Key result
Nebivolol protected rats against cisplatin-induced nephrotoxicity, significantly reducing serum creatinine, urea, and markers of oxidative stress and inflammation compared to untreated rats.
Why the study?
Does nebivolol prevent cisplatin-induced nephrotoxicity in Wistar rats?
Does nebivolol prevent cisplatin-induced nephrotoxicity in Wistar rats?
Nebivolol protects against cisplatin-induced nephrotoxicity in rats through antioxidant, anti-inflammatory, and antiapoptotic effects.
Nebivolol attenuates cisplatin nephrotoxicity in rats; hypothesis-generating and should not change clinical practice.
Treatment with cisplatin is associated with dose-limiting side effects, mainly nephrotoxicity. On the other hand, nebivolol, a β1 -adrenoceptor antagonist, exhibits vasodilatory and antioxidative properties. This study aimed to determine whether nebivolol possesses a protective effect against cisplatin nephrotoxicity and explore many mechanisms underlying this potential effect. Nephrotoxicity was induced in Wistar rats by a single intraperitoneal injection of cisplatin (6 mg/kg) on day 2. Nebivolol (10 mg/kg) was administered orally for 7 consecutive days. Nebivolol showed a nephroprotective effect as demonstrated by the significant reduction in the elevated levels of serum creatinine and urea as well as renal levels of malondialdehyde, nitric oxide products (nitrite/nitrate), inducible nitric oxide synthase, tumour necrosis factor-alpha, caspase-3, angiotensin II and endothelin-1 with a concurrent increase in renal levels of reduced glutathione and endothelial nitric oxide synthase compared to untreated rats. Histopathological examination confirmed the nephroprotective effect of nebivolol. Pre-treatment with Nω -nitro-L-arginine methyl ester, the non-specific nitric oxide synthase inhibitor, partially altered the protection afforded by nebivolol. In conclusion, nebivolol protects rats against cisplatin-induced nephrotoxicity that is most likely through its antioxidant, anti-inflammatory and antiapoptotic effects as well as by abrogation of the augmented angiotensin II and endothelin-1 levels.
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Morsy et al. (2015) studied Cisplatin-induced nephrotoxicity. Nebivolol vs. untreated rats was evaluated on Nephrotoxicity (serum creatinine, urea, and renal markers). Nebivolol protected rats against cisplatin-induced nephrotoxicity, significantly reducing serum creatinine, urea, and markers of oxidative stress and inflammation compared to untreated rats.
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