Printer Friendly

Topographic anatomy of the spinal cord and vertebromedullary relationships in Mazama gouazoubira Fisher, 1814 (Artiodactyla; Cervidae)/Anatomia topografica da medula espinal e relacoes vertebromedulares em Mazama gouazoubira Fisher, 1814 (Artiodactyla; Cervidae).

Introduction

Brazil has the most varied mastofauna of the entire Neotropical region (ROCHA; DALPONTE, 2006). Cervids are a group of animals that belong to the order Artiodactyla and the family Cervidae is distributed worldwide in a variety of biomes, although they are becoming rare in several areas of natural occurrence (MARQUES et al., 2007). According to Melo et al. (2007), six different genera are endemic to South America: Blastocerus, Hippocamelus, Ozotoceros, Pudu, Odocoileus and Mazama. The cervid Mazama gouazoubira, known popularly as brocket deer, is grayish brown and the ventral side of its tail is white. Its antlers are short simple straight spikes, and it has characteristic odor glands behind its eyes and in its hocks (NASCIMENTO et al., 2000).

The degree of threat and ecological importance of this group have highlighted the need to include information about these animals in environmental inventories and diagnoses. Moreover, knowledge of the topography of the spinal cord is indispensable in clinical practice for the diagnosis, prognosis and treatment of vertebromedullary injuries, and it is sometimes necessary to locate injuries of the central nervous system at a vertebral level, a method that is possible by associating specific sensory and motor deficiencies in a given spinal segment (DYCE et al., 2004; MACHADO, 2003), especially in anesthesiology, in order to block specific spinal nerves (DYCE et al., 2004).

The anatomy of the medullary segments has been studied and described in humans (WILLIAMS et al., 1995), felines, monkeys (CARVALHO-BARROS et al., 2003), sheep (RAO, 1990), coatis (GREGORES et al., 2010), freshwater dolphins (MACHADO et al., 2003) and sea lions (FETTUCCIA; SIMOES-LOPES, 2004) , but the pattern of the medullary topography of M. gouazoubira has not yet been reported. Several aspects such as the macroscopy of the brachial plexus (MELO et al., 2007), the biology (RICHARD; JULIA, 2001) and the incidence of parasites (DEEM et al., 2004; MARQUES et al., 2007) of this deer have been reported, but there is a paucity of information about its anatomy, particularly about its nervous system.

Considering the importance of detailed knowledge about the comparative anatomy of the nervous system of vertebrates and its use in veterinary medicine, the purpose of this investigation was to describe the segments of the spinal cord and the vertebromedullary relationships in M. gouazoubira.

Material and methods

This study was based on three specimens of M. gouazoubira which were sent by the Environmental Police to the Federal University of Uberlandia Faculty of Veterinary Medicine in Uberlandia, State of Minas Gerais, Brazil. The cervids were dubbed E1--adult female, E2--adult male, and E3--young female.

The skin, epaxial muscles, vertebral arches and epidural fatty tissue were removed from the back, exposing the spinal cord and the spinal nerve roots. The craniosacral (CS) length of the animals was measured with a pachymeter with 0.05 mm precision, starting from the external occipital protuberance to the sacrocaudal interarch space. The medullary segments evaluated were the cervical (CS), thoracic (TS), lumbar (LS), and sacrocaudal (SCS) segments and the medullary cone (CM). The indices of each segment of the spinal cord were then calculated, in percentage, by dividing the length of the medullary segment by the sacrocaudal length. The mean lengths of the medullary segments were determined by applying a simple descriptive statistic, and the distances between the nerve roots were determined based on an analysis of variance and on Tukey's test with 5% significance.

Results and discussion

Table 1 lists the mean values of the length of the segments of the spinal cord of M. gouazoubira, while Table 2 shows the percent index of each segment in relation to the craniocaudal length, and Table 3 indicates the topography of the medullary segments.

The spinal column of M. gouazoubira has seven cervical, thirteen thoracic, six lumbar, and five sacral vertebrae. Thirty-two pairs of spinal nerves were measured, eight cervical, thirteen thoracic, six lumbar and five sacral pairs.

In domestic animals, the spinal cord is divided into cervical, thoracic, lumbar, sacral, and caudal or coccygeal segments. Wild animals such as Chrysocium brachiurus (MACHADO et al., 2002), Arctocephalus australis (MACHADO et al., 2003), Tamandua tetradactila and M. gouazoubira show the same segmentation, but the two last segments are considered a single fraction (Figures 1 and 2).

[FIGURE 1 OMITTED]

[FIGURE 2 OMITTED]

The spinal cord of M. gouazoubira is an elongated and cylindroidal mass, dorsoventrally flattened, with two dilatations called the cervical and lumbar intumescences, like those of other animals (Figures 1 and 2). The cord ends between S3 and S4 in M. gouazoubira (Table 3), at the level of the second sacral vertebra in horses, cattle (DEEM et al., 2004) and sheep (RAO, 1990), in the cranial portion of the seventh lumbar vertebra in dogs (GETTY et al., 1986), at S3 in buffalos (RAO, 1976) and impalas (RAO et al., 1993), and between L1 and L2 in humans (WILLIAMS et al., 1995).

In the relationship between the medullary segments and the length of the vertebral column, the indices of the cervical, thoracic, lumbar and sacrocaudal segments are, respectively, 18.47, 35.26, 34.17 and 12.02% in Oryctolagus cuniculus (SANTOS et al., 1999), 22.40, 49.32; 24.07 and 3.68% in Felis concolor, 21.97, 50.83, 11.20 and 15.97% in Tamandua tetradactyla, and 28.02, 35.34, 19.68 and 6.93% in M. gouazoubira (Table 2).

The average lengths of the medullary segments are 175.07 mm for the cervical, 226.03 mm for the thoracic, 123.47 mm for the lumbar and 43.63 mm for the sacrocaudal segment. Notable differences have been found between the indices of the segments of the spinal cord of M. gouazoubira and those of other species.

The funneling of the lumbar segment of the spinal cord originates in the medullary cone (ERHART, 1992; GETTY et al., 1986; GODINHO et al., 1987), which begins between L5 and L6 in Equus caballus and Chrysocium brachiurus (MACHADO et al., 2002), between L6 and L7 in Oryctolagus cuniculus (SANTOS et al., 1999), in L5 of Arctocephalus australis (MACHADO et al., 2003), L6 of Herpailurus yagouaroundi (CARVALHO et al., 2003) and Felis catus (CAMARA-FILHO et al., 1998), varies between L5 and L7 in pacas (SCAVONE et al., 2007) and between L2 and L6 in M. gouazoubira (Table 3, Figures 2 and 3).

[FIGURE 3 OMITTED]

The apex of the medullary cone occurs between the fifth or sixth lumbar vertebra in pigs, between the sixth or seventh lumbar vertebra in dogs, the second sacral vertebra in horses, and more variably between the sixth lumbar and third sacral vertebrae in cats (DYCE et al., 2004). However, Camara-Filho et al. (1998) describe the end of the medullary cone in Felis catus as occurring in the first sacral vertebra. In A. australis, the medullary cone ends in the body of the sixth lumbar vertebra (MACHADO et al., 2002), in H. yagouaroundi in the second lumbar vertebra (CARVALHO et al., 2003), in pacas it varies between L7 and S1 (SCAVONE et al., 2007), and in rabbits (SANTOS et al., 1999) between S1 and S4, as it does in M. gouazoubira, where it extends to the sacral portion of the vertebral column, more specifically between S2 and S3 (Figures 2 and 3). This arrangement differs from other ruminants, since Dyce et al. (2004) reported that in the latter, the medullary cone ends at the level of the sixth lumbar vertebra.

The reported lengths of the medullary cone are 100 mm in horses, 45.1 mm in rabbits (SANTOS et al., 1999), 88.5 mm in sheep (SANTOS et al., 1999); and 33.9 mm in Agouti paca (SCAVONE et al., 2007). The medullary cone lengths measured in M. gouazoubira were 35.1 mm, 44.3 mm and 59.4 mm in specimens E1, E2 and E3, respectively, with a mean length index of 7.53%.

In M. gouazoubira, thickening of the spinal cord corresponding to the cervical intumescence was found between segments C4-T1 and of lumbar intumescence between L3-L6 (Figures 1 and 2). In buffalos, this thickening includes segments C6-T1 for the cervical and L3-S1 for the lumbar intumescence (RAO, 1976). In sheep, these dilatations correspond to C5-T2 and L4-S1, respectively (RAO, 1990), while in cats the cervical segment in C3 showed the largest volume (THOMAS; COMBS, 1962), and in impala these values were reported in C3-L13 and L2, respectively (RAO et al., 1993). In M. gouazoubira, the two intumescences represent only a small portion of each segment of the spinal cord and are shorter than in the other aforementioned animals.

The distances between the spinal nerve roots (Figure 4) vary conspicuously along the length of the spinal cord (Table 4).

The measurements of segment C2-C6 show the longest distances between nerve roots. There is a stable decrease between the values measured in the region of the thoracic segment and an increase in the region comprised between segments L2-L5. However, the space between C2-C3 shows the longest distances between nerve roots. The longest distances between nerve roots have been reported in segments C2-C6 in buffalos (RAO, 1976), C2-C3 in dogs (FLETCHER; KITCHELL, 1966), C2-C4 in sheep (RAO, 1990) and C2-C3 impalas (RAO et al., 1993).

The distances between nerve roots are similar in buffalos (RAO, 1976), sheep (RAO, 1990), impalas (RAO et al., 1993) and dogs (FLETCHER; KITCHELL, 1966). In buffalos, impalas and dogs, the highest values are found in the cervical region, precisely between C2-C3, as in M. gouazoubira. In sheep, the longest distances between nerve roots are also found between C3-C4, i.e., a distance of 2.97 cm (RAO, 1990). Generally speaking, the measurements described for buffalos, sheep, impalas and dogs are similar to those of M. gouazoubira.

[FIGURE 4 OMITTED]

In cats, Thomas and Combs (1962) stated these distances decreased between segments T10-T12. In impalas, Rao et al. (1993) confirmed a decrease of these values in the craniocaudal direction, and reported that the smallest distances were found between T1-T2. This statement cannot be made for M. gouazoubira, since the distance between nerve roots varies constantly along the length of the spinal cord (Figure 4). One can therefore only infer that these values are stable or tend to vary toward lower values in the craniocaudal direction, except for segments L3-L6, which present the lumbar intumescence.

No significant variations were found in the distances of the nerve roots of the cervical segment in the two antimeres, where the overall average distance was 2.23 cm. The analysis of the thoracic segment showed a significant variation in the right and left antimeres of specimen E3, in which the measured values were smaller than in E1 and E2. The mean index of the distances was 2.06 cm. The lumbosacral segment of specimen E1 varied significantly in relation to that of E2 and E3. The overall average in this segment was 1.98 cm.

Conclusion

The indices of the length of the cervical, thoracic, lumbar and sacrocaudal segments of the spinal cord of M. gouazoubira are similar to those reported for other animals, especially ruminants, albeit with some peculiarities.

The distances measured between the spinal nerve roots show a tendency to decrease in the craniocaudal direction, except for the portions comprised between the cervical and lumbar intumescences.

In rare cases, no significant variations were found in the distances between the nerve roots in the various segments (cervical, thoracic and lumbosacral) in the different specimens (E1, E2 and E3).

DOI: 10.4025/actascibiolsci.v32i2.5061

Received on September 12, 2008.

Accepted on March 2, 2009.

References

CAMARA-FILHO, J. A.; RODRIGUES, M.; SILVEIRA, R. Determinacao morfologica do cone medular espinhal no espaco da primeira vertebra sacral. Revista do Centro de Ciencias Medicas da EFF, v. 2, n. 2, p. 55-59, 1998.

CARVALHO, S. F. M.; SANTOS, A. L. Q.; AVILA-JUNIOR, R. H.; ANDRADE, M. B.; MAGALHAES, L. M.; MORAIS, F. M.; RIBEIRO, P. I. R. Topografia do cone medular em um gato mourisco, Herpailurus yagouaroundi (Severtzow, 1858) (FELIDAE). Archives of Veterinary Sicience, v. 8, n. 2, p. 35-38, 2003.

CARVALHO-BARROS, R. A.; PRADA, I. L. S.; SILVA, Z.; RIBEIRO, A. R.; SILVA, D. C. O. Constituicao do plexo lombar do macaco Cebus apella. Brazilian Journal of Veterinary Research and Animal, v. 40, n. 5, p. 373-381, 2003.

DEEM, S. L.; NOSS, A. J.; VILLARROEL, R.; UHART, M. M.; KARESH, W. B. Disease survey of free-ranging Grey Brocket Deer (Mazama gouazoubira) in the Gran Chaco, Bolivia. Journal of Wildlife Diseases, v. 40, n. 1, p. 92-98, 2004.

DYCE, K. M.; SACK, O. W.; WENSING, C. J. G. Tratado de anatomia veterinaria. Rio de Janeiro: Elsevier, 2004.

ERHART, E. A. Elementos de anatomia humana. Sao Paulo: Atheneu, 1992.

FETTUCCIA, D. C.; SIMOES-LOPES, P. C. Morfologia da coluna vertebral do boto cinza, Sotalia guianensis (Cetacea, Delphinidae). Biotemas, v. 17, n. 2, p. 125-148, 2004.

FLETCHER, T. F.; KITCHELL, R. L. Anatomical studies on the spinal cord segments of the dog. American Journal of Veterinary, v. 27, n. 121, p. 1759-1767, 1966.

GETTY, R.; ROSENBAUM, C. E.; GHOSHAL, N. G.; HILLMANN, D. Anatomia dos animais domesticos. Rio de Janeiro: Guanabara Koogan, 1986.

GODINHO, H. P.; CARDOSO, F. M.; NASCIMENTO, J. F. Anatomia dos ruminantes domesticos. Belo Horizonte: ICB-UFMG, 1987.

GREGORES, G. B.; BRANCO, E.; CARVALHO, A. F.; OLIVEIRA, P. C.; FERREIRA, G. J.; CABRAL, R.; FIORETTO, E. T.; MIGLINO, M. A.; CORTOPASSI, S. R. G. Topografia do cone medular do quati. Biotemas, v. 23, n. 2, p. 35-42, 2010.

MACHADO, A. B. M. Neuroanatomia functional. Sao Paulo: Atheneu, 2003.

MACHADO, G. V.; FONSECA, C. C.; NEVES, M. T. D.; PAULA, T. A. R.; BENJAMIN, L. A. Topografia do cone medular no lobo-guara (Chrysocyum brachyurus Illiger, 1815). Revista Brasileira de Ciencias Veterinaria, v. 9, n. 2, p. 107-109, 2002.

MACHADO, G. V.; LESNAU, G. G.; BIRCK, A. J. Topografia do cone medular no lobo marinho (Arctocephalus australis Zimmermann, 1783). Arquivos de Ciencias Veterinarias e Zoologia da Unipar, v. 6, n. 1, p. 11-14, 2003.

MARQUES, S. M. T.; QUADROS, R. M.; MAZZOLLI, M.; JESUS, J. R. Parasitos gastrintestinais em veados (Mazama gouazoubira) de areas nativas no planalto de Santa Catarina, Brasil. Veterinaria em Foco, v. 5, n. 1, p. 3-9, 2007.

MELO, S. R.; GONCALVES, A. F. N.; CASTRO SASAHARA, T. H.; FIORETTO, E. T.; GERBASI, S. H.; MACHADO, M. R. F.; GUIMARAES, G. C.; RIBEIRO, A. A. C. Sex-related macrostructural organization of the deer's brachial plexus. Anatomia Histologia Embryologia, v. 36, n. 4, p. 295-299, 2007.

NASCIMENTO, A. A.; BONUTI, M. R.; MAPELI, E. B. ; TEBALDI, J. H.; ARANTES, I. G.; ZETTERMANN, C. D. Infeccoes naturais em cervideos (Mammalia, Cervidae) procedentes dos estados do Mato Grosso do Sul e Sao Paulo, por nematoideos Trichostrongyloidea Cram, 1927. Brazilian Journal of Veterinary Research and Animal Science, v. 37, n. 2, p. 12-31, 2000.

RAO, G. S. A study of spinal cord segments in the Indian Buffalo. Journal of the Anatomical Society of India, v. 16, n. 1, p. 43-50, 1976.

RAO, G. S. Anatomical studies on ovine spinal cord. Anatomischer Anzeiger, v. 171, p. 261-264, 1990.

RAO, G. S.; KALT, D. J.; KOCH, M.; MOJOK, A. A. Anatomical studies on the spinal cord segments of the Impala (Aepyceros melampus). Anatomia, Histologia, Embryologia, v. 22, p. 273-278, 1993.

RICHARD, E.; JULIA, R. P. Dieta de Mazama gouazoubira (Mammalia, Cervidae) En un ambiente secundario de yungas. Iheringia. Serie Zoologia, n. 90, p. 147-156, 2001.

ROCHA, E. C.; DALPONTE, J. C. Composicao e caracterizacao da fauna de mamiferos de medio e grande porte em uma pequena reserva de cerrado em Mato Grosso, Brasil. Revista Arvore, v. 30, n. 4, p. 669-678, 2006.

SANTOS, A. L. Q.; LIMA, E. M. M.; SANTANA, M. I. S. Length of spinal cord and topography of medullar cone in rabbit (Oryctolagus cuniculus). Bioscience Jornal, v. 15, n. 2, p. 45-62, 1999.

SCAVONE, A. R.; GUIMARAES, G. C.; RODRIGUES, V. H. V.; SASAHARA, T. H. C.; MACHADO, M. R. F. Topografia do cone medular da paca (Agouti paca, Linnaeus --1766). Brazilian Journal of Veterinary Research and Animal Science, v. 44, supl., p. 53-57, 2007.

THOMAS, C. E.; COMBS, C. M. Spinal cord segments: A gross structure in adult cat. American Jorunal of Anatomy, v. 110, n. 1, p. 37-47, 1962.

WILLIANS, P. L.; WARWICK, L.; DYSON, M.;BANNISTER, L. H. Gray anatomia. Rio de Janeiro: Guanabara Koogan, 1995.

Fabiano Campos Lima, Andre Luiz Quagliatto Santos *, Betania Carvalho Lima, Lucelia Goncalves Vieira and Liria Queiroz Luz Hirano

Laboratorio de Pesquisa em Animais Silvestres, Faculdade de Medicina Veterinaria, Universidade Federal de Uberlandia, Av. Amazonas, 2245, 38405-302, Jardim Umuarama, Uberlandia, Minas Gerais, Brazil, *Author for correspondence. E-mail: quagliatto@famev.ufu.br
Table 1. Length, in millimeters, of the cervical (CS), thoracic
(TS), lumbar (LS), sacrocaudal (SCS), medullary cone (CM), and
craniosacral (CS) segments and the spinal cord (SpC) of M.
gouazoubira.

        E1       E2       E3

SC    184.4    173.9    166.9
TS    255.4    228.4    194.3
LS    139.1    123.3    108.0
SCS    39.0     37.7     54.2
CM     35.1     44.3     59.4
CS    658.8    652.4    567.6
SpC   617.9    563.3    523.4

Table 2. Index, in percentage, of the cervical (CS), thoracic (TS),
lumbar (LS), and sacrocaudal (SCS) segments and the medullary
cone (CM) in relation to the craniosacral (CS) length of M.
gouazoubira.

        E1       E2       E3

CS    28.00    26.65    29.40
TS    38.77    35.01    32.23
LS    21.11    18.90    19.03
SCS    5.46     5.78     9.55
CM     5.33     9.55    10.46

Table 3. Topography of the beginning (B) and end (E) of the
cervical (CS), thoracic (TS), lumbar (LS) and sacrocaudal (SCS)
segments of the spinal cord and the medullary cone (CM) in M.
gouazoubira. FM- foramen magnum, C7- seventh cervical
vertebra, T1- first thoracic vertebra, T13- thirteenth thoracic
vertebra, L1- first lumbar vertebra, L2- second lumbar vertebra,
L3- third lumbar vertebra, L5- fifth lumbar vertebra, L6- sixth
lumbar vertebra, S1- first sacral vertebra, S2- second sacral
vertebra, S3- third sacral vertebra, S4- fourth sacral vertebra.

           E1              E2              E3

        B       E       B       E       B       E

CS     FM      T1      FM      T1      FM      C7
TS     T1      T13     T1      L1      C7      L1
LS     T13     L5      L1      L5      L1      L5
SCS    L5      S3      L5      S4      L5      S3
CM    L6/S1   S2/S3    L6     S2/S3    L2      S2

Table 4. Mean distances between the right (R) and left (L) spinal
nerve roots in M. gouazoubira. E1 (specimen 1), E2 (specimen 2),
E3 (specimen 3). Cervical (CS), thoracic (TS) and lumbosacral
segments (LSS) of the spinal cord.

           E1     E2     E3

CS    R   2.25   2.22   2.06
      L   2.49   2.13   2.21

TS    R   2.18   2.18   1.76
      L   2.39   2.11   1.76

LSS   R   2.26   1.62   1.88
      L   2.73   1.48   1.91
COPYRIGHT 2010 Universidade Estadual de Maringa
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2010 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:texto en ingles
Author:Lima, Fabiano Campos; Santos, Andre Luiz Quagliatto; Lima, Betania Carvalho; Vieira, Lucelia Goncalv
Publication:Acta Scientiarum Biological Sciences (UEM)
Date:Apr 1, 2010
Words:3128
Previous Article:Seasonal variation of metazoan parasites of Geophagus brasiliensis (Perciformes: Cichlidae) from the Guandu river, State of Rio de Janeiro,...
Next Article:Population structure of Kielmeyera rugosa Choisy (Clusiaceae) at Serra de Itabaiana National Park, Sergipe State/Estrutura populacional de Kielmeyera...
Topics:

Terms of use | Copyright © 2017 Farlex, Inc. | Feedback | For webmasters