Key result
High-dose estrogen improves renal and lung damage after ischemia-reperfusion in rats by reducing oxidative stress.
Why the study?
Renal ischemia-reperfusion injury induces remote lung complications in a hormone-dependent manner, prompting investigation into the effect of estrogen on RIR-induced pulmonary injury in ovariectomized rats.
Does estradiol valerate improve renal ischemia-reperfusion-induced pulmonary injury in ovariectomized female rats?
Does estradiol valerate improve renal ischemia-reperfusion-induced pulmonary injury in ovariectomized female rats?
Estrogen acts as an antioxidant to reduce oxidative stress and ameliorate remote lung injury caused by renal ischemia-reperfusion in ovariectomized rats.
Estrogen may attenuate remote lung injury in experimental renal ischemia-reperfusion; leaves open clinical translation in humans.
Renal ischemia-reperfusion injury (RIRI) as a pathological process induces remote organ injury such as lung complications and it is regulated in a hormone-dependent manner. This study investigates the effect of estrogen on RIR-induced pulmonary injury in ovariectomized (OV) rats. A total of 60 female Wistar rats were divided into six groups: (i) intact sham, (ii) OV sham, (iii) OV sham + estradiol valerate (E), (iv) intact ischemia, (v) OV ischemia, and (vi) OV ischemia + E. Bilateral ischemia was performed for 45 min in all groups except sham. Before the ischemia, OV groups received an intramuscular (i.m.) injection of E. After reperfusion, blood samples were collected for serum analysis and kidney and lung tissue were separated for pathological experiment and malondialdehyde (MDA) and nitrite measurement. The left lung was weighed to measure pulmonary edema. Estrogen deficiency caused a greater increase in blood urea nitrogen and creatinine levels during IRI. Ischemia reduced nitrite of serum and lung tissue. The increased level of MDA during ischemia, returned to normal levels via estrogen injection. The severity of renal and lung damage in ischemic groups increased significantly, and estrogen improved this injury. Estrogen as an antioxidant agent can reduce oxidative stress and may improve renal function and ameliorating lung damage caused by RIR.
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Nahavandi et al. (2021) studied Renal ischemia-reperfusion-induced pulmonary injury (n=60). Estradiol valerate (estrogen) vs. Sham and ischemia groups without estrogen was evaluated on Renal and lung damage, oxidative stress markers (MDA, nitrite), and renal function (BUN, creatinine). High-dose estrogen administration in ovariectomized female rats reduced oxidative stress and significantly improved renal function and lung damage caused by renal ischemia-reperfusion injury.
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