Taurine and hesperidin rescues carbon tetrachloride-triggered testicular and kidney damage in rat via modulating oxidative stress and inflammation.

This study assessed the prophylactic or therapeutic effects of taurine (TR) and/or hesperidin (HES) on carbon tetrachloride (CCl₄) induced acute kidney and testicular injury in rats.

Rats were randomly divided into nine experimental groups including control; corn oil; CCl₄; HES/CCl₄; TR/CCl₄; HES + TR/CCl₄; CCl₄/HES; CCl₄/TR; and CCl₄/HES + TR groups. CCl₄ was intraperitoneally injected with a single dose of 2 ml /kg b.w. HES and TR were orally gavaged twice weekly 100 mg/kg b.w. for four weeks. Kidney function, inflammatory response, sexual hormones, and oxidative stress indicators were assessed. Histomorphological and immune-histochemical studies of the inflammatory marker nuclear factor kappa (NF-κB) in renal and testicular tissues were performed.

The results showed that the TR and/or HES treatment significantly suppressed CCl₄ induced rise of urea, uric acid, potassium, and follicle-stimulating hormone levels. However, significant restoration of sodium, testosterone, and luteinizing hormone was apparent in CCl₄ exposed rats received HES and/or TR. Also, the HES and/or TR treatment significantly rescues CCl₄ induced oxidative stress and inflammation. Moreover, the HES and/or TR dosing significantly repaired the CCl₄ evoked altered renal and testicular architecture and suppressed NF-κB immunoexpression. Notably, alleviating CCl₄ induced renal and testicular damage was more effective in the prophylactic groups than the therapeutic groups. Also, most of the estimated parameters of the HES + TR group did not significantly vary from those of single TR or HES.

In conclusion, HES or TR could efficiently guard against CCl₄ nephro-and reprotoxic effects, but both bioactive combinations afford only a limited synergistic outcome.