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10.1016/j.soard.2017.03.014

http://scihub22266oqcxt.onion/10.1016/j.soard.2017.03.014
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suck abstract from ncbi


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pmid28552742
      Surg+Obes+Relat+Dis 2017 ; 13 (7 ): 1152-1157
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  • Oxalobacter formigenes colonization normalizes oxalate excretion in a gastric bypass model of hyperoxaluria #MMPMID28552742
  • Canales BK ; Hatch M
  • Surg Obes Relat Dis 2017[Jul]; 13 (7 ): 1152-1157 PMID28552742 show ga
  • BACKGROUND: Hyperoxaluria and oxalate kidney stones frequently develop after Roux-en-Y gastric bypass (RYGB). Oxalobacter formigenes can degrade ingested oxalate. OBJECTIVES: Examine the effect of O. formigenes wild rat strain (OXWR) colonization on urinary oxalate excretion and intestinal oxalate transport in a hyperoxaluric RYGB model. SETTING: Basic Science Laboratory, United States. METHODS: At 21 weeks of age, 28 obese male Sprague-Dawley rats survived Sham (n = 10) or RYGB (n = 18) surgery and were maintained on a 1.5% potassium oxalate, 40% fat diet. At 12 weeks postoperatively, half the animals in each group were gavaged with OXWR. At 16 weeks, percent dietary fat content was lowered to 10%. Urine and stool were collected weekly to determine oxalate and colonization status, respectively. At week 20, [14 C]-oxalate fluxes and electrical parameters were measured in vitro across isolated distal colon and jejunal (Roux limb) tissue mounted in Ussing Chambers. RESULTS: RYGB animals lost 22% total weight while Shams gained 5%. On a moderate oxalate diet, urinary oxalate excretion was 4-fold higher in RYGB than Sham controls. OXWR colonization, obtained in all gavaged animals, reduced urinary oxalate excretion 74% in RYGB and 39% in Sham and was further augmented by lowering the percentage of dietary fat. Finally, OXWR colonization significantly enhanced basal net colonic oxalate secretion in both groups. CONCLUSIONS: In our model, OXWR lowered urinary oxalate by luminal oxalate degradation in concert with promotion of enteric oxalate elimination. Trials of O. formigenes colonization and low-fat diet are warranted in calcium oxalate stone formers with gastric bypass and resistant hyperoxaluria.
  • |*Gastric Bypass [MESH]
  • |Animals [MESH]
  • |Creatinine/urine [MESH]
  • |Disease Models, Animal [MESH]
  • |Eating [MESH]
  • |Feces/microbiology [MESH]
  • |Hyperoxaluria/*microbiology [MESH]
  • |Male [MESH]
  • |Obesity, Morbid/*surgery [MESH]
  • |Oxalates/*urine [MESH]
  • |Oxalobacter formigenes/*physiology [MESH]
  • |Random Allocation [MESH]
  • |Rats, Sprague-Dawley [MESH]


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