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Journal articles on the topic 'Bullfrog – Anatomy'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Davim, André, Tereza Dantas, and Márcia Pereira. "Analysis of the Anti-Inflammatory Potential of Pure and Microemulsified Bullfrog Oil in Acute Lung Injury." Journal of Morphological Sciences 35, no. 02 (June 2018): 102–5. http://dx.doi.org/10.1055/s-0038-1669933.

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AbstractInfectious diseases account for more than a third of all hospital admissions, and are highly prevalent in intensive care units. Currently, sepsis is one of the diseases with the highest morbidity and mortality rates worldwide, with death rates reaching up to 60% among intensive care patients, according to statistics from low-income countries. The prominence of multi-resistant microorganisms is rising, while the possibilities of development of new target drugs are being exhausted. Thus, the objective of the present study was to evaluate the anti-inflammatory potential of bullfrog oil in its pure state and in a microemulsion system in an experimental model of sepsis. Mice were separated into three groups and treated with bullfrog oil in its pure state, in a microemulsion, and with saline solution, and subsequently submitted to induction of sepsis. Bronchoalveolar lavages were performed for cell counts, as well as analyses of lung tissue samples. When the washings were analyzed, no statistically significant difference was observed in cell migration between the experimental groups, but a difference was observed between these groups and the saline solution group. When the lung tissue samples were analyzed, intense tissue wear was observed in the bullfrog oil groups, with the presence of cellular infiltrate and rupture of respiratory bronchioles and alveoli. However, in the microemulsion group, no major tissue wear was observed, and the pulmonary parenchyma was more preserved. Thus, we concluded that bullfrog oil in pure form and in a microemulsion system are good modulators of the inflammatory response, with the microemulsion system being more efficient in protecting lung tissue.

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2

Rizzi, G., E. Silva-Zacarin, C. Oliveira, M. Costa, R. Salla, and F. Abdalla. "Morphological characterization of the gonads of bullfrog tadpoles (Lithobates catesbeianus)." Journal of Morphological Sciences 32, no. 04 (October 2015): 245–52. http://dx.doi.org/10.4322/jms.074214.

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Abstract Introduction: This work describes various aspects of early gonadal development of female and male in pre-metamorphic tadpoles (Lithobates catesbeianus) at Gosner stage 25. Materials and Methods: Ovaries and testicles were prepared for routine light microscopy for morphological study and for acridine orange technique fluroescent microscopy for observation of RNA cytoplasm activity. Results: The results showed that female gonads at Gosner stage 25 predominated primary and secondary oogonias, as well as primary, secondary and tertiary oocytes. The developing testicle presented primary spermatogonia (I or A) and secondary spermatogonia (II or B), and as well as primary and secondary spermatocyte. All this cell phases were morphologically characterized and the cell sizes measured. In pre-metamorphic testes the somniferous duct are not developed and the vasa deferentia is opened. Conclusion: At this point, it was possible differentiate ovary from testes does not for the gonadal cells, but for the general anatomy of the organs, being the ovary a spheroid structure and the testicle an elongated tubule.

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3

Yaoi, Yuichi, Tomoaki Onda, Yoshie Hidaka, Shinya Yajima, Masakazu Suzuki, and Shigeyasu Tanaka. "Developmental Expression of Otoconin-22 in the Bullfrog Endolymphatic Sac and Inner Ear." Journal of Histochemistry & Cytochemistry 52, no. 5 (May 2004): 663–70. http://dx.doi.org/10.1177/002215540405200510.

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4

Bowers, C. W., L. Y. Jan, and Y. N. Jan. "A substance P-like peptide in bullfrog autonomic nerve terminals: Anatomy biochemistry and physiology." Neuroscience 19, no. 1 (September 1986): 343–56. http://dx.doi.org/10.1016/0306-4522(86)90026-6.

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5

Fujitsuka, Noriaki, Chie Fujitsuka, Yoshiharu Shimomura, Taro Murakami, Atsushi Yoshimura, Keisuke Kawakami, Woodrow F. Ritchie, Nobuhiro Kaneko, and Masahiro Sokabe. "Intramembrane structure of the sensory axon terminals in bullfrog muscle spindles." Anatomical Record 252, no. 3 (November 1998): 340–54. http://dx.doi.org/10.1002/(sici)1097-0185(199811)252:3<340::aid-ar2>3.0.co;2-p.

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6

Yaoi, Yuichi, Masakazu Suzuki, Hideaki Tomura, Shingo Kurabuchi, Yuichi Sasayama, and Shigeyasu Tanaka. "Expression and Localization of Prohormone Convertase PC1 in the Calcitonin-producing Cells of the Bullfrog Ultimobranchial Gland." Journal of Histochemistry & Cytochemistry 51, no. 11 (November 2003): 1459–66. http://dx.doi.org/10.1177/002215540305101106.

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7

Collings, Amber J., and Christopher T. Richards. "Digital dissection of the pelvis and hindlimb of the red-legged running frog, Phlyctimantis maculatus, using Diffusible Iodine Contrast Enhanced computed microtomography (DICE μCT)." PeerJ 7 (June 7, 2019): e7003. http://dx.doi.org/10.7717/peerj.7003.

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Background The current study applies both traditional and Diffusible Iodine Contrast Enhanced computed microtomography (DICE µCT) techniques to reveal the musculoskeletal anatomy of Phlyctimantis maculatus. DICE µCT has emerged as a powerful tool to visualise intricate musculoskeletal anatomy. By generating 3D digital models, anatomical analyses can be conducted non-destructively, preserving the in situ 3D topography of the system, therefore eliminating some of the drawbacks associated with traditional methods. We aim to describe the musculature of the spine, pelvis, and hindlimb, compare the musculoskeletal anatomy and pelvic morphology of P. maculatus with functionally diverse frogs, and produce 3D digital anatomy reference data. Method An adult frog was stained using an aqueous Lugol’s solution and scanned in a SkyScan1176 in vivo µCT scanner. Scan images were reconstructed, resampled, and digitally segmented to produce a 3D model. A further adult female frog was dissected traditionally for visualisation of tendinous insertions. Results Our work revealed three main findings: (1) P. maculatus has similar gross muscular anatomy to Rana catesbeiana (bullfrog) but is distinct from those species that exhibit ancestral traits (leopelmids) and those that are highly specialised (pipids), (2) P. maculatus’s pelvic anatomy best fits the description of Emerson’s walking/hopping pelvic morphotype IIA, and (3) a split in the semimembranosus and gracilis major muscles is consistent with the reported myology in other anuran species. Discussion While DICE µCT methods were instrumental in characterising the 3D anatomy, traditional dissection was still required to visualise important structures such as the knee aponeurosis, tendinous insertions, and fasciae. Nonetheless, the anatomical data presented here marks the first detailed digital description of an arboreal and terrestrial frog. Further, our digital model presents P. maculatus as a good frog model system and as such has formed a crucial platform for further functional analysis within the anuran pelvis and hindlimb.

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8

Seixas Filho, José Teixeira de, Silvia Conceição Reis Pereira Mello, Fabiane Toste Cardoso, and Rodrigo Otavio Lopes de Souza. "Functional anatomy and intestinal morphometry of bullfrog tadpoles subjected to a dietary regime with commercial feeds." Ciência e Agrotecnologia 40, no. 4 (August 2016): 464–74. http://dx.doi.org/10.1590/1413-70542016404001116.

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ABSTRACT One of the main hindrances to frog farming is the lack of knowledge of the nutritional requirements of tadpoles that allow nutritionists to formulate the ideal diet for this phase, reducing operational costs and providing homogeneity to the shoal. This study aimed at evaluating the anatomy of the digestive tract and morphometry of the midgut and hindgut of bullfrog (Lithobates catesbeianus) tadpoles to provide subsidies for nutritionists to make adjustments in the balancing of suitable diets for this species. The population of tadpoles that received the dietary regimen named DR3, which consisted of a fortnight increase of the dietary protein levels (from 32 to 45% of CP) for 60 days, showed the best results regarding weight gain, survival rate, and homogeneity in the passage of the larval stages as compared with the other dietary regimens tested. Additionally, the morphometry of the intestines of the animals subjected to DR3 showed a greater length (419.2 mm) and higher caliber of the midgut portion where most of the nutrient absorption takes place. It can thus be inferred that this fact is related to the height of the absorptive intestinal folds resulting from the supply of a diet with better quality, confirmed by the weight of the juveniles.

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9

Fernandez, Sthefanie, Rosângela Felipe Rodrigues, Rose Eli Grassi Rici, Phelipe Oliveira Favaron, and Alan Peres Ferraz De Melo. "Ultrastructure of the bullfrog (Lithobates catesbeianus-Shaw, 1802) oviduct in different seasons." Microscopy Research and Technique 76, no. 5 (March 1, 2013): 523–32. http://dx.doi.org/10.1002/jemt.22195.

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10

Carvalho, Hernandes Faustino, and Sérgio Luis Felisbino. "The development of the pressure-bearing tendon of the bullfrog, Rana catesbeiana." Anatomy and Embryology 200, no. 1 (May 20, 1999): 55–64. http://dx.doi.org/10.1007/s004290050259.

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11

Herbener, G. H., M. Bendayan, and R. C. Feldhoff. "Albumin localization in the frog hepatocyte during vitellogenesis as revealed by protein A-gold immunocytochemistry." Journal of Histochemistry & Cytochemistry 34, no. 5 (May 1986): 665–71. http://dx.doi.org/10.1177/34.5.3486212.

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The protein A-gold immunocytochemical technique was used to localize albumin in the hepatocyte of the normal male American bullfrog, Rana catesbeiana, and also in the hepatocyte of this animal 8 days after treatment with estradiol-71 beta. Albumin concentration in plasma also was estimated biochemically. In the normal animal, specific immunolabeling for albumin was present in the intracellular compartments involved in protein secretion, i.e., rough endoplasmic reticulum (RER), Golgi apparatus and secretory granules, and also in lysosomes. Density of labeling increased as it progressed along the secretory pathway. In the hepatocyte of the estrogen-treated frog, specific immunolabeling for albumin was also present along the entire secretory pathway and in the lysosomes. Density of labeling over the RER was similar to that seen for this organelle in normal tissue; however, no progressive increase, but rather significant decreases, in labeling density occurred further along the secretory pathway. The biochemical data demonstrated no change in the concentration of plasma albumin in the treated frog, compared with the normal one. These observations localize albumin along its secretory pathway in frog hepatocyte and demonstrate a perturbation in its secretion in response to estrogen treatment.

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12

Gracia-Navarro, F., and P. Licht. "Subcellular localization of gonadotrophic hormones LH and FSH in frog adenohypophysis using double-staining immunocytochemistry." Journal of Histochemistry & Cytochemistry 35, no. 7 (July 1987): 763–69. http://dx.doi.org/10.1177/35.7.3108366.

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We applied double post-embedding immunocytochemical methods using specific antibodies against bullfrog (Rana catesbeiana) luteinizing hormone (LH) and follicle-stimulating hormone (FSH) with immunogold staining (5- and 20-nm particles) to determine the subcellular localization of both gonadotropins and to observe their immunostaining patterns in anterior pituitary of the frog Rana pipiens. Results showed that individual gonadotrophs may store either one or both gonadotropins in a given secretory granule and in large globules (lysosomes?). Most gonadotrophs (50-88%) contain both hormones; 12-50% contain only FSH, and only a few (0-7%) contain LH alone. Individual secretory granules, even in cells that contain both hormones, may contain only one or both gonadotropin molecules. Evaluation of the percentage of monohormonal and multihormonal secretory granules revealed that multihormonal secretory granules were the most numerous and that LH monohormonal secretory granules were the least numerous. These results indicate that cellular storage of gonadotropin in amphibian pituitary is similar to that described for mammals, where a single cell type containing both gonadotropins predominates. Variability in hormone content both of cells and of granules in all individuals is consistent with the hypothesis that frog pituitary possesses a single multipotential gonadotroph.

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13

Yaoi, Yuichi, Sakae Kikuyama, Hiroaki Hayashi, Yoichi Hanaoka, Makoto Sakai, and Shigeyasu Tanaka. "Immunocytochemical Localization of Secretory Phospholipase A2-like Protein in the Pituitary Gland and Surrounding Tissue of the Bullfrog, Rana catesbeiana." Journal of Histochemistry & Cytochemistry 49, no. 5 (May 2001): 631–37. http://dx.doi.org/10.1177/002215540104900510.

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14

Tanaka, Shigeyasu, Shingo Kurabuchi, Hiroshi Mochida, Hiroaki Hayashi, and Katsumi Wakabayashi. "Production and Characterization of Specific Anti-peptide Antiserum Against Free α-subunit of Rat Pituitary Glycoprotein Hormones." Journal of Histochemistry & Cytochemistry 45, no. 7 (July 1997): 985–90. http://dx.doi.org/10.1177/002215549704500708.

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To obtain an antibody specific for the α-subunit of rat pituitary glycoprotein hormones, we synthesized a peptide corresponding to the sequence 37–53 (ST-7: Phe-Ser-Arg-Ala-Tyr-Pro-Thr-Pro-Ala-Arg-Ser-Lys-Lys-Thr-Met-Leu-Val) of the rat α-subunit. The polyclonal antiserum against this peptide was generated in rabbits. This region is hydrophilic and highly conserved among several mammalian species. Noncompetitive binding tests showed that the ST-7 antiserum had specific affinity for the rat free α-subunit, but not for rat intact LH, FSH, and TSH. The ST-7 antiserum immunostained two types of cells in the rat anterior pituitary, i.e., gonadotrophs and thyrotrophs. This was also the case in mouse, cattle, sheep, and pig, which have an identical sequence of ST-7 in their α-subunit. The pituitary cells of horse (Arg substituted for Lys as residue 48 of the rat α-subunit), human, and eel (Leu for Ala at residue 45), chicken (Met for Ala at residue 45), and bullfrog (Tyr for Phe at residue 37 and Met for Ala at residue 45) were not stained with the ST-7 antiserum. This study indicated that the ST-7 antiserum is sequence-specific for the α-subunit and is therefore useful for immunohistochemical studies on the secretory pathway of the free α-subunit.

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15

Kusakabe, Tatsumi. "Morphogenesis of the carotid labyrinth in the bullfrog,Rana catesbeinna, during larval development and metamorphosis." Anatomy and Embryology 184, no. 2 (1991): 133–39. http://dx.doi.org/10.1007/bf00942744.

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16

Watanabe, Hiroshi, Hiroshi Washioka, and Akira Tonosaki. "?Cholinergic? postsynaptic membranes of bullfrog sympathetic ganglia: Electron microscopy of thin sections and freeze-fracture replicas." Anatomical Record 214, no. 1 (January 1986): 82–88. http://dx.doi.org/10.1002/ar.1092140114.

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17

Bennett, G., and R. Hemming. "Ultrastructural localization of CMPase, TPPase, and NADPase activity in neurons, satellite cells, and Schwann cells in frog dorsal root ganglia." Journal of Histochemistry & Cytochemistry 37, no. 2 (February 1989): 165–72. http://dx.doi.org/10.1177/37.2.2536056.

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Sections of bullfrog dorsal root ganglia were analyzed for cytidine monophosphatase (CMPase), thiamine pyrophosphatase (TPPase), and nicotinamide adenine dinucleotide phosphatase (NADPase) activity, and the distributions of these enzymatic activities were compared with those traditionally found in other cell types (e.g., CMPase: Golgi trans-sacculotubular network; TPPase: trans-Golgi saccule(s); NADPase: intermediate Golgi saccules). In the present study, CMPase activity in neurons was localized mainly to the Golgi trans-sacculotubular network and lysosomes, but sometimes also occurred at the ends of the trans and most distal intermediate Golgi saccules. A similar distribution was found in satellite and Schwann cells. TPPase activity in neurons occurred not only in the trans-Golgi saccule but also in the trans-sacculotubular network, lysosomes, and scattered tubular elements. In satellite and Schwann cells, activity was found in both the trans saccule and trans-sacculotubular network, and substantial activity often appeared in the more distal of the intermediate saccules. NADPase activity in neurons was usually absent from the intermediate Golgi saccules and was confined to the trans-sacculotubular network and lysosomes; however, activity was sometimes also found in the intermediate and/or trans-Golgi saccules. In satellite and Schwann cells, activity appeared consistently in both the trans-sacculotubular network and intermediate saccules, as well as in lysosomes. These distributions, especially in the case of TPPase and NADPase, differ substantially from the most frequently reported localizations of the above enzymes, indicating that the Golgi complex may exhibit considerable plasticity of structure and function in different cell types.

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18

Kusakabe, Tatsumi, Tadashi Kawakami, Michio Ono, Hajime Sawada, and Toshifumi Takenaka. "Distribution of peptidergic nerve fibres in bullfrog lingual papillae demonstrated by a combination of double immunofluorescence labelling and a multiple dye filter." Histochemical Journal 28, no. 4 (April 1996): 289–97. http://dx.doi.org/10.1007/bf02409017.

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19

Sasso-Cerri, E., E. Freymuller, and S. M. Miraglia. "Testosterone-immunopositive primordial germ cells in the testis of the bullfrog, Rana catesbeiana." Journal of Anatomy 206, no. 6 (June 2005): 519–23. http://dx.doi.org/10.1111/j.1469-7580.2005.00419.x.

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20

Bałuk, Peter. "Scanning electron microscopic studies of bullfrog sympathetic neurons exposed by enzymatic removal of connective tissue elements and satellite cells." Journal of Neurocytology 15, no. 1 (February 1986): 85–95. http://dx.doi.org/10.1007/bf02057907.

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21

Tadokoro, Osamu, Hiroshi Ando, Ichiro Kawahara, Naokazu Asanuma, Masayo Okumura, Junichi Kitagawa, Eiji Kondo, and Hiroshi Yagasaki. "Distribution and Origin of VIP-, SP-, and Phospholipase Cβ2-Immunoreactive Nerves in the Tongue of the Bullfrog,Rana catesbeiana." Anatomical Record 299, no. 7 (April 8, 2016): 929–42. http://dx.doi.org/10.1002/ar.23334.

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22

ICHIMURA, KOICHIRO, KENJI KOIZUMI, HIROYUKI KUDOH, TAKAYOSHI MIYAKI, and TATSUO SAKAI. "A novel branching pattern of the superior mesenteric artery found in the bullfrog (Rana catesbeiana ) amphibian." Journal of Anatomy 198, no. 5 (May 2001): 625–33. http://dx.doi.org/10.1046/j.1469-7580.2001.19850625.x.

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23

Eidietis, Laura. "The tactile-stimulated startle response of tadpoles: acceleration performance and its relationship to the anatomy of wood frog (Rana sylvatica), bullfrog (Rana catesbeiana), and American toad (Bufo americanus) tadpoles." Journal of Experimental Zoology Part A: Comparative Experimental Biology 305A, no. 4 (2006): 348–62. http://dx.doi.org/10.1002/jez.a.269.

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24

Honrubia, V., L. F. Hoffman, S. Sitko, and I. R. Schwartz. "Anatomic and physiological correlates in bullfrog vestibular nerve." Journal of Neurophysiology 61, no. 4 (April 1, 1989): 688–701. http://dx.doi.org/10.1152/jn.1989.61.4.688.

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1. The correlations between anatomic and physiological characteristics of primary afferent neurons innervating the anterior semicircular canal in the bullfrog were investigated. These characteristics were examined separately in large groups of neurons, and the direct correlations between them were established in a subset of neurons by means of intraaxonal recording and labeling. 2. Anatomic features of the anterior canalicular nerve that were related with fiber diameter were studied. This nerve was composed of an average of 1,142 fibers (standard deviation of 171 in 5 samples), of which 42% were less than 2 microns in diameter and 8% were greater than 7 microns. The nerve branched into 6 clearly defined bundles, whose fiber diameter-dependent composition could be determined in 5 samples. In the 2 center bundles, 32% of the fibers had diameters greater than 7 microns. In contrast, these thick fibers comprised only 4% of the fiber population in the 2 lateralmost bundles, in which 44% of the fibers had diameters less than 2 microns. The projections of labeled afferent fibers were traced into the neuroepithelium, and it was demonstrated that all thick fibers, even those of the lateral bundles, turned toward more central regions of the crista. Consequently, in the bullfrog, there is a clear predominance of thick afferent fibers innervating the anterior crista's central region and thin fibers in the peripheral region. 3. The dendritic morphology of the broad classes of afferent fibers (i.e., thick and thin) was elucidated. Individually labeled thick afferents possessed dendrites forming short, thick, clawlike extensions to contact a few hair cells. The thinnest afferents were labeled through extracellular horseradish peroxidase (HRP) injections. In contrast to the thick fibers, thin afferents were characterized by an unbranched trajectory with serially located bouton-like structures that were apposed to successive hair cells. 4. The characteristics of spontaneous firing and the responses to rotational stimuli were determined for 138 anterior canalicular neurons. Spontaneous firing rates ranged from 0 to 95 spikes.s-1. The coefficient of variation (CV) of spontaneous firing ranged from 0.12 to 2.5. Response gains to high- (0.5 and 0.4 Hz) and medium- (0.05 Hz) frequency sinusoidal acceleration stimuli were positively correlated with CV (P less than 0.001) for neurons with a CV value less than or equal to 0.5. The gain of neurons characterized by more irregular spontaneous firing (CV values greater than 0.5) was uncorrelated with CV.(ABSTRACT TRUNCATED AT 400 WORDS)

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25

Newman, Anita, Alexander Kuruvilla, Alberto Pereda, and Vicente Honrubia. "REGENERATION OF THE EIGHTH CRANIAL NERVE. I. ANATOMIC VERIFICATION IN THE BULLFROG." Laryngoscope 96, no. 5 (May 1986): 484–93. http://dx.doi.org/10.1288/00005537-198605000-00003.

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26

Davis, Andrew K. "Metamorphosis-related changes in leukocyte profiles of larval bullfrogs (Rana catesbeiana)." Comparative Clinical Pathology 18, no. 2 (October 24, 2008): 181–86. http://dx.doi.org/10.1007/s00580-008-0773-8.

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27

Ko, Chien Ping. "Formation of the active zone at developing neuromuscular junctions in larval and adult bullfrogs." Journal of Neurocytology 14, no. 3 (June 1985): 487–512. http://dx.doi.org/10.1007/bf01217757.

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28

Kusakabe, Tatsumi. "Ultrastructural characteristics of glomus cells in the external carotid artery during larval development and metamorphosis in bullfrogs,Rana catesbeiana." Anatomical Record 233, no. 3 (July 1992): 461–66. http://dx.doi.org/10.1002/ar.1092330313.

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29

Kusakabe, Tatsumi. "Intimate apposition of the glomus and smooth muscle cells (g-s connection) in the carotid labyrinth of juvenile bullfrogs." Anatomy and Embryology 185, no. 1 (1992): 39–44. http://dx.doi.org/10.1007/bf00213599.

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