Alleviation of pre-exposure of mouse brain with low-dose 12C6+ ion or 60Co gamma-ray on male reproductive endocrine damages induced by subsequent high-dose irradiation

International Journal of Andrology

Volumn 29, Issue 6, 2006, Pages 592-596

  Zhang, Hong ^a   Liu, Bing ^a   Zhou, Qingming ^a   Zhou, Guangming ^a   Yuan, Zhigang ^a   Li, Wenjian ^a   Duan, Xin ^a   Min, Fengling ^a   Xie, Yi ^a   Li, Xiaoda ^a  

^a INSTITUTE OF MODERN PHYSICS   (China)

Author keywords

12C6+ heavy ion; Adaptive response; Irradiation; Low dose pre exposure; Male reproductive endocrine capacity; Mouse brain

Indexed keywords

CARBON; COBALT 60; FOLLITROPIN; GONADOTROPIN; LUTEINIZING HORMONE; TESTOSTERONE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN RADIATION; COBALT THERAPY; CONTROLLED STUDY; ENDOCRINE FUNCTION; ENDOCRINE SYSTEM; FOLLITROPIN BLOOD LEVEL; GAMMA RADIATION; GONADOTROPIN BLOOD LEVEL; HORMONE BLOOD LEVEL; LOW ENERGY RADIATION; LUTEINIZING HORMONE BLOOD LEVEL; MALE; MALE GENITAL SYSTEM; MALE GENITAL SYSTEM DISEASE; MEASUREMENT; MOUSE; MOUSE STRAIN; NONHUMAN; PRIORITY JOURNAL; RADIATION DOSE; RADIATION EXPOSURE; SPERMATOZOON ABNORMALITY; SPERMATOZOON COUNT; TESTIS WEIGHT; TESTOSTERONE BLOOD LEVEL;

ANIMALS; BRAIN; COBALT RADIOISOTOPES; DOSE-RESPONSE RELATIONSHIP, RADIATION; FOLLICLE STIMULATING HORMONE; GAMMA RAYS; HEAVY IONS; LUTEINIZING HORMONE; MALE; MICE; MICE, INBRED STRAINS; ORGAN SIZE; SPERM COUNT; SPERMATOZOA; TESTIS; TESTOSTERONE;

EID: 33751301793     PISSN: 01056263     EISSN: 13652605     Source Type: Journal    
DOI: 10.1111/j.1365-2605.2006.00698.x     Document Type: Article

References (28)

1. Bartosz, G., Leyko, W. & Fried, R. (1979) Is superoxide dismutase a physiological radioprotector? Experientia 35, 1194.
2. Bragg, W. & Kleemann, R. (1905) On the α-particles of radium and their loss of range in passing through various atoms and molecules. Philosophical Magazine 10, 146-189.
3. Brooks, A., Bao, S., Rithidech, K., Couch, L. A. & Braby, L. A. (2001) Relative effectiveness of HZE iron-56 particles for the induction of cytogenetic damage in vivo. Radiation Research 155, 353-359.
4. Cai, L. & Liu, S. Z. (1992) Study on the mechanism of cytogenetic adaptive response induced by low dose radiation. Chinese Medical Journal (English) 105, 277-283.
5. Castro, J. R., Phillips, T. L., Prados, M., Gutin, P., Larson, D. A., Petti, P. L., Daftari, I. K., Collier, J. M. & Lillis-Hearne, P. (1997) Neon heavy-charged particle radiotherapy of glioblastoma of the brain. International Journal of Radiation Oncology, Biology, Physics 38, 257-261.
6. Constine, L. S., Woolf, P. D., Cann, D., Mick, G., McCormick, K., Raubertas, R. F. & Rubin, P. (1993) Hypothalamic-pituitary dysfunction after radiation for brain tumors. The New England Journal of Medicine 328, 87-94.
7. Kraft, G. (2002) Radiobiological effects of highly charged ions. In: The Physics of Highly and Multiply Charged Ions, Chapter 10 (ed. F. J. Currell), pp. 1-49. Kluwer Academic Publisher, Dordrecht.
8. Lee, J. H., Choi, I. Y., Kil, I. S., Kim, S. Y., Yang, E. S. & Park, J. W. (2001) Protective role of superoxide dismutases against ionizing radiation in yeast. Biochimica et Biophysica Acta 1526, 191-198.
9. Liu, S. Z., Liu, W. H. & Sun, J. B. (1987) Radiation hormesis: its expression in the immune system. Health Physics 52, 579-583.
10. Liu, S. Z., Han, Z. B. & Liu, W. H. (1994) Changes in lymphocyte reactivity to modulatory factors following low-dose ionizing radiation. Biomedical and Environmental Science 7, 13013-13015.
11. Mehta, M. P., Tsao, M. N., Whelan, T. J., Morris, D. E., Hayman, J. A., Flickinger, J. C., Mills, M., Rogers, C. L. & Souhami, L. (2005) The American Society for Therapeutic Radiology and Oncology (ASTRO) evidence-based review of the role of radiosurgery for brain metastases. International Journal of Radiation Oncology, Biology, Physics 63, 37-46.
12. Miura, Y. (2004) Oxidative stress, radiation-adaptive responses, and aging. Journal of Radiology Research 45, 357-372.
13. Miura, Y. & Suzuki, S. (2002) Radiation adaptive response of glial cells. Biological Sciences in Space 16, 193-194.
14. Muller, J. (2003) Impact of cancer therapy on the reproductive axis. Hormone Research 59 (Suppl. 1), 12-20.
15. Ogilvy-Stuart, A. L. & Shalet, S. M. (1993) Effect of radiation on the human reproductive system. Environmental Health Perspectives 101 (Suppl. 2), 109-116.
16. Okayasu, R., Okada, M., Okabe, A., Noguchi, M., Takakura, K. & Takahashi, S. (2006) Repair of DNA damage induced by accelerated heavy ions in mammalian cells proficient and deficient in the non-homologous end-joining pathway. Radiation Research 165, 59-67.
17. Ritter, M. A., Cleaver, J. E. & Tobias, C. A. (1977) High-LET radiations induce a large proportion of non-rejoining DNA breaks. Nature 266, 653-655.
18. Sagan, L. A. & Cohen, J. J. (1990) Biological effects of low-dose radiation: overview and perspective. Health Physics 59, 11-13.
19. Schulz-Ertner, D., Nikoghosyan, A., Thilmann, C., Haberer, T., Jakel, O., Karger, C., Kraft, G., Wannenmacher, M. & Debus, J. (2004) Results of carbon ion radiotherapy in 152 patients. International Journal of Radiation Oncology, Biology, Physics 58, 631-640.
20. Sengupta, S. & Bhattacharjee, S. B. (1990) Effects of low-dose hydrogen peroxide treatment of V79 cells on killing and mutation by different agents. Mutation Research 243, 81-85.
21. Wang, Z. Q., Saigusa, S. & Sasaki, M. S. (1991) Adaptive response to chromosome damage in cultured human lymphocytes primed with low doses of X-rays. Mutation Research 246, 179-186.
22. Wyrobek, A. J. & Bruce, W. R. (1975) Chemical induction of sperm abnormalities in mice. Proceedings of the National Academy of Sciences of the United States of America 72, 4425-4429.
23. Wyrobek, A. J., Watchmaker, C. & Gordon, L. (1984) Sperm morphology testing in mice. In: Handbook of Mutagenicity Test Procedures (eds B. J. Kilbey, M. Legator, W. Nichol & C. Ramel), pp. 739-750. Elsevier Science Publishers, Amsterdam.
24. Yamaoka, K., Edamatsu, R. & Mori, A. (1991) Increased SOD activities and decreased lipid peroxide levels induced by low dose X irradiation in rat organs. Free Radical Biology & Medicine 11, 299-306.
25. Yamaoka, K., Komoto, Y., Suzuka, I., Edamatsu, R. & Mori, A. (1993) Effects of radon inhalation on biological function - lipid peroxide level, superoxide dismutase activity, and membrane fluidity. Archives of Biochemistry and Biophysics 302, 37-41.
26. Youngblom, J. H., Wiencke, J. K. & Wolff, S. (1989) Inhibition of the adaptive response of human lymphocytes to very low doses of ionizing radiation by the protein synthesis inhibitor cycloheximide. Mutation Research 227, 257-261.
27. 60Co gamma-rays on sperm shape abnormalities, lipid peroxidation and superoxide dismutase (SOD) activity induced by subsequent high-dose irradiation. International Journal of Radiation Biology 73, 163-167.
28. Zhou, H., Randers-Pehrson, G., Waldren, C. A. & Hei, T. K. (2004) Radiation-induced bystander effect and adaptive response in mammalian cells. Advances in Space Research 34, 1368-1372.