The nephroprotective effects of allicin and ascorbic acid against cisplatin-induced toxicity in rats

被引:56
作者
Abdel-Daim, Mohamed M. [1 ]
Abushouk, Abdelrahman Ibrahim [2 ]
Donia, Thoria [3 ]
Alarifi, Saud [4 ]
Alkahtani, Saad [4 ]
Aleya, Lotfi [5 ]
Bungau, Simona G. [6 ]
机构
[1] Suez Canal Univ, Fac Vet Med, Pharmacol Dept, Ismailia, Egypt
[2] Ain Shams Univ, Fac Med, Ramsis St, Cairo 11566, Egypt
[3] Tanta Univ, Fac Sci, Chem Dept, Tanta, Egypt
[4] King Saud Univ, Sci Coll, Dept Zool, Riyadh, Saudi Arabia
[5] Bourgogne Franche Comte Univ, CNRS, UMR 6249, Chronoenvironm Lab, F-25030 Besancon, France
[6] Univ Oradea, Fac Med & Pharm, Dept Pharm, Oradea, Romania
关键词
Allicin; Ascorbic acid; Cisplatin; Inflammation; Nephrotoxicity; Oxidative stress; INDUCED OXIDATIVE STRESS; INDUCED NEPHROTOXICITY; VITAMIN-C; LIPID-PEROXIDATION; GARLIC POWDER; RENAL INJURY; ANTIOXIDANT; DAMAGE; INFLAMMATION; PROTECTS;
D O I
10.1007/s11356-019-04780-4
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Cisplatin (CDDP) may induce nephrotoxicity through oxidative stress, DNA damage, and inflammation. This study was performed to evaluate the antioxidant and anti-inflammatory effects of allicin and ascorbic acid (AA) and investigate the nephroprotective efficacy of their combination against CDDP-induced intoxication. Rats were divided into seven groups: control, allicin (10mg/kg for 14days), AA (20mg/kg for 14days), CDDP (7mg/kg as a single dose on the seventh experimental day), CDDP-allicin, CDDP-AA, and CDDP-allicin-AA (at the aforementioned doses). The administration of CDDP induced marked body weight loss and renal damage, manifested by significant increases (p<0.05) in serum creatinine, urea, and uric acid levels and significant reductions in serum Na, Ca, and phosphorus concentrations, in addition to severe alterations in serum and renal tissue levels of tumor necrosis factor- in comparison with control rats. Moreover, CDDP-intoxicated rats exhibited significantly (p<0.05) higher lipid peroxidation, as well as lower levels of reduced glutathione and activities of glutathione peroxidase, superoxide dismutase, and catalase enzymes in the renal tissue, compared with control rats. The administration of allicin or AA significantly reduced (p<0.05) the CDDP-induced changes in all the aforementioned parameters. Interestingly, allicin achieved comparable nephroprotection to AA in most assessed parameters; however, the restoration of normal serum and renal tissue concentrations of these parameters was more frequent in the CDDP-AA group. In conclusion, both allicin and AA showed significant nephroprotective effects against CDDP intoxication and their combination exhibited better protection than either agent alone. These results are probably mediated by their antioxidant and anti-inflammatory activities.
引用
收藏
页码:13502 / 13509
页数:8
相关论文
共 54 条
  • [1] Influence of Spirulina platensis and ascorbic acid on amikacin-induced nephrotoxicity in rabbits
    Abdel-Daim, Mohamed M.
    Ahmed, Amira
    Ijaz, Hira
    Abushouk, Abdelrahman Ibrahim
    Ahmed, Hussien
    Negida, Ahmed
    Aleya, Lotfi
    Bungau, Simona G.
    [J]. ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH, 2019, 26 (08) : 8080 - 8086
  • [2] Allicin ameliorates doxorubicin-induced cardiotoxicity in rats via suppression of oxidative stress, inflammation and apoptosis
    Abdel-Daim, Mohamed M.
    Kilany, Omnia E.
    Khalifa, Hesham A.
    Ahmed, Amal A. M.
    [J]. CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2017, 80 (04) : 745 - 753
  • [3] Antagonistic activity of dietary allicin against deltamethrin-induced oxidative damage in freshwater Nile tilapia; Oreochromis niloticus
    Abdel-Daim, Mohamed M.
    Abdelkhalek, Nevien K. M.
    Hassan, Ahmed M.
    [J]. ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, 2015, 111 : 146 - 152
  • [4] AEBI H, 1984, METHOD ENZYMOL, V105, P121
  • [5] Alam R, 2018, OXID MED CELL LONGEV, V2018, P1, DOI DOI 10.1155/2018/1780956
  • [6] The ameliorative effect of cysteine prodrug L-2-oxothiazolidine-4-carboxylic acid on cisplatin-induced nephrotoxicity in rats
    Ali, B. H.
    Al Moundhri, M. S.
    Eldin, M. Tag
    Nemmar, A.
    Tanira, M. O.
    [J]. FUNDAMENTAL & CLINICAL PHARMACOLOGY, 2007, 21 (05) : 547 - 553
  • [7] Antunes LMG, 2000, PHARMACOL RES, V41, P405, DOI 10.1006/phrs.1999.0600
  • [8] Cisplatin nephrotoxicity
    Arany, I
    Safirstein, RL
    [J]. SEMINARS IN NEPHROLOGY, 2003, 23 (05) : 460 - 464
  • [9] Arunkumar P. A., 2012, Asian Pacific Journal of Tropical Biomedicine, V2, P640, DOI 10.1016/S2221-1691(12)60112-9
  • [10] Naringenin attenuates cisplatin nephrotoxicity in rats
    Badary, OA
    Abdel-Maksoud, S
    Ahmed, WA
    Owieda, GH
    [J]. LIFE SCIENCES, 2005, 76 (18) : 2125 - 2135