The aim of this work was to study the topography, morphology, vascularisation, histology and innervation of the lungs in the ground squirrel (Spermophilus citellus) and compare these data with those concerning the rat, mole rat, rabbit and mouse. The research was carried out on 15 animals. It was revealed that the right lung has four lobes (cranial, middle, caudal and accessory lobes), while the left lung is not divided into segments. The functional vessels are a. pulmonalis dextra et sinistra and vv. pulmonales (5-6), while the nutritive vessels of the lungs are a. bronchoesophagea dextra and v. bronchoesophagea dextra. Histological tissue sections of the lungs revealed that the wall of terminal bronchioles contains no cartilage and the mucosal epithelium is pseudostratified, cubic and ciliated. Clara cells (club cells, bronchiolar exocrine cells) are present but have no cilia. The lung alveolar diameter is 37 μm on average, and the thickness of the alveolar wall and the interalveolar septa is 1.38 μm. Destruction of the alveolar walls, accumulation of erythrocytes in the capillaries of alveolar septa and destruction of the cytolemma of the capillary endothelium were detected. In addition, connective tissue fibres and peripheral nerves were detected by silver impregnation.
Hippopotamidae family is nowadays represented by two species within two different genera: pygmy hippopotamus (Choeropsis liberiensis) and common hippopotamus (Hippopotamus amphibius). The common hippopotamus has a very unique anatomy, and the shape of the body, especially the head is adapted for a semi-aquatic life style. The morphological examination and description of the gross anatomical features of the hippopotamus skull is described in this paper. The shape of the skull is adapted for the amphibian way of life. Their eyes, ears and nostrils are placed high on the roof of the skull which allows these organs to remain above the surface of the water while the animal is being submerged underwater. The skull is massive, but the brain case (neurocranium) is extremely small compared with the splanchnocranium and complete head. The dental formula of the common hippopotamus is: incisors (I) 2/2, canines (C) 1/1, premolars (P) 3-4/3-4 and molars (M) 3/3. Incisors and canine teeth are formed in the shape of tusks and are used for threat or “demonstration of power” among animals when vigorously fi ghting. Incisor teeth grow continuously and are twice bigger in males than in females.
The structure of heterochromatin protects genome from undesirable recombinations, while estrogen and luteinizing-releasing hormone (LHRH) cause changes in structure of chromatin. The objective of this study was to prove the connection of neonatally applied estrogen and LHRH, with shown effects on chromatin in hippocampus of adult male rats. Stereological results have shown that total surface of neuron area in estrogen treated animals significantly reduced in regard to the control group as well as groups treated with LHRH. The number of heterochromatin granules in either estrogen or LHRH treated groups significantly increased, while in the last fourth group treated with both estrogen and LHRH the difference is even more expressed, both in regard to the control group and other groups. [Projekat Ministarstva nauke Republike Srbije, br. 173034]
In this study the effects of a neonatally (3rd day of life) administered single dose (1 mg) of estradiol dipropionate (E2) on the parietal cortex of juvenile (16 days of life) female rats were investigated. The morphology the volume of the soma and the thickness of the apical dendrite were studied in Golgi impregnated pyramidal neurons from both the external and internal pyramidal layers. In the treated female rats the volume of the soma and the thickness of the apical dendrite of pyramidal neurons was increased surpassing the values in the corresponding controls. These findings indicated significant and prolonged effects of a single dose of estrogen administered in the neonatal period, on the parietal neocortical pyramidal neurons of female rats
Metatarsal bones and finger articles of roe deer and sheep are rarely used for animal identification. In practice there are frequent cases where on a corpse the head and distal parts of the limbs are missing. That is in order to prevent the identification of the bones, by which it is easiest to determine the animal species. For identification of metatarsal bones (Ossa metatarsi) as well as finger articles (Os?sa digitorum pedis seu phalanges digitorum) there were used distal parts of hindlimb bones, taken from 6 roe deers and 7 sheep. Afer the separation from the soft tissues, the bones were boiled in an autoclave, and for bleaching and degreasing they were kept in 3% solution of hydrogen peroxide (H2O2). The bones were air dried, and then photographed. In roe deer, four metatarsal bones are developed: the second (Os metatarsale secundum), the third (Os metatarsale tertium), the fourth (Os metatarsale quartum) and the fifth (Os metatarsale quintum). In sheep, the third (Os metatarsale tertium) and the fourth (Os metatarsale quartum) metatarsal bones are developed. Both in roe deer and sheep, the third and the fourth metatarsal bones are fused into one single bone - main metatarsal bone. In sheep, on dorsal and plantar side of these bones there are grooves which are more shallow and wider than in roe deer. In roe deer, hindlimbs have four fingers, and in sheep two. In roe deer there is also the difference in the number of articles on the second and fifth finger. In this animal the second and fifth finger have coalesced the first and second article (Ph1 + Ph2) and the third article(Ph3). Based on the third article of the third and fourth finger, it may be distinguished one animal from another. Margo solearis in roe deer is peaky and in sheep it is blunt. In roe deer Processus extensorius is peaky on Margo coronalis, while in shee it is blunt. In the cases when material (fresh meat, blood, hair) necessary for some laboratory methods is missing, there is used the method of animal species determination based on morphological differences between the bones of these two animals. By this method it can be with certainty determined which animal the bones belong to.
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