Novel Therapeutic Approaches of Sildenafil Against Rhabdomyolysis-Associated Acute Kidney Injury | ||||
| Journal of Advanced Pharmacy Research | ||||
| Article 5, Volume 6, Issue 3, July 2022, Page 144-154 PDF (908.03 K) | ||||
| Document Type: Research Article | ||||
| DOI: 10.21608/aprh.2022.136558.1174 | ||||
 View on SCiNiTO | ||||
| Authors | ||||
Ghada Samy El-Tanbouly   ; Rania Khalil
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| Department of Pharmacology, Faculty of Pharmacy, Delta University for Science and Technology, Gamasa 11152, Egypt | ||||
| Abstract | ||||
| Objectives: Rhabdomyolysis-associated acute kidney injury (AKI) is a manifestation frequently observed in many cases. Sildenafil (Sild) is a phosphodiesterase-5 inhibitor selected in this study for its experimental protective effects in muscle and kidney injury experimental models. The current study aimed to hypothesize that Sild had a renoprotective effect through the anti-oxidant, anti-inflammatory, and anti-apoptotic mechanisms in glycerol (Gly)-induced rhabdomyolysis rat model. Methods: Male Sprague Dawley rats were allocated into four groups: control group (saline, i.p); Sild control group (5 mg/kg, orally); glycerol (Gly) group (50%, 10 ml/kg, i.m.); prophylactic Sild plus glycerol group (5 mg/kg, orally, 1 hr before glycerol). All treatments were applied as a single dose. Blood samples and renal tissues were collected 24 hr following glycerol injection. Results: Gly produced renal morphological changes, muscle, and renal dysfunction, in addition to increased mortality rates, oxidative stress, renal inflammatory responses, and renal apoptosis. Sild reduced muscle/kidney function disturbances (serum total CK, CK-MB, creatinine, BUN, in addition to urinary creatinine levels), reduced oxidative stress in renal tissue, increased antioxidant defense (TAC, SOD, NRF-2/HO-1), decreased mortality rates, and accelerated renal histological recovery. Additionally, inflammatory mediator levels of TNF-α, NF-κB, and COX-2 were suppressed. Moreover, the study revealed new insights into protection from rhabdomyolysis-associated AKI, through reduction of renal apoptosis by decreasing levels of BAX and increasing levels of BCL-2. Conclusions: Sild protected against rhabdomyolysis-linked renal morphological damage, renal and muscle function disturbances, by decreasing renal oxidative stress, inflammation, and apoptosis. Therefore, Sild proved its muscle/reno-protective impacts, and possibly can be used as a new therapeutic approach for acute muscle and kidney injuries, which represents a new benefit for a common and widely used medication. | ||||
| Keywords | ||||
| Sildenafil; Rhabdomyolysis; BCL-2; BAX; NRF-2/HO-1 | ||||
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