Department of Physiology, Medical College of Georgia at Augusta University, Augusta, GA, USA.
Department of Physiology, Medical College of Wisconsin, Milwaukee, WI, USA.
Acta Physiol (Oxf). 2021 Aug;232(4):e13662. doi: 10.1111/apha.13662. Epub 2021 Apr 26.
Our previous studies have demonstrated the importance of dietary factors in the determination of hypertension in Dahl salt-sensitive (SS) rats. Since the gut microbiota has been implicated in chronic diseases like hypertension, we hypothesized that dietary alterations shift the microbiota to mediate the development of salt-sensitive hypertension and renal disease.
This study utilized SS rats from the Medical College of Wisconsin (SS/MCW) maintained on a purified, casein-based diet (0.4% NaCl AIN-76A, Dyets) and from Charles River Laboratories (SS/CRL) fed a whole grain diet (0.75% NaCl 5L79, LabDiet). Faecal 16S rDNA sequencing was used to phenotype the gut microbiota. Directly examining the contribution of the gut microbiota, SS/CRL rats were administered faecal microbiota transfer (FMT) experiments with either SS/MCW stool or vehicle (Vehl) in conjunction with the HS AIN-76A diet.
SS/MCW rats exhibit renal damage and inflammation when fed high salt (HS, 4.0% NaCl AIN-76A), which is significantly attenuated in SS/CRL. Gut microbiota phenotyping revealed distinct profiles that correlate with disease severity. SS/MCW FMT worsened the SS/CRL response to HS, evidenced by increased albuminuria (67.4 ± 6.9 vs 113.7 ± 25.0 mg/day, Vehl vs FMT, P = .007), systolic arterial pressure (158.6 ± 5.8 vs 177.8 ± 8.9 mmHg, Vehl vs FMT, P = .09) and renal T-cell infiltration (1.9-fold). Amplicon sequence variant (ASV)-based analysis of faecal 16S rDNA sequencing data revealed taxa that significantly shifted with FMT: Erysipelotrichaceae_2, Parabacteroides gordonii, Streptococcus alactolyticus, Bacteroidales_1, Desulfovibrionaceae_2, Ruminococcus albus.
These data demonstrate that dietary modulation of the gut microbiota directly contributes to the development of Dahl SS hypertension and renal injury.
我们之前的研究表明,饮食因素在决定达尔盐敏感(SS)大鼠高血压中起重要作用。由于肠道微生物群与高血压等慢性疾病有关,我们假设饮食改变会改变微生物群,从而介导盐敏感高血压和肾脏疾病的发生。
本研究利用来自威斯康星医学院(SS/MCW)的 SS 大鼠,这些大鼠以纯化的基于酪蛋白的饮食(0.4%NaClAIN-76A,Dyets)维持,来自查尔斯河实验室(SS/CRL)的 SS 大鼠以全谷物饮食(0.75%NaCl5L79,LabDiet)维持。使用粪便 16S rDNA 测序对肠道微生物群进行表型分析。直接检查肠道微生物群的贡献,SS/CRL 大鼠接受粪便微生物群移植(FMT)实验,用 SS/MCW 粪便或载体(Veh1)与高盐(HS,4.0%NaClAIN-76A)饮食联合。
当 SS/MCW 大鼠喂食高盐(HS,4.0%NaClAIN-76A)时,会出现肾脏损伤和炎症,而 SS/CRL 大鼠则明显减轻。肠道微生物群表型分析显示出与疾病严重程度相关的独特特征。SS/MCW FMT 加重了 SS/CRL 对 HS 的反应,表现为蛋白尿增加(67.4±6.9 与 113.7±25.0mg/天,Veh1 与 FMT,P=0.007)、收缩压升高(158.6±5.8 与 177.8±8.9mmHg,Veh1 与 FMT,P=0.09)和肾 T 细胞浸润增加(1.9 倍)。粪便 16S rDNA 测序的扩增子序列变异(ASV)分析显示,FMT 后显著改变的分类群有:Erysipelotrichaceae_2、Parabacteroides gordonii、Streptococcus alactolyticus、Bacteroidales_1、Desulfovibrionaceae_2、Ruminococcus albus。
这些数据表明,饮食对肠道微生物群的调节直接导致了达尔 SS 高血压和肾脏损伤的发生。