Increased clearance of indoxyl sulfate in renal failure rats with the addition of watersoluble poly‐β‐cyclodextrin to the dialysate

Nephrology ◽  
2021 ◽  
Author(s):  
Shuxin Liu ◽  
Lingyun Jia ◽  
Jia Xiao ◽  
Jingyu Li ◽  
Fangfang Mei ◽  
...  
2007 ◽  
Vol 24 (4) ◽  
pp. 662-671 ◽  
Author(s):  
Kazufumi Iwata ◽  
Hiroshi Watanabe ◽  
Takafumi Morisaki ◽  
Takanobu Matsuzaki ◽  
Takafumi Ohmura ◽  
...  

2011 ◽  
Vol 152 (43) ◽  
pp. 1724-1730 ◽  
Author(s):  
István Kiss

Uremic syndrome and condition is primarily a result of kidney failure in which uremic toxins are accumulated. More and more attention is paid to possibilities for removal of uremic toxins, which not only means dialysis, but also takes into account special dietary considerations and treatments, which aim to absorb the toxins or reduce their production. These uremic toxins, which also increase the cardiovascular risks, play a major part in morbidity and mortality of patients suffering from chronic renal failure and those receiving renal replacement therapy. One of them is a member of the indol group, the indoxyl sulfate. This toxin is difficult to remove with dialysis and is an endogenous protein-bound uremic toxin. Today we know that indoxyl sulfate is a vascular-nephrotoxic agent, which is able to enhance progression of cardiovascular and renal diseases. It is of particular importance that because of its redox potency, this toxin causes oxidative stress and antioxidant effects at the same time and, on top of that, it is formed in the intestinal system. Its serum concentration depends on the nutrition and the tubular function and, therefore, it can also signal the progression of chronic renal failure independently of glomerular filtration rate. Successful removal of indoxyl sulfate reduces the morbidity and mortality and improves survival. Therefore, it could be a possible target or area to facilitate the reduction of uremia in chronic renal failure. The use of probiotics and prebiotics with oral adsorbents may prove to be a promising opportunity to reduce indoxyl sulfate accumulation. Orv. Hetil., 2011, 152, 1724–1730.


2012 ◽  
Vol 31 (2) ◽  
pp. A26
Author(s):  
Chuan Zou ◽  
Fuhua Lu ◽  
Yuchi Wu ◽  
Qizhan Lin ◽  
Xusheng Liu

2018 ◽  
Vol 315 (4) ◽  
pp. F824-F833 ◽  
Author(s):  
Eikan Mishima ◽  
Shinji Fukuda ◽  
Yoshitomi Kanemitsu ◽  
Daisuke Saigusa ◽  
Chikahisa Mukawa ◽  
...  

Accumulation of uremic toxins, which exert deleterious effects in chronic kidney disease, is influenced by the intestinal environment; the microbiota contributes to the production of representative uremic toxins, including p-cresyl sulfate and indoxyl sulfate. Canagliflozin is a sodium-glucose cotransporter (SGLT) 2 inhibitor, and it also exerts a modest inhibitory effect on SGLT1. The inhibition of intestinal SGLT1 can influence the gastrointestinal environment. We examined the effect of canagliflozin on the accumulation of uremic toxins in chronic kidney disease using adenine-induced renal failure mice. Two-week canagliflozin (10 mg/kg po) treatment did not influence the impaired renal function; however, it significantly reduced the plasma levels of p-cresyl sulfate and indoxyl sulfate in renal failure mice (a 75% and 26% reduction, respectively, compared with the vehicle group). Additionally, canagliflozin significantly increased cecal short-chain fatty acids in the mice, suggesting the promotion of bacterial carbohydrate fermentation in the intestine. Analysis of the cecal microbiota showed that canagliflozin significantly altered microbiota composition in the renal failure mice. These results indicate that canagliflozin exerts intestinal effects that reduce the accumulation of uremic toxins including p-cresyl sulfate. Reduction of accumulated uremic toxins by canagliflozin could provide a potential therapeutic option in chronic kidney disease.


2006 ◽  
Vol 16 (3) ◽  
pp. 199-203 ◽  
Author(s):  
Kentaro Taki ◽  
Sakurako Nakamura ◽  
Marius Miglinas ◽  
Atsushi Enomoto ◽  
Toshimitsu Niwa

2006 ◽  
Vol 10 (4) ◽  
pp. 262-267 ◽  
Author(s):  
Shuji Iida ◽  
Keisuke Kohno ◽  
Junko Yoshimura ◽  
Seiji Ueda ◽  
Michiaki Usui ◽  
...  

1999 ◽  
Vol 25 (1-2) ◽  
pp. 118-122 ◽  
Author(s):  
Toshimitsu Niwa ◽  
Isao Aoyama ◽  
Fumio Takayama ◽  
Saori Tsukushi ◽  
Takashi Miyazaki ◽  
...  

2019 ◽  
Vol 4 (7) ◽  
pp. S223
Author(s):  
M. Satoh ◽  
M. Kondo ◽  
Y. Wada ◽  
S. Itano ◽  
K. Kidokoro ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document