4.7 Article

Stenocereus huastecorum-fruit juice concentrate protects against cisplatin-induced nephrotoxicity by nitric oxide pathway activity and antioxidant and antiapoptotic effects

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FOOD RESEARCH INTERNATIONAL
卷 160, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.foodres.2022.111337

关键词

Renal dysfunction; Cisplatin; Nitric oxide; Pitaya; Stenocereus huastecorum; Cisplatin-induced nephrotoxicity

资金

  1. CONACyT [637582, 767356, 632340, FORDECYT 296354, FORDECYT-PRONACES 101732, DFG 2016/277850, FORDECYT-292399]

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This study aimed to investigate the effect of pitaya juice concentrate (PJC) on cisplatin-induced nephrotoxicity. The results showed that PJC had a renoprotective effect by attenuating renal dysfunction, structural damage, apoptosis activation, and oxidative stress, and it was related to changes in the tumor necrosis factor-alpha and renal nitric oxide pathways.
Cisplatin (CP) is an antineoplastic agent used to treat solid tumors, that has high nephrotoxicity caused by physiologic, hemodynamic, and biochemical alterations. Some studies have shown that naturally derived bioactive compounds in CP-induced nephrotoxicity reduce the side effects of this antineoplastic drug. Pitaya is an endemic fruit from Mexico with a high bioactive compound content, including betalains and phenolic com-pounds, with reports of antioxidant and anti-inflammatory properties. In this study, the aim was to establish the effect of a pitaya juice concentrate (PJC) on CP-induced nephrotoxicity in Wistar male rats through the iden-tification of metabolites, determination of its chemical composition and antioxidant activity, and evaluation of the protective effect of a PJC on CP-induced nephrotoxicity in rats. The PJC showed a high content of betanins with antioxidant activity by an oxygen radical absorbance capacity assay (1299.6 +/- 2.80 Trolox equivalents/g). PJC was administered daily (400 mg day-1, p. o.) for 3 days before CP administration until the end of the experiment. On day four, rats were administered a single injection of CP (6 mg kg, i.p.-1) and sacrificed 72 h later. We observed that CP provoked renal dysfunction (1.0 +/- 0.1 vs. 0.4 +/- 0.07 serum creatinine levels), oxidative stress, a decrease in nitrate and nitrite over line over line 2/NO3) levels (0.1 +/- 0.08 vs. 0.4 +/- 0.3) and activation of apoptosis stress, a decrease in nitrate and nitrite (NO and immune responses in kidney tissue. In addition, CP treatment induced tubular damage threefold. PJC administration prevented renal dysfunction (0.5 +/- 0.06 vs. 1.0 +/- 0.1), normalized degenerative structural damage prevented the increase in lipoperoxidation levels (0.04 +/- 0.01 vs. 0.2 +/- 0.1) and reduced the apoptosis index by 2.5 in kidney tissue. However, it did not modify the immune response caused by CP. Furthermore, PJC treatment increased nuclear factor erythroid two related factors two protein levels two times and NO2/NO3 22 times in kidney tissue, which may play a role in the renoprotective effect. In conclusion, the renoprotective effect of PJC on CP-induced nephrotoxicity was associated with the attenuation of dysfunction, structural damage, apoptosis activation, and oxidative stress and was related to changes in the tumor necrosis factor-alpha and renal nitric oxide (NO) pathways. The changes in the NO pathway may be involved in renal hemodynamics. Pitaya could be used as a functional food and therapeutic coadjuvant during CP treatments due to its high bioactive levels and renoprotective compounds. over line levels

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