<abstract xmlns="http://www.w3.org/1999/xhtml"><sec id="j_1905-7415.1005.507_s_001_w2aab3b7b3b1b6b1aab1c17b1Aa"><h3>Background</h3><p>Biomarkers for the early diagnosis of chronic kidney disease (CKD) will lead to its better management. Rodent models will be helpful for biomarker discovery. Urinary exosomes, membrane bound vesicles, may contain interesting biomarkers.</p></sec><sec id="j_1905-7415.1005.507_s_002_w2aab3b7b3b1b6b1aab1c17b2Aa"><h3>Objective</h3><p>To produce a mouse model of CKD with sufficient urine volume for exosome studies.</p></sec><sec id="j_1905-7415.1005.507_s_003_w2aab3b7b3b1b6b1aab1c17b3Aa"><h3>Methods</h3><p>We characterized a mouse models of CKD induced by 55 min ischemia–reperfusion injury and contralateral nephrectomy at 1 wk after the chronic ischemia–reperfusion injury (Chr IR) in 7 mice and other 7 sham-operated control mice. We collected 24 h urine for urine exosome extraction.</p></sec><sec id="j_1905-7415.1005.507_s_004_w2aab3b7b3b1b6b1aab1c17b4Aa"><h3>Results</h3><p>Blood urea nitrogen, serum creatinine, and proteinuria increased as early as 2 wk, and reciprocally lower hematocrit. The renal injury, proteinuria, and anemia persisted 12 wk after nephrectomy as consistent with uremic symptoms. The mouse model of CKD showed renal histopathology of interstitial fibrosis with mild glomerular injury, and failure to grow. At 12 wk, the volume of urine collected in 24 h was sufficient for exosome extraction. Urinary exosomes were demonstrated by western blots showing tumor susceptibility gene 101 protein.</p></sec><sec id="j_1905-7415.1005.507_s_005_w2aab3b7b3b1b6b1aab1c17b5Aa"><h3>Conclusions</h3><p>Mice with renal injury induced by Chr IR showed renal injury and proteinuria as early as 2 wk
with uremic symptoms and tubulointerstitial fibrosis. Most importantly, the 24 h volume of urine at 12 wk was sufficient for exosome extraction.</p></sec></abstract>

BackgroundBiomarkers for the early diagnosis of chronic kidney disease (CKD) will lead to its better management. Rodent models will be helpful for biomarker discovery. Urinary exosomes, membrane bound vesicles, may contain interesting biomarkers.ObjectiveTo produce a mouse model of CKD with sufficient urine volume for exosome studies.MethodsWe characterized a mouse models of CKD induced by 55 min ischemia–reperfusion injury and contralateral nephrectomy at 1 wk after the chronic ischemia–reperfusion injury (Chr IR) in 7 mice and other 7 sham-operated control mice. We collected 24 h urine for urine exosome extraction.ResultsBlood urea nitrogen, serum creatinine, and proteinuria increased as early as 2 wk, and reciprocally lower hematocrit. The renal injury, proteinuria, and anemia persisted 12 wk after nephrectomy as consistent with uremic symptoms. The mouse model of CKD showed renal histopathology of interstitial fibrosis with mild glomerular injury, and failure to grow. At 12 wk, the volume of urine collected in 24 h was sufficient for exosome extraction. Urinary exosomes were demonstrated by western blots showing tumor susceptibility gene 101 protein.ConclusionsMice with renal injury induced by Chr IR showed renal injury and proteinuria as early as 2 wk
with uremic symptoms and tubulointerstitial fibrosis. Most importantly, the 24 h volume of urine at 12 wk was sufficient for exosome extraction.

Urinary exosomes from a mouse model of chronic tubulointerstitial kidney disease induced by chronic renal ischemia–reperfusion injury and nephrectomy

Chulalongkorn University, and King Chulalongkorn Memorial Hospital

Asian Biomedicine

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

BackgroundBiomarkers for the early diagnosis of chronic kidney disease (CKD) will lead to its better management. Rodent models will be helpful for biomarker...

Urinary exosomes from a mouse model of chronic tubulointerstitial kidney disease induced by chronic renal ischemia–reperfusion injury and nephrectomy

Article Category: Brief communication (Original)

Publicado en línea: 31 mar 2017

Páginas: 447 - 454

DOI: https://doi.org/10.5372/1905-7415.1005.507

Palabras clave
Chronic ischemic reperfusion injury, chronic kidney disease, mouse model, urinary exosome

© 2016 Asada Leelahavanichkul, Wiwat Chancharoenthana, Somchai Eiam-Ong

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Urinary exosomes from a mouse model of chronic tubulointerstitial kidney disease induced by chronic renal ischemia–reperfusion injury and nephrectomy

Article Category: Brief communication (Original)

Publicado en línea: 31 mar 2017

Páginas: 447 - 454

DOI: https://doi.org/10.5372/1905-7415.1005.507

Palabras claveChronic ischemic reperfusion injury, chronic kidney disease, mouse model, urinary exosome

© 2016 Asada Leelahavanichkul, Wiwat Chancharoenthana, Somchai Eiam-Ong

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Palabras clave
Chronic ischemic reperfusion injury, chronic kidney disease, mouse model, urinary exosome