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西红花苷和藏红花醛作为小鼠γ射线、氨基甲酸乙酯和丙卡巴肼诱导的遗传毒性应激保护剂的功效。

Efficacy of crocin and safranal as protective agents against genotoxic stress induced by gamma radiation, urethane and procarbazine in mice.

作者信息

Koul A, Abraham S K

机构信息

School of Life Sciences, Jawaharlal Nehru University, New Delhi, India.

出版信息

Hum Exp Toxicol. 2018 Jan;37(1):13-20. doi: 10.1177/0960327116689715. Epub 2017 Jan 23.

DOI:10.1177/0960327116689715
PMID:28111973
Abstract

Crocin (CRO) and safranal (SAF) are bioactive constituents of saffron (dried stigma of Crocus sativus flower), an expensive spice with medicinal properties. Aqueous extract of saffron is known for its antigenotoxic effect against environmental genotoxins/carcinogens. However, there is need to identify saffron constituents responsible for this antigenotoxic effect. The aim of our investigation was to ascertain the role of CRO and SAF as inhibitors of in vivo genotoxic stress. For this purpose, Swiss albino mice were pretreated with CRO (50-mg/kg body weight (bw))/SAF (0.025- and 0.25-ml/kg bw) by gavage for 2 days. Thereafter, the pretreated mice were exposed to the genotoxic agents: (1) gamma radiation (GR; 2 Gy), (2) urethane (URE; 800 mg/kg) and (3) procarbazine (PCB; 60 mg/kg). In addition, CRO (50 mg/kg) was co-administered with the nitrosation reaction mixture of methylurea (MU; 300-mg/kg bw) + sodium nitrite (15 mg/kg) which can form N-nitroso-N-MU in the stomach. Genotoxic damage was measured by performing the bone marrow micronucleus test. Results obtained demonstrated significant reductions in the incidence of micronucleated polychromatic erythrocytes in the bone marrow of mice pretreated with CRO/SAF before exposure to the above DNA damaging agents, GR, URE and PCB. Co-administration of CRO with the nitrosation reaction mixture led to significant decrease in genotoxicity when compared to nitrosation reaction mixture alone. Histopathological studies revealed that these saffron constituents reduced testicular cell damage induced by the test genotoxins. The cell-free DNA-nicking assay using pBR322 DNA showed significant protective effects of CRO against hydroxyl radical-induced strand breaks.

摘要

藏红花素(CRO)和藏红花醛(SAF)是藏红花(番红花干燥柱头)的生物活性成分,藏红花是一种具有药用特性的昂贵香料。藏红花水提取物以其对环境基因毒素/致癌物的抗基因毒性作用而闻名。然而,需要确定导致这种抗基因毒性作用的藏红花成分。我们研究的目的是确定CRO和SAF作为体内基因毒性应激抑制剂的作用。为此,通过灌胃法给瑞士白化小鼠预处理CRO(50毫克/千克体重(bw))/SAF(0.025和0.25毫升/千克bw),持续2天。此后,将预处理的小鼠暴露于基因毒性剂:(1)γ射线辐射(GR;2戈瑞),(2)氨基甲酸乙酯(URE;800毫克/千克)和(3)丙卡巴肼(PCB;60毫克/千克)。此外,将CRO(50毫克/千克)与甲基脲(MU;300毫克/千克bw)+亚硝酸钠(15毫克/千克)的亚硝化反应混合物共同给药,该混合物可在胃中形成N-亚硝基-N-MU。通过进行骨髓微核试验来测量基因毒性损伤。获得的结果表明,在暴露于上述DNA损伤剂GR、URE和PCB之前,用CRO/SAF预处理的小鼠骨髓中微核多色红细胞的发生率显著降低。与单独的亚硝化反应混合物相比,CRO与亚硝化反应混合物共同给药导致基因毒性显著降低。组织病理学研究表明,这些藏红花成分减少了受试基因毒素诱导的睾丸细胞损伤。使用pBR322 DNA的无细胞DNA切口试验表明,CRO对羟基自由基诱导的链断裂具有显著的保护作用。

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