Absence of genotoxicity of sea water from Coveñas:in vitro study on human leukocytes and erythrocytes

Authors

  • Wilmer Soler T
  • Nelly Velásquez E
  • Luis Francisco Miranda R
  • Diana Zuluaga G

DOI:

https://doi.org/10.17533/udea.rfnsp.473

Keywords:

Sea water, antioxidant activity, genotoxicity, comet assay

Abstract

In Latin America, Colombia included, the use of natural sea water has been recently introduced for nutritional and therapeutics purposes due to its high content of minerals and oligoelements. This practice has also been used in Europe during the last century. Objective: to evaluate potential toxicity in sea water from Coveñas
(Colombian Atlantic coast). Methods: erythrocytes and leukocytes were incubated in sea water samples collected in Coveñas to evaluate osmotic fragility, viability, and DNA damage (by comet technique). Atioxidant properties of this water were additionally studied. Results: erythrocytes presented a higher index of hemolysis in sea water compared with phosphate buffer (PBS) with a similar hypertonic concentration (4,3% y 2,8% respectively, P=0,00001); however, median differences were very low. Lymphocytes viability in sea water was 95% after one hour of incubation at 4ºC and it was similar to the percentage observed in isotonic PBS. Sea water did not cause damage on DNA as tested one hour after treatment of lymphocytes according to the “Olive moment” averages. Sea water did not present any pro-oxidant or antioxidant capacity as tested with the ABTS+technique. Conclusions: these results suggest that sea water from this area in the Colombian Atlantic cast is bio-safe for human consumption but it is necessary to test concentrated organic fraction and determine in vivo toxic effects
|Abstract
= 242 veces | PDF (ESPAÑOL (ESPAÑA))
= 65 veces|

Downloads

Download data is not yet available.

Author Biography

Wilmer Soler T

Profesor Facultad Nacional de Salud Pública

References

(1). Quinton R. L’eau de mer milieu organique. Constancedu milieu marin originel comme milieu vital des cellu-les, à travers la série animale. 39.a ed. París: Editions Encre; 1995. p. 503.

(2). Mahé A. El plasma de Quinton: el agua de mar nuestromedio interno. Barcelona: Icaria; 1999. p. 190.

(3). Giese AC. Fisiología general: estructura y dinámica celular. 3.ª ed. México: Interamericana; 1968. p. 603.

(4). Arslan Z, Ertas N, Tyson JF, Uden PC, Denoyer ER.Determination of trace elements in marine plankton byinductively coupled plasma mass spectrometry (ICP-MS).Fresenius J Anal Chem. 2000;366(3):273-282. DOI: https://doi.org/10.1007/s002160050053

(5). Fenical W. Chemical studies of marine bacteria: develo-ping a new resource. Chem Rev 1993;93(5):1673-1638. DOI: https://doi.org/10.1021/cr00021a001

(6). Kimata H, Tai H, Nakagawa K, Yokoyama Y, Nakajima H,Ikegami Y. Improvement of skin symptoms and mineralimbalance by drinking deep sea water in patients withatopic eczema/dermatitis syndrome (AEDS). Acta Medi-ca (Hradec Kralove) 2002;45(2):83-84. DOI: https://doi.org/10.14712/18059694.2019.59

(7). Kimata H, Tai H, Nakajima H. Reduction of allergic skinresponses and serum allergen-specific IgE and IgE-in-ducing cytokines by drinking deep-sea water in patientswith allergic rhinitis. Otorhinolaryngol Nova 2001;11:302-303. DOI: https://doi.org/10.1159/000068306

(8). Tai H, Nakagawa K, Watanabe Y, Yokoyama Y, Nakaji-ma H, Ikegami Y, Nozaki Y, Kikuchi Y. Effect of highmineral water prepared from deep-sea water on humanblood pressure and hemorheological parameter. DeepOcean Water Res 2000;1:53-55.

(9). Harari M, Shani J, Seidl V, Hristakieva E. Climatothera-py of atopic dermatitis at the dead sea: demographic eva-luation and cost-efectiveness. Int J Dermatol 2000;39(1):59-69. DOI: https://doi.org/10.1046/j.1365-4362.2000.00840.x

(10). Holmstrom M, Rosen G, Wahlander L. Effect of nasallavage on nasal symptoms and physiology in wood in-dustry workers. Rhinology 1997;35(3):108-112.

(11). Seppey M, Schweri T, Hausler R. Comparative rando-mised clinical study of tolerabilitiy and efficacy of rhi-nomer force 3 versus a reference product in post-opera-tive care of the nasal fossae after endonasal surgery. ORLJ Otorhinolaryngol Relat Spec 1996;58(2):87-92. DOI: https://doi.org/10.1159/000276805

(12). Laboratoires Quinton International S.L. Almoradí (CE).Laboratorios Quinton. [Sitio en internet]. Disponible en:www.quinton.es. Consultado: 18 de octubre de 2005.

(13). Rojas E, Lopez MC, Valverde M. Single cell gel electro-phoresis assay, methodology and applications. J Chromatogr B Biomed Sci Appl 1999;722(1-2):225-254. DOI: https://doi.org/10.1016/S0378-4347(98)00313-2

(14). Roldán GE. Actividad antibacteriana del agua de mar invitro, frente a Pseudomonas aeruginosa, Staphylococ-cus aureus y Escherichia coli. Medellín, 2003. Trabajode grado (bióloga). Universidad de Antioquia. Facultadde Ciencias Exactas y Naturales.

(15). Singh NP, McCoy MT, Tice RR, Schneider EL. A simpletechnique for quantitation of low levels of ADN damagein individual cells. Exp Cell Res 1988;175(1):184-191. DOI: https://doi.org/10.1016/0014-4827(88)90265-0

(16). Duthie SJ, Ross M, Collins A R. The influence of smo-king and diet on the hypoxanthine phosphoribosyl trans-ferase (hprt) mutant frecuency in circulating T lympho-cytes from a normal human population. Mutat Res1995;331(1):55-64. DOI: https://doi.org/10.1016/0027-5107(95)00051-J

(17). Konca K, Lankoff A, Banasik A, Lisowska H, Kuszews-ki T, Gózdz S, Koza Z, Wojcik A. A cross-platform pu-blic domain PC image-analysis program for the cometassay. Mutat Res 2003;534(1-2):15-20. DOI: https://doi.org/10.1016/S1383-5718(02)00251-6

(18). Beresford RA, Fastier FN. Effects of some s-alkylthio-uroniums and related compounds on the osmotic fragility and the membrane expansion of human erythrocytes.Br J Pharmacol 1980;71(1):253-258. DOI: https://doi.org/10.1111/j.1476-5381.1980.tb10933.x

(19). Re R, Pellegrini N, Proteggente A, Pannala A, Yang M,Rice-Evans C. Antioxidant activity applying an impro-ved ABTS radical cation decolorization assay. Free Ra-dic Biol Med 1999;26(9-10):1231-1237. DOI: https://doi.org/10.1016/S0891-5849(98)00315-3

(20). Colombia. Ministerio de Salud. Perfiles epidemiológicos:región costa Atlántica. Bogotá, D.C: El Ministerio; 1996.

(21). Hood DW. Los ciclos químicos del mar. p. 30-40. En: Vet-ter RC. Oceanografía: la última frontera. Buenos Aires: ElAteneo; 1976.

(22). Groff JL, Gropper SS, Hunt SM. Advanced nutrition andhuman metabolism. 2nd ed. St. Paul, MN: West Publis-hing; 1995. p 575.

(23). Vasant C, Balamurugan K, Rajaram R, Ramasami T. Apop-tosis of lymphocytes in the presence of Cr(V) complexes:role in Cr (VI)-induced toxicity. Biochem Biophys ResCommun 2001;285(5):1354-1360. DOI: https://doi.org/10.1006/bbrc.2001.5335

(24). Turekian KK. Los océanos. Barcelona: Omega; 1974.

(25). Piperakis SM, Visvardis EE, Tassiou AM. Comet assayfor nuclear DNA damage. Methods Enzymol 1999;300:184-194. DOI: https://doi.org/10.1016/S0076-6879(99)00125-1

(26). Hartmann A, Speit G. Genotoxic effects of chemical inthe single cell gel (SCG) test with human blood cells inrelation to the induction of sisterchromatid exchange(SCE). Mutat Res 1995;346(1):49-56. DOI: https://doi.org/10.1016/0165-7992(95)90068-3

(27). Márquez ME, López JB, Correa G, Pareja A, GiraldoNA. Detección del daño genotóxico agudo y crónico enuna población de laboratoristas ocupacionales expuestos. Iatreia 2003;16(4):275-282.

(28). Velásquez N. Mutagenicidad y genotoxicidad de extrac-tos de agua tratada para el consumo humano y de subpro-ductos de la cloración. Medellín, 2000. Trabajo de grado (bióloga). Universidad de Antioquia. Facultad deCiencias Exactas y Naturales.

Published

2009-02-02

How to Cite

1.
Soler T W, Velásquez E N, Miranda R LF, Zuluaga G D. Absence of genotoxicity of sea water from Coveñas:in vitro study on human leukocytes and erythrocytes. Rev. Fac. Nac. Salud Pública [Internet]. 2009 Feb. 2 [cited 2025 Feb. 6];23(2):1-6. Available from: https://revistas.udea.edu.co/index.php/fnsp/article/view/473

Issue

Section

Research