Portuguese Version

Year:  2006  Vol. 72   Ed. 4 - (13º)

Artigo Original

Pages: 523 to 527

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Histological and ultrastructural aspects of the tongue in undernourished rats

Author(s): Marilda Aparecida Milanez Morgado de Abreu1, Luc Louis Maurice Weckx2, Cleonice Hitomi Watashi Hirata3

Keywords: protein-energy malnutrition, histology, tongue, scanning electron microscopy.

Abstract:
There are few published studies on the effects of protein-caloric undernourishment on the oral mucosa. Objectives: The objective of this study is to verify the histological and ultrastructural aspects of the tongue mucosa in protein-caloric undernourished adult rats. Material and Methods: A clinical experimental study was done in thirty Wistar rats, 15 controls and 15 with protein-caloric undernourishment. The last group received ration in small amounts, with a reduced casein content, during 45 days. Rats were weighed every 3 days, from the first (90 days of life) to the last day of a 45-day dietary period, when they were sacrificed. Plasma was used for protein electrophoresis and their tongues were prepared for light and scanning electron microscopy. Analysus of variance and Student's t-test were used for statistical analysis. Results: A significant decrease in weight and in plasma proteins was found in protein-caloric undernourished rats compared to the control group. Histological findings revealed no differences between the two groups and there were no statistically significant differences in the filiform papilla count under the scanning electron microscopy. Conclusion: Protein-caloric undernourishment does not cause alterations in the tongue mucosa of adult rats.

INTRODUCTION

Although clinical findings in the mouth such as tongue mucosa atrophy, loss of papillae, and angular cheilitis, are frequently related to nutrition, there are few studies on the effect of protein-energy malnutrition over the oral mucosa and the tongue1-4.

Winkler and Nakamoto in 19825 studied the effects of prenatal malnutrition on tissue development in the mouth of newborn rats. They described histological alterations on the tongue such as reduced cell numbers and the increased size of these cells. Malnutrition also affected incisor and molar dental bacteria. Results suggested that adequate protein intake was extremely important for the healthy development of teeth and the tongue.

Aldred et al. in 19896 reported an increase in yeasts in the mouth of malnourished children, but found no other clear clinical signs.

The aim of this paper is to study the effect of protein-energy malnutrition on the mucosa of the tongue of adult rats, using optical and scanning electron microscopy.

MATERIAL AND METHODS

This is an experimental study made on thirty "WISTAR" rats aged 90 days and weighing between 180 and 220 grams. Animals were placed in individual cages measuring 40 x 20 x 13 cm each, containing sawdust and water with no restrictions.

Animals were randomly divided into two groups each containing 15 rats. The first group (control) received ration composed of casein (18%), corn (4%), salt (4%), multivitamins (1%), benzoate (0.1%), oil (8%), sugar (10%), corn starch excipient qs (100%). The second group (with protein-energy malnutrition) received a similar ration but with changes in the relative components of casein (1%), given as ration weighing 6 grams/day.

Rats were weighed every 3 days from the first day (age 90 days) until the final day of the 45-day diet period. At this point, having been weighed, the animals were guillotined. Blood was collected and plasma was obtained by centrifugation for protein electrophoresis.

The tongue was sectioned and completely removed. The anterior region of the tongue was sectioned for light and electron microscopy.

Fragments were included in paraffin for microtome sectioning and hematoxylin-eosin (HE) stained. Slides were studied under a common optical microscopy at 50 and 400 times amplification. The following parameters were assessed: epithelial layer uniformity or lack thereof, the presence or absence of an inflammatory infiltrate in the lamina propria, and areas with or without filiform and fungiform papillae in the anterior region of the tongue. Uniformity was considered as the regular distribution of layers with similar cell maturity.

Seven cases in each group (control and malnourished) were assessed by electron microscopy. The number of filiform papillae was one of the study parameters; counts were obtained from electron microscopy pictures taken using VP 120 black-and-white film. Inclusion criteria were: the number of whole filiform papillae (which included a base and a conical projection) counted on pictures magnified 100 times, measuring 9 x 9 cm, using a 2.3 cm2 area, in each case counting 5 to 10 regions. Tangential papillae in the left and lower borders were included; tangential papillae in the right and upper borders were excluded; regions with fungiform papillae were excluded7.

Statistical analysis included the analysis of variance to compare average rat weight, protein electrophoresis and the papillary count. Student's T-test was used to study the difference between two independent samples8 with a 0.05 or 0.5% significance level.

RESULTS

Weight increased in the control group and decreased in the protein-energy malnutrition group after 45 days. Statistical analysis revealed a significant difference between both samples on the 45th day, as shown on Chart 1.

The plasma protein electrophoresis profile disclosed a significant reduction in total plasma proteins in the protein-energy malnutrition group on the 45th day compared to controls (Tables 1 and 2).

Common light microscopy histology revealed no differences between the control group and the protein-energy malnutrition group for the parameters we studied (Figures 1 and 2).

Common light microscopy histology of the tongues of rats in both groups showed stratified epithelium with uniform layers in 15 cases. Neither group had an inflammatory infiltrate or areas of papillary loss in the tongue. Keratinization of the ventral surface of the tongue was seen in 2 cases in the control group (with thickening of the keratin layer in 1 control group case) and in no case of the protein-energy malnutrition group.

There were no statistically significant differences in the filiform papillae count by electron microscopy on the tongue in both the control group (7 cases) and the protein-energy malnutrition group (7 cases), as seen on Tables 3, 4 and 5 (Figures 3 and 4).

Figure 1. Photomicrograph of a sagittal section of a filiform papilla. Stratified epithelium of the normal tongue mucosa in the control group - Magnification - 100X.


Figure 2. Photomicrograph of a sagittal section of a filiform papilla. Stratified epithelium of the normal tongue mucosa of rats with protein-energy malnutrition - Magnification - 100X.


Figure 3. Photomicrograph of the anterior dorsal surface of the adult rat tongue. Filiform and fungiform papillae over which are taste buds. Control group. Original Magnification - 200X.


Figure 4. Photomicrograph of the anterior dorsal surface of the adult rat tongue showing a papilla inclined antero-posteriorly. Protein-energy malnutrition group. Original Magnification - 200X.


Chart 1. Histogram of rat body weight averages in the control group and the protein-energy malnutrition during the 45-day period.

DISCUSSION

Malnutrition is a significant public health problem in the world; protein-energy malnutrition is one of the most severe forms of this condition. It affects mostly children in poorer coutries, where the prevalence is estimated as 1/3 of children between birth and five years of age9.

The World Health Organization defines protein-energy malnutrition as "the range of pathological conditions arising from a deficiency of cell intake, transport or use of nutrients, commonly associated with infection, occurring with greater frequency in infants and pre-school children"10.

Protein-energy malnutrition causes a variety of clinical conditions, the most apparent being effects on body measurements and weight as a whole or for specific organs. Malnutrition develops in a sequence starting from exclusive protein deficiency (kwashiorkor) to protein-energy deficiency (marasmus)11. In man, nutritional deficiency is never an exclusively caloric or protein deficiency; both are usually associated.

Clinically there is a strong association between protein-energy malnutrition and hypovitaminosis, and glossities and stomatitis1-4. In out study the 45-day protein-energy deficient diet effectively produced malnutrition in rats aged 90 days, as shown in the statistically significant differences between the control group and the protein-energy malnutrition group; there was both weight loss and a reduction in total proteins. However, the histological study of the tongue of protein-energy malnutrition rats, both under common optical microscopy and electron microscopy did not reveal changes such as glossitis or loss or filiform papillae.

There are no published papers on the effects of protein-energy malnutrition specifically on the mucosa of the mouth or tongue. There is one paper describing changes in prenatal malnutrition5. In contrast, there are many reports on the clinical, histological and ultra-structural changes of the tongue mucosa in iron deficiency, particularly during pregnancy and the postnatal period1-4,12, and vitamin deficiency, in particular vitamin B deficiency12,13, both of which describe tongue mucosa alterations such as lobulation, fissures, edema and loss of papillae. These studies corroborate our daily clinical findings, where glossitis and loss of papillae are seen in patients with iron deficiency, whereas no evident tongue alterations are seen in patients with protein-energy malnutrition.

Methodological limitations do not allow us to state with certainty that there are no alterations of the tongue mucosa in animals subjected to protein-energy malnutrition, as we studied only adult animals. If our study had included animals in the growing or prenatal phases, which are more sensitive to malnutrition, we might have found some evident change. A further point is the duration of malnutrition. Chronic malnutrition could possibly lead to such changes, as described by some authors11,14. Therefore, our investigation opens the door for further studies and new methods.

Using other animal species to understand what happens on the tongue in protein-energy malnutrition leads to a further issue, which is to extrapolate such results to human beings. Although we found no published papers comparing the tongue mucosa between these species, it is known that rats have biological similarities to human beings, which is why it is used so frequently as an experimantal animal15.

Regardless of our belief that glossitis is connected to malnutrition and hypovitaminosis in general, we do not exclude the possibility of further reviews on this subject, as other causes are certainly a matter for research. Studies involving prolonged or chronic protein-energy malnutrition, or conducted in prenatal or growing animals, could add further elements to clarify such issues.

CONCLUSION

Histology and ultra-structural studies of the anterior region of the tongue in 90-day rats subjected to protein-energy malnutrition for 45 days reveal that:

 Protein-energy malnutrition does not alter the tongue mucosa in adult rats.

REFERENCES

1. Steele B, Sofaer JA, Southam JC. Short communication lingual epithelial thickness in mice with inherited iron-deficiency anaemia (sla). Archs Oral Biol 1981;26:343-4.

2. Rennie JS, MacDonald DG. Cell kinectics of hamster ventral tongue epithelium in iron deficiency. Archs Oral Biol 1984;29(3):195-9.

3. Rennie JS, MacDonald DG. Quantitative histological analysis of the epithelium of the ventral surface of hamster tongue in experimental iron deficiency. Archs Oral Biol 1982;27:393-7.

4. Scott J, Valentine JA, Hill CA et al. Morphometric analysis of atrophic changes in human lingual epithelium in iron deficiency anaemia. J Clin Path 1985;38:1025-9.

5. Winkler MM, Nakamoto T. Effects of prenatal malnutrition on development of oral tissue in neonatal rats. Ann Nutr Metab 1982;26:248-53.

6. Aldred MJ, Arendorf TM, Wade WG et al.. Frequency and density of yeasts in the mouths of malnourished children. Comm Dent Oral Epid 1989;17(3):136-8.

7. Loud AV, Anversa P. Biology of disease. Morphometric analysis of biologic processes. Lab Invest 1984;50:250-61.

8. Sieger S. Estatística no paramétrica aplicada a las ciencias de la conduta. 2ª ed., Editorial Trillas: México, 1975; p.346.

9. Onis M, Habicht J. Anthropometric reference data for international use: recommendations from a World Health Organization Expert Committee. Am J Clin Nutr 1996;64(4):650-8.

10. SISVAN. Sistema de Vigilância Alimentar e Nutricional. Ministério da Saúde. Instituto Nacional de Alimentação e Nutrição. Brasília: SISVAN-INAN 1991: [Boletim Nacional nº1].

11. Alves DC. Desnutrição. In: Augusto ALP, Alves DC, Mannarino IC, Gerude M, organizadores. Terapia nutricional. São Paulo: Atheneu; 1995. p.220.

12. Hjorting-Hansen E, Bertram V. Oral aspect of pernicious anaemia. Brit Dent J 1968;125(6):266-70.

13. Pindborg JJ. Atlas of diseases of the oral mucosa, 4th., Saunders: Copenhagen, 1985; p.130-49.

14. Batista Filho M. Prevalência e estágios da desnutrição protéico-calórica em crianças da cidade de São Paulo [tese]. São Paulo: Faculdade de Saúde Pública da Universidade de São Paulo; 1976.

15. Fagundes DJ, Taha MO. Modelo animal de doença: critérios de escolha e espécies de animais de uso corrente / Animal disease model: choice s criteria and current animals specimens. Acta Cir Brs 2004;19(1):59-65.


1 Master's degree, graduate studies at the Stomatology Sector, Otorhinolaryngology and Disturbances of Human Communication Department and the Dermatology Department; Sao Paulo Federal University/Paulista Medical School.
2 Lecturer, Full Professor of the Pediatric Otorhinolaryngology and Disturbances of Human Communication Department; Hea of the Otorhinolaryngology and Head & Neck Surgery Department, Sao Paulo Federal University/Paulista Medical School.
3 Master's, Doctor, Head of the Stomatology Sector, Otorhinolaryngology and Disturbances of Human Communication Department and the Dermatology Department; Sao Paulo Federal University/Paulista Medical School.
Sao Paulo Federal University/Paulista Medical School (UNIFESP/EPM).
Address for correspondence: Marilda Aparecida Milanez Morgado de Abreu - Rua Brasil 1599 Centro Dracena SP 17900-000
Telephone: (0xx18) 3821-4630 - Fax: (0xx18) 3821-2276 - E-mail: lfmabreu@uol.com.br
This paper was submitted to the ABORL-SGP (Publication Management System) of the RBORL on 17/10/2005 and approved on 5/5/2006.
Paper submitted to the ABORL-CCF SGP (Management Publications System) on October 17th, 2005 and accepted for publication on May 5th, 2006.

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