Abstract
Radiation-induced double-strand modification of DNA was studied in the absence and presence of sodium 1,4-dihydroxy-9,10-anthraquinone-2-sulfonate (NaQSH2) and its metal (Cu2+ and Ni2+) complexes in aerated, de-aerated (Argon saturated) and N2O saturated aqueous media at pH 7.4. Ethidium bromide, an established DNA intercalator was used to estimate DNA remaining after interaction with γ-radiation, by measuring loss of fluorescence of the ethidium bromide–DNA adduct. In de-aerated (Argon saturated) and N2O saturated aqueous media radiation-induced double-strand modification of calf thymus DNA was comparatively less in presence of NaQSH2 and its Ni(II) complex than standard control indicating the compounds behaved as radio-protectors. However, in presence of the Cu(II) complex radiation-induced double-strand modification increased significantly. In N2O saturated medium, double-strand modification of DNA was almost double in all cases than that observed in de-aerated (Argon saturated) medium indicating OH radicals played a major role in modifying DNA. That OH radicals were important was verified by repeating experiments using tertiary-butanol that showed significant decrease in DNA modification. Another important observation was in aerated medium NaQSH2, Ni(II)–NaQSH2 did not show radioprotection while Cu(II)–NaQSH2 was an almost equally effective radiosensitizer as that observed in N2O saturated medium. Role of molecular oxygen as radiosensitizer was thus realized.
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