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Effects of Fecal Microbiota Transplantation on Composition in Mice with CKD
- Source :
- Toxins, Vol 12, Iss 741, p 741 (2020), Toxins, Toxins, MDPI, 2020, 12 (12), pp.741. ⟨10.3390/toxins12120741⟩, Toxins, 2020, 12 (12), pp.741. ⟨10.3390/toxins12120741⟩, TOXINS, Volume 12, Issue 12
- Publication Year :
- 2020
- Publisher :
- MDPI AG, 2020.
-
Abstract
- International audience; Background: Chronic kidney disease (CKD) is a renal disorder characterized by the accumulation of uremic toxins with limited strategies to reduce their concentrations. A large amount of data supports the pivotal role of intestinal microbiota in CKD complications and as a major source of uremic toxins production. Here, we explored whether fecal microbiota transplantation (FMT) could be attenuated in metabolic complication and uremic toxin accumulation in mice with CKD. Methods: Kidney failure was chemically induced by a diet containing 0.25% (w/w) of adenine for four weeks. Mice were randomized into three groups: control, CKD and CKD + FMT groups. After four weeks, CKD mice underwent fecal microbiota transplantation (FMT) from healthy mice or phosphate buffered saline as control. The gut microbiota structure, uremic toxins plasmatic concentrations, and metabolic profiles were explored three weeks after transplantation. Results: Associated with the increase of alpha diversity, we observed a noticeable improvement of gut microbiota disturbance, after FMT treatment. FMT further decreased p-cresyl sulfate accumulation and improved glucose tolerance. There was no change in kidney function. Conclusions: These data indicate that FMT limited the accumulation of uremic toxins issued from intestinal cresol pathway by a beneficial effect on gut microbiota diversity. Further studies are needed to investigate the FMT efficiency, the timing and feces amount for the transplantation before, to become a therapeutic option in CKD patients.
- Subjects :
- CHRONIC KIDNEY-DISEASE
Male
IMPACT
Health, Toxicology and Mutagenesis
uremic toxins
030232 urology & nephrology
lcsh:Medicine
Urine
Gut flora
Kidney
Toxicology
Gastroenterology
Feces
Mice
0302 clinical medicine
RNA, Ribosomal, 16S
Medicine and Health Sciences
p-cresyl-sulfate
INSULIN-RESISTANCE
0303 health sciences
biology
fecal microbiota transplantation
3. Good health
[SDV.TOX] Life Sciences [q-bio]/Toxicology
medicine.anatomical_structure
[SDV.TOX]Life Sciences [q-bio]/Toxicology
Metabolome
medicine.symptom
DNA, Bacterial
medicine.medical_specialty
P-CRESYL SULFATE
Renal function
Inflammation
Article
03 medical and health sciences
Insulin resistance
INFLAMMATION
Metabolic Diseases
Internal medicine
Glucose Intolerance
medicine
Animals
INDOXYL SULFATE
MODULATION
Renal Insufficiency, Chronic
Uremia
030304 developmental biology
business.industry
lcsh:R
medicine.disease
biology.organism_classification
Gastrointestinal Microbiome
Mice, Inbred C57BL
Transplantation
[SDV.AEN] Life Sciences [q-bio]/Food and Nutrition
Disease Models, Animal
UREMIC SOLUTE
business
[SDV.AEN]Life Sciences [q-bio]/Food and Nutrition
Biomarkers
chronic kidney disease
Kidney disease
Subjects
Details
- Language :
- English
- ISSN :
- 20726651
- Volume :
- 12
- Issue :
- 741
- Database :
- OpenAIRE
- Journal :
- Toxins
- Accession number :
- edsair.doi.dedup.....5011c905e5c232cea123d628728f8ec8
- Full Text :
- https://doi.org/10.3390/toxins12120741⟩