<?xml version="1.0" encoding="utf-8"?>
 <records>
	<record>
	<language>eng</language>
	<publisher>4</publisher>
	<journalTitle>Anatomical Sciences Journal</journalTitle>
	<issn>17286158</issn>
	<eissn>17286158</eissn>
	<publicationDate>2013-02</publicationDate>
	<volume>10</volume>
	<issue>1</issue>
	<startPage>1</startPage>
	<endPage>6</endPage>
	<documentType>article</documentType>
	<title language="eng">Evalauation of Laminin Expression during Mouse Lens Development</title>


	<authors>
	<author>
	<name>Houshang Rafighdoost</name>
	<email></email>
	<affiliationId>1</affiliationId>
	 </author>
	<author>
	<name>Mehdi Jalali</name>
	<email></email>
	<affiliationId>2</affiliationId>
	 </author>
	<author>
	<name>Mohammad Reza Nikravesh</name>
	<email></email>
	<affiliationId>3</affiliationId>
	 </author>
	</authors>
	 <affiliationsList>
	      <affiliationName affiliationId="1">
                 
	      </affiliationName>
	      <affiliationName affiliationId="2">
                 
	      </affiliationName>
	      <affiliationName affiliationId="3">
                 
	      </affiliationName>
    </affiliationsList>


	<abstract language="eng">Introduction: Among the components of the extracellular matrix (ECM) and basement membrane (BM), laminitis heterotrimeric glycoprotein (laminin) and collagen type IV are the most important. In a previous study we have examined the role of collagen type IV in the developing lens capsule. The present study aims to determine the appearance and distribution of laminin in the BM and ECM of lenses during visual system morphogenesis. Materials and Methods: Pregnant Balb/C mice were randomly selected and maintained under normal conditions. The presence of a vaginal plug was assumed as day zero of pregnancy. From embryonic days 11 to 20, pregnant animals were sacrificed and their fetuses were collected for histotechnical prossessing. Results: Our data revealed that laminin appeared during the early stage of gestation (day 12) in the BM of the anterior epithelial lens cells. The amount of laminin gradually increased in the ECM and posterior lens capsule epithelial cells until days 14-18. After this period, a strongly positive laminin reaction was not observed in any part of the lens structure. Conclusion: These findings establish the importance of the laminin molecule in the developing optic cup (OC) and lens differentiation. It could be assumed that any changes in the presence of laminin during the critical period of eye development may result in visual system defects such as cataracts or congenital eye abnormalities.</abstract>
	<fullTextUrl format="pdf">http://anatomyjournal.ir/article-1-30-en.pdf</fullTextUrl>
	<keywords>
	<keyword>Laminin</keyword>
	<keyword>Mice</keyword>
	<keyword>Lenses</keyword>
	<keyword>Growth and development</keyword>
	</keywords>


	</record>
	<record>
	<language>eng</language>
	<publisher>4</publisher>
	<journalTitle>Anatomical Sciences Journal</journalTitle>
	<issn>17286158</issn>
	<eissn>17286158</eissn>
	<publicationDate>2013-02</publicationDate>
	<volume>10</volume>
	<issue>1</issue>
	<startPage>7</startPage>
	<endPage>14</endPage>
	<documentType>article</documentType>
	<title language="eng">Melatonin Impact on In Vitro Development of Mouse Preantral Follicles and Oocyte Maturation</title>


	<authors>
	<author>
	<name>Mohammad Nabiuni</name>
	<email></email>
	<affiliationId>1</affiliationId>
	 </author>
	<author>
	<name>Roya Ganji</name>
	<email></email>
	<affiliationId>2</affiliationId>
	 </author>
	<author>
	<name>Mohammadhadi Bahadori</name>
	<email></email>
	<affiliationId>3</affiliationId>
	 </author>
	</authors>
	 <affiliationsList>
	      <affiliationName affiliationId="1">
                 
	      </affiliationName>
	      <affiliationName affiliationId="2">
                 
	      </affiliationName>
	      <affiliationName affiliationId="3">
                 
	      </affiliationName>
    </affiliationsList>


	<abstract language="eng">Introduction: Melatonin acts as an indirect antioxidant and is a powerful direct free radical scavenger and
direct responses to melatonin in the gonads are detected. This study aims to investigate the influence of
different doses of melatonin on preantral follicle development and oogenesis of in vitro cultured mouse
ovarian follicles.
Materials and Methods: Preantral follicles with diameters of 150–175 μm were mechanically isolated from
NMRI mouse ovaries. Follicles were cultured in droplets of α-minimal essential medium (α-MEM)
supplemented with 5% FBS, 100 mIU/ml rhFSH, 1% ITS, 100 IU/ml penicillin and 100 μg/ml streptomycin
in conjunction with varying doses of melatonin (0, 1, 10, 100 nM and 100, 500 pM) for six days. On day six,
in vitro ovulation was induced by the addition of hCG/rEGF to the culture medium and after 16-20 h the
maturation state of the oocytes was assessed.
Results: There was a significant (P&#60;0.05) decrease in the number of surviving follicles in the groups that
received 10, 100 nM and 500 pM melatonin compared to the other groups. After induction of in vitro
ovulation, follicles in groups that received 1, 10, and 100 nM melatonin had higher ovulation rates (P&#60;0.05)
compared with the other groups. Oocyte maturation capacity was adversely influenced by five concentrations
of melatonin and GV arrest was significantly higher compared to the control group (P&#60; 0.01).
Conclusions: Our data indicates that a dose of 100 pM melatonin has no toxic effects on follicular
development and can be used to reduce oxidative stress in follicle culture systems.</abstract>
	<fullTextUrl format="pdf">http://anatomyjournal.ir/article-1-31-en.pdf</fullTextUrl>
	<keywords>
	<keyword>Ovarian follicle</keyword>
	<keyword>Melatonin</keyword>
	<keyword>Ovulation</keyword>
	<keyword>Oocytes</keyword>
	</keywords>


	</record>
	<record>
	<language>eng</language>
	<publisher>4</publisher>
	<journalTitle>Anatomical Sciences Journal</journalTitle>
	<issn>17286158</issn>
	<eissn>17286158</eissn>
	<publicationDate>2013-02</publicationDate>
	<volume>10</volume>
	<issue>1</issue>
	<startPage>15</startPage>
	<endPage>24</endPage>
	<documentType>article</documentType>
	<title language="eng">The Effects of Pentoxifylline on the Wound Healing Process in a Rat Experimental Pressure Sore Model</title>


	<authors>
	<author>
	<name>Abdollah Amini</name>
	<email></email>
	<affiliationId>1</affiliationId>
	 </author>
	<author>
	<name>Kobra Velaei</name>
	<email></email>
	<affiliationId>2</affiliationId>
	 </author>
	<author>
	<name>Mohammad Bayat</name>
	<email></email>
	<affiliationId>3</affiliationId>
	 </author>
	<author>
	<name>Masoomeh Dadpay</name>
	<email></email>
	<affiliationId>4</affiliationId>
	 </author>
	<author>
	<name>Mohsen Nourozian</name>
	<email></email>
	<affiliationId>5</affiliationId>
	 </author>
	</authors>
	 <affiliationsList>
	      <affiliationName affiliationId="1">
                 
	      </affiliationName>
	      <affiliationName affiliationId="2">
                 
	      </affiliationName>
	      <affiliationName affiliationId="3">
                 
	      </affiliationName>
	      <affiliationName affiliationId="4">
                 
	      </affiliationName>
	      <affiliationName affiliationId="5">
                 
	      </affiliationName>
    </affiliationsList>


	<abstract language="eng">Introduction: The present study used a histological evaluation method to examine the effects of
pentoxifylline (PTX) on healing an experimentally-induced pressure sore in a rat model.
Materials and Methods: There were 36 adult male rats used in this study. Under general anesthesia and
sterile conditions, we used forceps to create one pressure sore on each rat. A double layer of folded skin from
the dorsal region was held with the highest forceps pressure grade for two hours, followed by 30 minutes of
relaxation. This was repeated 12 times over three consecutive working days, and created a pressure sore after
seven days. Next, rats were randomly divided into three control and three experimental groups. The
experimental groups received intraperitoneal injections of PTX (50 mg/kg) for 14, 21, and 28 days after the
pressure sore was created. Control groups received a similar volume of saline solution. Rats were euthanized,
after which samples were extracted from the wound area and prepared for light microscopy examination. We
calculated the number of neutrophils, macrophages, fibroblasts, blood vessel sections, and thicknesses of the
newly formed epidermis and dermis.
Results: Although the values of some studied parameters were higher in the experimental group, there were
no significant differences noted between the experimental and control groups.
Conclusion: In this study PTX did not increase any histological parameters. Thus, the effects of PTX on the
pressure sore model seem to result from different mechanisms.</abstract>
	<fullTextUrl format="pdf">http://anatomyjournal.ir/article-1-32-en.pdf</fullTextUrl>
	<keywords>
	<keyword>Pentoxifylline</keyword>
	<keyword>Histology</keyword>
	<keyword>Rats</keyword>
	</keywords>


	</record>
	<record>
	<language>eng</language>
	<publisher>4</publisher>
	<journalTitle>Anatomical Sciences Journal</journalTitle>
	<issn>17286158</issn>
	<eissn>17286158</eissn>
	<publicationDate>2013-02</publicationDate>
	<volume>10</volume>
	<issue>1</issue>
	<startPage>25</startPage>
	<endPage>36</endPage>
	<documentType>article</documentType>
	<title language="eng">Study of the Effect of Hypothyroidism on the Apoptotic Index in Rat Ovarian Follicles, Using the TUNEL Technique</title>


	<authors>
	<author>
	<name>Mahmoud Moghaddam-Dorafshani</name>
	<email></email>
	<affiliationId>1</affiliationId>
	 </author>
	<author>
	<name>Medi Jalali</name>
	<email></email>
	<affiliationId>2</affiliationId>
	 </author>
	<author>
	<name>Mohammad Reza Nikravesh</name>
	<email></email>
	<affiliationId>3</affiliationId>
	 </author>
	<author>
	<name>Ali Reza Ebrahimzadeh</name>
	<email></email>
	<affiliationId>4</affiliationId>
	 </author>
	</authors>
	 <affiliationsList>
	      <affiliationName affiliationId="1">
                 
	      </affiliationName>
	      <affiliationName affiliationId="2">
                 
	      </affiliationName>
	      <affiliationName affiliationId="3">
                 
	      </affiliationName>
	      <affiliationName affiliationId="4">
                 
	      </affiliationName>
    </affiliationsList>


	<abstract language="eng">Introduction: Among the endocrine diseases, hypothyroidism is the commonest after diabetes.Thyroid
hormones (T3,T4) are essential for genital organs function. Apoptosis process in ovarian cells plays a
significant role of development in ovarian follicles. The aim of the present study was determine the apoptotic
index induced by hypothyroidism in rat ovarian follicles.
Materials and Methods: In the present study, twenty female mature wistar rats were used with age of 2.5
months and weight of 200-250 (g). Rats were divided into test and control groups. In test group chemical
hypothyroidism induced by propylthiouracil (PTU500 mg/L) in drinking water. The control group only
received normal drinking water. After three weeks the rats were killed and their ovaries removed and were
fixed for tissue preparation. TUNEL technique were used for determine of apoptosis. Cells count done by
stereological method. Data were analyzed by t-test and one-way ANOVA followed by Tukey test.
Significance was accepted at P&#60;0.05.
Results: The findings showed that the apoptotic index had a significant decrease in late antral and graffian
follicles (P=0.000) and no significant decrease in preantral and early antral follicles (P&#62;0.05) in hypothyroid
group. All granulosa cells were TUNEL-positive in primary follicles but no cell was seen in primordial
follicles in groups.
Conclusion: The results of the present study showed that the hypothyroidism may be vigorous decreased of
apoptotic index in antral and graffian follicles. Hypothyroidism increased the number of luteal bodies and
decreased the number of graffian follicles in ovarian tissue.</abstract>
	<fullTextUrl format="pdf">http://anatomyjournal.ir/article-1-33-en.pdf</fullTextUrl>
	<keywords>
	<keyword>Hypothyroidism</keyword>
	<keyword>Apoptosis</keyword>
	<keyword>Ovarian Follicle</keyword>
	<keyword>Thyroid Gland</keyword>
	<keyword>Rats</keyword>
	</keywords>


	</record>
	<record>
	<language>eng</language>
	<publisher>4</publisher>
	<journalTitle>Anatomical Sciences Journal</journalTitle>
	<issn>17286158</issn>
	<eissn>17286158</eissn>
	<publicationDate>2013-02</publicationDate>
	<volume>10</volume>
	<issue>1</issue>
	<startPage>37</startPage>
	<endPage>42</endPage>
	<documentType>article</documentType>
	<title language="eng">The Role of Wnt Signaling Pathway on the Expression of TGFβ 1 and TGFβ 2 in Cultured Rat Cortical Astrocytes</title>


	<authors>
	<author>
	<name>Sina Bozorgmehr</name>
	<email></email>
	<affiliationId>1</affiliationId>
	 </author>
	<author>
	<name>Azita Parvaneh Tafreshi</name>
	<email></email>
	<affiliationId>2</affiliationId>
	 </author>
	<author>
	<name>Shahsanam Abbasi</name>
	<email></email>
	<affiliationId>3</affiliationId>
	 </author>
	<author>
	<name>Bahman Zeynali</name>
	<email></email>
	<affiliationId>4</affiliationId>
	 </author>
	</authors>
	 <affiliationsList>
	      <affiliationName affiliationId="1">
                 
	      </affiliationName>
	      <affiliationName affiliationId="2">
                 
	      </affiliationName>
	      <affiliationName affiliationId="3">
                 
	      </affiliationName>
	      <affiliationName affiliationId="4">
                 
	      </affiliationName>
    </affiliationsList>


	<abstract language="eng">Introduction: Astrocytes, the most abundant glia in the central nervous system, modulate neuronal survival
and function. Astrocytic functions are mediated by synthesis and secretion of wide ranges of polypeptides
through mechanism (s) poorly understood. Among these, TGFβs are synthesized and released by the
astrocytes. In this study, the involvement of Wnt signaling pathway on the synthesis of TGFβs by the
astrocyte was investigated.
Materials and Methods: Cultured rat astrocytes were therefore treated either with Wnt3a (20 ng/ml) alone for
24 hours or in combination with sFRP-1 (400 ng/ml) for a further 24 hours. Cells were then harvested and
examined for the expression of TGFβs and the Wnt target gene, cyclin D1.
Results: In this study, we were able to show that 1) treatment Wnt3a alone for 24 hours induced the
expressions of TGFβs and cyclin D1 2) The effect of Wnt was inhibited by pre-treatment with sFRP-1, that
is, sFRP-1 pre-treatment significantly blocked the Wnt-induced expressions of TGFβs and cyclin D1.
Conclusion: This study therefore provides the first evidence for the involvement of Wnt signaling pathway in
the synthesis of TGFβ proteins by cortical rat astrocytes.</abstract>
	<fullTextUrl format="pdf">http://anatomyjournal.ir/article-1-34-en.pdf</fullTextUrl>
	<keywords>
	<keyword>Astrocytes</keyword>
	<keyword>Wnt3a Protein</keyword>
	<keyword>Transforming Growth Factor beta (TGF beta)</keyword>
	<keyword>Secreted frizzled related protein-1 (sFRP-1)</keyword>
	<keyword>Cyclin D1</keyword>
	</keywords>


	</record>
	<record>
	<language>eng</language>
	<publisher>4</publisher>
	<journalTitle>Anatomical Sciences Journal</journalTitle>
	<issn>17286158</issn>
	<eissn>17286158</eissn>
	<publicationDate>2013-02</publicationDate>
	<volume>10</volume>
	<issue>1</issue>
	<startPage>51</startPage>
	<endPage>56</endPage>
	<documentType>article</documentType>
	<title language="eng">The Cephalometric Neurocranial Index of One-day-old Male Newborns in Kermanshah by Anthropometry</title>


	<authors>
	<author>
	<name>Sara Eivazi</name>
	<email></email>
	<affiliationId>1</affiliationId>
	 </author>
	<author>
	<name>Reza Mastery Farahani</name>
	<email></email>
	<affiliationId>2</affiliationId>
	 </author>
	</authors>
	 <affiliationsList>
	      <affiliationName affiliationId="1">
                 
	      </affiliationName>
	      <affiliationName affiliationId="2">
                 
	      </affiliationName>
    </affiliationsList>


	<abstract language="eng">Introduction: The findings of cephalometry studies are widely applied in medical and engineering fields.
Cephalometry measurements are affected by genetics‚ age‚ gender‚ and social‚ economic and geographic
factors.This study assesses cephalometry of the neurocranium in male newborns in Kermanshah,Iran by an
anthropometry method to confirm or reject the theory of brachycephalization (i.e., a spread in the width of
the average head).
Materials and Methods: This was a cross–sectional, descriptive study conducted on 103 healthy male
newbornsborn by natural childbirth in Kermanshah during 2012. The newborns’ heights were measured by a
stadiometer and their weight was obtained by using a newborn's scale.The neurocranium circumference was
determined by a millimeter scaled tape. and the length and breadth of the neurocranium by Martin Saler
cephalometry.Data were analyzed by SPSS. cephalic index and neurocranium classification were determined
by the classical cephalometry method.
Results: The mean and standard deviation of the newborns’ anthropometry and cephalometry measurements
were: 506±20 cm (height), 3219±35 g (weight), 352±12 cm (head circumference), 115±4 mm (neurocranium
length), 94±3 mm (neurocranium breadth), and 81±3 (cephalic index). A total of 49% of the newborns were
brachycephalic and 3% were dolichocephalic.
Conclusion: the results shows that the cephalic index of Kermanshahi male newborns are larger than those of
Turkman Qazvin, Native Fars and Tehran.whereas thay are less than observed in Sistan and Baluchistan.The
study confirms that anthropometry factors (i.e. age, genetic, etc.)impact these newborns. The cephalization
theories in these newborns are also confirmed.</abstract>
	<fullTextUrl format="pdf">http://anatomyjournal.ir/article-1-36-en.pdf</fullTextUrl>
	<keywords>
	<keyword>Cephalometry</keyword>
	<keyword>Male</keyword>
	<keyword>Newborn</keyword>
	<keyword>Iran</keyword>
	</keywords>


	</record>
	<record>
	<language>eng</language>
	<publisher>4</publisher>
	<journalTitle>Anatomical Sciences Journal</journalTitle>
	<issn>17286158</issn>
	<eissn>17286158</eissn>
	<publicationDate>2013-02</publicationDate>
	<volume>10</volume>
	<issue>1</issue>
	<startPage>57</startPage>
	<endPage>62</endPage>
	<documentType>article</documentType>
	<title language="eng">A Study of the Anatomic Variations in Extrahepatic Bile Ducts in 50 Adults Referred to Kerman Forensic Medicine Organization</title>


	<authors>
	<author>
	<name>Seyed Hassan Eftekhar-Vaghefi</name>
	<email></email>
	<affiliationId>1</affiliationId>
	 </author>
	<author>
	<name>Ali Shams-Ara</name>
	<email></email>
	<affiliationId>2</affiliationId>
	 </author>
	<author>
	<name>Mahdiye Jamalizade</name>
	<email></email>
	<affiliationId>3</affiliationId>
	 </author>
	</authors>
	 <affiliationsList>
	      <affiliationName affiliationId="1">
                 
	      </affiliationName>
	      <affiliationName affiliationId="2">
                 
	      </affiliationName>
	      <affiliationName affiliationId="3">
                 
	      </affiliationName>
    </affiliationsList>


	<abstract language="eng">Anatomic variations in forensic extrahepatic bile ducts is common. Knowledge of extrahepatic bile duct variations is important for surgeons in order to prevent iatrogenic damage during surgery. This study aims to determine the variations in extrahepatic bile ducts among 150 cadavers located at the Kerman Medicine Organization. We performed autopsies on 150 cadavers. Bile ducts were exposed and studied to determine their anatomic variants and diameters. We observed anatomic variants of the biliary tree in 7 cadavers (4.6%). In 3 (2%) cadavers, the right hepatic duct was missing, in 2 (1.33%) the left hepatic duct was missing and 6 (4%) did not have a common hepatic duct. In one case the common bile duct was absent. We may conclude that the Variation of bile duct is different in multiple population.</abstract>
	<fullTextUrl format="pdf">http://anatomyjournal.ir/article-1-37-en.pdf</fullTextUrl>
	<keywords>
	<keyword>Anatomic variation</keyword>
	<keyword>Bile ducts</keyword>
	</keywords>


	</record>
 </records>
 
  
  
  
  
 