Morfologia y Ultraestructura de la Hipofisis en Camellos Bactrianos (Camelus bactrianus).
The hypophysis plays a major role in regulating important physical functions and general wellbeing. It is referred to as the body's 'master gland' because its secretion regulates the activity of most other hormone-secreting glands. It senses the body's needs and sends signals to different organs and glands throughout the body to regulate their function and maintain an appropriate environment. It secretes a variety of hormones into the bloodstream which act as messengers to transmit information from the hypophysis to distant cells, regulating their activity (Martinez-Lage, 2011; Marieb & Hoehn, 2012).
The Bactrian camels (Camelus bactrianus) live in the arid and semiarid areas of the northwest China and Mongolia, where feeding resources are generally scattered and poor. Although the complexity the hypophysis in Bactrian camel is considered to be most important for their adaption to extreme environment, it has received little attention. Related researches of hypophysis on large artiodactyls, such as buffalo, sheep, pigs, dig and others were often found in publications (Dorst, 1968; Li et al, 2008). Whereas, studies on the brain, hypothalamus and adrenal gland in Bactrian camel have been more detailed report (Xie et al., 2006; Ye et al., 2014, 2015, 2017). So we systematically investigated the hypophysis from healthy adult Bactrian camel by anatomical, histological and electron microscopical approaches, and obtained the quantitative data for comparison among artiodactyls. The purpose of this study is to provide credible anatomic and morphological data, the cellular and subcellular structures of the hypophysis, which will contribute to the future research on the physiology and pathology of hypophysis structures and will provide a theoretical basis for ongoing investigations for the relationship between environment adaptation of the Bactrian camels and their special organ structure.
MATERIAL AND METHOD
Materials. Ten specimens of the adult Bactrian camels were obtained from the slaughterhouse of the Right Alashan Banner Food Company in Inner Mongolia Autonomous Region, China, the average age was 9 years old. As soon as the animals were killed by exsanguination in the local slaughterhouse, four specimens were removed intact and rapidly, then the different parts of the hypophysis separated and soaked in 3% glutaraldehyde solution and 10% neutral formalin solution fixative respectively, for microscopic and ultrastructural study.
The remaining specimens of the head of Bactrian camels were fixed at 5 to 15 min after death. Both internal carotid arteries were isolated by blunt dissection. Cannula coupled by surgical tubing to a pressure-driven perfusion device, were inserted into each vessel. Pressure was maintained at a constant value of 130 mmHg for both the initial rinse solution, which was a mixture of 0.5 L of 0.85 % sodium chloride, 0.1% sodium nitrite and 0.1% sodium heparin, and the final fixative which consisted of 3 L of 0.1 M phosphate buffered 10% formalin (pH 7.4).
Gross anatomy. The brains and hypophysis were removed from the cranium at one week after death. The hypophysis was kept intact and weighted. The length parameters were measured by vernier caliper, and photos were taken by digital camera.
Microstructure. Samples of hypophysis for light microscope (LM) were fixed in 10% formaldehyde for 72 h, dehydrated, cleared and embedded in paraffin. Embedded tissues of were cut into 7 mm thick sections and stained with hematoxylin and eosin (HE) or special stain (SS) (Wang et al., 2006).
SS: form step 1 to 3
Step 1. Alcian blue staining: tissue sections of 7 [micro]m's thick were dewaxed in xylene, soaked into the solution of formic acid (88% formic acid 40 ml + [H.sub.2][O.sub.2] 4 ml + [H.sub.2]S[O.sub.4] 0.5 ml) for 5 min, and then washed 10 min. The samples were stained by alcian blue (alcian blue 2 g + 2 N [H.sub.2]S[O.sub.4] 100 ml) for at least 12 h, and then washed 10 min.
Step 2. Periodic acid-Schiff staining (FAS): The samples were soaked into 1% periodic acid for 5 min, water rinsed several times, then stained by Schiff reagents (water 200 ml + Basic fuchsin 1 g + 1 N HCl 20 ml + potassium metabisulfite 1 g + activated carbon 2 g) for 10 min of water rinse.
Step 3. Azocarmine and orange G staining: The samples stained by 0.5% azocarmine for 30 s, water rinsing, stained by 2% orange G (orange G 2 g + phosphotungstic acid 1 g + water 100 ml) for 30 min. The sections were dehydrated through increasing concentrations of ethanol and xylene, coverslip slides using permount.
Ultrastructure. The samples were prepared for Transmission electron microscope (TEM) with three major procedures, post processing, semi-thin sectioning and ultrathin sectioning. In post processing, small pieces were first fixed in 3% glutaraldehyde buffer for 1 week; second, they were washed in 0.1 M phosphate buffer; third, the pieces were cut into 1 [mm.sup.3] lumps and post-fixed with osmium tetroxide for 1 h; fourth, the samples were washed twice in 0.1 M phosphate buffer and then dehydrated in ascending grades of ethanol before being embedded in epon 812. Semithin sections of different samples were collected and stained with toluidine blue. Ultra-thin sections were then collected on copper grids. The ultra-thin sections were stained with a saturated solution of uranyl acetate for 30 min, followed by lead citrate for 7 min in a carbon dioxide-free environment. The end-products were examined under a transmission electron microscope (JEOL, JEM-1230).
Data analysis. All the sections were photographed and analyzed by MOTIC Images Advanced 3.0 and the data obtained were statistically analyzed using the SPSS in version 19.
Anatomy. The hypophysis of Bactrian camel rests upon the hypophysial fossa of the sphenoid bone in the center of the middle cranial fossa attaching to the hypothalamus by hypophysis stalk. And it was surrounded by sella turcica covered diaphragma sellae. The gland was oval in shape with the same size of a peanut. The terminal of hypophysis was a tiny protuberance, which was the terminal of neurohypophysis. The hypophysis was about 1.54 g in weight with the weight ratio of 0.0045 g/kg to body (AGW/BW). Its volume was about 2~3 [cm.sup.3] with different radial lines of 1.68'1.43'1.14 cm. Moreover, the hypophysis stalk was 0.55 cm in diameter and 1.09 cm in length. The hypophysis could be dividedinto two parts, the outer adenohypophysis and the inner neurohypophysis (Table I) (Figs. 1 and 2).
Observation from the median sagittal plane, the hypophysis in Bactrian camel is bilaterally symmetrical. The cavum infundibular visibly extended to the distal of infundibular stalk, with a portion deep inside of the hypophysis. The hypophysis in Bactrian camel could be divided into three parts: pars nervosa, pars distalis and pars intermedia. The pars distalis was biggest, located in ventral surface of the hypophysis, and surrounding the pars intermedia excluding the top of the hypophysis. The hypophyseal cleft was obvious and big between pars distalis and pars intermedia, and it was filled with gelatinous substances. The pars intermedia is a narrow region between the pars distalis and pars nervosa, which surrounding the pars nervosa excluding hypophysis stalk and the tiny protuberance at the terminal of pars nervosa. The pars nervosa was water drop shape, located in the centre of the gland, and surrounded by the pars intermedia and the pars distalis. Furthermore, the pars tuberalis that surrounds the neural stalk, was an intrusion of the pars distalis to the hypothalamus. The neurohypophysis consisted of the pars nervosa, the infundibular stalk and the median eminence. The infundibular stalk and the pars tuberalis together comprise the hypophysis stalk. Besides, on the dorsum of the hypophysis, filled with gelatinous substance, a big cavity formed between the capsule and the pars intermedia, or between the pars intermedia and the pars nervosa (Figs. 2 and 3).
LM and TEM. The hypophysis was covered by a thinner layer of capsule with connective tissue, which consisted of mainly collagen fibers and reticular fiber. The parenchyma had two anatomically distinct zones, the outer adenohypophysis and the inner neurohypophysis, which had different histological and cytological structures in LM and TEM.
Adenohypophysis. The adenohypophysis constituted 80% of the volume of the hypophysis with fasciculate or irregular anastomosing reticulum, less connective tissue and affluent blood sinuses present. The cells of adenohypophysis arranged in clusters, and formed the following parts: the pars distalis and the pars intermedia (Figs. 3 and 4).
Pars distalis (PaD). The pars distalis was the largest portion of the whole gland. Clusters of cells were arranged here, fasciculately or reticulumly, with blood sinuses affluently mingled (Figs. 4A and 4B). According to the colors after HE staining, the cells could be divided into chromophobe cells, acidophil cells and basophil cells. The cytoplasmic of the acidophil cells were red, and the nuclei were deep blue. The cytoplasmic of the basophil cells were light blue, and the nuclei were deep blue. Moreover, the chromophobe cells were hard staining by HE, the cytoplasmic were light blue or colorless, and the nuclei were light blue. In general, the chromophobe cells accounts for above 50% of the cells of pars distalis, the acidophil cells were 40%, and the basophil cells were less than 10 % (Figs. 4C-L). Furthermore, a thin layer of cells that was similar with ependymal cells located in the interior marginal area of the pars distalis, and margin on hypophyseal cleft. The cells were triangle, round or ovoid in shape, and palisading closely. The nuclei were rounded or oval and the nucleo-cellula ratio (N/C ratio) was larger (Fig. 4K).
Chromophobe cell (CC). Half and more of the pars distalis are the chromophobe cell, which arranged in clusters. The chromophobe cells were small in size with rounded or polygonal-shaped and with a lighter HE staining (Figs. 4CL). Some publication indicated that chromophobe cells were undifferentiated to reserve for transforming into acidophilic cell and basophilic cell. Ultrastructural examinations confirmed that the chromophobe cells were rounded or polyhedral, whose nuclei were rounded or oval with a larger N/C ratio. It is worth noting that underdeveloped organelles and absence of secretory granules was the most prominent feature of the chromophobe cells (Fig. 5A).
Acidophil cell (AC). The majority of acidophil cells were located in the lateral and central parts of the pars distalis, and the minority were in the interior part. The acidophil cells were triangle, round or ovoid in shape, and medium-sized or somewhat larger. The nuclei were rounded or oval, dyed with various shades, and usually one or two were in a cell. The cytoplasmic of acidophil cells could be stained by eosin at HE. The results of azocarmine and orange G staining could demonstrate the difference of two types of acidophil cells: Orange somatotropic cells and nacarat lactotrophic cells (Figs. 4C-L). Further, a relationship of the secretory granules identified by the electron microscopy has also been demonstrated (Ciocca et al., 1979).
Somatotropic cell (SC) .The somatotropic cells constitute over 50% of the acidophil cells, and arranged in clusters along the capillary. The cytoplasmic of somatotropic cells could be stained orange by orange G (Figs. 4F and 4J). In electron micrographs, the somatotropic cells were rounded or polyhedral, the nuclei were round and located centrally. Many secretory granules ultra structurally visible were electron-dense, uniformly spherical and generally 240 to 410 nm in diameter, with no gap between membrana limitans and endocrine (Fig. 5B).
Lactotrophic cell (LC). The lactotrophic cells always arranged singularly, and tended to be randomly distributed within the pars distalis. The cytoplasmic of lactotrophic cells could be stained nacarat by azocarmine and orange G (Figs. 4F and 4J). Ultra structurally, the size and shape of the secretory granules were non-uniform and generally spherical, ovoid, or rhabditiform in diameters of 300 to 430 nm, as well as 100 to 200 nm (Fig. 5C).
Basophil cell (BC). In general, the basophil cells were slightly larger than the acidophil cells, and round, ovoid or polygon in shape. The cytoplasmic could be stained light blue by HE, and the nuclei were dark blue. Three types of basophil cells could be distinguished with immunohistochemical techniques and electron micrographs: thyrotrophic cells, gonadotrophic cells and corticotrophic cells (Figs. 4C-L and 5D-F).
Thyrotrophic cell (TC). The thyrotrophic cells were round or polyhedral in shape, and medium-sized or somewhat larger. They often formed small nests occupying a fairly area of the anterior-median portion of the pars distalis. The nuclei were rounded or oval with a small N/C ratio. After the procedure of SS staining, the cytoplasmic were dark blue, especially the cytoplasm marginal area, and the nuclei were light red (Figs. 4F and 4J). Ultrastructurally, the thyrotrophic cells showed small and less secretory granules measuring generally 70 to 150 nm in diameter, and the secretory granules were the smallest. The secretory granules were electron-dense and uniform, spherical, and located in the cytoplasm marginal area (Fig. 5D).
Gonadotrophic cell (GC). The gonadotrophic cells were round, ovoid or long strip in shape, larger-sized, and medium-sized, and widely distributed throughout the pars distalis. By SS staining, the cytoplasmic were fuchsia, and the nuclei were crimson (Figs. 4F and 4J). In electron micrographs, a lot of secretory granules were electron-dense, spherical, and visible in the cytoplasm. The size of secretory granules varies considerably, generally divided into large granules and small granules. The diameter of large granules generally were 200 to 250 nm, small granules were about 80 to 150 nm (Fig. 5E).
Corticotrophic cell (ACTH). The corticotrophic cells were ovoid in shape, smaller-sized, amount was less, and usually located within the central part of the pars distalis. After SS staining, the cytoplasmic were light blue, and the nuclei were light red (Figs. 4F and 4J). Ultrastructurally, these cells showed small and less secretory granules in diameters of generally 80~250 nm. The secretory granules were electrondense and nouniform, spherical locating in the cytoplasm marginal area (Fig. 5F).
Stellate cells. The stellate cells could not be clearly distinguished under light microscopy. In electron micrographs, the stellate cells looked similar to the chromophobe cells, as they were absence of secretory granules. Their differences were that the chromophobe cells were rounded or polygonal-shaped arranging in clusters, but the stellate cells were irregular-shape, with long protuberance arranging as a single cell. Furthermore, the organelles of chromophobe cells were more developed than the chromophobe cells (Fig. 5G).
Pars intermedia (PaI). The pars intermedia of the hypophysis in Bactrian camel was narrow situated between the pars distalis and the pars nervosa, approximately 730 um in thickness, and composed of basophil cells and many crevices with different sizes. These cells arranged in cords or clusters. There was an obvious and big cleft between pars distalis and the pars intermedia, which named hypophyseal cleft. There was also a cleft between the pars intermedia and the pars nervosa, which was smaller than the hypophyseal cleft. The pars intermedia was developed and surrounding the pars nervosa except hypophysis stalk and the tiny protuberance at the terminal of pars nervosa. The basophil cells were the only type observed after HE and SS staining in the pars intermedia, the cells were irregular polygon, larger-sized, and the nuclei were round or oval (Fig. 6).
Neurohypophysis (PN). The neurohypophysis consists of the pars nervosa, the infundibular stalk and the median eminence. They contained large numbers of unmyelinated nerve fibres, pituicytes, rich in capillaries and connective tissue. The nerve fibre bundles environ the capillarie, which was located centrally, surrounded by connective tissue and unmyelinated nerve fibers, radiated out from internal neurohypophysis to external neurohypophysis, and were dyed deep by SS. By SS staining, the nerve fibres were deep blue, the connective tissues were red, and the pituicytes were red or blue and tended to be randomly distributed within the nerve fibres. The corpusculum neurosecretorium (Herring bodies) were rare in the external neurohypophysis, and mainly distributed in the internal neurohypophysis (Figs. 7 and 9).
Nerve fibres. The nerve fibers of the neurohypophysis mainly started from the hypothalamus, and branchily radiated out from internal neurohypophysis to external neurohypophysis. The pituicytes and some narrow clefts were randomly distributed within the nerve fibre bundles. The cells of internal neurohypophysis were loose, and filled with a lot of blood sinus and cavity. The corpusculum neurosecretorium were different in size and shape, and mainly distributed in the internal neurohypophysis, which were stained deep eosinophilic masses by HE (Figs. 7A-D and 9) (Dellmann & Rodriguez, 1970; Vazquez & Amat, 1978).
Pituicyte. Pituicytes were glial cells with irregular shapes and some protuberances. Their cytoplasm often contains lipid droplets and pigments. Two types of pituicytes could be distinguished by HE and TEM: protoplasmic pituicytes and fibrous pituicytes (Figs. 7E-F and 8).
Protoplasmic pituicyte (PP). The protoplasmic pituicyte constitute most of the pituicyte with larger size, different protuberances, and long elliptic in the nuclei. In electron micrographs, the cells and its nuclei were irregular in shape. The cytoplasm contained numerous lipid droplets. many pigments with electron-dense and irregular shapes which were visible in the cytoplasm (Figs. 7E-F and 8A).
Fibrous pituicyte (FP). The fibrous pituicyte constitute a handful of pituicyte, with smaller size and less protuberances. The nuclei were irregular round or ovoid, and the marginal area was dyed deep by HE. In electron micrographs, the cells and nuclei were irregular in shape with a larger N/C ratio. A lot of lipid droplets with irregular shapes were visible in the cytoplasm. Furthermore, the cytoplasm of fibrous pituicyte included numerous ribosomes, abundant round or oval mitochondria, and developed endoplasmic reticulum (Figs. 7EF and 8B).
Although the hypophysis showed great differences in morphological characters in mammals, Bactrian camel possessed one similar to Chinese buffalo (Kang & Liu, 1992). There were great differences in the gland weights of mammals, and generally large body with big one but a small ratio of AGW/BW (Table II) (Francis & Mulligan, 1949; Dorst; Kang & Liu; Takano et al., 1999; Li et al.). The hypophysis of Bactrian camel was about 1.54 g in weight, its AGW/BW was 0.0045 g/kg, and it was similar with herbivores that had the similar body size to Bactrian camel. The weight and morphological characters of the hypophysis would be greatly influenced by seasons, age and sex (Dent, 1961).
The Bactrian camel had fully developed adenohypophysis that constituted 80% of the volume of the hypophysis. It was worth noting that the pars intermedia was more developed than in humans and in most domestic animals (Hewitt, 1950; Dorst). We noticed an interesting phenomenon: some mammals that live in arid and semiarid areas had developed pars intermedia, like rodent and Bactrian camel, while undeveloped ones existed in humans, primates and domestic animals, or were even missing in elephants and whales. We hypothesized that the evolution level of pars intermedia might be related to thirst resistance ability. However, the neurohypophysis was undeveloped, which was related to low fertility of Bactrian camel.
Seven type of cells in pars distalis could be distinguished by immunohistochemical techniques and electron micrographs, and the constitution was similar with the most of mammals (Moriarty, 1973). Among them, the stellate cells were contradictory due to the absence of secretory granules, some scholars think it belonged to the chromophobe cells, but others disagreed with it (Soji & Herbert, 1989; Allaertset al., 1996). The difference between them was that the chromophobe cells were rounded or polygonal-shaped with arrangement of clusters, but the stellate cells were irregular-shape, usually had long protuberance, and were always arranged in a single cell. Furthermore, the organelles of stellate cells were more developed than the chromophobe cells. Therefore, they could easily be differentiated in terms of morphology, but the functions of the former were unclear. Soji & Herbert found that the stellate cells could transmit signals via the network of protuberance in rats. It was reported that: the dendritic cells were visible in the adenohypophysis, and its functions were not only the antigen presenting, but also could regulate the development, hormone secretion and feedback, etc. (Allaerts et al.; Hoek et al, 1997).
The neurosecretory granules are transported axonally down to the pars nervosa, and they often accumulate in the dilated portions of the axons near their terminals named corpusculum neurosecretorium. The corpusculum neurosecretorium, in Bactrian camel which was different from most mammals, were rare in the external neurohypophysis, and mainly distributed in the internal neurohypophysis.
Our study would provide a comprehensive assessment of hypophysis in Bactrian camel, and all of these morphological characteristics of the hypophysis, might have evolved to assist the camel in adapting to a particular environmental niche. However, further studies are necessary to better understand the biological characteristics and regulation mechanisms of this organ.
ACKNOWLEDGEMENTS. This study received financial support from National Natural Science Foundation of China (39300097), and Open Foundation of Chinese Educational Department Key Laboratory of Arid and Grassland Agroecology. The authors are also grateful to Dr. Lei Zhu, Chun Yang and Zhongtian Bai for the collection of specimens.
Allaerts, W.; Fluitsma, D. M.; Hoefsmit, E. C.; Jeucken, P H.; Morreau, H.; Bosman, F. T. & Drexhage, H. A. Immunohistochemical, morphological and ultrastructural resemblance between dendritic cells and folliculo-stellate cells in normal human and rat anterior pituitaries. J. Neuroendocrinol., 8(1):17-29, 1996.
Ciocca, D. R.; Rodriguez, E. M. & Cuello, C. A. Comparative light- and electronmicroscopical study of the normal adenohypophysis in the human. Acta Anat. (Basel), 103(1):83-99, 1979.
Dellmann, H. D. & Rodriguez, E. M. Herring bodies; an electron microscopic study of local degeneration and regeneration of neurosecretory axons. Z. Zellforsch. Mikrosk. Anat., 111(3) :293-315, 1970.
Dent, J. N. Seasonal and sexual variation in the hypophysis of Triturusviridescens Anat. Rec., 141:85-95, 1961.
Dorst, J. On the macroscopic and topographic anatomy of the hypophysis of the domestic pig (Sus scrofa domestica) with particular reference to comparative-morphological aspects. Arch. Exp. Vterinarmed., 22(4):777-803, 1968.
Francis, K. C. & Mulligan, R. M. The weight of the hypophysis of the male dog in relation to body weight and age, with a differential cell count of the anterior lobe. J. Morphol., 85(1):141-61, 1949.
Hewitt, W. F. Jr. Age and sex differences in weight of hypophysis in dogs. Proc. Soc. Exp. Biol. Med., 74(4):781-2, 1950.
Hoek, A.; Allaerts, W.; Leenen, P J.; Schoemaker, J. & Drexhage, H. A. Dendritic cells and macrophages in the pituitary and the gonads. Evidence for their role in the fine regulation of the reproductive endocrine response. Eur. J. Endocrinol., 136(1):8-24, 1997.
Kang, S. Z. & Liu, J. H. Observation of the histological structures of Chinese buffalo pituitarium. J. Hunan Agric. Coll., 18:337-42, 1992.
Li, J. X.; Qin, J.; Song, X. B.; Wei, Q. N.; Pan, T. F.; Han, T.; Pan, Q. & Li, R. M. Comparision research on histology of Murrah hybrid buffalo an bubalus bubalis in Guangxi. J. Guangxi Agric. Biol. Sci., 27:16-20, 2008.
Marieb, E. N. & Hoehn, K. Human Anatomy & Physiology. 9th ed. Boston, Pearson, 2012. pp.629.
Martinez-Lage, M. The Pituitary. 3rd ed. San Diego, Elsevier, 2011. pp. 23-5.
Moriarty, G. C. Adenohypophysis: ultrastructural cytochemistry. A review. J. Histochem. Cytochem., 21(10):855-94, 1973.
Soji, T. & Herbert, D. C. Intercellular communication between rat anterior pituitary cells. Anat. Rec., 224(4):523-33, 1989.
Takano, K.; Utsunomiya, H.; Ono, H.; Ohfu, M. & Okazaki, M. Normal development of the hypophysis: assessment with three-dimensional MR volumetry. A. J. N. R. Am. J. Neuroradiol., 20(2):312-5, 1999.
Vazquez, R. & Amat, P The ultrastructure of the Herring bodies in rats subjected to different experimental conditions. Cell Tissue Res., 189(1):41-51, 1978.
Wang, X. C.; Gao, H. Y.; Li, Y. L.; Zeng, Y. D.; Yin, J. J. & Bi, C. Improvement and application of the histological stain method in adenohypophysis. J. Taishan Med. Coll., 127:715-6, 2006.
Xie, Z. H.; Li, H. Y. & Wang, J. L. Morphological study on the cerebrum of Bactrian camel (Camelus bactrianus) with particular reference to sulci. J. Camel Pract. Res., 13(1):61-6, 2006.
Ye, W. L.; Wang, F. L.; Wang, H. J. & Wang, J. L. Morphology and ultrastructure of the adrenal gland in Bactrian camels (Camelus bactrianus). Tissue Cell, 49(2 Pt. B):285-95, 2017.
Ye, W. L.; Xie, Z. H.; Wang, F. L.; Gen, X.; Dong, S. & Wang, J. L. Studies on Morphology of Hypothalamus in Bactrian Camels (Camelus bactrianus). J. Camel Pract. Res., 21(1):103-9, 2014.
Ye, W.; Wang, F.; Lv, S.; Wang, Y.; Dong, S. & Wang, J. A novel path of communication from kidney to the adrenal gland in bactrian camels (Camelus bactrianus). Int. J. Morphol., 33(4):1460-2, 2015.
222 Tianshui Road
Lanzhou 730000, CHINA
Wenling Ye (1,2); Hongju Wang (1); Fengling Wang (1) & Jianlin Wang (2)
(1) School of Medicine, Henan University, Kaifeng 475001, P. R. China.
(2) Key Lab of Arid and Grassland Agroecology, School of Life Sciences, Lanzhou University, Lanzhou 730000, P. R. China.
Caption: Fig. 1. Ventral view of the brain. Bar. 1 cm.
Caption: Fig. 2. Gross anatomic of the hypophysis in Bactrian camel: A. The dorsal surfaces of the pituitary gland. Bar. 0.5 cm; B. The ventrical surfaces of the pituitary gland. Bar. 0.5 cm; C. The medial sagittal of the pituitary gland. Bar. 0.5 cm; D. pars distal part and nerve (involved middle part) dissected are separated from hypophyseal cleft. Bar. 0.5 cm.
Caption: Fig. 3. Medial sagittal surface of hypophysis gland.
Caption: Fig. 4. Light micrograph of the pars distalis in hypophysis: A-F. The lateral part of the pars distalis: pars distalis (PaD), acidophilic cell (AC), basophilic cell (BC), chromophobe cell (CC), sinusoid (Sin), somatotroph cell (SC), thyrotroph cell (TC), gonadotroph cell (GC), corticotroph cell (ACTHC). (A, HE x40; B, SS x40; C, HE x400; D, HE x1000; E, SS x400; F, SS x1000); G-J. The center part of the pars distalis: pars distalis (PaD), acidophilic cell (AC), basophilic cell (BC), chromophobe cell (CC), sinusoid (Sin), somatotroph cell (SC), lactotroph cell (LC). (G, HE x400; H, HE x1000; I, SS x400; J, SS x1000); K-L. The interior part of the pars distalis: pars distalis (PaD), hypophyseal cleft (HypC), acidophilic cell (AC), basophilic cell (BC), chromophobe cell (CC), sinusoid (Sin). (K, HE x400; L, HE x1000).
Caption: Fig. 5. Ultrastructure of the pars distalis cells in hypophysis gland: A. Chromophobe cell, TEM (x6000); B. Somatotroph cell, (TEM x 10000); C. lactotroph cell, (TEM x 12000); D. Thyroid stimulating hormone cell, (TEMx15000); E. Gonadotroph cell, (TEM x 12000); F. Corticotroph cell, (TEM x 10000); G. Stellate cell, (TEM x 12000).
Caption: Fig. 6. Light micrograph of the pars intermedia in hypophysis: A-F: pars distalis (PaD), hypophyseal cleft (HypC), pars intermedia (PaI), parsnervosa(PN), sinusoid (Sin). (A, HE x40; B, SS x40; C, HE x400; D, SS x400; E, HE x1000; F, SS x1000).
Caption: Fig. 7. Light micrograph of the pars nervosa in hypophysis: A-F: hypophyseal cleft (HypC), pars intermedia (PaI), pars nervosa (PN), protoplasmic pituicyte (PP), fibrous pituicyte (FP), herring body (HB), unmyelinated nerve fiber (Unf). (A, HE x40; B, SS x40; C, HE x400; D, SS x400; E, HE x400; F, HE x1000).
Caption: Fig. 8. Ultrastructure of the pars nervosa cells in hypophysis: A. Protoplasmic pituicyte, (TEMx6000); B. Fibrous pituicyte, (TEMx6000).
Caption: Fig. 9. Light micrograph of the corpusculum neurosecretorioum in hypophysis: A-B: pars nervosa (PN), corpusculum neurosecretorioum (HB), unmyelinated nerve fiber (Unf). (A, HE x100; B, HE x400).
Table I. Biometry of the hypophysis gland. Items N Mean SD Min-Max Gross weight (kg) 10 345.0 44.72 300-400 Weight (g) 10 1.54 0.24 1.30-1.80 AGW/BW (g/kg) 10 0.0045 0.0011 0.0036-0.0054 Volume (cm3) 10 2.60 0.73 1.70-3.52 Length (cm) 10 1.68 0.31 1.42-2.38 Breadth (cm) 10 1.43 0.29 1.26-1.53 Thickness (cm) 10 1.14 0.25 0.84-1.25 Length of pituitary stalk (cm) 10 1.09 0.18 0.95-1.28 Diameter of pituitary stalk (cm) 10 0.55 0.06 0.50-0.62 Weight of adenohypophysis (g) 10 0.90 0.02 0.78-1.03 Volume of adenohypophysis 10 2.00 0.66 1.30-2.90 ([cm.sup.3]) Length of adenohypophysis (cm) 10 1.57 0.34 1.41-2.18 Breadth of adenohypophysis (cm) 10 1.43 0.37 1.26-1.53 Thickness of adenohypophysis 10 1.14 0.14 0.84-1.25 (cm) Weight of neurohypophysis (g) 10 0.60 0.08 0.48-0.65 Volume of neurohypophysis 10 0.60 0.16 0.40-0.87 ([cm.sup.3]) Length of neurohypophysis (cm) 10 1.65 0.28 1.42-2.38 Breadth of neurohypophysis (cm) 10 0.93 0.10 0.76-1.21 Thickness of neurohypophysis 10 0.81 0.11 0.69-1.04 (cm) AGW/BW: the ratio of the hypophysis gland weight/body weight. Table II. Comparison of the weight and AGW/BW in some animals' hypophysis Animals Gross Weight of AGW/BW weight (kg) pituitary (g) (g/kg) Rat 0.2 0.01 0.05 Dog 10 0.077 0.0077 Pig 100 0.25 0.0025 Human 60 0.55 0.0092 Sheep 70 1.75 0.025 Mongolian pony 300 1.97 0.0066 Murrah hybrid buffalo 200 1.415 0.0071 Guangxi bubalus buffalo 200 1.37 0.0069 India buffalo 550 0.886 0.0016 Chinese buffalo 500 2.55 0.0051 Bactrian Camel 345 1.54 0.00446 AGW/BW: the ratio of the hypophysis weight / body weight.
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|Author:||Ye, Wenling; Wang, Hongju; Wang, Fengling; Wang, Jianlin|
|Publication:||International Journal of Morphology|
|Date:||Dec 1, 2018|
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