Karakoc Habib T E, Altintas Ramazan, Parlakpinar Hakan, Polat Alaaddin, Samdanci Emine, Sagir Mustafa, Duran Zeynep R
Student, Medical Faculty, Inonu University, Malatya, Turkey.
Department of Urology, Medical Faculty, Inonu University, Malatya, Turkey.
Adv Clin Exp Med. 2015 Jul-Aug;24(4):585-93. doi: 10.17219/acem/47742.
Cisplatin, an effective chemotherapeutic agent, is used for the treatment of several types of cancers. However, cisplatin has some severe side effects such as nephrotoxicity. On the other hand, molsidomine, a NO donor, has anti-oxidative and vasodilator effects.
The aim of this study was to estimate the protective effects of molsidomine on cisplatin-induced nephrotoxicity.
Thirty-two rats were randomly divided into 4 groups as follows: (1) control; (2) received a single-dose intraperitoneal (i.p.) injection of 5 mg/kg cisplatin; (3) received single i.p. dose of molsidomine (4 mg/kg/day) for 3 consecutive days before cisplatin treatment; (4) received single i.p. dose of molsidomine (4 mg/kg/day) for 3 consecutive days. The specific biochemical markers, including antioxidants, and the histopathological alterations were evaluated.
Cisplatin significantly increased malondialdehyde (MDA) and myeloperoxidase (MPO) levels and decreased glutathione peroxidase (GPX) level. Molsidomine significantly decreased MPO level nearly to control level; however, its ameliorating effects on MDA, SOD, CAT and GPX did not reach to significant levels. Cisplatin-induced elevation of blood-urea-nitrogen and serum-creatinine were diminished after molsidomine administration. Cisplatin also induced severe tubular degeneration, nuclear condensation, apoptosis and scattered patchy inflammation in the histological examination. Molsidomine improved all of these histological damages.
In this study, the beneficial effect of molsidomine against cisplatin nephrotoxicity has been evaluated for the first time.
顺铂是一种有效的化疗药物,用于治疗多种类型的癌症。然而,顺铂有一些严重的副作用,如肾毒性。另一方面,吗多明是一种一氧化氮供体,具有抗氧化和血管舒张作用。
本研究旨在评估吗多明对顺铂诱导的肾毒性的保护作用。
32只大鼠随机分为4组,如下:(1)对照组;(2)腹腔注射单剂量5mg/kg顺铂;(3)在顺铂治疗前连续3天腹腔注射单剂量吗多明(4mg/kg/天);(4)连续3天腹腔注射单剂量吗多明(4mg/kg/天)。评估了包括抗氧化剂在内的特定生化标志物和组织病理学改变。
顺铂显著提高丙二醛(MDA)和髓过氧化物酶(MPO)水平,降低谷胱甘肽过氧化物酶(GPX)水平。吗多明显著降低MPO水平,几乎降至对照水平;然而,其对MDA、超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和GPX的改善作用未达到显著水平。给予吗多明后,顺铂诱导的血尿素氮和血清肌酐升高有所减轻。在组织学检查中,顺铂还诱导了严重的肾小管变性、核浓缩、凋亡和散在的片状炎症。吗多明改善了所有这些组织学损伤。
在本研究中,首次评估了吗多明对顺铂肾毒性的有益作用。