased plasma TMA levels but decreased the plasma TMAO-to-TMA ratio. Although resveratrol had negligible effect on fecal concentrations of SCFAs, it increased G-protein coupled receptor-41 (GPR41) protein levels in the offspring's kidneys. Additionally, resveratrol therapy increased plasma levels of L-arginine and the L-arginine-to-ADMA ratio (AAR), and decreased oxidative stress. Overall, the protective effects of resveratrol against programmed hypertension are related to gut microbiome remodeling, including an increased abundance of beneficial microbes, mediation of the TMA-TMAO pathway, and alterations of SCFA receptors. Our results highlighted that targeting the microbiome and their metabolites might be potential therapeutic strategies to prevent maternal CKD-induced adverse pregnancy and offspring outcomes.
肠道微生物群在肾脏疾病和高血压中起着关键作用;然而,母体慢性肾脏病(CKD)诱发的子代高血压是否与微生物群及其代谢产物的改变有关仍不清楚。我们以大鼠作为动物模型,构建了母体腺嘌呤诱导的CKD模型,以研究成年雄性子代是否会发生高血压和肾脏疾病。由于白藜芦醇具有抗氧化和益生元特性,我们还旨在阐明孕期和哺乳期使用白藜芦醇是否可通过调节肠道微生物群和氧化应激,使母体CKD引发的高血压得到改善。从怀孕前3周直到哺乳期,雌性Sprague-Dawley大鼠分别给予普通饲料(C组)或添加0.5%腺嘌呤的饲料(CKD组)。一组腺嘌呤诱导的CKD怀孕大鼠在妊娠和哺乳期饮用含白藜芦醇(R组;50 mg/L)的水。雄性子代分为三组:C组、CKD组和CKD+R组。分析的微生物代谢产物包括粪便中的短链脂肪酸(SCFAs)和血浆中的三甲胺(TMA)/氧化三甲胺(TMAO)。我们发现围产期白藜芦醇治疗可预防母体CKD诱导成年雄性子代发生高血压。三组中细菌群落的总体微生物组成和多样性存在差异。白藜芦醇治疗增加了α多样性,降低了 与 的比例,并增加了 属和 属的丰度。围产期白藜芦醇治疗增加了血浆TMA水平,但降低了血浆TMAO与TMA的比例。虽然白藜芦醇对粪便中SCFAs浓度的影响可忽略不计,但它增加了子代肾脏中G蛋白偶联受体41(GPR41)的蛋白水平。此外,白藜芦醇治疗增加了血浆L-精氨酸水平和L-精氨酸与不对称二甲基精氨酸的比例(AAR),并降低了氧化应激。总体而言,白藜芦醇对程序性高血压的保护作用与肠道微生物群重塑有关,包括有益微生物丰度增加、TMA-TMAO途径的调节以及SCFA受体的改变。我们的结果强调,针对微生物群及其代谢产物可能是预防母体CKD引起的不良妊娠和子代结局的潜在治疗策略。