2000
DOI: 10.1016/s0027-5107(00)00117-2
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In vivo rodent micronucleus assay: protocol, conduct and data interpretation

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Cited by 384 publications
(242 citation statements)
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“…Cyclophoshamide is an atineoplastic agent with alkylating properties, which indiscriminately complexes with DNA among normal and cancerous cells and is inactive until it is metabolized in the liver by mixed function oxidases of the cytochrome P-450 (Valadares, Castro, Cunha, 2007;Rang et al, 2003). The acute toxicity of cyclophosphamide is primarily associated with its genotoxicity Hayashi, 2000). In somatic cells, it provokes gene mutations, chromosomal aberrations, micronuclei and exchanges of sister chromatids in a variety of cell cultures with and without the presence of metabolic activation (Monteith, Vanstone, 1995;Elhajouji et al, 1994;Madle et al, 1986).…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Cyclophoshamide is an atineoplastic agent with alkylating properties, which indiscriminately complexes with DNA among normal and cancerous cells and is inactive until it is metabolized in the liver by mixed function oxidases of the cytochrome P-450 (Valadares, Castro, Cunha, 2007;Rang et al, 2003). The acute toxicity of cyclophosphamide is primarily associated with its genotoxicity Hayashi, 2000). In somatic cells, it provokes gene mutations, chromosomal aberrations, micronuclei and exchanges of sister chromatids in a variety of cell cultures with and without the presence of metabolic activation (Monteith, Vanstone, 1995;Elhajouji et al, 1994;Madle et al, 1986).…”
Section: Discussionmentioning
confidence: 99%
“…It is recommended for renal lithiasis to help remove small kidney stones but contraindicated for large stones, as well as during pregnancy. Main adverse reactions include diarrhea and hypotension and it should not be used for more than three weeks .Among genotoxicity tests recommended by international regulatory agencies and government institutions, the in vivo Micronucleus Test (MN) in rat bone marrow is widely accepted and recommended to assess and record new chemical and pharmaceutical products that enter the world market (Krishna, Hayashi, 2000; Ribeiro, 2003;Speit, Zeller, Neuss, 2011). This test is frequently used to detect clastogenic agents (which break chomosomes) and aneugenic agents (which induce aneuploidy or abnormal chromosome segregation due to mitotic spindle dysfunction) (Macgregor et al, 1987;Hayashi et al;.…”
mentioning
confidence: 99%
“…Micronuclei (MN) are caused by chromosome breakage and disturbance of the mitotic apparatus (Heddle, 1973;Schmid, 1973;Krishna and Hayashi, 2000). The MN assay, therefore, detects both clastogenicity (chromosome breakage) and aneugenicity (alteration of chromosome number due to chromosome lagging that results from dysfunction of the mitotic apparatus) when performed appropriately (Krishna and Hayashi, 2000).…”
Section: Introductionmentioning
confidence: 99%
“…The significance of the cytological and chromosomal aberrations such as chromosomal stickiness, chromosome fragments, lagging chromosomes, binucleated cells and micronuclei (MN) observed in these studies has been discussed by other authors (Patil and Bhat, 1992;Singh, 2003;Krishna and Hayashi, 2000;Çelik and Aslantürk, 2010). Inhibition of cytokinesis and occurrence of binucleated cells following treatment of root tip cells with plant extracts have been reported (Kaushik, 1996;Gömürgen et al, 2005).…”
Section: Discussionmentioning
confidence: 84%