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Journal of physiology and pharmacology : an official journal of the Polish Physiological Society · 2026

Stable pentadecapeptide therapy counteracts gentamicin-induced nephrotoxicity via nitric oxide-system modulation: evidence from a triple nitric oxide-agent approach in rats.

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Vukoja I, Vlainic J, Francina M, Barisic I, Zukanovic G, Miskulin I, Kralj L, Popovic Dolic M, Dulcic D, Tubikanec A M, Sikiric S, Krezic I, Kordic M, Beketic Oreskovic L, Oreskovic I, Strbe S, Staresinic B, Pavelic Turudic T, Perovic D, Bilic V, Stancic Rokotov D, Boban Blagaic A, Seiwerth S, Sikiric P, Skrtic A

Аннотация

In rats, stable gastric pentadecapeptide (BPC 157) therapy may resolve severe gentamicin nephrotoxicity (100 mg/kg ip/daily through 8 days) and the nitric oxide (NO)-system relation. We applied BPC 157 (10 µg/kg, 10 ng/kg, in drinking water or daily intraperitoneally) along with a triple NO-agent approach. Triple NO-agent approach captures NO-system, as a whole, simultaneously the inhibition (N(G)-nitro-L-arginine methylester (L-NAME) 5 mg/kg ip/daily), the overstimulation (L-arginine, 100 mg/kg ip/daily), and the immobilization (L-NAME + L-arginine/daily). BPC 157 therapy counteracted gentamicin nephrotoxicity clinical presentation (i.e., close to normal), serum urea, and creatinine (i.e., values close to normal preserved), maintained diuresis (polyuria/oliguria completely avoided), and no renal mass increase. Finally, fully preserved normal tubular epithelium cells and nephron presentation were present in the microscopy. Counteracted were in kidney gentamicin-increased malondialdehyde (MDA)-levels, and gentamicin-decreased NO-, and superoxide dismutase (SOD)-levels. NO-agents exhibited the opposite (worsening/attenuation) relations: L-arginine (a further increase of urea and creatinine serum values, polyuria, oliguria) vs. L-NAME relations (decrease of the increased urea and creatinine serum values, delayed polyuria, avoided oliguria, less tubular necrosis). These opposite points, combined (L-NAME + L-arginine), resulted in even stronger lesions, and more pronounced oliguria occurred, indicating the annihilation of the beneficial effect of L-NAME when it was combined with L-arginine. BPC 157 regimens (peroral or intraperitoneal) overwhelmed these NO-agents' effects. Thereby, in general, a triple NO-agent approach can reveal all essential gentamicin points of the NO-system (attenuation (L-NAME)/worsening (L-arginine)), revealing the full spectrum of the NO-system functions. Combined with the BPC 157 application, the triple NO-agent approach shows BPC 157's full efficacy in maintaining and/or reestablishing NO-system effects and functions, and kidney integrity in the gentamicin-rats.

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