Genotoxic and Cytotoxic Activity of Cyanobacterial (Blue-Green Algal) Toxin BMAA in Human Lymphocyte Cells
Abstract
Cyanobacteria, one of the oldest life forms, are also known as blue-green algae. Many species of cyanobacteria produce metabolites called cyanotoxin, which are classified as hepatotoxins, neurotoxins and cytotoxins and are highly toxic to vertebrate organisms. One of these toxins is the Beta-N-methyl-amino-L-alanine (BMAA). Blooms (large numbers or colonies) of the cyanobacteria or related organisms produce one or more toxins that can be dangerous to fish, wild animals and humans. There is not enough information in the literature related to the genotoxic effect of this toxin. In this study, it was aimed to determine investigation of the cytotoxic and genotoxic activity of cyanobacterial toxin BMAA in human lymphocyte cells by micronucleus assay. Different concentrations (20, 10, 5 and 1 μg/ml) of BMAA cyanotoxin were applied to human lymphocyte cell culture and micronucleus frequencies (MN) and nuclear division index (NDI) were calculated to determine genotoxic and cytotoxic effects. The data obtained from our study were compared with the negative control group prepared with dimethyl sulfoxide (DMSO) and with the well known ethyl methanesulfonate (EMS) with genotoxic effect and positive control group. According to these results; increasing the frequency of micronucleus according to the whole control negative control group that we used BMAA was not statistically significant compared with the EMS (positive control group) (p>0.05). However, no significant cytotoxic effect was found when the results of the NDI were examined (p>0.05).
Keywords
Supporting Institution
Project Number
References
- Al-Sammak, M.A. 2012. Occurrence and effect of algal neurotoxins in Nebraska freshwater ecosystems. PhD. Thesis. University of Nebraska-Lincoln, USA.
- Buenz, E. J., and Howe, C.L. 2007. Beta-methylarnino-alanine (BMAA) injures hippocampal neurons in vivo. Neurotoxicology, 28(3): 702-704.
- Chang, Y.C., Chiu, S.-J., and Kao, K.P. 1993. Beta-N-methylamino-L-alanine (L-BMAA) decreases brain glutamate receptor number and induces behavioral changes in rats. The Chinese journal of physiology, 36(2): 79-84.
- Cox, P.A., Kostrzewa, R.M., Guillemin, G.J. 2017. BMAA and neurodegenerative illness. Neurotox. Res.,1: 1-6.
- Dawson, R., Marschall, E.G., Chan, K.C., Millard, W.J., Eppler, B., and Patterson, T.A. 1998. Neurochemical and neurobehavioral effects of neonatal administration of β-N-methylamino-l-alanine and 3,3'-iminodipropionitrile. Neurotoxicology and Teratology, 20(2): 181-192.
- de Munck, E., Muñoz-Sáez, E., Miguel, B.G., Solas, M.T., Ojeda, I., Martínez, A., et al. 2013. β-N-methylamino-l-alanine causes neurological and pathological phenotypes mimicking Amyotrophic Lateral Sclerosis (ALS): The first step towards an experimental model for sporadic ALS. Environmental toxicology and pharmacology, 36(2): 243-255.
- Esterhuizen-Londt, M., Pflugmacher, S., and Downing, T.G. 2011. β-N-Methylamino-L-alanine (BMAA) uptake by the aquatic macrophyte Ceratophyllum demersum. Ecotoxicology and Environmental Safety, 74(1): 74-77.
- Esterhuizen-Londt, M., Pflugmacher, S., and Downing, T.G. 2011b. The effect of β-N-methylamino-L-alanine (BMAA) on oxidative stress response enzymes of the macrophyte Ceratophyllum demersum. Toxicon, 57(5): 803-810.
Details
Primary Language
English
Subjects
-
Journal Section
Research Article
Authors
Arif Ayar
*
0000-0001-7849-4459
Türkiye
Deniz Altun Colak
Türkiye
Handan Uysal
Türkiye
Vahit Konar
This is me
Türkiye
Publication Date
August 30, 2019
Submission Date
July 29, 2019
Acceptance Date
August 29, 2019
Published in Issue
Year 2019 Volume: 1 Number: 1