Literature DB >> 9804941

In vivo and in vitro antigenotoxic effect of nordihydroguaiaretic acid against SCEs induced by methyl methanesulfonate.

E Madrigal-Bujaidar1, S Díaz Barriga, M Cassani, P Márquez, P Revuelta.   

Abstract

Nordihydroguaiaretic acid (NDGA) is a phenolic lignan which has shown to cause a variety of actions potentially useful for human health; therefore, in this investigation we determined its capacity for inhibiting the rate of sister chromatid exchanges (SCEs) induced by methyl methanesulfonate (MMS). We tested the effect of 0.25, 0.50, 1.0, and 2.0 microM of NDGA on the damage exerted by 55 microM of MMS. Cultured human lymphocytes from two female donors were used for the experiment. The best result concerning its modulatory action was obtained with 1.0 microM of NDGA; with this dose the mean inhibitory index including both donors reached 68.2%. The values obtained for the mitotic and proliferative indexes were not significantly modified with respect to the basal data. We also used the mouse bone marrow in vivo system to evaluate the inhibitory effect of the chemical. In this study we tested 1.0, 6.0, and 11.0 mg/kg of NDGA intraperitoneally (i.p.) administered 1 h before an i.p. injection of MMS (40 mg/kg). The best inhibitory index in this model corresponded to the dose of 11 mg/kg of NDGA (86.9%). The mitotic index and the average generation time showed no significant variation with respect to the control data. Our study established that NDGA produces antigenotoxic action in mammalian cells in vitro and in vivo. Copyright 1998 Elsevier Science B.V.

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Year:  1998        PMID: 9804941     DOI: 10.1016/s1383-5718(98)00128-4

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  4 in total

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Authors:  Maha A Fahmy; Ayman A Farghaly; Entesar E Hassan; Emad M Hassan; Zeinab M Hassan; Khaled Mahmoud; Enayat A Omara
Journal:  Asian Pac J Cancer Prev       Date:  2022-04-01

4.  Epigallocatechin gallate attenuates arsenic induced genotoxicity via regulation of oxidative stress in balb/C mice.

Authors:  Surbhi Kaushal; Aitizaz Ul Ahsan; Vijay Lakshmi Sharma; Mani Chopra
Journal:  Mol Biol Rep       Date:  2019-07-26       Impact factor: 2.316

  4 in total

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