Evaluation of the rat bone marrow and peripheral blood micronucleus test using monocrotaline

Author(s):  
Raymond J Proudlock ◽  
Joanne Statham ◽  
Wayne Howard
2019 ◽  
Vol 102 ◽  
pp. 13-22 ◽  
Author(s):  
Bernd-Wolfgang Igl ◽  
Annette Bitsch ◽  
Frank Bringezu ◽  
Steffi Chang ◽  
Martina Dammann ◽  
...  

1999 ◽  
Vol 24 (SupplementI) ◽  
pp. 103-106 ◽  
Author(s):  
Naoki TORITSUKA ◽  
Hirohiko DAIMON ◽  
Shigeki SAWADA ◽  
Fumio SAGAMI ◽  
Piero TIRONE ◽  
...  

Author(s):  
Lucas Rodrigues do Rego ◽  
Everton Pantoja Vale ◽  
Danilo Dheyvison Nascimento Pureza ◽  
Moacir de Azevedo Bentes Monteiro Neto ◽  
Fernando Antônio de Medeiros ◽  
...  

The Amazon Rainforest has a great variety of medicinal plants, among them we can highlight the “Almecegueira” or “Breu Branco” (Protium heptaphylum) in Portuguese, the producer of a greenish-white resin that hardens when it touches the air, known by its gastroprotective and anti-inflammatory effects. These effects are attributed to a triterpene mixture of α and β amirine, predominant in the resin. The purpose of the study is to obtain a cytogenetic profile to the α, β-amirine mixture obtained in the resin of P. heptaphylum. For this, the micronucleus test was used in peripheral blood and bone marrow; administering solution in Swiss mice with the dosages of 1mg/Kg, 3mg/Kg, and 10mg/Kg, diluted in 5% DMSO, the effects were observed in 24h and 48h after the treatment. For the test in peripheral blood the mice’s caudal vein was punctured, while for the bone marrow test, the femurs of the animals were obtained from which bone marrow samples were taken. It was found that in peripheral blood, the administration of the compounds did not cause genotoxicity in 24h and 48h, in contrast, antigenotoxicity was, for concentrations 1; 3 and 10mg/kg, respectively 10%; 12%; 67% in 24h and 9%; 15%; 73% in 48h.  In the bone marrow, no genotoxicity was observed, as for antigenotoxicity was observed that for concentrations 1; 3 e 10mg/kg the percentage of reduction was respectively: 11%, 15%, and 30% in 24h and 13% 16% 33% in 48h. It is concluded that the studied compound can be an alternative for treatments in the future since it presents low toxicity and high antigenotoxic potential.


Mutagenesis ◽  
2009 ◽  
Vol 24 (5) ◽  
pp. 419-424 ◽  
Author(s):  
J. Hayes ◽  
A. T. Doherty ◽  
D. J. Adkins ◽  
K. Oldman ◽  
M. R. O'Donovan

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