The Toxicity Effect of Echium amoenum on the Liver and Kidney of Mice

Page: [548 - 553] Pages: 6

  • * (Excluding Mailing and Handling)

Abstract

Aims: The aim of this study was to investigate the toxic effect of Echium amoenum plants on the liver and kidney of the animal model.

Background: Echium amoenum is one of the medicinal plants containing pyrrolizidine alkaloids with several properties which has widely consumed among different communities.

Objective: The toxic effects of Echium amoenum on the liver and kidney were investigated in this study.

Methods: Sixty mice were kept for 28 days under the appropriate laboratory conditions. Echium amoenum extract (25, 12.5, 50 mg / kg, ip.) was administered for 28 days. At the end of the experiment, blood samples were drawn and liver and kidneys were removed for evaluating hepatotoxicity and nephrotoxicity of extract. Additionally, experiments were conducted to assay the enzymatic and oxidative activities.

Results: There was no significant difference in the levels of copper ion in the liver and kidneys among all groups. There was a significant difference in the levels of lipid peroxidation in the liver of treated groups versus the control group. The significant difference was not observed in the levels of glutathione of the liver of all groups. However, the levels of glutathione of the kidney significantly decreased in the treated groups versus the control group. There was no significant difference in the liver enzymes, including ALP, SGOT, and SGPT, between all groups. This indicates that damage increases with enhancing the time and concentrations of the extract. Biochemical analysis showed the creatinine and urea levels did not change in the treated groups versus the control group.

Conclusion: According to the present findings, it is suggested that Echium amoenum causes hepatotoxicity and nephrotoxicity effects in dose and time-dependent manner.

Keywords: Echium Amoenum, nephrotoxicity, hepatotoxicity, histopathology, oxidative stress, toxic effect.

Graphical Abstract

[1]
Naseri N, Kalantar K, Amirghofran Z. Anti-inflammatory activity of Echium amoenum extract on macrophages mediated by inhibition of inflammatory mediators and cytokines expression. Res Pharm Sci 2018; 13(1): 73-81.
[http://dx.doi.org/10.4103/1735-5362.220970] [PMID: 29387114]
[2]
Sadeghi L, Yousefi Babadi V, Tanwir F. Improving effects of Echium amoenum aqueous extract on rat model of Alzheimer’s disease. J Integr Neurosci 2018; 17(3-4): 661-9.
[http://dx.doi.org/10.3233/JIN-180093] [PMID: 30103344]
[3]
Heidari MR, Mandegary A, Hosseini A, Vahedian M. Anticonvulsant effect of methanolic extract of Echium amoenum and C.A. Mey. Against seizure induced by picrotoxin in mice. Pak J Biol Sci 2006; 9: 772-6.
[http://dx.doi.org/10.3923/pjbs.2006.772.776]
[4]
Neuman MG, Cohen L, Opris M, Nanau RM, Hyunjin J. Hepatotoxicity of pyrrolizidine alkaloids. J Pharm Pharm Sci 2015; 18(4): 825-43.
[http://dx.doi.org/10.18433/J3BG7J] [PMID: 26626258]
[5]
Abu Bin Nyeem M, Sadul Haque M, Abdul Hoque M, Islam M, Islam S. Phytoconstituents and pharmacological activity of Gauzaban (Borago officinalis Linn). Int J Food Sci Nutr 2: 148-52.
[6]
Gholamzadeh S, Zare S, Ilkhanipoor M. Evaluation of the anxiolytic effect of Echium amoenum petals extract, during chronic treatment in rat. Res Pharm Sci 2007; 2: 91-5.
[7]
Sicińska P, Bukowska B, Michałowicz J, Duda W. Damage of cell membrane and antioxidative system in human erythrocytes incubated with microcystin-LR in vitro. Toxicon 2006; 47(4): 387-97.
[http://dx.doi.org/10.1016/j.toxicon.2005.12.006] [PMID: 16457864]
[8]
Gibson XA, Shartava A, McIntyre J, et al. The efficacy of reducing agents or antioxidants in blocking the formation of dense cells and irreversibly sickled cells in vitro. Blood 1998; 91(11): 4373-8.
[http://dx.doi.org/10.1182/blood.V91.11.4373] [PMID: 9596687]
[9]
Apak R, Guclu K, Ozyürek M, Çelik S. Mechanism of antioxidant capacity assays and the CUPRAC (cupric ion reducing antioxidant capacity) assay. Mikrochim Acta 2008; 160: 413-9.
[http://dx.doi.org/10.1007/s00604-007-0777-0]
[10]
Sadighara P, Jahanbakhsh M, Araghi A, Jahed Khaniki GH, Sharieatifar N. Investigation of the hepatic effects of stevioside on chicken embryo method. Published online. Jundishapur J Nat Pharm Prod 2017; 12: 1-4.
[11]
Sadighara P, Araghi A, Sayrafi R, Sepehri Moghaddam H. The injection of rice bran oil to avian egg: focus on carotenoids content of liver and brain in embryonic period. J HerbMed Pharmacol 2015; 4: 53-5.
[12]
Gupta E, Purwar S, Sundaram S, Rai GK. Nutritional and therapeutic values of stevia rebaudiana. J Med Plants Res 2013; 7: 3343-53.
[13]
Ozbek E. Induction of oxidative stress in kidney. Int J Nephrol 2012.2012465897
[http://dx.doi.org/10.1155/2012/465897] [PMID: 22577546]
[14]
Waring WS, Moonie A. Earlier recognition of nephrotoxicity using novel biomarkers of acute kidney injury. Clin Toxicol (Phila) 2011; 49(8): 720-8.
[http://dx.doi.org/10.3109/15563650.2011.615319] [PMID: 21970770]
[15]
Al-Attar AM, Abu Zeid IM. Effect of tea (Camellia sinensis) and olive (Olea europaea L.) leaves extracts on male mice exposed to diazinon. BioMed Res Int 2013.2013461415
[http://dx.doi.org/10.1155/2013/461415] [PMID: 23691503]
[16]
Abu Bin Nyeem M, Sadul Haque M, Abdul Hoqu M, Islam M, Islam S. Phytoconstituents and pharmacological activity of Gauzaban (Borago officinalis Linn): A review. Int J Food Sci Nutr 2017; 2: 148-52.