Histological Study of Ostrich Skin after Biopsy
IJVS 2013; 8(1); Serial No:18
IRANIAN JOURNAL OF
VETERINARY SURGERY
(IJVS)
WWW.IVSA.IR
Histological Study of Ostrich Skin after Biopsy
Foroogh Sadat Mansoori1, Sara Dehyadegari2, Mahsa Mohtadi2
Abstract
Objective- To investigate histological structure of Ostrich skin was done. Ostrich leathers are of exotic leather types,
which are in increasing demand due to their outstanding natural gain patterns formed by large feather follicles on the
leather surface.
Animals-Ten mature ostriches were selected from ostrich breeding center in Jupar, Kerman, Iran, all of which were
in good shape and healthy condition.
Procedure- For this study, some samples of ostrich skin were made from ostriches aged about 1 year old.0.5 * 0.5
cm sample of different areas of skin was made and kept in 10% formalin solution for 7 days; then, the samples were
taken out. Routine histological techniques were done and 6 micron-thickness sections were cut. The sections were
stained with standard Haematoxilin and Eosin (H&E) and masson trichrome and Periodic acid-Sciff(pas). The
histological study was done using a light microscope and the photographs were taken for detailed illustration of the
results.
Results- Microscopic studies showed that the skin consisted of 2 different layers as epidermis and dermis. Epidermis
consisted of the following different groups of cells, form depth to surface: basal cell – granular cell – chondrocyte
shape cells and keratin cells. Dermis consisted of a dense connective tissue with both regular and irregular fibers in
which the irregular part was near the epidermis.
Conclusions and clinical relevance- The results of this study suggested that ostrich’s skin in either dermis or
epidermis is very different from other domesticated animals; and the development of dermal connective tissue makes
this skin a good model for studying wound healing and skin grafting.
Key words: Ostrich, skin, Histology.
Indeed, while production of leather and fur products
decreased between 1975 and 1992 in developed countries, it
increased in the developing world from 4.4% (1975–1985) to
5.3% (1985–1992) (14).and this trend was expected to
continue.3 Small economies like Kenya and Ethiopia may not
affect global business cycles and the specific factors for
improving leather industry, such as enhancing value-addition
to the leather production process, encouraging uptake and
effective use of cleaner technologies to improve product
quality and diversifying finished leather products, respond to
policy entrepreneurship by various stakeholders involved in
leather industry.2Behzat Oral Bitlisli conducted a study and
found that neck, leg and back sides of ostrich skins differed
physically and chemically from each other. In terms of area
and strength characteristics of leathers, back and leg sides
were appropriate for upper leather production whereas neck
sides could be used for accessories.4 He found that ostrich
skins were heavier than sheep and goat skins but lighter than
calf and cattle hides.4 This work aimed to detect some
characteristics of ostrich skins which were valuable for leather
industry.
Introduction
Ostrich leathers are of exotic leather types, which are in
increasing demand due to their outstanding natural gain
patterns formed by large feather follicles on the leather
surface.1 Approximately, 700,000 ostrich skins are introduced
to the global market every year, out of which 300,000 are
obtained from South Africa. It is evident that ostrich skins have
a small share of market compared to the nearly 330 million
hides and 850 million skins, which constitutes the raw material
for leather industry in the world.1
Leather industry produces a range of indispensable consumer
goods including footwear, garments, handbags and luggage.2
1Department of Basic Science, School of Veterinary, Shahid
Bahonar University of Kerman,Kerman, Iran.
2Graduate Studant of Veterinary, Shahid Bahonar University
of Kerman,Kerman, Iran.
Address all correspondence to Dr. Foroogh Sadat Mansoori
(DVM, PhD) E-mail:
53
IJVS 2013; 8(1); Serial No:18
consisted of several keratinized cells. The outermost strata
tended to break away from the surface in flakes and gave rise
to the dry scurfy appearance of the skin.
Value of epidermis thickness in the feather’s follicle area was
very thin (Fig.1). Stratum basal consisted of basophilic
nucleus and very little cytoplasma. The line between epiderm
and derm was not very folded.
The dermis consisted of dense connective tissue and was
clearly observed in staining. Two models of fibers were visible;
both of them were collagen and elastic. All areas of dermis
were made up of dense connective tissues; but definitely, in
its deep part (about one forth of thickness of total tissue), the
dense regular connective tissue was visible and they were
parallel to skin surface. At the dermal-epidermal junction, the
basal layer of cells were placed on the basal lamina,
consisting of a thin layer of fine filamentouce.5 (Masoltsy
1969) in dermal layer, the dense connective tissue in masson
trichrome were green and pink. Also, there were many vessels
which were small arteriols.
Nerves:
The mutual nerves were in the dermis. There was a circular
shape. (Fig.4) on the line between papillar and reticular, there
was an organization which gave the corpuscle a crosssectional appearance, like that of an onion. One of them was
between two follicles and was so large. It had small arteriol
and was right on top of papillary region. It was ladder-like
cross-striation in routine haematoxilin and eosin preparations.
(Fig.5)
Materials and methods
Ten mature ostriches were selected from ostrich breeding
center in Jupar, Kerman, Iran, all of them were in good shape
and healthy condition.
The ostriches were obtained from a slaughterhouse for getting
samples from the skin of body, back of head and between two
eyes. These samples were transmitted to Histotechnic
Laboratory of Veterinary Faculty.
Their heads were kept in 10% formalin solution for 7 days and
this formalin was changed every day. The samples were cut
into 1*1 cm very carefully in order not to be hurt at dermal
layer. They were placed in 10% solution of neutral-buffered
formalin which consisted of 10 volumes of commercial
formalin (40% formaldehyde in water) and 90 volumes of
phosphate-buffered water for 24 h; then, their formalin solution
was changed and, after fixation, 1 cm segment was dissected
from each part and sections of 6 micron thickness were
prepared from the samples through routine histological
techniques .Then, all of the samples were numbered and put
in the tissue process system.
The sections were stained with standard Haematoxilin and
Eosin (H&E), masson trichrome (for the connective tissue)
and Periodic acid-Sciff for protein granules. The histological
study was done using a light microscopy and the photographs
were taken for detailed illustration of the results.
Results
Microscopic studies showed that skin consisted of two
distinguish layers; (...truncated)