Antigenotoxic effect of the Plumbago zeylanica extract against the genotoxic damage induced by potassium canrenoate in cultured human peripheral blood lymphocytes

References

• Asolkar, A. V., Kakkar, K. K., Charke, O. J. (1992). Glossary of Indian medicinal plants with active principles, part I (p. 187). New Delhi: CSIR.
   Google Scholar
• Beg, A. Z., Ahmad, I. (2000). Effect of Plumbago zeylanica extract and certain agents on multidrug resistant bacteria of clinical origin. World J Microbiol Biotechnol 16:841–844.
   Web of Science ®Google Scholar
• Brambilla, G., Martelli, A. (2002). Are some progestins genotoxic liver carcinogens? Mutat Res 512:155–163.
   PubMed Web of Science ®Google Scholar
• Carballo, M. A., Alvarez, S., Boveris, S. (1993). Cellular stress by light and rose bengal in human lymphocytes. Mutat Res 288:215–222.
   PubMed Web of Science ®Google Scholar
• Carrano, A. V., Natarajan, A. T. (1988). Consideration for population monitoring using cytogenetic technique, ICPEMC Publication No. 14, International Commission for protection against Environmental Mutagens and Carcinogens. Mutat Res 204:379–406.
   PubMed Web of Science ®Google Scholar
• Chitravadivu, C., Manian, S., Kalaichelvi, K. (2009). Quantitative analysis of selected medicinal plants, Tamil Nadu, India. Middle-East J Sci Res 4:144–146.
   Google Scholar
• Chopra, R. N., Nayer, S. L., Chopra, I. C. (1992). Glossary of Indian medicinal plants, 3rd ed. (pp. 7–246). New Delhi: CSIR.
   Google Scholar
• Cook, C. S., Hauswald, C., Oppermann, J. A., Schoenhard, G. L. (1993). Involvement of cytochrome P450 IIIA in metabolism of potassium canrenoate to an epoxide: mechanism of inhibition of the epoxide formation by spironolactone and its sulfur containing metabolite. J Pharmacol Exp Ther 266:1–7.
   PubMed Web of Science ®Google Scholar
• Cook, C. S., Hauswald, C. L., Schoenhard, G. L., Piper, C. F., Patel, A., Radzialowski, E. M., et al. (1988). Difference in metabolic profile of potassium canrenoate and spironolactone in the rat: mutagenic metabolites unique to potassium canrenoate. Arch Toxicol 61:201–212.
   PubMed Web of Science ®Google Scholar
• Crossen, P. E., Morgan, M. F. (1977). Analysis of human lymphocyte cell cycle time in culture measures by sister chromatid differential staining. Exp Cell Res 104:453–457.
   PubMed Web of Science ®Google Scholar
• Dearfield, K. L., Cimino, M. C., McCarroll, N. E., Mauer, I., Valcovic, L. R. (2002). Genotoxicity risk assessment: a proposed classification strategy. Mutat Res 521:121–125.
   PubMed Web of Science ®Google Scholar
• Hagmar, L., Bonassi, S., Stromberg, U., Brogger, A., Knudson, J. E., Norppa, H., et al. (1998). Chromosomal aberrations in human lymphocytes predict human cancer: a report from the European Study Group on cytogenetic biomarkers and health (ESCH). Can Res 58:4113–4121.
   PubMedGoogle Scholar
• IARC. (1999). International Agency for Research on Cancer, oral contraceptives, combined (group 1) (vol. 72, p. 49). Lyon, France: IARC.
   Google Scholar
• IPCS. (1985). International Programme on Chemical Safety: Environmental Health Criteria 46. Guidelines for the study of genetic effects in human populations (pp. 25–54). Geneva: WHO.
   Google Scholar
• Kuroda, Y., Jain, A. K., Tezuka, H., Kada, T. (1992). Antimutagenicity in cultured mammalian cells. Mutat Res 267:201–209.
   PubMed Web of Science ®Google Scholar
• Martelli, A., Carrozzino, R., Mattioli, F., Bucci, G., Lanarino, G., Brambilla, G. (2002). DNA damage in tissues of rat treated with potassium canrenoate. Toxicology 171:95–103.
   PubMed Web of Science ®Google Scholar
• Martelli, A., Mattioli, F., Carrozzino, R., Ferraris, E., Marchese, M., Angiola, M., et al. (1999). Genotoxicity testing of potassium canrenoate in cultured rat and human cells. Mutagenesis 14:463–472.
   PubMed Web of Science ®Google Scholar
• Maurich, T., Pistelli, L., Turchi, G. (2004). Anti-clastogenic activity of two structurally related pterocarpans purified from Bituminaria bituminosa in cultured human lymphocytes. Mutat Res 561:75–81.
   PubMed Web of Science ®Google Scholar
• Morse, M. A., Stoner, G. D. (1993). Cancer chemoprevention: principles and prospects. Carcinogenesis 14:1737–1746.
   PubMed Web of Science ®Google Scholar
• Muraki, T., Nakadate, T., Kubota K., Tokunaga, Y., Kato R. (1980). Effects of repeated administration of potassium canrenoate (SC-14266) on serum gonadotrophin, prolactin, testosterone, and progesterone in male rats. Experientia 36:68–69.
   PubMedGoogle Scholar
• Noel, S., Kasinathan, M., Rath, S. K. (2006). Evaluation of apigenin using in vitro cytochalasin blocked micronucleus assay. Toxicol In Vitro 20:1168–1172.
   PubMed Web of Science ®Google Scholar
• Perry, P., Wolff, S. (1974). New Giemsa methods for differential staining of sister chromatids. Nature 261:156–158.
   Web of Science ®Google Scholar
• Ramsay, L., Shelton, J., Harrison, I., Tidd, M., Asbury, M. (1976). Spironolactone and potassium canenoate in normal man. Clin Pharmacol Ther 20:167–177.
   PubMed Web of Science ®Google Scholar
• RomeroJimenez, M., Sanchez, J. C., Analla, M., Serrano, A. M., Moraga, A. A. (2005). Genotoxicity and antigenotoxicity of some traditional medicinal herbs. Mutat Res 585:147–155.
   PubMed Web of Science ®Google Scholar
• Roncada, T., Vicentini, V. E. P., Mantovani, M. S. (2004). Possible modulating actions of plants extracts, on the chromosome breaking activity of MMC and Ara C in human lymphocytes in vitro. Toxicol In Vitro 16:617–622.
   Google Scholar
• Siddique, Y. H., Afzal, M. (2009). Antigenotoxic effect of apigenin against mitomycin C induced genotoxic damage in mice bone marrow cell. Food Chem Toxicol 47:536–539.
   PubMed Web of Science ®Google Scholar
• Siddique, Y. H., Ara, G., Beg, T., Afzal M. (2007a). Antigenotoxic effect of Ocimum sanctum L. extract against cyproterone acetate induced genotoxic damage in cultured mammalian cell. Acta Biol Hung 58:397–409.
   PubMed Web of Science ®Google Scholar
• Siddique, Y. H., Ara, G., Beg, T., Afzal, M. (2007b). Protective role of nordihydroguaiaretic acid (NDGA) against the genotoxic damage induced by ethynodiol diacetic in human lymphocytes in vitro. J Env Biol 28:279–282.
   PubMed Web of Science ®Google Scholar
• Siddique, Y. H., Ara, G., Beg, T., Afzal, M. (2008b). Antigenotoxic effect of nordihydroguaiaretic acid (NDGA) against chlormadinone acetate induced genotoxic damage in mice bone marrow cells. J Nat Med 62:52–56.
   PubMed Web of Science ®Google Scholar
• Siddique, Y. H., Ara, G., Beg, T., and Afzal, M. (2010). Anticlastogenic effect of apigenin in human lymphocytes treated with ethinylestradiol. Fitoterapia 81:590–594.
   PubMed Web of Science ®Google Scholar
• Siddique, Y. H., Ara, G., Beg, T., Faisal, M., Ahmad, M., Afzal, M. (2008a). Antigenotoxic role of Centella asiatica L. extract against cyproterone acetate induced genotoxic damage in cultured human lymphocytes. Toxicol In Vitro 22:10–17.
   PubMed Web of Science ®Google Scholar
• Siddique, Y. H., Beg, T., Afzal, M. (2005). Antigenotoxic effects of ascorbic acid against megestrol acetate induced genotoxicity in mice. Hum Exp Toxicol 24:121–127.
   PubMed Web of Science ®Google Scholar
• Siddique, Y. H., Beg, T., Afzal, M. (2006). Protective effect of nordihydroguaiaretic acid (NDGA) against norgestrel induced genotoxic damage. Toxicol In Vitro 20:227–233.
   PubMed Web of Science ®Google Scholar
• Sivakumar, V., Prakash, R., Murali, M. R., Devaraj, H., Niranjali Devaraj, S. (2005). In vivo micronucleus assay and GST activity in assessing genotoxicity of plumbagin in Swiss albino mice. Drug Chem Toxicol 28:499–507.
   PubMed Web of Science ®Google Scholar
• Sivakumar, V., Devaraj, S. N. (2006). Protective effect of Plumbago zeylanica against cyclophosphamide induced genotoxicity and oxidative stress in Swiss albino mice. Drug Chem Toxicol 29:279–288.
   PubMed Web of Science ®Google Scholar
• Tice, R. R., Schneider, E. L., Rary, J. M. (1976). The utilization of bromodeoxyuridine incorporation in DNA for the analysis of cellular kinetics. Exp Cell Res 102:232–236.
   PubMed Web of Science ®Google Scholar