Abstract

BackgroundOral charcoal adsorbent AST-120 (AST) is reported to ameliorate renal dysfunction by the absorption of toxic substance in the gut. Recent study revealed that, in CKD, gut environment is disturbed including the decrease in tight junctions and Lactobacillus (Lact). In this study, we examined whether AST improves the renal dysfunction through gut environment.MethodSix-week-old spontaneously hypertensive rats (SHR) were rendered CKD by 5/6th nephrectomy (Nx). SHRs were divided into SHR (Sham), SHR with Nx (Nx), and Nx given AST (Nx + AST) (n = 10, each). After 12 weeks, rats were killed and biochemical parameters were explored. The gut flora was analyzed. Furthermore, gut molecular changes in tight junctions and toll-like receptors were examined. We also investigated the effects of the combination therapy with AST and Lact.ResultsThe increase in serum urea nitrogen and urinary protein excretion in Nx was restored in Nx + AST. The increased renal glomerulosclerosis in Nx was ameliorated in Nx + AST. Increases in serum uremic toxins and IL-6 in Nx were ameliorated in Nx + AST. The gut flora analysis revealed that the decrease in Lact in Nx was restored in Nx + AST. The downregulation in the tight junction and TLR2 in Nx was mitigated by AST. However, combination therapy failed to exhibit additional effects.ConclusionAST ameliorated renal function with the restoration of Lact and tight junction through TLR pathway, which would mitigate systemic inflammation and contributed to their renoprotective effects. Our study provides a novel mechanism of the renoprotective effects by AST.

Highlights

  • The increase of chronic kidney disease (CKD) patients becomes the serious problem for humans because CKD elevates cardiovascular events and causes end-stage kidney disease [1]

  • We demonstrated that AST elevates the population of Lact in CKD rats, which improved the disruption of intestinal barrier and systemic inflammation through TLR2 and TLR4

  • We investigated the effects of AST on the progression of CKD

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Summary

Introduction

The increase of chronic kidney disease (CKD) patients becomes the serious problem for humans because CKD elevates cardiovascular events and causes end-stage kidney disease [1]. Clinical and Experimental Nephrology (2018) 22:1069–1078 beneficial to the maintenance of gut barrier function and inhibit the systemic inflammation evoked by the intrusion of various toxins from leaky gut [10]. In this way, the organ interrelationship between gut and kidney has been gaining the scientific interest, coined as ‘the intestinal-renal syndrome’ [12]. We demonstrated that AST elevates the population of Lact in CKD rats, which improved the disruption of intestinal barrier and systemic inflammation through TLR2 and TLR4. The present study provides the novel mechanism of AST through the modulation of gut environment

Materials and methods
A Systolic blood pressure B CreaƟnine
Discussion
F Plasma Indoxyl sulafate
Compliance with ethical standards
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