College of Veterinary Medicine / University of Mosul
  • Register
  • Login
  • العربیة

Iraqi Journal of Veterinary Sciences

Notice

As part of Open Journals’ initiatives, we create website for scholarly open access journals. If you are responsible for this journal and would like to know more about how to use the editorial system, please visit our website at https://ejournalplus.com or
send us an email to info@ejournalplus.com

We will contact you soon

  1. Home
  2. Volume 34, Issue 2
  3. Authors

Current Issue

By Issue

By Subject

Keyword Index

Author Index

Indexing Databases XML

About Journal

Aims and Scope

Editorial Board

Facts and Figures

Publication Ethics

Indexing and Abstracting

Related Links

FAQ

Peer Review Process

News

Authorship

Document Download Center

Anticlastogenic properties of Quercus infectoria galls extract against DMBA induced genotoxicity in bone marrow cells of mice in vivo

    Sherzad I Amedi Bushra M. Mohammed

Iraqi Journal of Veterinary Sciences, 2020, Volume 34, Issue 2, Pages 279-285
10.33899/ijvs.2019.125930.1188

  • Show Article
  • Highlights
  • References
  • Download
  • Cite
  • Statistics
  • Share

Abstract

This study aimed to evaluate the aqueous extract of Quercus infectoria galls extract (QIGE) as anticlastogenic. The effect of QIGE was tested in mice (5 groups for each test) treated with 7, 12-dimethylbenz (a) anthracene (DMBA), the strong site-specific carcinogenic agent. In this study, the QIGE show no signs of toxicity, a single dose of DMBA (50 mg/kg) was injected intraperitoneally to Swiss albino mice caused a great increase in number of chromosomal aberrations, micronucleated polychromatic erythrocytes (MnPCEs) and reduction in the percentage of mitotic index (MI) (cytogenetic markers). Oral pre-treatment and post-treatment of QIGE for 14 days at dose 2 gm/kg b.w. daily to DMBA-treated animals greatly reduced in number of micronucleus formation, chromosomal abnormalities such as chromosomal break, chromatid breaks, ring chromosome, dicentric chromosome and fragments. Besides, mitotic index frequency increased comparing with the positive control. The data suggest that QIGE has potent anti-clastogenic effect against DMBA-induced genotoxicity in bone marrow cells of albino male mice and it may have a protective effect against the mutagenicity of the polynuclear aromatic hydrocarbons (PAH).
Keywords:
    <i>Quercus infectoria</i> galls Anticlastogenic Mutagenicity Chromosome aberration Micronucleus
Main Subjects:
  • Animal Toxicology

1.This study aimed to evaluate the anticlastogenic effect of the aqueous extract of Quercus infectoria galls extract (QIGE) against 7, 12-dimethylbenz (a) anthracene (DMBA).

2.Different QIGE doses of Quercus infectoria galls extract (QIGE) 2, 4, 6, 8, 10 and 12 gm/kg b.w. show no signs of toxicity; the recorded data suggested that the aqueous extract of QIG is safe.

3.A single dose of DMBA (50 mg/kg) caused a great increase in number of chromosomal aberrations, micronucleate polychromatic erythrocytes (MnPCEs) and reduction in the percentage of mitotic index (MI) in bone marrow cells of albino mice.

4.The present study found that the Oral pre-treatment and post-treatment of QIGE for 14 days at the dose 2 gm/kg b.w. daily to DMBA-treated animals reported inhibitory and protective effects on the cytotoxic and DNA damage induced by DMBA.

  • PDF (631 K)
  • XML
(2020). Anticlastogenic properties of Quercus infectoria galls extract against DMBA induced genotoxicity in bone marrow cells of mice in vivo. Iraqi Journal of Veterinary Sciences, 34(2), 279-285. doi: 10.33899/ijvs.2019.125930.1188
Sherzad I Amedi; Bushra M. Mohammed. "Anticlastogenic properties of Quercus infectoria galls extract against DMBA induced genotoxicity in bone marrow cells of mice in vivo". Iraqi Journal of Veterinary Sciences, 34, 2, 2020, 279-285. doi: 10.33899/ijvs.2019.125930.1188
(2020). 'Anticlastogenic properties of Quercus infectoria galls extract against DMBA induced genotoxicity in bone marrow cells of mice in vivo', Iraqi Journal of Veterinary Sciences, 34(2), pp. 279-285. doi: 10.33899/ijvs.2019.125930.1188
Anticlastogenic properties of Quercus infectoria galls extract against DMBA induced genotoxicity in bone marrow cells of mice in vivo. Iraqi Journal of Veterinary Sciences, 2020; 34(2): 279-285. doi: 10.33899/ijvs.2019.125930.1188
  • RIS
  • EndNote
  • BibTeX
  • APA
  • MLA
  • Harvard
  • Vancouver

  1. Baharuddin N, Abdullah H, Abdul Wahab WN. Anti-Candida activity of Quercus infectoria gall extracts against Candida species. J Pharma Bio Sci. 2015;7(1):15. 10.4103/0975-7406.148742
  2. Srivastava RC, Husain MM, Hasan SK, Athar M. Green tea polyphenols and tannic acid act as potent inhibitors of phorbol ester-induced nitric oxide generation in rat hepatocytes independent of their antioxidant properties. Cancer Letters. 2000;153(1-2):1-5. 10.1016/s0304-3835(99)00400-0
  3. Hussein G, Miyashiro H, Nakamura N, Hattori M, Kakiuchi N, Shimotohno K. Inhibitory effects of Sudanese medicinal plant extracts on hepatitis C virus (HCV) protease. Phytotherap Res. 2000;14(7):510-6. 10.1002/1099-1573(200011)
  4. Mengeloğlu F. Antimicrobial activity of galls of Quercus infectoria. Dicle Med J. 2011;38(3):309-11. 10.5798/0921.2011.03.0038
  5. Redwane A, Lazrek HB, Bouallam S, Markouk M, Amarouch H, Jana M. Larvicidal activity of extracts from Quercus lusitania var. infectoria galls (Oliv.). J Ethnopharmacol. 2002;79(2):261-3. 10.1016/s0378-8741(01)00390-7
  6. Guerin MR. Energy sources of polycyclic aromatic hydrocarbons. In: Environment, chemistry, and metabolism. New York: Academic Press; 1978. 3-42 p. 10.1016/B978-0-12-279201-4.50008-6
  7. Clarke CH, Shankel DM. Antimutagenesis in microbial systems. Bacteriol Rev. 1975;39(1):33-53. 10.1128/mmbr.39.1.33-53.1975
  8. Abdel-Shafy HI, Mansour MS. A review on polycyclic aromatic hydrocarbons: Source, environmental impact, effect on human health and remediation. Egyptian J Petroleum. 2016;25:107-23. 10.1016/j.ejpe.2015.03.011
  9. Yu H, Yan J, Jiao Y, Fu PP. Photochemical reaction of 7,12-dimethylbenz[a]anthracene (DMBA) and formation of DNA covalent adducts. Inter J Environ Res Pub Heal. 2005;2(1):114-22. 10.3390/ijerph2005010114
  10. Schieber M, Chandel NS. ROS function in redox signaling and oxidative stress. Cur Biol. 2014;24(10):R453-62.  10.1016/j.cub.2014.03.034
  11. Iminjan M, Amat N, Li XH, Upur H, Ahmat D, He B. Investigation into the toxicity of traditional Uyghur medicine Quercus infectoria galls water extract. PLoS ONE. 2014;9(3):e90756. 10.1371/journal.pone.0090756
  12. Valdiglesias V, Mndez J, Psaro E, Laffon B. The importance of the in vitro genotoxicity evaluation of food components: The selenium. J Nutr. 2009;140(1):213-233. 10.3945/jn.109.110569
  13. Thakkar JH, Solanki HK, Tripathi P, Patel NJ. Evaluation of antimutagenic potential of Annona squamosa leaf extract. Inter J Biol Pharma Res. 2010;1(2):114-23. 10.22159/ajpcr.2019.v12i2.29026
  14. Berti AP, Palioto GF, Rocha CLMSC. Antimutagenicity and antigenotoxicity of Aloe arborescens miller and Aloe barbadensis miller in Aspergillus nidulans and wistar rats. Gen Mol Res. 2016;15(3). 3-5. 10.4238/gmr.15038522
  15. De Flora S. Mechanisms of inhibition of mutagenesis and carcinogenesis: Classification. Mut Res Environ Mut Rel Sub. 2003;203(3):205. 10.1016/s0027-5107(97)00292-3
  16. McClure JW. Physiology and functions of flavonoids. In: Boston, MA. The flavonoids. New York: Springer; 1975. 970-1055 p.
  17. Bannerman RM. Mutagenicity: New horizons in genetic toxicology. Am J Med Gen. 2005;15(2):350-1. 10.1002/ajmg.1320150224
  18. Shubber EK, Juma AS. Cytogenetic effects of plant extract of Urtica dioca on mouse somatic cells. Nucleus. 1999;42(3)182-187. 10.1508%2Fcytologia.70.385
  19. Evans EP, Breckon G, Ford CE. An air-drying method for meiotic preparations from mammalian testes. Cytogen Gen Res. 1964;3(5):289-94. 10.1159/000129818
  20. Schmid W. The micronucleus tests. Mut Res. 1975;31(1):9-15. 10.1016/0165-1161(75)90058-8
  21. Bhuvaneswari V, Velmurugan B, Abraham SK, Nagini S. Tomato and garlic by gavage modulate 7,12-dimethylbenz[a]anthracene-induced genotoxicity and oxidative stress in mice. Brazilian J Med Biol Res. 2004;37(7):1029-34. 10.1590/s0100-879x2004000700012
  22. Mayer C, Schmezer P, Freese R, Mutanen M, Hietanen E, Obe G. Lipid peroxidation status, somatic mutations and micronuclei in peripheral lymphocytes: A case observation on a possible interrelationship. Cancer Let. 2000;152(2):169-73. 10.1016/s0304-3835(00)00332-3
  23. Iminjan M, Amat N, Li XH, Upur H, Ahmat D, He B. Investigation into the toxicity of traditional uyghur medicine Quercus infectoria galls water extract. PLoS ONE. 2014;9(3) 10.1371/0090756.e90756
  24. Fathabada AE, Shariatifar N, Mardania K and Mohammad PI. Study on antibacterial and antioxidant activity of Oak gall (Quercus infectoria) extracts from Iran. Int J Curr Sci. 2015;14:44-50. https://www.researchgate.net/publication/338336622
  25. Kaur G, Athar M, Alam MS. Quercus infectoria galls possess antioxidant activity and abrogates oxidative stress-induced functional alterations in murine macrophages. Chem Bioll Inter. 2008;171(3):272-82. 10.1016/j.cbi.2007.10.002
  26. Mathew S, Kuttan G. Antioxidant activity of Tinospora cordifolia and its usefulness in the amelioration of cyclophosphamide induced toxicity. J Exp Clin Can Res. 1997;16(4):407-11.
  27. Premkumar K, Pachiappan A, Abraham SK, Santhiya ST, Gopinath PM, Ramesh A. Effect of Spirulina fusiformis on cyclophosphamide and mitomycin-C induced genotoxicity and oxidative stress in mice. Fitoterapia. 2001;72(8):906-11. 10.1016/s0367-326x(01)00340-9
  28. Oh HT, Kim SH, Choi HJ, Chung MJ, Ham SS. Antioxidative and antimutagenic activities of 70% ethanol extract from masou salmon (Oncorhynchus masou). Toxicol Vitro. 2008;22(6):1484-8. 10.1590/S1516-89132015060309
  29. Gupta S, Chaudhuri T, Seth P, Ganguly DK, Giri AK. Antimutagenic effects of black tea (World blend) and its two active polyphenols theaflavins and the amrubicin's in Salmonella assays. Phytotherapy Res. 2002;16(7):655-61. 10.1002/ptr.1038
  30. Hemmati AA, Houshmand G, Nemati M, Bahadoram M, Dorestan N, Rashidi-Nooshabadi MR. Wound healing effects of Persian oak (Quercus brantii) ointment in rats. Jundishapur J Nat Pharm Prod. 2015;10(4):e25508. 10.17795/jjnpp-25508

  • Article View: 349
  • PDF Download: 507
  • LinkedIn
  • Twitter
  • Facebook
  • Google
  • Telegram
  • Home
  • Glossary
  • News
  • Aims and Scope
  • Privacy Policy
  • Sitemap

 

© 2020, College of Veterinary Medicine, University of Mosul

 
This journal is licensed under a Creative Commons Attribution 4.0 International (CC-BY 4.0)

Powered by eJournalPlus