El-Shorbagy Haidan M
Cairo University, Giza, Egypt.
Cytotechnology. 2017 Feb;69(1):89-102. doi: 10.1007/s10616-016-0039-2. Epub 2016 Nov 30.
Sodium butyrate (SB) is one of the histone deacetylase inhibitors (HDACi's) that is recently evidenced to have a prooxidant activity and an ability to reduce hydrogen peroxide-induced DNA damage. Since the majority of estrogen receptor positive breast cancer patients are treated with tamoxifen citrate (TC), which exerts well established oxidative and genotoxic effects, thus the basic objective of this study is to determine whether SB could ameliorate or curate tamoxifen citrate-induced oxidative DNA damage and genotoxic effect in vivo through up-regulation of some antioxidant enzymes. The individual and combined effects of SB and TC have been examined on rat bone marrow cells, using Micronucleus assays (MN), Comet assay, DNA fragmentation, expression of some antioxidant genes using Real time-PCR and finally, oxidative stress analysis. SB significantly increased the mitotic activity (P < 0.05), while TC induced marked micronuclei and oxidative DNA damage, in the SB post-treatment group, the combination of SB (300 mg/kg) and TC (40 mg/kg) was able to decrease the induction of MN and oxidative DNA damage through up-regulation of Cat, Sod and Gpx1 genes significantly at (P < 0.05) more efficiently than that in the SB pre-treatment one. Therefore, we postulate that SB can be used therapeutically in combination with TC treatment to modulate TC genotoxic effect by reducing its oxidative stress, and thus being an appropriate agonist agent to combine with TC than each compound alone.
丁酸钠(SB)是组蛋白去乙酰化酶抑制剂(HDACi)之一,最近有证据表明其具有促氧化活性以及降低过氧化氢诱导的DNA损伤的能力。由于大多数雌激素受体阳性乳腺癌患者接受柠檬酸他莫昔芬(TC)治疗,而该药物具有公认的氧化和遗传毒性作用,因此本研究的基本目的是确定SB是否可以通过上调某些抗氧化酶来改善或减轻柠檬酸他莫昔芬在体内诱导的氧化DNA损伤和遗传毒性作用。使用微核试验(MN)、彗星试验、DNA片段化分析、通过实时聚合酶链反应检测一些抗氧化基因的表达以及最后进行氧化应激分析,研究了SB和TC对大鼠骨髓细胞的单独及联合作用。SB显著提高了有丝分裂活性(P < 0.05),而TC诱导了明显的微核和氧化DNA损伤。在SB后处理组中,SB(300 mg/kg)和TC(40 mg/kg)的组合能够通过显著上调Cat、Sod和Gpx1基因(P < 0.05)来降低MN的诱导和氧化DNA损伤,比SB预处理组更有效。因此,我们推测SB可与TC联合用于治疗,通过降低其氧化应激来调节TC的遗传毒性作用,因此与单独使用每种化合物相比,SB是与TC联合使用的合适激动剂。