Akihiro Kurishita
Tohoku University
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Featured researches published by Akihiro Kurishita.
Mutation Research\/dnaging | 1995
Tetsuya Ono; Yoshinori Miyamura; Hironobu Ikehata; H. Yamanaka; Akihiro Kurishita; Kazuo Yamamoto; T. Suzuki; T. Nohmi; Makoto Hayashi; Toshio Sofuni
Spontaneous mutant frequency of lacZ gene in spleen of transgenic MutaTM mouse was examined at different ages. It was (3.2 +/- 1.3 (SD)) x 10(-5) at newborn and increased almost linearly with age up to (8.3 +/- 1.8) x 10(-5) at one year. Since the mutation of the gene is not likely to be subject to selection in vivo, the data support the idea that spontaneous mutation takes place throughout aging process and accumulates with age if not selected out by cell death.
Mutation Research\/dnaging | 1993
Yoshinori Miyamura; Riichi Tawa; Akio Koizumi; Yoshihiko Uehara; Akihiro Kurishita; Hiromu Sakurai; Shigetoshi Kamiyama; Tetsuya Ono
DNA methylation is known to change with age in several mammalian species. Here we have examined the effect of dietary energy restriction on this age-associated change in liver DNA of C3H/SHN mice. The total 5-methyldeoxycytidine level in the genome decreased slightly soon after energy restriction started. The effect, however, diminished with time and no appreciable difference was detected at middle and old ages. The degree of methylation at the c-myc gene, on the other hand, was not affected by energy restriction at early periods, but the age-dependent alterations at later ages were repressed. This is a new finding to show that DNA methylation is one of the molecular indices of aging affected by energy restriction. It suggests an importance of DNA methylation in the aging process.
Acta Oncologica | 1992
Y. Hosor; Akihiro Kurishita; Tetsuya Ono; Kiyohiko Sakamoto
Repeated injections of recombinant human granulocyte colony-stimulating factor (rhG-CSF) to lethally irradiated mice increased the rate of animal survival. Dose modification factor was 1.20 when 4.5 micrograms/mouse of rhG-CSF was given daily for 14 days after whole body irradiation. Haematological examinations revealed that rhG-CSF increased the number of blood-circulating leukocytes, neutrophils, monocytes and erythrocytes, but not that of lymphocytes and thrombocytes. Spleen weight and number of endogenous spleen colonies were also increased by rhG-CSF treatment compared with the values for mice irradiated only.
Gerontology | 1993
Yoshinori Miyamura; H. Ohtsu; O. Niwa; Akihiro Kurishita; H. Watanabe; T. Sado; Tetsuya Ono
Study of DNA methylation of the c-myc gene in liver tumors of BCF1 mice treated with various agents revealed frequent alteration from that in normal liver. The alteration, however, was complex and showed either an increase or a decrease of methylation to various degrees. On the other hand, the tumors obtained from middle-aged C3H/He mice, which develop liver tumors spontaneously at a high incidence rate starting in middle age, showed predominantly increases of methylation in the c-myc gene, while the large tumors found in older mice revealed decreases. The normal part of the liver showed a slight gradual age-dependent increase. These suggest that hypermethylation of the c-myc gene is common to aging and early tumor development in liver. Thus the alteration of DNA methylation seems to be a good clue to investigate why the tumor incidence rate increases rapidly as individuals grow older.
Mutation Research | 1992
Akihiro Kurishita; Tetsuya Ono; Shigefumi Okada; Yuriko Mori; Syozo Sawada
To assess the genetic effects of fission neutron, the induction of external malformations was studied in F1 fetuses after F0 male mice were irradiated. Male mice of the ICR:MCH strain were irradiated with 252Cf neutron at doses of 0.238, 0.475, 0.95 and 1.9 Gy. They were mated with non-irradiated female mice at 71-120 days after the irradiation. Pregnant females were autopsied on day 18 of gestation and their fetuses were examined for deaths and external abnormalities. No increases of pre- and post-implantation losses were noted at any dose. External abnormalities were observed at rates of 1.40% in the 0.238 Gy, 2.23% in the 0.475 Gy, 3.36% in the 0.95 Gy and 3.26% in the 1.9 Gy groups; the rate in the control group was 1.65%. The dose-response curve was linear up to 0.95 Gy, and then flattened out; the induction rate of external abnormalities was 2.7 x 10(-4)/gamete/cGy based on the linear regression. These results indicated that fission neutron effectively induces external abnormalities in F1 fetuses after spermatogonial irradiation.
International Journal of Radiation Biology | 1993
Akihiro Kurishita; Tetsuya Ono; A. Uchida
The effects of combined treatment with OK-432, an immunomodulator prepared from Streptococcus haemolyticus, and aztreonam, a monobactum antibiotic, in the prevention of radiation-induced bacteraemia and mortality were examined in ICR-MCH mice irradiated with 9.5 Gy. The organisms recovered from the irradiated mice were Streptococcus faecalis and Proteus mirabilis. Treatment with aztreonam reduced the incidence of mice infected with Proteus mirabilis (p < 0.01), but it showed no efficacy on Streptococcus faecalis. OK-432 could reduce the frequency of bacteraemia attributed to both organisms (p < 0.05). Combined treatment with OK-432 and aztreonam further decreased the incidence of bacteraemia by both organisms; no organisms were recovered at 14 days following irradiation. The survival rate at 30 days following irradiation was 80% in mice treated with OK-432 plus aztreonam and 55% with OK-432 alone, while it was 0% in the groups treated with aztreonam or saline alone. These results indicated that combined treatment with OK-432 and a suitable antibiotic such as aztreonam is more effective than OK-432 or aztreonam alone.
Differentiation | 1990
Riichi Tawa; Tetsuya Ono; Akihiro Kurishita; Shigefumi Okada; Shingo Hirose
Journal of Radiation Research | 1998
Riichi Tawa; Yutaka Kimura; Jun-ichiro Komura; Yoshinori Miyamura; Akihiro Kurishita; Masao S. Sasaki; Hiromu Sakurai; Tetsuya Ono
Age and Ageing | 1993
Tetsuya Ono; Yoshihiko Uehara; Akihiro Kurishita; Riichi Tawa; Hiromu Sakurai
Teratogenesis Carcinogenesis and Mutagenesis | 2005
Akihiro Kurishita