scholarly journals Analysis of parameters characterizing argyrophilic zones in intact lymphocytes of domestic sheep (Ovis aries L., 1758) and their hybrids with argali (Ovis ammon L., 1758)

2021 ◽  
Vol 344 (1) ◽  
pp. 52-56
Author(s):  
P. M. Klenovitsky ◽  
B. S. Iolchiev ◽  
A. N. Vetokh

Relevance and research material. The study of the characteristics of the nucleolus in cells of various tissues allows us to assess the intensity of the processes of protein proliferation and biosynthesis in animals. In interphase cells, the nucleoli correspond to argyrophilic zones (AgNOR) stained with silver nitric acid. The purpose of this study is to determine the characteristics of AgNOR in sheep interphase lymphocytes of different genotypes based on computer analysis and to select parameters for functional evaluation of nucleoli. AgNOR status was studied in peripheral blood lymphocytes from hybrid sheep four genotypes: purebred Romanov sheep, and their F1 hybrids with argali (groups 1 and 2), hybrids, bearing 3/4 of Romanov sheep blood and 1/4 blood argali (group 3), and hybrids that had 7/8 of domestic sheep and 1/8 blood argali (group 4). The number of argyrophilic zones (AgNOR), their total area (SSNOR), their average color density (DNOR), and the average color density of the core (DN) and its AgNOR-free area (DF) were taken into account.Results. Image processing and analysis were performed using the Image Scope 1.0 program. The average AgNOR value in the studied groups of sheep ranges from 2.64 (group 1) to 3.50 in hybrids in groups 2 and 3. There were no significant differences in the value of SSNOR between the groups. In terms of DN and DF, all hybrids were significantly inferior to purebred sheep (р < 0.001). In terms of DNOR, the sheep of group 2 were significantly inferior to the animals of the other groups (р < 0.001). When evaluating the state of the nucleolus-forming system, it is advisable to take into account the AgNOR number, as well as the average optical densities DN and DF.

2021 ◽  
Vol 77 (04) ◽  
pp. 6512-2021
Author(s):  
XIAOHUA DU ◽  
XIA LIU ◽  
JAMES BLACKAR MAWOLO

Neuroglobin (Ngb) is a member of the globin member that is mainly expressed in the brain and retina. The expression in the retina is greater than it is in the brain because of the high demand for oxygen by the retina. This protein reversibly binds oxygen and is involved in oxygen transport or protection against oxidative stress. The study aims to explore the pattern of Ngb expression in Tibetan sheep (Ovis ammon or argali ) living in a plateau region and domestic sheep (Ovis aries) dwelling on low land. The study also provides detailed insight into the morphological characteristics of Ngb distribution closely related to oxygen metabolism in the retina of Tibetan and domestic sheep. Immunohistochemical staining procedures were performed to detect the Ngb protein expression in the retinae of both sheep, while the Inter’s integrated performance primitives (IPP) semi-quantitative analysis was employed to compare the quantities of Ngb expressed in the retinae of the two types of sheep. The outer nuclear layer and the outer segment of the photoreceptor showed a negative Ngb expression, while a weak positive expression was observed in the inner core layer and ganglion cell layer, while a strong positive expression was found in the other layers. The independent T-test revealed that the expression intensity in the nerve fiber layer, inner and outer plexus layers, inner segment of the photoreceptor, and superior pigment cortex were significantly higher in the Tibetan sheep as compared to the domestic sheep. The overall Ngb expression in the Tibetan sheep was higher than the domestic sheep. The study emphasized that the different Ngb expression in the Tibetan and domestic sheep may influence their adaptation to the respective environments. The stronger Ngb expression in the retina of Tibetan sheep may indicate that Ngb is closely related to the oxygen metabolism of these animals and has a function during oxygen transport.


2018 ◽  
Vol 14 (1) ◽  
Author(s):  
Hui Dong ◽  
Ruijing Su ◽  
Yinghua Wang ◽  
Zongxi Tong ◽  
Longxian Zhang ◽  
...  

Oryx ◽  
2010 ◽  
Vol 44 (3) ◽  
pp. 366-375 ◽  
Author(s):  
Pranav Chanchani ◽  
Gopal S. Rawat ◽  
Surendra P. Goyal

AbstractWe conducted surveys in the Trans-Himalayan Tso Lhamo plateau in Sikkim, India, to ascertain the status and distribution of some of India’s last surviving populations of wild ungulates (numbers in brackets are estimates for Sikkim): Tibetan argali Ovis ammon hodgsoni (c. 177 individuals), Tibetan gazelle Procapra picticaudata (c. 77), and kiang Equus kiang polyodon (c. 18). Topography appears to have an important influence on ungulate distribution, and populations of these species are aggregated in a small region along the northern boundary of the plateau. Persistence of the wild ungulates in this area can be attributed to the non-hunting tradition of local residents and to the seasonal absence of livestock (yak Bos grunniens and domestic sheep Ovis aries) and grazing. Nonetheless, wild ungulates remain vulnerable because of their small populations and anthropogenic pressure on their habitats. We recommend that conservation be prioritized in important wildlife habitats through partnerships with local communities.


2016 ◽  
Vol 28 (2) ◽  
pp. 144
Author(s):  
A. L. Green ◽  
F. C. Oback ◽  
J. E. Oliver ◽  
L. Popovic ◽  
L. T. McGowan ◽  
...  

Interspecies somatic cell NT (SCNT) can be used in the conservation of endangered animals but only when there is an abundant source of compatible oocytes and recipients. The objective of this study was to compare the efficiency of intra- and interspecies SCNT in sheep using zona-free embryo reconstruction methods. Skin fibroblasts from either an argali (Ovis ammon) or control (Ovis aries) ram were used as donor cells for SCNT between passages 2 to 5 and following culture in medium containing 0.5% FCS for 4 to 6 days. Single cells were electrically fused to cytoplasts prepared following enucleation of in vitro-matured zona-free metaphase II-arrested oocytes obtained from domestic ewes. In an additional experiment with argali, a double cytoplast (DC-SCNT) procedure was used whereby a second cytoplast was fused to the first reconstruct within 1 h. Reconstructs were artificially activated ~25 h after the start of maturation using ionomycin and 6-DMAP. Zona-free parthenogenote (PG) control oocytes were activated around the same time. In each treatment, 10 to 12 zona-free embryos where cultured in microwells formed in 20-μL drops of modified synthetic oviduct fluid under oil. Half the medium was replaced on Day 3, and developing embryos were transferred to individual 5-μL drops on Day 6. Development on Day 7 was expressed as a percentage of cleaved embryos. Statistical significance was determined using Fisher’s exact test for embryo development and two-tailed t-test for embryo cell numbers. Total embryo development on Day 7 was significantly greater with intraspecies sheep SCNT compared with interspecies argali SCNT (34/157 = 21.7% v. 34/363 = 9.4%, respectively; P < 0.001). Moreover, SCNT embryo development was significantly less than PG controls (122/360 = 33.9%; P < 0.001). Although argali DC-SCNT had no effect on total embryo development compared with SCNT (9/69 = 13.0% v. 7/56 = 12.5%, respectively), doubling cytoplasm volume increased the proportion of grade 1 and 2 embryos on Day 7 (8.7 v. 0%; P < 0.05). Consequently, DC-SCNT blastocysts had greater numbers of nuclei compared with SCNT (108 ± 47 v. 65 ± 9; n = 6, n = 6, respectively; P = 0.054). In comparison, PG blastocysts possessed on average 122 ± 27 nuclei (n = 7). A sample of 14 argali cloned blastocysts were all confirmed to have been derived from the respective ram after genotyping ~6000 ovine single nucleotide polymorphisms on a custom-made chip (Illumina, San Diego, CA, USA). Chromosome spreads of argali embryos revealed a modal number of 4 bi-armed autosomes as opposed to 6 in Ovis aries. In conclusion, in vitro development following interspecies SCNT in argali was about half that compared with domestic sheep. Blastocyst quality was improved by increasing oocyte cytoplasmic volume facilitated by zona-free cloning. Alternative sources of cytoplasm may further improve development. Confirmation that Ovis aries cytoplasm can fully reprogram a differentiated argali nucleus remains to be determined. This research was supported by AgResearch Core Funding.


Author(s):  
P. Bagavandoss ◽  
JoAnne S. Richards ◽  
A. Rees Midgley

During follicular development in the mammalian ovary, several functional changes occur in the granulosa cells in response to steroid hormones and gonadotropins (1,2). In particular, marked changes in the content of membrane-associated receptors for the gonadotropins have been observed (1).We report here scanning electron microscope observations of morphological changes that occur on the granulosa cell surface in response to the administration of estradiol, human follicle stimulating hormone (hFSH), and human chorionic gonadotropin (hCG).Immature female rats that were hypophysectcmized on day 24 of age were treated in the following manner. Group 1: control groups were injected once a day with 0.1 ml phosphate buffered saline (PBS) for 3 days; group 2: estradiol (1.5 mg/0.2 ml propylene glycol) once a day for 3 days; group 3: estradiol for 3 days followed by 2 days of hFSH (1 μg/0.1 ml) twice daily, group 4: same as in group 3; group 5: same as in group 3 with a final injection of hCG (5 IU/0.1 ml) on the fifth day.


Author(s):  
E.J. Prendiville ◽  
S. Laliberté Verdon ◽  
K. E. Gould ◽  
K. Ramberg ◽  
R. J. Connolly ◽  
...  

Endothelial cell (EC) seeding is postulated as a mechanism of improving patency in small caliber vascular grafts. However the majority of seeded EC are lost within 24 hours of restoration of blood flow in previous canine studies . We postulate that the cells have insufficient time to fully develop their attachment to the graft surface prior to exposure to hemodynamic stress. We allowed EC to incubate on fibronectin-coated ePTFE grafts for four different time periods after seeding and measured EC retention after perfusion in a canine ex vivo shunt circuit.Autologous canine EC, were enzymatically harvested, grown to confluence, and labeled with 30 μCi 111 Indium-oxine/80 cm 2 flask. Four groups of 5 cm x 4 mm ID ePTFE vascular prostheses were coated with 1.5 μg/cm.2 human fibronectin, and seeded with 1.5 x 105 EC/ cm.2. After seeding grafts in Group 1 were incubated in complete growth medium for 90 minutes, Group 2 were incubated for 24 hours, Group 3 for 72 hours and Group 4 for 6 days. Grafts were then placed in the canine ex vivo circuit, constructed between femoral artery and vein, and subjected to blood flow of 75 ml per minute for 6 hours. Continuous counting of γ-activity was made possible by placing the seeded graft inside the γ-counter detection crystal for the duration of perfusion. EC retention data after 30 minutes, 2 hours and 6 hours of flow are shown in the table.


VASA ◽  
2020 ◽  
Vol 49 (4) ◽  
pp. 281-284
Author(s):  
Atıf Yolgosteren ◽  
Gencehan Kumtepe ◽  
Melda Payaslioglu ◽  
Cuneyt Ozakin

Summary. Background: Prosthetic vascular graft infection (PVGI) is a complication with high mortality. Cyanoacrylate (CA) is an adhesive which has been used in a number of surgical procedures. In this in-vivo study, we aimed to evaluate the relationship between PVGI and CA. Materials and methods: Thirty-two rats were equally divided into four groups. Pouch was formed on back of rats until deep fascia. In group 1, vascular graft with polyethyleneterephthalate (PET) was placed into pouch. In group 2, MRSA strain with a density of 1 ml 0.5 MacFarland was injected into pouch. In group 3, 1 cm 2 vascular graft with PET piece was placed into pouch and MRSA strain with a density of 1 ml 0.5 MacFarland was injected. In group 4, 1 cm 2 vascular graft with PET piece impregnated with N-butyl cyanoacrylate-based adhesive was placed and MRSA strain with a density of 1 ml 0.5 MacFarland was injected. All rats were scarified in 96th hour, culture samples were taken where intervention was performed and were evaluated microbiologically. Bacteria reproducing in each group were numerically evaluated based on colony-forming unit (CFU/ml) and compared by taking their average. Results: MRSA reproduction of 0 CFU/ml in group 1, of 1410 CFU/ml in group 2, of 180 200 CFU/ml in group 3 and of 625 300 CFU/ml in group 4 was present. A statistically significant difference was present between group 1 and group 4 (p < 0.01), between group 2 and group 4 (p < 0.01), between group 3 and group 4 (p < 0.05). In terms of reproduction, no statistically significant difference was found in group 1, group 2, group 3 in themselves. Conclusions: We observed that the rate of infection increased in the cyanoacyrylate group where cyanoacrylate was used. We think that surgeon should be more careful in using CA in vascular surgery.


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