Augustine U. Nnama , Ifeanyi O. Aguzie , Chike F. Oguejiofor , Gladys Ndidiamaka Ugwu , Maureen N. Chukwu , Christopher D. Nwani
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引用次数: 0
Abstract
Vanadium pentoxide (V2O5) is one of the compounds that have been reported to pose varying degrees of toxicity upon exposure; thus, making it a challenging environmental hazard that affects living organisms. This study investigated the cytotoxicity effects of daily sub-lethal oral doses of V2O5 on the bone marrow of male Oryctolagus cuniculus after 21 days. Male O. cuniculus (n = 60, ∼ 6 week old, 433.45 ± 5.00 g body weight) were simply randomized into four experimental groups and a control with three replicates of four animals each. Based on the estimated 96-h LD50 value of 119.0 mg/kg, sub-lethal doses of V2O5 were prepared as 1 mg/kg, 5 mg/kg, 10 mg/kg and 20 mg/kg, and administered to the test animals daily by oral gavage for 21 days. Vanadium pentoxide induced cytotoxicity in the bone marrow cells (BMCs) of exposed groups, with significant changes in all evaluated haemopoietic bone marrow stem cells (erythrocytes, leukocytes, thrombocytes and plasma cells). There were mixed trends in the values of leucocyte differentials in the exposed animal. Oral exposure to V2O5 exerts cytopathologic effects in the forms of DNA damage on the bone marrow of O. cuniculus. These findings support previous reports on the environmental hazards vanadium pentoxide poses to living organisms.
据报道,五氧化二钒(V2O5)是一种暴露后会产生不同程度毒性的化合物;因此,使其成为影响生物体的具有挑战性的环境危害。本实验研究了每日亚致死剂量V2O5口服21 d后对雄性小黄蚕骨髓细胞毒性的影响。选取60只雄性,6周龄,体重433.45±5.00g,随机分为4个试验组和1个对照组,每组3个重复,每个重复4只。以估计的96 h LD50值119.0mg/kg为基础,分别配制为1mg/kg、5mg/kg、10mg/kg和20mg/kg的V2O5亚致死剂量,每天灌胃给药21 d。五氧化二钒诱导暴露组骨髓细胞(BMCs)细胞毒性,所有评估的造血骨髓干细胞(红细胞、白细胞、血小板和浆细胞)发生显著变化。在暴露的动物中,白细胞的差异值有不同的趋势。口服暴露于V2O5对小丘蛙骨髓产生细胞病理学影响,表现为DNA损伤。这些发现支持了先前关于五氧化二钒对生物体造成环境危害的报道。
期刊介绍:
Environmental Toxicology and Pharmacology publishes the results of studies concerning toxic and pharmacological effects of (human and veterinary) drugs and of environmental contaminants in animals and man.
Areas of special interest are: molecular mechanisms of toxicity, biotransformation and toxicokinetics (including toxicokinetic modelling), molecular, biochemical and physiological mechanisms explaining differences in sensitivity between species and individuals, the characterisation of pathophysiological models and mechanisms involved in the development of effects and the identification of biological markers that can be used to study exposure and effects in man and animals.
In addition to full length papers, short communications, full-length reviews and mini-reviews, Environmental Toxicology and Pharmacology will publish in depth assessments of special problem areas. The latter publications may exceed the length of a full length paper three to fourfold. A basic requirement is that the assessments are made under the auspices of international groups of leading experts in the fields concerned. The information examined may either consist of data that were already published, or of new data that were obtained within the framework of collaborative research programmes. Provision is also made for the acceptance of minireviews on (classes of) compounds, toxicities or mechanisms, debating recent advances in rapidly developing fields that fall within the scope of the journal.