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Revista Brasileira de Hematologia e Hemoterapia

Print version ISSN 1516-8484

Rev. Bras. Hematol. Hemoter. vol.34 no.4 São Paulo  2012

http://dx.doi.org/10.5581/1516-8484.20120068 

SCIENTIFIC COMMENTS

 

Animal models of human nutritional diseases: a short overview

 

 

Carlos Augusto Carvalho de Vasconcelos

Universidade Federal de Pernambuco - UFPE, Recife, Brazil

Corresponding author

 

 

The long history of animal experimentation describes the use of a series of methods that not only include the use of whole animals but isolated organs, isolated tissues, tissue cultures, isolated cells, subcellular components, modeling and structure-activity relationships. Data from government reports, from medical research council reports and from scientific publications point to the extent to which these methods are used. A study of the revolution of therapeutics and of the recent decline in drug innovation, raises the question as to whether the trend away from experimentation on the whole organism may have gone too far(1).

Several factors were very important in the discovery of essential nutrients including the recognition that certain diseases are directly associated to diet. Subsequently, the development of suitable animal models investigated animals that have specific requirements for the nutrient in question, the use of bioassay procedures to first produce and then ameliorate one or more of the symptoms related to deficiency and the development of defined purified diets that could be made singly deficient in a nutritional entity. Generally, the diet-disease association preceded both isolation of the nutrient per se as well as the establishment of nutrient function(2,3).

The STZ-diabetes model is widely used to investigate diabetic peripheral neuropathies by transmission electron microscopy (TEM). Morphological alterations of the vestibulocochlear nerve in experimental diabetes are being described for the first time and such information corroborates to a better understanding of the changes in hearing observed in diabetic patients(4). The nutritional status of animals can change these results, as can the cellular composition and emerging inflammatory reactions. Leukocyte counts can easily be studied by TEM and with the advancing age of mice the results may be different. There are several forms of causing undernourishment in animals with the most common being protein malnutrition caused by the ingestion of small quantities of milk protein - casein (about 8%), as described in the original article by Viana et al. published in this issue of the Revista Brasileira de Hematologia eHemoterapia(5).

This scientific paper shows the importance of physical training on the physiological adaptation of leukocytes in situations of neonatal malnutrition. Currently many experiments are underway to try to reconcile animal research to effectively and ethically extrapolate the results to humans.

 

References

1. Paton W. Man and mouse: animals in medical research. Oxford: Oxford University Press; 1984.         [ Links ]

2. Combs GF Jr. The vitamins. San Diego: Academic Press; 1992.         [ Links ]

3. Baker DH. Animal models in nutrition research. J Nutr. 2008;138(2):391-6. Review.         [ Links ]

4. Vasconcelos CA, Fazan VP, Moore KC, Nessler RA, Valença MM. Transmission electron microscopy studies of the vestibulocochlear nerve in chronic diabetic rats. Int J Morphol [Internet]. 2011[cited 2012 Jun 21];29(1):272-7. Available from: http://www.scielo.cl/pdf/ijmorphol/v29n1/art45.pdf        [ Links ]

5. Viana MT, Perez MC, Ribas VR, Martins GF, de Castro CM. Leukocyte, red blood cell and morphological adaptation to moderate physical training in rats undernourished in the neonatal period. Rev Bras Hematol Hemoter. 2012;34(4):285-91.         [ Links ]

 

 

Corresponding author:
Carlos Augusto Carvalho de Vasconcelos
Universidade Federal de Pernambuco - UFPE Laboratório de Nutrição Experimental e Dietética/LNED
Prof. Nelson Chaves, s/n Cidade Universitária
50670-901 Recife, PE, Brazil
Phone: 55 81 21268470
cacv@ufpe.br

Conflict-of-interest disclosure: The authors declare no competing financial interest
Submitted: 8/3/2012
Accepted: 8/6/2012

 

 

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