Rosmarinus officinalis essential oil modulates renal toxicity and oxidative stress induced by potassium dichromate in rats

被引:32
作者
El-Demerdash, Fatma M. [1 ]
El-Sayed, Raghda A. [1 ]
Abdel-Daim, Mohamed M. [2 ]
机构
[1] Alexandria Univ, Inst Grad Studies & Res, Dept Environm Studies, 163 Horreya Ave,POB 832, Alexandria 21526, Egypt
[2] Suez Canal Univ, Dept Pharmacol, Fac Vet Med, Ismailia, Egypt
关键词
Chromium hexavalent; rosemary essential oil; oxidative stress; antioxidant enzymes; nephrotoxicity; CHROMIUM-INDUCED NEPHROTOXICITY; ANTIOXIDANT PROPERTIES; PHENOLIC FRACTION; PROTECTIVE ROLE; ROSEMARY; EXTRACTS; DAMAGE; L; HEPATOTOXICITY; APOPTOSIS;
D O I
10.1016/j.jtemb.2021.126791
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
BACKGROUND: Chromium hexavalent (CrVI) is known as a toxic contaminant that induced oxidative stress and nephrotoxicity in humans and animals. Rosmarinus officinalis is a perennial herb rich in biologically active constituents that have powerful antioxidant properties. So, the current work evaluated the effectiveness of Rosmarinus officinalis essential oil (REO) against alterations induced by potassium dichromate in the kidney of male rats. METHODS: GC-MS analysis, in vitro total phenol contents, and DPPH scavenging activity of REO were estimated. Thirty-five Wistar male rats were categorized into 5 groups. The first group was the control, the second one was orally administered rosemary essential oil (REO; 0.5 mL/kg BW), the third group was injected intraperitoneally with hexavalent chromium (CrVI; 2 mg/kg BW) for 14 days, the fourth group used as the protective group (REO was administrated 30 min before i.p. injection of CrVI) and the fifth group applied as the therapeutic group (rats injected with CrVI 30 min followed by oral administration of REO), respectively. RESULTS: Twenty-nine components were detected with high total phenolic contents and high DPPH scavenging activity. Results revealed that CrVI- intoxicated rats showed a valuable increase in oxidative stress profile (TBARS and H2O2) and a notable decline in glutathione (GSH), total protein content, and enzymatic antioxidants (SOD, CAT, GPx, and GST). Furthermore, serum kidney functions biomarkers (urea, creatinine, and uric acid) were increased significantly. Also, the administration of CrVI showed histological and immunohistochemical (PCNA-ir) changes in rat kidney tissue. Otherwise, administration of REO pre or post-treatment with CrVI significantly restored most of the biochemical parameters in addition to improvement in kidney tissue architecture. Moreover, individual intake with REO exhibited an amendment in oxidative stress markers. CONCLUSION: Conclusively, REO had a potential antioxidant capacity in ameliorating K2Cr2O7-induced nephrotoxicity, especially in the protection group.
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页数:9
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