Key result
Alprostadil significantly reduced inflammation and necrosis compared to vehicle in a rat model of renal ischemia and reperfusion injury (p=0.025).
Why the study?
Does alprostadil reduce inflammatory aspects and tissue injury in a rat model of renal ischemia and reperfusion injury?
RCT
randomized
Does alprostadil reduce inflammatory aspects and tissue injury in a rat model of renal ischemia and reperfusion injury?
In a rat model of renal ischemia-reperfusion injury, intravenous alprostadil administered immediately before reperfusion significantly attenuated histological inflammation, necrosis, and CPK levels.
Answers are grounded in this paper and cite their sources.
Alprostadil attenuates renal IRI in rats; hypothesis-generating and requires clinical trials before any human application.
PURPOSE: To evaluate the effects of alprostadil in an experimental model of ischemia and reperfusion injury (IRI) in rat renal tissue. METHODS: Adult male Wistar rats were randomized into three groups Vehicle-treated group(Veh), Alprostadil-treated(Al), and sham(Sh) group. Veh and Al groups had suprarenal aorta occluded for 30 minutes and reperfused for 60 minutes. Saline or 20 µg/kg of Alprostadil was intravenously infused immediately before declamping. Sh group animals underwent similar procedure without aortic occlusion. Left nephrectomy and blood sampling were performed after 60 minutes of reperfusion. Renal ICAM-1 expression and histological analysis were performed to estimate inflammatory response and tissue disarrangement. Serum biochemical markers for IRI were also measured. Kruskal-Wallis test was used to assess differences between the groups. RESULTS: There was lower expression of ICAM-1 in groups Veh and Sh. On histologically evaluation, inflammation and necrosis in the Veh group was significantly higher (grades III/IV) than Al group (Veh>Al=Sh; p = 0.025), as well as CPK levels (Veh>Al=Sh; p = 0.03). CONCLUSION: Alprostadil attenuates the immunohistochemical and histological repercussions in the renal tissue of rats submitted to a post-ischemic reperfusion with supra-renal aortic clamping.
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Freitas et al. (2014) conducted an RCT in renal ischemia and reperfusion injury. Alprostadil vs. Vehicle (saline) and sham was evaluated on inflammation and necrosis on histological evaluation (p=0.025). Alprostadil significantly reduced inflammation and necrosis compared to vehicle in a rat model of renal ischemia and reperfusion injury (p=0.025).
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