Changes of concentration, total content of histones and relative portions of histone fractions were investigated in the liver of rats after administration of the hepatoprotective substance silymarin (70 mg/kg) and after gamma-irradiation of the whole body at a dose of 3 Gy, which were examined in 30 hours and in 7 days. Administration of silymarin alone considerably increased the concentration, particularly total content of extractable histones in the liver of rats examined in hour 30 (Fig. 1). They decreased below the level of control values after 7 days. The whole body irradiation at a dose 3 Gy of gamma-radiation caused a steep fall of the concentration and total content of histones in hour 30, which persisted also on day 7. Silymarin administered 1 hour before irradiation prevented quantitative changes of histones in hour 30, after irradiation the fall was still steeper than after irradiation without silymarin administration. As Tab. I shows, a significant decrease in the relative portion of histone fractions H2A + H2B was found in the extracted histone of the experimental animals of all 3 groups in hour 30, as well as a decrease in the fraction H1 after irradiation without silymarin administration. A decrease in the lysin-rich histone portion was related to an increase in the relative portion of histone H3. In the rats which were administered silymarin 1 hour before irradiation these changes were found to persist until day 7, and they were related to an increase in the subfraction H1-degrees within the histone fraction H1 (Tab. II). Hence the results document that silymarin administration 1 hour before irradiation had a positive effect which was observed in all the investigated parameters in hour 30 after irradiation. But the radioprotective effect of silymarin was only temporary while until day 7 after irradiation histone variations were identical or still larger than after irradiation without silymarin administration.
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Department of Clinical Sciences, School of Veterinary Medicine, Islamic Azad University-Kazerun Branch, KazerunDepartment of Clinical Sciences, School of Veterinary Medicine, Islamic Azad University-Kazerun Branch, Kazerun
Ghasrodashti A.R.
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Esfandiari A.
Mohebbi-Fani M.
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Department of Food Hygiene, School of Veterinary Medicine, University of Shiraz, ShirazDepartment of Clinical Sciences, School of Veterinary Medicine, Islamic Azad University-Kazerun Branch, Kazerun
Mohebbi-Fani M.
Hoshyar M.B.
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Department of Clinical Sciences, School of Veterinary Medicine, Islamic Azad University-Kazerun Branch, KazerunDepartment of Clinical Sciences, School of Veterinary Medicine, Islamic Azad University-Kazerun Branch, Kazerun
Hoshyar M.B.
Nayeri K.
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Department of Food Hygiene, School of Veterinary Medicine, University of Shiraz, ShirazDepartment of Clinical Sciences, School of Veterinary Medicine, Islamic Azad University-Kazerun Branch, Kazerun
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Univ Madras, Inst Basic Med Sci, Dept Pharmacol & Expt Toxicol, Madras 600113, Tamil Nadu, IndiaUniv Madras, Inst Basic Med Sci, Dept Pharmacol & Expt Toxicol, Madras 600113, Tamil Nadu, India
Pradeep, Kannampalli
Mohan, Chandrasekaran Victor Raj
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Univ Madras, Inst Basic Med Sci, Dept Pharmacol & Expt Toxicol, Madras 600113, Tamil Nadu, IndiaUniv Madras, Inst Basic Med Sci, Dept Pharmacol & Expt Toxicol, Madras 600113, Tamil Nadu, India
Mohan, Chandrasekaran Victor Raj
Gobianand, Kuppannan
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Univ Madras, Inst Basic Med Sci, Dept Pharmacol & Expt Toxicol, Madras 600113, Tamil Nadu, IndiaUniv Madras, Inst Basic Med Sci, Dept Pharmacol & Expt Toxicol, Madras 600113, Tamil Nadu, India
Gobianand, Kuppannan
Karthikeyan, Sivanesan
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Univ Madras, Inst Basic Med Sci, Dept Pharmacol & Expt Toxicol, Madras 600113, Tamil Nadu, IndiaUniv Madras, Inst Basic Med Sci, Dept Pharmacol & Expt Toxicol, Madras 600113, Tamil Nadu, India