Drug Res (Stuttg) 2015; 65(11): 561-566
DOI: 10.1055/s-0034-1384533
Original Article
© Georg Thieme Verlag KG Stuttgart · New York

Evaluation of Protein Ubiquitylation in Heart Tissue of Rats Exposed to Diazinon (an Organophosphate Insecticide) and Crocin (an Active Saffron Ingredient): Role of HIF-1α

B. M. Razavi
1   Targeted Drug Delivery Research Center, Department of Pharmacodinamy and Toxicology, Mashhad University of Medical Sciences, Mashhad, Iran
,
H. Hosseinzadeh
2   Pharmaceutical Research Center, Department of Pharmacodinamy and Toxicology, Mashhad University of Medical Sciences, Mashhad, Iran
,
M. Imenshahidi
1   Targeted Drug Delivery Research Center, Department of Pharmacodinamy and Toxicology, Mashhad University of Medical Sciences, Mashhad, Iran
,
M. Malekian
1   Targeted Drug Delivery Research Center, Department of Pharmacodinamy and Toxicology, Mashhad University of Medical Sciences, Mashhad, Iran
,
M. Ramezani
3   Nanotechnology Research Center, Department of Biotechnology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran
,
K. Abnous
4   Pharmaceutical Research Center, Department of Medicinal Chemistry, Mashhad University of Medical Sciences, Mashhad, Iran
› Author Affiliations
Further Information

Publication History

received 27 February 2014

accepted 21 June 2014

Publication Date:
04 November 2014 (online)

Abstract

Introduction:  Organophosphate compounds, such as diazinon (DZN), are widely used in agriculture and can lead to formation of reactive oxygen species (ROS) in cardiovascular system. ROS are highly toxic since they can cause serious changes in proteins including ubiquitylation. Crocin (a carotenoid isolated from saffron), has protective effects against DZN cardiotoxicity. In this study level of total protein ubiquitylation as markers of oxidative stress and level of ubiquitin-HIF-1α and P53, known substrates of ubiquitylation, in rat hearts exposed to DZN and crocin were evaluated.

Methods:  Rats were divided into 7 groups: corn oil (control), DZN (15 mg/kg/day, gavage), crocin (12.5, 25, 50 mg/kg/day, i. p.) plus DZN, vitamin E (200 IU/kg, i. p., 3 days a week) plus DZN and crocin (50 mg/kg/day, i. p.). Treatments were continued for 4 weeks. Total protein ubiquitylation, total HIF-1α and P53 were analyzed by western blotting. Total HIF-1α and P53 were purified by immunoprecipitation (IP) and ubiquitin- HIF-1α and P53 were analyzed by western blotting.

Results:  Higher protein ubiquitylation levels were observed in DZN treated rats. Decrease in ubiquitin-HIF-1α was also shown, and leads to higher HIF-1α protein levels in DZN group. Crocin (50 mg/kg) and vit. E protected cells against DZN protein ubiquitylation. Significant differences were not observed between the ubiquitin – P53 and total P53 protein levels.

Conclusion:  Our results showed that ubiquitylation could be considered as a marker of oxidative stress in rats exposed to DZN. Increase in level of HIF-α may compensate adverse effect of DNZ in rat heart.

 
  • References

  • 1 Passmore L, Barford D. Getting into position: the catalytic mechanisms of protein ubiquitylation. Biochem J 2004; 379: 513-525
  • 2 Haglund K, Dikic I. New EMBO Member’s Review Ubiquitylation and cell signaling. EMBO J 2005; 24: 3353-3359
  • 3 Trachootham D, Lu W, Ogasawara M et al. Redox Regulation of Cell Survival. Antioxid Redox Signal 2008; 10: 1344-1373
  • 4 Yang Y, Yu X. Regulation of apoptosis: the ubiquitous way. FASEB J 2003; 17: 790-799
  • 5 Pialoux A, Mounier R, Brown A et al. Relationship between oxidative stress and HIF-1α mRNA during sustained hypoxia in humans. Free Rad Biol Med 2009; 46: 321-326
  • 6 Wang KS, Chen G, Shen HL et al. Insulin receptor tyrosine kinase substrate enhances low levels of MDM2-mediated P53 ubiquitination. Plos One 2011; 6: e23571
  • 7 Liu D. Xu YP53, Oxidative Stress, and Aging. Antioxid Redox Signal 2011; 2069-1678
  • 8 Zhou S, Liu L, Yang X et al. Paraoxon Attenuates Vascular Smooth Muscle Contraction through Inhibiting Ca2+Influx in the Rabbit Thoracic Aorta. J Biomed Biotechnol 2010; 2010 DOI: 829190. doi: 10.1155/2010/829190. Epub 2010 Apr 22.
  • 9 Ogutcu A, Uzunhisarcikli M, Kalender S et al. The effects of organophosphate insecticide diazinon on malondialdehyde levels and myocardial cells in rat heart tissue and protective role of vitamin E. Pest Biochemi Physiol 2006; 86: 93-98
  • 10 Abdou H, El Mazoudy R. Myotoxic and hyperlipidemic effects of diazinon in female rats. J Med Res Institue 2007; 28: 292-298
  • 11 Razavi BM, Hosseinzadeh H, Movassaghi AR et al. Protective effect of crocin on diazinon induced cardiotoxicity in subcronic exposure. Chem boil inter 2013; 25: 547-55
  • 12 Razavi M, Hosseinzadeh H, Abnous Kh et al. Crocin restores hypotensive effect of subchronic administration of diazinon in rats. Iran J Basic Med Sci 2013; 16: 64-72
  • 13 Soeda S, Ochiai T, Shimeno H et al. Pharmacollogical activities of crocin in saffron. J Nat Med 2007; 61: 102-111
  • 14 Alavizadeh SH, Hosseinzadeh H. Bioactivity assessment and toxicity of crocin: A comprehensive review. Food Chem Toxicol 2013;
  • 15 Hosseinzadeh H, Shamsaie F, Mehri S. Antioxidant activity of aqueous and ethanolic extracts of Crocus sativus L. stigma and its bioactive constituents crocin and safranal. Pharmacogn Mag 2010; 5: 419-424
  • 16 Shen X, Qian Z. Effects of crocetin on antioxidant enzymatic activities in cardiac hypertrophy induced by norepinephrine in rats. Pharmazie 2006; 61: 348-352
  • 17 Hariri A, Moallem S, Mahmoudi M et al. Sub-acute effects of diazinon on biochemical indices and specific biomarkers in rats: Protective effects of crocin and safranal. Food Chem Toxicol 2010; 48: 2803-2808
  • 18 Hadizadeh F, Mohajeri S et al. Extraction and purification of crocin from saffron stigmas employing a simple and efficient crystallization method. Pak J Biol Sci 2010; 13: 691-698
  • 19 Akturk O, Demirin H, Sutcu R et al. The effects of diazinon on lipid peroxidation and antioxidant enzymes in rat heart and ameliorating role of vitamin E and vitamin C. Cell Biol Toxicol 2006; 22: 455-461
  • 20 Halliwell B, Chirico S. Lipid peroxidation: its mechanism, measurement, and significance. Am J Clin Nutr 1993; 57: 715S-724S
  • 21 Galanis A, Pappa A, Giannakakis A et al. Reactive oxygen species and HIF-1 signalling in cancer. Cancer Letters 2008; 266: 12-20
  • 22 Chene P. Inhibiting the p53–MDM2 interaction: an important target for cancer. Nat Rev Cancer 2003; 3: 102-109
  • 23 Michael DO. The p53–Mdm2 module and the ubiquitin system. Semin Cancer Biol 2003; 13: 49-58
  • 24 Hrelajac I, Zajc I, Filipic M. Effects of model organophosphorous pesticides on DNA damage and proliferation of HepG2 cells. Environ Mol Mutagen 2008; 49: 360-367
  • 25 Brooks CL, Gu W. Ubiquitination, phosphorylation and acetylation: the molecular basis for P53 regulation. Curr Opin Cell Biol 2003; 15: 164-171
  • 26 Yang Y, Li CC, Weissman AM. Regulation the P53 system through ubiquitination. Oncogene 2004; 23: 2096-2106
  • 27 Zhang B, Tanaka J, Yang L et al. Protective effect of vitamin E against focal brain ischemia and neuronal death through induction of target genes of hypoxia-inducible factor-1. Neuroscience 2004; 126: 433-440
  • 28 Wu Y, Pan RR, Geng P. The effect of Crocin against hypoxia damage of myocardial cell and its mechanism. Zhongguo Ying Yong Sheng Li Sheng Li Xue Za Zhi 2010; 26: 453-457