de Assis Braga Daiane Cristina, Carlos Batista Marcos Adriano, Guerra-Sá Renata, Alves da Silva Thayane Christine, Carneiro Marco Antônio Alves, da Silva Lanna Maria Célia, Azevedo Vasco Ariston, de Oliveira Carvalho Rodrigo Dias, Souza Gustavo Henrique Bianco de, Antunes Vagner Roberto, Aparecida Lima de Moura Sandra, Ceron Carla Speroni, Cardoso Leonardo Máximo
Department of Biological Sciences, Institute of Exact and Biological Sciences, Federal University of Ouro Preto, Ouro Preto, MG 35,402-136, Brazil.
Department of Biodiversity, Evolution and Environment, Institute of Exact and Biological Sciences, Federal University of Ouro Preto, Ouro Preto, MG 35,402-136, Brazil.
J Pharm Pharmacol. 2025 Jan 6;77(1):111-126. doi: 10.1093/jpp/rgae137.
High sodium intake is a major risk factor for hypertension and renal diseases. Previous studies have shown that a suspension of ethanolic extract of Psidium guajava (guava) leaves (PsE) has antihypertensive effects in rats on a high-sodium diet (HSD), but some mechanisms to that remain unexplored. This study explored whether oral PsE treatment affects sodium handling by the intestine and alters the gut microbiome in HSD-fed rats.
Male Wistar rats were divided into two groups: standard salt diet (SSD) and HSD (0.9% Na+), from weaning. After 12 weeks, both groups received PsE (200 mg/kg) or a vehicle for an additional 4 weeks.
Sodium excretion was measured using flame photometry, and sodium absorption was assessed by intestinal perfusion technique. The gut microbiome was analysed through 16S ribosomal gene sequencing. HSD increased faecal sodium, further elevated by PsE, which inhibited intestinal sodium absorption in HSD rats. HSD altered the abundance of specific bacterial families, which PsE partially reversed. No changes in alpha diversity were noted among groups.
These findings suggest that PsE inhibited intestinal sodium handling and that PsE, combined with increased faecal sodium, may reshape the gut microbiome of HSD rats to resemble that of SSD rats.
高钠摄入是高血压和肾脏疾病的主要危险因素。先前的研究表明,番石榴叶乙醇提取物(PsE)悬浮液对高钠饮食(HSD)大鼠具有降压作用,但其部分机制仍未得到探索。本研究探讨了口服PsE治疗是否会影响HSD喂养大鼠肠道对钠的处理并改变其肠道微生物群。
雄性Wistar大鼠从断奶开始分为两组:标准盐饮食(SSD)组和HSD(0.9% Na+)组。12周后,两组均再接受4周的PsE(200 mg/kg)或赋形剂处理。
使用火焰光度法测量钠排泄,并通过肠道灌注技术评估钠吸收。通过16S核糖体基因测序分析肠道微生物群。HSD增加了粪便中的钠含量,PsE进一步升高了该含量,且PsE抑制了HSD大鼠的肠道钠吸收。HSD改变了特定细菌家族的丰度,PsE部分逆转了这种改变。各组间的α多样性没有变化。
这些发现表明,PsE抑制肠道对钠的处理,并且PsE与粪便钠含量增加相结合,可能会使HSD大鼠的肠道微生物群重塑为类似于SSD大鼠的肠道微生物群。