2011
DOI: 10.1002/nau.20855
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Unilateral ureteral obstruction evokes renal tubular apoptosis via the enhanced oxidative stress and endoplasmic reticulum stress in the rat

Abstract: Our data suggest that renal tubular apoptosis induced by oxidative stress and ER stress occurred in the UUO kidney.

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Cited by 54 publications
(47 citation statements)
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“…It was also consistent with other studies. 46,51,62,63 We might draw a stable conclusion that the increased expression of PAX2 was associated with cell apoptosis, especially with RTEC apoptosis, but the decreased expression of PAX2 did not take part in the progression of RIF. However, the exact mechanism is complicated and not well elucidated at the moment and more studies are needed in the future.…”
Section: Mrna Expression Of Pax2mentioning
confidence: 97%
See 1 more Smart Citation
“…It was also consistent with other studies. 46,51,62,63 We might draw a stable conclusion that the increased expression of PAX2 was associated with cell apoptosis, especially with RTEC apoptosis, but the decreased expression of PAX2 did not take part in the progression of RIF. However, the exact mechanism is complicated and not well elucidated at the moment and more studies are needed in the future.…”
Section: Mrna Expression Of Pax2mentioning
confidence: 97%
“…We speculated that the mechanism was as follows: The generation of ROS was increased in the renal tissue of UUO rats. 51,52 The increased ROS might upregulate the gene expression of PAX2, 49,50 which regulated the expression of TGF-β1. 53,54 The disorder of TGF-β1 might induce the expressions of α-SMA, Col-IV, and FN, [21][22][23] and the increased TGF-β1 upregulated the expression of caspase-3.…”
Section: Mrna Expression Of Pax2mentioning
confidence: 99%
“…Increased hydrostatic pressure causes damage to the tubulointerstitial compartment of the kidney. 3 Apoptosis in tubular cells, capillary rarefaction, and interstitial cell inflammatory infiltration can be observed. The ensuing progressive fibrosis results in loss of parenchyma.…”
Section: Introductionmentioning
confidence: 99%
“…4) and are regulated by NFE2L2, which is activated upon exposure to ROS to effect transcriptional changes in response to oxidative stress (21). Oxidative stress has been implicated in the pathogenesis of UPJO and animal models previously (22)(23)(24). A total of 24 statistically significant proteins were associated with oxidative stress, of which 13 are represented in the putative biomarker panel (Table III).…”
Section: Discussionmentioning
confidence: 99%