Key result
Exendin-4 significantly attenuated tubular injury and interstitial fibrosis in a mouse model of unilateral ureteral obstruction by regulating the intrarenal renin-angiotensin system.
Why the study?
Does exendin-4 prevent interstitial fibrosis and regulate the intrarenal renin-angiotensin system in a mouse model of unilateral ureteral obstruction?
Does exendin-4 prevent interstitial fibrosis and regulate the intrarenal renin-angiotensin system in a mouse model of unilateral ureteral obstruction?
Exendin-4 attenuates interstitial fibrosis in a mouse model of unilateral ureteral obstruction by regulating the balance of the intrarenal renin-angiotensin system and inhibiting the Ang II-mediated TGF-β1/Smad3 signaling pathway.
Answers are grounded in this paper and cite their sources.
Hypothesis-generating in obstructive nephropathy models; leaves open translation of intrarenal RAS modulation to human CKD.
OBJECTIVE: The objective of this article is to investigate the renoprotecive effects of exendin-4 in a mouse model of unilateral ureteral obstruction (UUO) and explore the putative mechanisms. METHODS: Male Balbc mice underwent sham operation or UUO surgery, and then received intraperitoneal injection of vehicle or exendin-4, respectively. After 14 days, mice were sacrificed and the left kidneys were collected and analyzed by histology, immunohistochemistry, Western blot, quantitative real-time reverse transcription polymerase chain reaction, radioimmunoassay and enzyme-linked immunosorbent assay. RESULTS: As compared to the sham group, mice that underwent UUO surgery developed more severe tubular injury and interstitial fibrosis, as well as higher expression of fibronectin (FN), collagen-1 (Col-1) and α-smooth muscle actin (α-SMA). Also, we observed higher expression of angiotensin-converting enzyme (ACE) while lower expression of angiotensin-converting enzyme 2 (ACE2), higher levels of intrarenal angiotensin II (Ang II) while lower levels of intrarenal angiotensin-(1-7), and higher expression of transforming growth factor β1 (TGF-β1) and phosphorylation of Smad3 (p-Smad3) in the obstructed kidneys. Impressively, these pathologic changes were significantly attenuated in the mice group of UUO treated with exendin-4. CONCLUSION: Our present study indicates for the first time that exendin-4 exerts renoprotective effects in an experimental model of UUO, partly through regulating the balance of the intrarenal renin-angiotensin system and then inhibiting the Ang II-mediated TGF-β1/Smad3 signaling pathway.
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Ying et al. (2016) studied Unilateral ureteral obstruction (UUO) / Chronic kidney disease (n=26). Exendin-4 vs. Vehicle was evaluated on Tubular injury, interstitial fibrosis, and expression of intrarenal renin-angiotensin system components (p=<0.05). Exendin-4 significantly attenuated tubular injury and interstitial fibrosis in a mouse model of unilateral ureteral obstruction by regulating the intrarenal renin-angiotensin system.
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