Paradoxical Effect of Grape Pomace Extract on Cisplatin-Induced Acute Kidney Injury in Rats

被引:6
|
作者
Neag, Maria Adriana [1 ]
Mitre, Calin Iosif [2 ]
Mitre, Andrei Otto [3 ]
Morhan, Vlad [3 ]
Catinean, Adrian [4 ]
Botan, Emil Claudiu [5 ]
Melincovici, Carmen Stanca [6 ]
Muntean, Dana Maria [7 ]
Buzoianu, Anca Dana [1 ]
机构
[1] Iuliu Hatieganu Univ Med & Pharm, Pharmacol Toxicol & Clin Pharmacol Dept, 23 Marinescu St, Cluj Napoca 400337, Romania
[2] Iuliu Hatieganu Univ Med & Pharm, Dept Anaesthesiol & Intens Care, 19-21 Croitorilor St, Cluj Napoca 400162, Romania
[3] Iuliu Hatieganu Univ Med & Pharm, Fac Med, 8 Babes St, Cluj Napoca 400012, Romania
[4] Iuliu Hatieganu Univ Med & Pharm, Dept Internal Med, 3-5 Clinicilor St, Cluj Napoca 400006, Romania
[5] Cty Emergency Hosp Cluj Napoca, 3-5 Clinicilor St, Cluj Napoca 400006, Romania
[6] Iuliu Hatieganu Univ Med & Pharm, Histol Dept, 4-6 Pasteur St, Cluj Napoca 400349, Romania
[7] Iuliu Hatieganu Univ Med & Pharm, Dept Pharmaceut Technol & Biopharmaceut, 12 Ion Creanga St, Cluj Napoca 400010, Romania
关键词
cisplatin; grape extract; resveratrol; nephrotoxicity; COPPER TRANSPORTER CTR1; INDUCED NEPHROTOXICITY; MITOCHONDRIAL-MEMBRANE; OXIDATIVE STRESS; SEED EXTRACT; RENAL INJURY; RED WINE; ANTIOXIDANT; RESVERATROL; CHEMOTHERAPY;
D O I
10.3390/pharmaceutics11120656
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cisplatin is one of the most used drugs in the therapy of different types of cancer. However, its use is limited by nephrotoxicity. This study investigated the effects of a commercially available grape pomace extract (GE) from Vitis vinifera on cisplatin-induced kidney toxicity in rats. Sixty-four male Wistar albino rats were randomly divided into eight groups. Groups 1-3 were controls, receiving 0.9% saline and doses 1 and 2 of GE respectively. Cisplatin was given to groups 4-8. Two groups received pretreatment with GE, while another two groups received pre- and post-treatment with GE. Blood samples were collected and all animals sacrificed. Kidneys were harvested for histopathological analysis. GE significantly increased blood creatinine and urea levels, the severity of kidney histopathological damage, and mortality in all cisplatin groups, except for group 7 which received pre- and post-treatment with a low dose of GE. Renal toxicity was determined by mortality and severe histopathological renal lesions. Additionally, the serum total antioxidant capacity (TAC) was not significantly modified in the treated groups compared to the control. These results indicate that the GE did not have a protective effect on cisplatin-induced nephrotoxicity; on the contrary, GE accentuated the toxic effect of cisplatin.
引用
收藏
页数:12
相关论文
共 50 条
  • [41] Protopanaxadiol prevents cisplatin-induced acute kidney injury by regulating ferroptosis
    Song, Zeyu
    Li, Zhenyuan
    Pan, Tao
    Liu, Teng
    Gong, Baifang
    Wang, Zhixia
    Liu, Ke
    Fan, Huaying
    JOURNAL OF PHARMACY AND PHARMACOLOGY, 2024, 76 (07) : 884 - 896
  • [42] Inhibiting glucosylceramide synthase exacerbates cisplatin-induced acute kidney injury
    Dupre, Tess V.
    Doll, Mark A.
    Shah, Parag P.
    Sharp, Cierra N.
    Siow, Deanna
    Megyesi, Judit
    Shayman, James
    Bielawska, Alicja
    Bielawski, Jacek
    Beverly, Levi J.
    Hernandez-Corbacho, Maria
    Clarke, Christopher J.
    Snider, Ashley J.
    Schnellmann, Rick G.
    Obeid, Lina M.
    Hannun, Yusuf A.
    Siskind, Leah J.
    JOURNAL OF LIPID RESEARCH, 2017, 58 (07) : 1439 - 1452
  • [43] Changes in zinc and manganese concentrations in cisplatin-induced acute kidney injury
    Yamamoto, Yuko
    Hotta, Yuji
    Tomita, Natsumi
    Naiki-Ito, Aya
    Kitagawa, Ayae
    Kuboshiki, Urara
    Hagita, Tamaki
    Noda, Misuzu
    Sanagawa, Akimasa
    Kataoka, Tomoya
    Kondo, Masahiro
    Furukawa-Hibi, Yoko
    Takahashi, Satoru
    Kimura, Kazunori
    BIOCHEMISTRY AND BIOPHYSICS REPORTS, 2023, 33
  • [44] The Nephroprotective Effects of α-Bisabolol in Cisplatin-Induced Acute Kidney Injury in Mice
    Zaaba, Nur Elena
    Beegam, Sumaya
    Elzaki, Ozaz
    Yasin, Javed
    Nemmar, Bilal Mohamed
    Ali, Badreldin H.
    Adeghate, Ernest
    Nemmar, Abderrahim
    BIOMEDICINES, 2022, 10 (04)
  • [45] Crucial roles of asprosin in cisplatin-induced ferroptosis and acute kidney injury
    Zheng, Fen
    Lei, Jian-Zhen
    Wang, Jing-Xiao
    Xu, Xiao-Yu
    Zhou, Bing
    Ge, Rui
    Dai, Min
    Dong, Hong-Ke
    Wu, Nan
    Li, Yue-Hua
    Zhu, Guo-Qing
    Zhou, Ye-Bo
    FREE RADICAL BIOLOGY AND MEDICINE, 2025, 227 : 296 - 311
  • [46] HYDROGEN SULFIDE AMELIORATES CISPLATIN-INDUCED ACUTE KIDNEY INJURY IN MICE
    Park, Dong Jun
    Cho, Hyun Seop
    Kim, Jin Hyun
    Jung, Myeong Hee
    Chang, Se-Ho
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2015, 30
  • [47] Prospective analysis of the risk factors for cisplatin-induced acute kidney injury
    Tsunoda, A.
    Oda, H.
    Mizuno, T.
    Yamashita, Y.
    Tamaru, S.
    Saito, K.
    Ishihara, M.
    Nishimura, Y.
    Nakatani, K.
    Katayama, N.
    ANNALS OF ONCOLOGY, 2017, 28
  • [48] CXCL16 regulates cisplatin-induced acute kidney injury
    Liang, Hua
    Zhang, Zhengmao
    He, Liqun
    Wang, Yanlin
    ONCOTARGET, 2016, 7 (22) : 31652 - 31662
  • [49] Antihypertensive Drug Combinations Modify Cisplatin-induced Acute Kidney Injury
    Takeuchi, Koji
    Sogawa, Rintaro
    Tsuruhashi, Satoko
    Motooka, Chika
    Kimura, Sakiko
    Shimanoe, Chisato
    IN VIVO, 2022, 36 (03): : 1391 - 1396
  • [50] ROLE OF METHIONINE SULFOXIDE REDUCTASE A ON CISPLATIN-INDUCED ACUTE KIDNEY INJURY
    Noh, Mi Ra
    Kim, Jee In
    Park, Kwon Moo
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2017, 32