Return to search

Estudo Histol?gico e localiza??o imuno-histoqu?mica de prote?nas do citoesqueleto em ov?rios, test?culos e epid?dimos de tr?s esp?cies de lagartos da Fam?lia Leiosauridae (Reptilia: Squamata). / Histological study and localization immunohistochemical of cytoskeleton proteins in testes and epididymis of three lizard species belonging to family leiosauridae (Reptilia: Squamata).

Submitted by Celso Magalhaes (celsomagalhaes@ufrrj.br) on 2018-09-24T15:13:44Z
No. of bitstreams: 1
2017 - Enely Maris da Silveira Firmiano.pdf: 12307016 bytes, checksum: d58bee7e5ddc0113fa072ab4e9aabc29 (MD5) / Made available in DSpace on 2018-09-24T15:13:44Z (GMT). No. of bitstreams: 1
2017 - Enely Maris da Silveira Firmiano.pdf: 12307016 bytes, checksum: d58bee7e5ddc0113fa072ab4e9aabc29 (MD5)
Previous issue date: 2017-08-29 / Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior - CAPES / Cap. I
The aim of the current study is to investigate the histological and histochemical description, as well as the presence and immunohistochemical distribution of cytoskeleton proteins such as alpha smooth muscle actin, desmin and vimentin in the ovaries, testes and epididymis of Enyalius bilineatus, Enyalius perditus and Urostrophus vautieri. These species are representatives of family Leiosauridae, in order to help developing a database on the reproductive biology of these lizards, which could be compared to that of other reptile species and vertebrates. The herein studied specimens are deposited in the Herpetological Collection of Federal University of Juiz de Fora. The animals? ovaries, epididymis and testes were removed and sent to the Histology and Embryology Laboratory (UFRRJ), where they were fixed, processed and then subjected to histological, histochemical and immunohistochemical techniques. The ovaries of these leiosauridae are functionally-active paired organs filled with ovarian follicles at different follicular development stages. These organs are covered by a simple cubic epithelium, which presents an underlying connective tissue layer called tunica albuginea. The testes are covered by the tunica albuginea and hold septa forming lobes where the seminiferous tubules are located in. The epididymis of these lizards are convolute ducts internally coated by an epithelium, whose shape ranges from simple cylindrical to simple cubic with stereocilia. The immunohistochemical analysis applied to the ovaries of the herein studied lizards showed moderate to strong reaction to the alpha smooth muscle actin in the teak layer and in endothelial cells of blood vessels. With respect to the species? testes, this cytoskeleton protein showed strong reaction in the tunica albuginea, interstitial tissue, and in endothelial cells of blood vessels. As for the epididymis, the alpha-actin showed immunohistochemical reaction in the capsule and in the interstitial tissue of the lizards. The antibody ?desmin? showed strong immunostaining in the albuginea and ovarian stroma of E. perditus, only; however, the endothelial cells in the blood vessels of the three herein analyzed species showed positive reaction to this intermediate filament. Desmin showed immunoreactivity in the testicular albuginea and in the endothelial cells of the blood vessels in the herein analyzed leiosauridae testes; however, only E. bilineatus showed immunostaining in the interstitial region. Desmin showed positive immunoreaction in the epididymis of E. perditus and E. bilineatus, only. Vimentin did not show immunostaining in the ovaries, testes and epididymis of the three analyzed lizards. The consistent results found in the current study provide additional data on the reproductive biology of the investigated species. These data may be used for phylogenetic and behavioral comparisons between the herein studied species and other species belonging to family Leiosauridae or other reptiles
Cap. II
The aim of the current study is to investigate the histological description, as well as the presence and immunohistochemical distribution of alpha smooth muscle actin, desmin and vimentin in the testes and epididymis of Enyalius bilineatus, Enyalius perditus and Urostrophus vautieri, which are representatives of family Leiosauridae, in order to help developing a database on the reproductive biology of these lizards, which could be compared to that of other reptile species and vertebrates. The herein studied specimens are deposited in the Herpetological Collection of Federal University of Juiz de Fora. The animals? epididymis and testes were removed and sent to the Histology and Embryology Laboratory (UFRRJ), where they were fixed, processed and then subjected to histological and immunohistochemical techniques. The shape of the testes varies reasonably among the studied leiosauridae. These organs are covered by the tunica albuginea and hold septa forming lobes, where the seminiferous tubules are located in. The epididymis of these lizards are convolute ducts internally coated by an epithelium, whose shape ranges from simple cylindrical to simple cubic with stereocilia. The immunohistochemical analysis applied to the testes of the herein studied lizards showed strong positive reaction to the alpha smooth muscle actin in the tunica albuginea, interstitial tissue, and in endothelial cells of blood vessels. Desmin showed strong immunoreactivity in the testicular albuginea of E. bilineatus and moderate immunoreactivity in E. perditus and U. vautieri; however, only E. bilineatus showed immunostaining in the interstitial tissue region. The endothelial cells of blood vessels showed positive immunoreaction to desmin in the three herein analyzed species. The epididymis showed moderate immunohistochemical reaction to alpha smooth muscle actin in the capsule and in the interstitial tissue, whereas desmin showed positive immunoreaction in the epididymis of E. perditus and E. bilineatus, only. Vimentin did not show immunostaining in the testes and epididymis of the three analyzed lizards. The consistent results found in the current study provide additional data on the reproductive biology of the investigated species. These data may be used for phylogenetic and behavioral comparisons between the herein studied species and other species belonging to family Leiosauridae or other reptiles. / Cap. I
Este trabalho investiga, al?m da descri??o histol?gica e histoqu?mica, a presen?a e distribui??o imuno-histoqu?mica de alfa-actina de m?sculo liso, desmina e vimentina nos ov?rios, test?culos e epid?dimos de Enyalius bilineatus, Enyalius perditus e Urostrophus vautieri, representantes da fam?lia Leiosauridae, para ajudar a formar uma base de dados sobre a biologia reprodutiva destes lagartos que possam ser comparados com outras esp?cies de r?pteis, bem como com outros vertebrados. Os esp?cimes estudados encontram-se depositados na Cole??o Herpetol?gica da UFJF. Os ov?rios, epid?dimos e test?culos dos animais foram removidos e encaminhados ao Laborat?rio de Histologia e Embriologia (UFRRJ), onde foram fixados, processados e ent?o submetidos ?s t?cnicas histol?gicas, histoqu?micas e imuno-histoqu?micas. Os ov?rios destes leiosaur?deos s?o ?rg?os pareados, repletos de fol?culos ovarianos, em distintos est?gios de desenvolvimento folicular. Estes s?o revestidos por epit?lio c?bico simples, com uma camada de tecido conjuntivo subjacente, a t?nica albug?nea. Os test?culos encontram-se envolvidos pela t?nica albug?nea e em seu interior cont?m septos que formam l?bulos, nos quais se localizam os t?bulos semin?feros. Os epid?dimos destes lagartos s?o ductos convolutos, revestidos internamente por um epit?lio que varia de cil?ndrico simples a c?bico simples com estereoc?lios. A imuno-histoqu?mica, nos ov?rios dos lagartos estudados, mostra uma rea??o moderada a acentuada para alfa-actina de m?sculo liso na camada da teca e em c?lulas endoteliais dos vasos sangu?neos, enquanto nos test?culos destas esp?cies nota-se uma acentuada rea??o para esta prote?na do citoesqueleto, na t?nica albug?nea, no tecido intersticial e nas c?lulas endoteliais dos vasos sangu?neos. Nos epid?dimos observa-se imunomarca??o para alfa-actina na c?psula e no tecido intersticial destes lagartos. Quanto ao anticorpo desmina, apenas em E. perditus, foi poss?vel imunorrea??o na albug?nea e no estroma ovariano, no entanto, nas tr?s esp?cies analisadas, as c?lulas endoteliais dos vasos sangu?neos demonstraram rea??o positiva a este filamento intermedi?rio. Nos test?culos dos leiosaur?deos estudados, a desmina foi imunolocalizada na albug?nea testicular e nas c?lulas endoteliais dos vasos sangu?neos, entretanto, apenas em E. bilineatus ocorreu imunomarca??o, na regi?o do interst?cio. Nos epid?dimos, a desmina demonstrou imunorrea??o positiva apenas em E. perditus e E. bilineatus. N?o houve rea??o imuno-histoqu?mica para vimentina nos ov?rios, test?culos e epid?dimos dos tr?s lagartos analisados. Este estudo obteve resultados consistentes, fornecendo assim mais dados sobre a biologia reprodutiva das esp?cies aqui investigadas, que poder?o ser utilizados para compara??es filogen?ticas e comportamentais com outras esp?cies da fam?lia Leiosauridae e outros r?pteis.

Cap. II

Este trabalho investiga, al?m da descri??o histol?gica, a presen?a e distribui??o imuno-histoqu?mica de alfa-actina de m?sculo liso, desmina e vimentina nos test?culos e epid?dimos de Enyalius bilineatus, Enyalius perditus e Urostrophus vautieri, representantes da fam?lia Leiosauridae, para ajudar a formar uma base de dados sobre a biologia reprodutiva destes lagartos que possam ser comparados com outras esp?cies de r?pteis, bem como com outros vertebrados. Os esp?cimes estudados encontram-se depositados na Cole??o Herpetol?gica da Universidade Federal de Juiz de Fora. Os epid?dimos e test?culos dos animais foram removidos e encaminhados ao Laborat?rio de Histologia e Embriologia (UFRRJ), onde foram fixados, processados e ent?o submetidos ?s t?cnicas histol?gicas e imuno-histoqu?micas. O formato dos test?culos varia razoavelmente entre os leiosaur?deos estudados. Estes ?rg?os encontram-se envoltos pela t?nica albug?nea e no seu interior cont?m septos que formam l?bulos incompletos, nos quais se localizam os t?bulos semin?feros. Os epid?dimos destes lagartos s?o ductos convolutos. Estes ductos s?o revestidos internamente por um epit?lio que varia de cil?ndrico simples a c?bico simples com estereoc?lios. A imuno-histoqu?mica revela uma acentuada rea??o positiva para alfa-actina de m?sculo liso nos test?culos dos leiosaur?deos analisados, na t?nica albug?nea e no tecido intersticial, assim como, nas c?lulas endoteliais dos vasos sangu?neos. A desmina apresentou acentuada imunorreatividade na albug?nea testicular em E. bilineatus e moderada em E. perditus e U. vautieri, entretanto, na regi?o do tecido intersticial, apenas em E. bilineatus ocorreu imunomarca??o. Nas tr?s esp?cies analisadas, as c?lulas endoteliais dos vasos sangu?neos demostraram imunorrea??o positiva para desmina. Nos epid?dimos observou-se rea??o imuno-histoqu?mica moderada para alfa-actina de m?sculo liso na c?psula e no tecido intersticial, enquanto a desmina demonstrou imunorrea??o positiva apenas em E. perditus e E. bilineatus. N?o houve imunomarca??o para vimentina nos test?culos e epid?dimos dos tr?s lagartos analisados. Este estudo obteve resultados consistentes, fornecendo assim mais dados sobre a biologia reprodutiva das esp?cies aqui investigadas, que poder?o ser utilizados para compara??es filogen?ticas e comportamentais com outras esp?cies da fam?lia Leiosauridae e outros r?pteis.

Identiferoai:union.ndltd.org:IBICT/oai:localhost:jspui/2467
Date29 August 2017
CreatorsFirmiano, Enely Maris da Silveira
ContributorsPinheiro, Nadja Lima, Nascimento, Aparecida Alves do, Santos, Marco Ant?nio Jos? dos, Mendes, Rosa Maria Marcos, Santos, Clarice Machado dos, Paoli, Severo de
PublisherUniversidade Federal Rural do Rio de Janeiro, Programa de P?s-Gradua??o em Bilogia Animal, UFRRJ, Brasil, Instituto de Ci?ncias Biol?gicas
Source SetsIBICT Brazilian ETDs
LanguagePortuguese
Detected LanguageEnglish
Typeinfo:eu-repo/semantics/publishedVersion, info:eu-repo/semantics/masterThesis
Formatapplication/pdf
Sourcereponame:Biblioteca Digital de Teses e Dissertações da UFRRJ, instname:Universidade Federal Rural do Rio de Janeiro, instacron:UFRRJ
Rightsinfo:eu-repo/semantics/openAccess
RelationABD-ELMAKSOUD, A. 2005. Morphological, glycohistochemical, immunohistochemical studies on the embryonic and adult bovine testis. Thesis, Institute of Veterinary Anatomy II, Faculty of Veterinary Medicine, LMU, Munich, Germany ABD-ELMAKSOUD, A. 2009. Comparative expression of laminin and smooth muscle actin in the testis and epididymis of poultry and rabbit. J Mol Hist. 40:407-416. AIRE, T. A., OZEGBE, P. C. 2007. The testicular capsule and peritubular tissue of birds: morphometry, histology, ultrastructure and immunohistochemistry. J. Anat. 210: 731-740. AIRE, T. A., OZEGBE, P. C. 2008. Immunohistochemistry of the cytoskeleton in the excurrent ducts of the testis in birds of the Galloanserae monophyly. Cell Tissue Res. 333: 311-321. AKBARSHA, M. A., KADALMANI, B., TAMILARASAN, V. 2006. Histological variation along and ultrastructural organization of the epithelium of the ductus epididymidis of the fan-throated lizard Sitana ponticeriana Cuvier. Acta Zoologica. 87:181-196. ALKAFAFY, M. 2005. Glycohistochemical, immunohistochemical and ultrastructural studies of the bovine epididymis. Thesis, Institute of Veterinary Anatomy II, Faculty of Veterinary Medicine, LMU, Munich, Germany. ANDREUCCETTI, P. 1992. An ultrastructural study of differentiation of pyriform cells and their contribution to oocyte growth in representative Squamata. Journal of Morphology. 212:1-11. ARENAS, M. I., FRAILE, B., DE MIGEL, M., PANIAGUA, R. 1995. Intermediate filaments in the testis of the teleost mosquito fish Gambusia affinis holbrooki: a light and electron microscope immunocytochemical study and Western blotting analysis. Histochemical Journal. 27: 329-337. ARENAS, M. I., BETENCOURT, F. R., FRAILE, B., PANAIGUA, R. 1997. Immunocytochemical and quantitative study of the tunica albuginea testis in young and ageing men. Histochem Cell Biol. 107: 469-477. BAKST, M. R. 1998. Structure of the avian oviduct with emphasis on sperm storage in poultry. Journal of Experimental Zoology. 282: 618-626. BANKS, F. C. L., KNIGHT, G. E., CALVERT, R. C., TURMAINE, M., THOMPSON, C. S., MIKHAILIDIS, D. P., MORGAN, R. J., BURNSTOCK, G. 2006. Smooth muscle and 96 purinergic contraction of the human, rabbit, rat, and mouse testicular capsule. Biol. Reprod. 74: 473?480. BAROUDI, R. 1970. Elementos da zoologia. 6. ed. S?o Paulo: Nobel. p.125-152. B?RNILS, R. S., GIRAUDO, A. R., CARREIRA S., CECHIN, S. Z. 2007. R?pteis das por??es subtropical e temperada da Regi?o Neotropical. Ci?ncia & Ambiente. 35: 101-136. B?RNILS, R. S., BATISTA, M. A., Bertelli, P. W. 2001. Cobras e lagartos do Vale: levantamento das esp?cies de Squamata (Reptilia, Lepidosauria) da Bacia do Rio Itajai, Santa Catarina, Brasil. Revista de estudos ambientais. 3: 69-79. B?RNILS, R. S., COSTA, H. C. (org.). 2012. Brazilian reptiles: List of species. Version 2012.1. Available at http://www.sbherpetologia.org.br/. Sociedade Brasileira de Herpetologia. BERTOLUCI, J., CANELAS, M. A. S., EISEMBERG, C. C., PALMUTI, C. F. S., MONTINGELLI, G. G. 2009. Herpetofauna of Esta??o Ambiental de Peti, an Atlantic Rainforest fragment of Minas Gerais State, southeastern Brazil. Biota Neotrop. 9(1). BETZ, T. W. 1963. The ovarian histology of the diamond-backed water snake. Natrix rhombifera during the reproductive cycle. Journal of Morphology. 113:245-260. BOCK, P., BREITTNECKER, G. LONGLMAYR, G. 1972. Kontraktile Fibroblasten (myofibroblasten) in der lamina propria der hodenkanalchen von Menchen. Zeitschrift fur Mikroskopisch. Anatomische Forschung. 133: 519-527. BORGES-NOJOSA, D. M., CARAMASCHI, U. 2004. Composi??o e an?lise comparativa da diversidade e afinidades biogeogr?ficas dos lagartos e anfisben?deos (Squamata) dos brejos nordestinos. In: Ecologia e Conserva??o da Caatinga. Editora Universit?ria da UFPE, Recife. BOTTE, V., ANGELINI, F. 1980. Endocrine control of reproduction in reptiles: the refractory period. In Delrio G, Brachet J, eds. Steroids and Their Mechanisms of Action in Nonmammalian Vertebrates. New York, Raven Press, 201-212. BOYD, M. M. M. 1940. The structure of the ovary and the formation of the corpus luteum in Hoplodactylus maculatus. Q J Microsc Sci. 82:337?376. CALLEBAUT, M., VAN NASSAUW, L. 1987. Demonstration by monoclonal antidesmin of a myoid tissue coat in the preovulatory ovarian tunica albuginea of the turtle Pseudemys scripta elegans. Med. Sci. Res. 15: 1129-1130. 97 COSTA, H. C., FERNANDES, V. D., RODRIGUES, A. C., FEIO, R. N. 2009. Lizards and Amphisbaenians, municipality of Vi?osa, state of Minas Gerais, southeastern Brazil. Check List. 5:3:732-745. CHAPONNIER, C., GABBIANI, G. 2004. Pathological situations characterized by altered actin isoform expression. J. Patholoy. 204:386-395. CZERNOBILSKY, B., MOLL, R., LEVY, R., FRANKE, W. W. 1985. Co-expression of cytokeratin and vimentin filaments in mesothelial, granulosa and rete ovarii cells of the human ovary. Eur. J. Cell Biol. 37: 175?190. DAVIS, J. R., LANGFORD, G A. 1970. Pharmacological studies of the testicular capsule in relation to sperm transport. In the human testis (eds Rosenberg E, Paulsen CA), 495-514. New York: Plenum. DE P?REZ, G., RAM?REZ M. P., CALDER?N M. L. 1999. Estudio preliminar de la ultraestructura de la pared del ovario y de fol?culos previtelog?nicos y vitelog?nicos tempranos de Caiman crocodilus fuscus. (Reptilia, Crocodylidae). Rev. Acad. Colomb. Cienci. 23: 453-464. DE P?REZ, G., RAM?REZ, M. P. 2002. El tracto reproductivo de la hembra en crocodylia: Estudio histol?gico y ultraestructural de Caiman crocodilus fuscus (Crocodylia: Alligatoridae) Acta Biol?gica Colombiana. 7:1:3-19. DESANTIS, S., LABATE, M., LABATE, G. M., CIRILLO, F. 2002 Evidence of regional differences in the lectin histochemistry along the ductus epididymis of the lizard, Podarcis sicula Raf. Histochem J. 34:123-130. DIKRANIAN, K., TROSHEVA, M., PETROV, M. 1993. Intermediate filaments and ATPase activity in the vascular wall of vertebrates. Acta Histochem. 94:13-9. DINGES, H. P., ZATLOUKAL, K., SCHMID, C., MAIR, S., WIRNSBEGER, G. 1991. Co-expression of cytokeratin and vimentin filaments in rete testis and epiddiymis. Virchows Archiv. A Path. Anat. Histopath. 418:119-127. DIOKMETZIDOU, A., TSIKITIS, M., NIKOULI, S., KLOUKINA, I., TSOUPRI, E., PAPATHANASIOU, S. 2016. Chapter Fifteen-Strategies to Study Desmin in Cardiac Muscle and Culture Systems. Methods in enzymology. 568:427-459. DYCE, K. M., SACK, W. O., WENSING, C. I. G. 1997. Tratado de anatomia veterin?ria. Rio de Janeiro: Guanabara Koogan p. 645-647. 98 DUFAURE, J., SAINT GIRONS, H. 1984. Histologie compare de l?epididyme et de ses secretions chez les reptiles (lezards et serpents). Archives d'anatomie microscopique et de morphologie exp?rimentale.73:15?26. EGGER, G. F., WITTER, K. 2009. Peritubular contractile cells in testis and epididymis of the Canis lupus familiaris. Acta Veterinaria Brno.78:3-11. ELLENPORT, C.R. Aparelho urogenital geral. 1986. In: GETTY, R. Anatomia dos animais dom?sticos. 5. ed. Rio de Janeiro: Guanabara Koogan. p.1813-1828. ETHERIDGE, R., WILLIAMS, E. E. 1991. A review of the South American lizard genera Urostrophus and Anisolepis (Squamata: Iguania: Polychridae). Bulletin of the Museum of Camparative Zoology. 152:317-361. FRAN?A, L.R., SILVA, JR. V.A., CHIARINI-GARCIA, H., GARCIA S. K., DEBELJUK, L. 2000. Cell proliferation and hormonal changes during postnatal development of the testis in the pig. Biol. Reprod. 63:1629-1636. FERREIRA, A., LAURA, I. A., DOLDER, H. 2002. Reproductive cycle of male green iguanas, Iguana iguana (Reptilia: S?uria: Iguanidae), in the Pantanal of Brasil. Brazilian Journal of Morphology Science. 19:1:23-28. FERREIRA, A., SILVA, D. N., VAN SLUYS, M., DOLDER, H. 2009. Seasonal Changes in Testicular and Epididymal Histology of the Tropical Lizard, Tropidurus itambere (Rodrigues, 1987), during its Reproductive Cycle. Brazilian Journal of Biology. 69:2:429-435. FERREIRA, A.; KIHARA, V. O.; MEHANNA, M. 2011.Reproductive strategies of brazilian lizards of the genus Tropidurus Rodrigues, 1987 (Squamata, Tropiduridae) in temporal and spatial. Int. J. Morphol. 29:4: 1414-1421. FROST, D. R., ETHERIDGE, R., JAMES, D. E., TITTUS, T. A. 2001. Total evidence, sequence alignment, evolution of Polychrotid Lizards, and a reclassification of the Iguania (Squamata: Iguania). Amer. Mus. Novitates. 3343:1-38. FOX H. 1977. The urogenital system of the reptiles. In: Gans C. (Ed.), Biology of Reptilia. Academic Press, New York, p.1-127. GALOU, M., GAO, J., HUMBERT, J., MERICSKAY, M., LI, Z., PAULIN, D., VICART, P. 1997. The importance of intermediate filaments in the adaptation of tissues to mechanical stress: evidence from gene knockout studies. Biology of Cell. 89:85-97. 99 GEISLER, N., KAUFMANN, E., WEBER, K. 1982. Proteinchemical characterization of three structurally distinct domains along the protofilament unit of desmin 10 nm filaments. Cell. 30:1: 277-286. GEOGARTOS, S. P. 1993. Dynamics of intermediate filaments: recent progress and unanswered questions. FEBS. 318:101-107. GIGON-DEPEIGES, A., DUFAURE, J. P. 1977. Secretory activity of the lizard epididymis and its control by testosterone. General and Comparative Endocrinology. 33:4:473-479. GOLDBERG, S. R. 1970. Seasonal ovarian histology of the viviparous iguanid lizard Sceloporus jarrovi. Journal of Morphology. 132:265-276. GOLDBERG, S. R. 1973. Ovarian cycle of the western fence lizard, Sceloporus occidentalis. Herpetologica. 29:284-289. GOLDMAN, R. D., KHUON, S., CHOU, Y. H., OPAL, P., STEINERT, P. M. 1996: The function of intermediate filaments in cell shape and cytoskeletal integrity. J. Cell Biol. 134: 971-983. GRIBBINS, K. M., GIST, D. H. 2003. Cytological evaluation of spermatogenesis within the germinal epithelium of the male european wall lizard, Podarcis muralis. Journal of Morphology. 258:296-306. GRIBBINS, K. M., GIST, D. H., CONGDON, J. 2003. Cytological evaluation of spermatogenesis in the red-eared slider. Trachemys scripta. Journal of Morphology. 255:337-346. GRIBBINS, K. M., ELSEY, R. M., GIST, D. H. 2006. Cytological evaluation of the germ cell development strategy within the testes of the American alligator, Alligator mississippiensis, Acta Zoology. 87:59-69. GRIBBINS, K. M., MILLS, E. M., SEVER, D. 2007. Ultrastructural examination of spermiogenesis within the testis of the ground skink, Scincella laterale (Squamata, Sauria, Scincidae), Journal of Morphology. 268:181-192. GRIBBINS, K., RHEUBERT, J., COLLIER, M., SIEGEL, D., SEVER, D. 2008. Histological analysis of spermatogenesis and the germ cell development strategy within the testis of the male western Cottonmouth Snake, Agkistrodon piscivorus. Annals of Anatomy. 190:461-476. GRIBBINS, K. M. 2011. Reptilian spermatogenesis: a histological and ultrastructural perspective. Spermatogenesis. 3:250?269. 100 GRIBBINS, K. M., MATCHETT, C. L., DELBELLO, K. A., RHEUBERT, J., VILLAGR?N-SANTACRUZ, M., GRANADOS-GONZ?LEZ, G., HERN?NDEZ-GALLEGOS, O. 2014. The ultrastructure of spermatid development during spermiogenesis within the rosebelly lizard, Sceloporus variabilis (Reptilia, Squamata, Phrynosomatidae). Journal of Morphology. 275:258?268. GRIER, H. J., URIBE, M. C, LO NOSTRO, F. L., MIMS, S. D., PARENTI, L. R. 2016. Conserved form and function of the germinal epithelium through 500 million years of vertebrate evolution. Journal of Morphology. 277:8:1014-44. G?MEZ, D., RAM?REZ-PINILLA, M. P. 2004. Ovarian Histology of the Placentotrophic Mabuya mabouya (Squamata, Scincidae). Journal of Morphology 259:90-105. GURAYA, S. S. 1989. Ovarian follicles in reptiles and birds. Springer-Verlag, Berlin: 287 p. HAHN, W. E. 1964. Seasonal changes in testicular and epididymal histology and spermatogenic rate in the lizard Uta stansburiana stejnegeri. Journal of Morphology. 115:3:447-459. HAMMOUCHE, S., GERNIGON, T., EXBRAYAT, J. M. 2009. Correlation between ovarian steroidogenesis and beta-endorphin in the Lizard Uromastyx acanthinura: Immunohistochemical approach. Folia Histochem Cytobiol. 47:5:S95-S100. HARGROVE, J. L., MACINDOE, J. H., ELLIS, L.C. 1977. Testicular contractile cells and sperm transport. Fertil Steril. 28:146-1157. HECKMANN, M., BAUER, R., JUNGMANN, A., WINTER, L., RAPTI, K., STRUCKSBERG, K. 2016. AAV9-mediated gene transfer of desmin ameliorates cardiomyopathy in desmin-deficient mice. Gene therapy. 23:8-9:673-9. HELFAND, B. T., CHANG, L., GOLDMAN, R. D. 2003. The dynamic and motile properties of intermediate filaments. Annual Review of Cell Developmental Biology. 19:445-467. HELFAND, B., CHANG, L., GOLDMAN, R. 2004. Intermediate filaments are dynamic and motile elements of cellular architecture. Cell science. 117:2:133-141. HENDERSON, D., WEBER, I. C. 1980. Immunoelectron microscopic studies of intermediate filaments in culture cells. Expl Cell Res. 129:441-53. HESS, R. A., THURSTON, R. J., BIELLER, H. V. 1976. Ultrastructure of the epididymal region and ductus deferens of the turkey (Meleagris gallopavo). J. Anat. 122:241-252. 101 HERRMANN, H., HESSE, M., REICHENZELLER, M., AEBI, U. 2003. Functional complexity of intermediate filament cytoskeletons: from structure to assembly to gene ablation. Int Rev Cytol. 223:83-175. HERRMANN, H., AEBI, U. 2004. Intermediate filaments: molecular structure, assembly mechanism, and integration into functionally distinct intracellular scaffolds, Annu Rev Biochem. 73:749-89. HERN?NDEZ-GALLEGOS O., M?NDEZ-DE LA CRUZ, F.M. R., VILLAGR?N-SANTACRUZ, M., RHEUBERT, J. L., GRANADOS-GONZ?LEZ, G., GRIBBINS, K. M. 2014. Seasonal spermatogenesis in the Mexican endemic oviparous lizard, Sceloporus aeneus (Squamata: Phrynosomatidae). Spermatogenesis. 4:3: 988585. HERN?NDEZ-FRANYUTTI A., URIBE ARANZ?BAL M. C., GUILLETTE L. J. JR. 2005. Oogenesis in the viviparous matrotrophic lizard Mabuya brachypoda. Journal of Morphology 265:152-164. HILDEBRAND, M. An?lise da estrutura dos vertebrados. S?o Paulo: Atheneu, 1995. p. 700. HINZ, B. 2007. Formation and function of the myofibroblast during tissue repair. J Invest Dermatol. 127:526-537. HOLSTEIN, A. F., MAEKAWA, M., NAGANO, T. 1996. Myofibroblasts in the lamina propria of human seminiferous tubules are dynamic structures of heterogeneous phenotype. Arch Histol Cytol. 59:109-125 HONDO, E., KITAMURA, N., TORIBA, M., KUROHMARU, M., HAYASHI, Y., YAMADA, J. 1997. Histological study of the seminiferous epithelium in the Japanese rat snake, Elaphe climacophora: identifation of spermatogonium. Journal of Veterinary Medical Science 59:23-29. HUBERT, J. 1985. Origin and development of oocytes. In: Gans C, editor. Biology of the Reptilia. New York: John Wiley & Sons. 14:41-74. IVASKA, A. J., PALLARIB, H-M., NEVOA, J., ERIKSSON, J. E. 2007. Novel functions of vimentin in cell adhesion, migration, and signaling. Exp Cell Res. 313:10:2050-62. JACKSON, J. F. 1978. Differentiation in the genera Enyalius and Strobilurus (Iguanidae): implications for Pleistocene climatic changes in eastern Brazil. Arquivos de Zoologia. 30: 1-40. 102 JEZEK, D., HITTMAIR, A., ROGATSCH, H. 1996. Lamina propria of sex cords in human fetal testis: an immunohistologial and stereological study. Anatomy and Embryology. 193:181-190. JONES, R. E. 1987. Ovulation: insights about the mechanisms based on a comparative approach. En D. O. Norris, R. E. Jones (eds.). Hormones and reproduction in fishes, amphibians and reptiles, 203-240. New York: Plenum Press. JONES, R. E., SWAIN, T., GUILLETTE, L. J., FITZGERALD, K. T. 1982. The comparative anatomy of lizard ovaries, with emphasis on the number of germinal beds. J Herpetol 16:240-252. JUNQUEIRA, L. C., CARNEIRO, J. 2013. Histologia B?sica. 12?ed. Rio de Janeiro: Guanabara Koogan. 538p. KABSCH, W., VANDEKERCKHOVE, J. 1992. Structure and function of actin. Annu Rev Biophys Biomol Struct. 21:49-76. KASPER, M., P. STOSIEK. 1989. Immunohistochemical investigation of different cytokeratins and vimentin in the human epididymis from the fetal period up to adulthood. Cell Tissue Res. 257:661-664. KHAN-DAWOOD, F. S., DAWOOD, M. Y., TABIBZADEH, S. 1996. Immunohistochemical analysis of the microanatomy of primate ovary. Biol. Reprod. 54:734-742. KIERSZENBAUM, A. L. Histologia e Biologia Celular - uma introdu??o ? patologia. 3? Edi??o. Rio de Janeiro: Elsevier, 2012. 704p. KINNER, B., ZALESKAS, J. M., SPECTOR, M. 2002. Regulation of smooth muscle actin expression and contraction in adult human mesenchymal stem cells. Exp Cell Res. 278:72-83. KLOSTERMAN, L. L. 1983. The ultrastructure of germinal beds in the ovary of Gerrhonotus coeruleus (Reptilia: Anguidae). Journal of Morphology. 178:247-266. LAZARIDES, E. 1980. Intermediate filaments as mechanical integrators of cellular space. Nature 283:249-256. LAZARIDES, E. 1982. Biochemical and immunocytological characterization of intermediate filaments in muscle cells. Methods Cell Biol. 25:333-57. LEESON, C. R., FORMAN, D. E. 1981. Postnatal development and differentiation of contractile cells within the rabbit testis. J Anat. 132: 491-511. 103 LYALL, F., ROBSON, S. C., BULMER, J. 2013. Spiral artery remodeling and trophoblast invasion in preeclampsia and fetal growth restriction relationship to clinical outcome. Hypertension. 2:6:1046-1054. LIANG, G., LIU, Q., YU, H., WANG, Q. 2011. Histological and immunocytochemical study of deferens ducts in the Chinese rat snake (Zaocys dhumnades). Zoological Research. 329:6:663-669. LIMA, A. F. B., SOUSA, B. M. 2006. Court and copulation behaviors of Enyalius perditus Jackson, 1978 (Squamata, Leiosauridae) in captivity conditions. Revista Brasileira De Zooci?ncias. 8:2:193-197. LOREDANA, R., VACCARO, M. C., PRISCO, M., CAROTENUTO, R., LIGUORO, A., ANDREUCCETTI, P. 2004. a and b Spectrin distribution during the differentiation of pyriform cells in follicles of lizard Podarcis sicula. Molecular Reproduction and Development. 67:101-107. LOUREN?O, L. 2008. Protocolos de rotina do laborat?rio de histologia e anatomia patol?gica. UTAD. Ed, Universidade de Tr?s-os-montes e Alto Douro. Vila Real. LUNA, E. J., HITT, A. L. 1992. Cytoskeleton-plasma membrane interactions. Science. 258: 955-963. MACHADO-SANTOS, C., SANTANA, L. N. S., VARGAS, R. F. G., ABIDU-FIGUEIREDO, M., BRITO-GITIRANA, L.,. CHAGAS, M. A. 2015. Histological and immunohistochemical study of the ovaries and oviducts of the juvenile female of Caiman latirostris (Crocodilia: Alligatoridae). Zoologia (Curitiba) [online]. 32:5: 395-402. MADEKUROZWA, M. C., KIMARO, W. H. 2006. A morphological and immunohistochemical study of healthy and atretic follicles in the ovary of the sexually immature ostrich (Struthio camelus). Anat. Histol. Embryol. 35: 253-258. MADEKUROZWA, M. C. 2007. An immunohistochemical study of the distribution of intermediate filaments in the ovary of the emu (Dromaius novaehollandiae). Anat. Histol. Embryol. 36: 336-342. MAEKAWA, M., NAGANO, T., KAMIMURA, T., ISHIKAWA, H., DEZAWA, M. 1991. Distribution of actin-filament bundles in myoid cells, Sertoli cells, and tunica albuginea of rat and mouse testes. Cell Tissue Res 266: 295?300. MAHMOUD, I. Y., CYRUS, R. V., BENNETT, T. M., WOLLER, M. J., MONTAG, D. M. 1985. Ultrastructural changes in testes of the snapping turtle, Chelydra serpentina in 104 relation to plasma testosterone, ? 5-3?-hydroxysteroid dehydrogenase, and cholesterol. General and comparative endocrinology, 57:3:454-464. MANES, M. E., NORIEGA, T., CASAL, F. C., APICHELA, S. 2007. Ovarian changes during the reproductive cycle of the Tupinambis merianae lizard raised in a temperate environment. Cuadernos de Herpetologia 21: 21-29. MARETTA, M., MARETTOVA, E. 2004. Immunohistochemical demonstration of myoid cells in the testis and its excurrent ducts in the domestic fowl. Br Poultry Sci 45: 585?589. MARETTOVA, E., MARETTA, M. 2002. Demonstration of intermediate filaments in sheep ovary. Acta Histochemica, 104:431-434. M MAURIZII, M. G., TADDEI, C. 1996. Immunolocalization of cytoskeletal proteins in the previtellogenic ovarian follicle of the lizard Podarcis sicula. Cell Tissue. 284:489-493. MENDES, R. M. M., PINHEIRO, N. L., NASCIMENTO, A. A., SANTOS, C. M., RIBEIRO, T. P., SANTOS, M. A. J., SALES, A. 2009. Histologia comparada de test?culo e do segmento sexual do rim de lagarto tropical Tropidurus torquatus Wied, 1820 (Squamata: Tropiduridae) adultos e imaturos. Revista Universidade Rural. S?rie Ci?ncias da Vida. 29:49-54. MESURE, M., CHEVALIER, M., DEPEIGES, A., FAURE, J., DUFAURE, J. P. 1991. Structure and ultrastructure of the epididymis of the viviparous lizard during the annual hormonal cycle: Changes of the epithelium related to secretory activity. J Morphol 210:133?145. MIETTINEN, M., VIRTANEN, I., TALERMAN, A. 1985. Intermediate filament proteins in human testis and testicular germ cell tumours. Am. I. Pathol. 120: 402-10. MOODLEY, G. K., VAN WYK, J. H. 2007. Folliculogenesis and ovarian histology of the oviparous gecko, Hemidactylus mabouia (Sauria: Gekkonidae). African Journal of Herpetology 56: 115-135. MOORE, R., CLARK, D., VODOPICH, D. S. 1998 - Botany - McGraw-Hill Education, 832 p. MOTTA, C. M., CASTRIOTA-SCANDERBEG, M., FILOSA, S., ANDREUCCETTI, P. 1995. Role of pyriform cells during the growth of oocytes in the lizard Podarcis sicula. J Exp Zool 273:247?256. 105 MOTTA, C. M., FILOSA, S., ANDREUCCETTI, P. 1996. Regression of the epithelium in the late previtellogenic follicles of Podarcis sicula: a case of apoptosis. J Exp Zool 276:233?241. MCHUGH, K. M., CRAWFORD, K., LESSARD, J. L. 1991. A Comprehensive Analysis of the Developmental and Tissue-Specific Expression of the Isoactin Multigene Family in the Rat. Developmental Biology 148:442-458. NEAVES, W. B. 1971. Intercellular bridges between follicle cells and oocyte in the lizard Anolis carolinensis. Anat Rec 170: 285?302. NOBLE, G. A., NOBLE, E. R. 1940. A brief anatomy of turtle. Stanford University Press, Stanford University California. London: Hamphrey Oxford University Press, 49p. NORRIS, D. O., JONES, R. E. 2012. Hormones and reproduction in fishes, amphibians, and reptiles. Springer Science & Business Media. 613 p. ORR, R. T. Biologia dos vertebrados. 5. ed. S?o Paulo: Livraria Rocca Ltda., 1986. p. 508. ORTEGA, H. H., SALVETTI, N. R., M?LLER, L. A., AMABLE, P., LORENTE, J. A., BARBEITO, C. G., GIMENO, E. J. 2007. Characterization of cytoskeletal proteins in follicular structures of cows with cystic ovarian disease. Journal of comparative pathology, 136:4: 222-230. O'SHEA, J., ROBSON, R., HARTZER, M., HUIATT, T., RATHBUN, W., STROMER, M. 1981. Purification of desmin from adult mammalian skeletal muscle. Biochemical Journal, 195:2: 345-356. OZEGBE, P. C., KIMARO, W., MADEKUROZWA, M. C., SOLEY, J. T., AIRE, T. A. 2010. The Excurrent Ducts of the Testis of the Emu (Dromaius novaehollandiae) and Ostrich (Struthio camelus): Microstereology of the Epididymis and Immunohistochemistry of its Cytoskeletal Systems. Anat. Histol. Embryol. 39:7?16. PALOMBI, F., FARINI, D., SALANOVA, M. DE GROSII, S., STEFANIN, M. 1992. Development and cytodifferentiation of peritubular myoid cells in the rat testis. Anatomical Record, 233: 32-41. PARANKO, J., PELLINIEMI, L. J. 1992. Differentiation of smooth muscle cells in the fetal rat testis and ovary: localization of alkaline phosphatase, smooth muscle myosin, F-actin, desmin. Cell Tissue Res 268: 521?530 PAULIN, D., LI, Z. 2004. Desmin: a major intermediate filamento protein essential for the structural integrity and function of muscle. Exp. Cell Res. 301: 1?7. 106 PFEIFFER, D. C., VOGL, A.W. 1992. Actin filaments associated with the basal Sertoli cell surface in the alligator and turtle. Tissue Cell. 24:5:643-54. PELLINIEMI, L. J., KUOPIO, T., FROJDMAN, K. 1996. The cell biology and function of the fetal Leydig cell. The Leydig cell. Cache River Press, Vienna, IL, 143-158. PERRY, M. M., GILBERT, A. B., EVANS, A. J. 1978. Electron microscope observations on the ovarian follicle of the domestic fowl during the rapid growth phase. Journal of Anatomy, 125:481-497. PIRES, M., COELHO, A. C., PALMEIRA, C., CARDOSO, M. N., SEIXAS, F., RODRIGUES, J. 2010. Protocolos de Imunologia. 49-55. POUGH, F. H.; JANIS, M. C.; HEISER, B. J. 2003. A vida dos vertebrados. 3. ed. S?o Paulo: Atheneu. p. 270-290. RAMAEKERS, F. C. S., FEITZ, W., MOESKE, O., SCHAART, G., HERMAN, C., DEBRUYNE, F., VOOIJES, G. P. 1985. Antibodies to cytokeratin and vimentin in testicular tumour diagnosis. Virchows Arch. A Pathol. Anat. 408: 127-142. RAM?REZ-PINILLA, M. P., DE P?REZ, G., RAM?REZ-PERILLA, J. 1989. Histolog?a del tracto reproductivo de la hembra del lagarto Phenacosaurus heterodermus (Reptilia: Sauria: Iguanidae). Trianea 3: 93?103. RAHIL, K. S. E NARBAITZ, R. 1973. Ultrastructural studies in the relationship between follicular cells and growing oocytes in the turtle Pseudemys scripta. Journal of Anatomy 115:175-186. RAUCCI, F., DI FIORE, M. M. 2010. The maturation of oocyte follicular epithelium of Podarcis s. sicula is promoted by d-aspartic acid. Journal of Histochemistry and Cytochemistry. 58:2:157-171. REDMER, D. A., V. DORAISWAMY, B. J. BORTNEM, K. FISHER, A. JABLONKA-SHARIFF, A. T. GRAZUL-BILSKA, L. P. REYNOLDS. 2001. Evidence for a role of capillary pericytes in vascular growth of the developing ovine corpus luteum. Biol. Reprod. 65: 879?889. RIBEIRO, L. B., SOUSA, B. M. 2006. Urostrophus vautieri (NCN). Skin shedding. Herpetological Review 37:3: 348. RODRIGUES, M. T., FREITAS, M. A., SILVA, T. F. S., BERTOLOTTO, C. E. V. 2006. A new species of lizard genus Enyalius (Squamata: Leiosauridae) from the highlands of Chapada Diamantina, state of Bahia, Brazil, with a key to species. Phyllomedusa, 5: 11-24. 107 ROGATSCH, H., JEZEK, D., HITTMAIR, A., MICUZ, G., FEICHTINGER, H. 1996. Expression of vimentin, cytokeratin, and desmin in Sertoli cells of human fetal, cryptorchid, and tumour-adjacent testicular tissue. Virchows Arch A Pathol Anat 427:497-502. ROSSI, F., FERRARESI, A., ROMAGNI, P., SILVESTRONI, L., SANTIEMMA, V. 2002. Angiotensin II stimulates contraction and growth of testicular peritubular myoid cells in vitro. Endocrinology. 143:8: 3096-3104. ROTHWELL, B., SOLOMON, S. E. 1977. The ultrastructure of the follicle wall of the domestic fowl during the phase of rapid growth. British Poultry Science, 18: 605-610. ROTHWELL, B., TINGARI, M. D. 1973. The ultrastructure of the boundary tissue of the seminiferous tubule in the testis of the domestic fowl (Gallus domesticus). J Anat 114: 321?328. RHEUBERT, J. L., TOUZINSKY, K., SEVER, D. M., ALDRIDGE, R. D., WILMES, A. J., SIEGEL, D. S., GRIBBINS, K. M. 2014. Reproductive Biology of Sceloporusconsobrinus (Phrynosomatidae): Male Germ Cell Development and Reproductive Cycle Comparisons within Spiny Lizards. Journal of Herpetology. 48:2:162-17. RUSSEL, L. D., SINHA-HIKIM, A. P., GHOSH, S., BARTKE, A. 1994. Structure-function relationships in somatic cells of the testis and accessory reproductive glands. In: BARTKE A. (eds). Function of somatic cells in the testis. Norwell: Spring-Verlag. p55-83. SADJIA, H., GERNIGON SPYCHALOWICZ, T., EXBRAYAT, J. M. 2007. Immunolocalization of estrogens and progesterone receptors within the ovary of the lizard Uromastyx acanthinura from vitellogenesis to rest season. Folia Histochemica et Cytobiologica. 45: 23-27. SANDLEIR, R. M. F. S. 1973. The reproduction of vertebrates. New York: Academic press. p. 56-59. SANTOS, R. C., LUCAS, P. S., SOUSA, B. M., NOVELLI, I. A. 2009. Reptilia, Squamata, Leiosauridae, Urostrophus vautieri: Distribution extension and geographic distribution map. Check List. 5:3: 533?536. SANTOS, H. S. et al. 2015. Ovarian follicular cycle of Tropidurus hispidus and Tropidurus semitaeniatus (Squamata: Tropiduridae) in a semiarid region of Brazil. Zoologia. 32:1: 86-92. 108 SAZIMA, I., HADDAD, C. F. B. 1992. R?pteis da Serra do Japi: notas sobre hist?ria natural. In Hist?ria natural da Serra do Japi: ecologia e preserva??o de uma ?rea florestal no sudeste do Brasil. (P. Morellato, org.). Editora da UNICAMP, Campinas, 212-235. SCHAFFELD, M., HERRMANN, H., SCHULTESS, J., MARKL, J. 2001. Vimentin and desmin of a cartilaginous fish, the shark Scyliorhinus stellaris: sequence, expression patterns and in vitro assembly. Eur J Cell Biol. 80: 692-702. SCHLATT, S., WEINBAUER, G. F., ARSLAN, M., NIESCHLAG, E. 1993. Appearance of ?-smooth muscle actin in peritubular cells of monkey testes is induced by androgens, modulated by follicle-stimulating hormone, and maintained after hormonal withdrawal. J Androl. 14: 340-350 SELSTAM, G., I. NILSSON, AND M. O. MATTSSON. 1993. Changes in the ovarian intermediate filament desmin during the luteal phase of the adult pseudopregnant rat. Acta Physiol. Scand. 147: 123-129. SEVER D. M. 2010. Ultrastructure of the reproductive system of the black swamp snake (Seminatrix pygaea). VI. Anterior testicular ducts and their nomenclature. Journal of Morphology. 271:104-115. SEVER, D. M., FREEBORN, L. R. 2012. Observations on the anterior testicular ducts in snakes with emphasis on sea snakes and ultrastructure in the yellow-bellied sea snake, Pelamis platurus. Journal of Morphology. 273: 324-336. SIEGEL, D. S., SEVER, D. M., RHEUBERT, J. L., GRIBBINS, K. M. 2009. Reproductive biology of Agkistrodon piscivorus Lac?p?de (Squamata, Serpentes, Viperidae, Crotalinae) Herpetol Monographs. 23:74?107. SINGH, D. K., MOHANTY, N., JENA, N. 2016. Reproductive cycle of male common Indian rock lizard, Psammophilus blanfordanus: Seasonal testis, epididymis and renal sex segment histology. The Journal of Zoology Studies, 3:6: 45-55. SILVA, D., RODRIGUES, M., MEHANNA, M., FERREIRA, A., DOLDER, H. 2016. C?lulas germinativas e espermatog?nese do lagarto Tropidurus torquatus (Tropiduridae) de uma ?rea urbana no bioma cerrado do centro-oeste brasileiro. Bioscience Journal. 32:6:1595-1603. SILVEIRA, J. A. 2009. Histologia testicular e caracteriza??o dos est?dios do ciclo do epit?lio semin?fero de Hemidactylus mabouia, (Moreau De Jonn?s, 1818) (Reptilia, Squamata, 109 Sauria, Gekkonidae). Disserta??o (mestrado em biologia celular e estrutural). Universidade Federal De Vi?osa, Minas Gerais, Brasil. 60p. SKALLI, O., ROPRAZ, P., TRZECIAK, A., BENZONANA, G., GILLESSEN, D., GABBIANI, G. 1986. A monoclonal antibody against -smooth muscle actin: A new probe for smooth muscle differentiation. J Cell Biol. 103:2787-2796. SOUSA, B. M. 2000. Aspectos ecol?gicos, comportamentais e morfol?gicos associados ? alimenta??o de Enyalius perditus Jackson, 1978 (Sauria: Polychrotidae). Tese de doutorado, UFRRJ, 168p. STEGER, K., WROBEL, K. H. 1994. Immunohistochemical demonstration of cytoskeletal proteins in the ovine testis during postnatal development. Anatomy and Embryology. 189: 521-530. STORER, T. I., USINGER, R. L., STEBBINS, R. C., NYBAKKEN, J. W. 2000. Zoologia geral. 6 ed. v. 8. S?o Paulo: Companhia Editora Nacional, p. 642-654. TAYLOR, C. 2014. Predictive Biomarkers and Companion Diagnostics. The Future of Immunohistochemistry - ?in situ proteomics?, or just a ?stain?? Appl Immunohistochem Mol Morphol. 22:8: 555-561. TEIXEIRA, R. L., ROLDI, K., VRCIBRADIC, D. 2005. Ecological Comparisons between the Sympatric Lizards Enyalius bilineatus and Enyalius brasiliensis (Iguanidae, Leiosaurinae) from an Atlantic Rain-Forest Area in Southeastern Brazil. Journal of Herpetology. 39:3: 504-509. TUMKIRATIWONG, P., MEESUK, W., CHANHOME, L., AOWPHOL, A. 2012. Reproductive patterns of captive male and female monocle cobra, Naja kaouthia (Lesson, 1831). Zoological Studies. 51:5: 692-700. UETZ, P., JIR? HO?EK (eds.), The Reptile Database, http://www.reptile-database.org, acessado em abril, 2017. URIBE, M. C., OMANA, M. E. M., QUINTERO, J. E. G., GUILLETTE, L. J. JR. 1995. Seasonal variation in ovarian histology of the viviparous lizard Sceloporus torquatus torquatus. Journal of Morphology 226:103-119. URIBE, M. C., PORTALES, G., GUILLETTE, L. J.

Page generated in 0.008 seconds