<?xml version="1.0" encoding="utf-8"?>
 <records>
	<record>
	<language>per</language>
	<publisher>4</publisher>
	<journalTitle>Anatomical Sciences Journal</journalTitle>
	<issn>17286158</issn>
	<eissn>17286158</eissn>
	<publicationDate>2006-05</publicationDate>
	<volume>4</volume>
	<issue>1</issue>
	<startPage>1</startPage>
	<endPage>9</endPage>
	<documentType>article</documentType>
	<title language="eng">Evaluation of Discontinues Puresperm Gradient in Separation of X And Y Bearing Human Spermatozoa by Fluorescent in Situ Hybridization (FISH)</title>


	<authors>
	<author>
	<name>Hamid Gourabi</name>
	<email></email>
	<affiliationId>1</affiliationId>
	 </author>
	<author>
	<name>Fatemeh Ale Ahmad</name>
	<email></email>
	<affiliationId>2</affiliationId>
	 </author>
	<author>
	<name>Bahman Zeyali</name>
	<email></email>
	<affiliationId>3</affiliationId>
	 </author>
	<author>
	<name>Saeed Kazemi</name>
	<email></email>
	<affiliationId>4</affiliationId>
	 </author>
	<author>
	<name>Hosein Bahar Vand</name>
	<email>Ashtiani</email>
	<affiliationId>5</affiliationId>
	 </author>
	</authors>
	 <affiliationsList>
	      <affiliationName affiliationId="1">
             Genetic Department, Royan Institue, Tehran, Iran.    
	      </affiliationName>
	      <affiliationName affiliationId="2">
                 
	      </affiliationName>
	      <affiliationName affiliationId="3">
                 
	      </affiliationName>
	      <affiliationName affiliationId="4">
                 
	      </affiliationName>
	      <affiliationName affiliationId="5">
                 
	      </affiliationName>
    </affiliationsList>


	<abstract language="eng">Introduction: To evaluate the 8 layer discontinues puresperm gradient in separation of human spermatozoa according to sex chromosomes by fluorescent in situ hybridization (FISH).
Material and Methods: This study was carried out on three patient referring to Royan fertility and infertility center. Semen analysis was assessed according to WHO criteria. Each sample was divided into two aliquots, one as a control was washed with phosphate bufer saline and another one for processing through 8- step discontinues puresperm gradient 35%-84% (7% differences between each subsequent layers). After centrifugation, sperm from top and bottom fraction was aspirated and fixed on slide, FISH procedure was performad by using X and Y specific probes. DNA probes bind to alpha satellite complementary sequence on centromeric region of X and Y chromosomes. More than 1000 sperm were scored for each sample. The proportion of X and Y bearing sperm chromosomes was determined by presence of red or green florescent signals.
Results: Statistical analysis by chi-square test revealed no significant differences in the X:Y probration in the 84% layer compared to the controls. But there were significantly differences in the 35% layer compared to 84% layers and the controls (P=0.001, P=0.006 respectively), and X bearing spermatozoa was enriched in bottom layer.
Conclusion: The result of this study showed that 8-step discontinues Puresperm gradient is not so reliable for separating X and Y bearings spermatozoa.</abstract>
	<fullTextUrl format="pdf">http://anatomyjournal.ir/article-1-433-en.pdf</fullTextUrl>
	<keywords>
	<keyword>Sex chromosome</keyword>
	<keyword>Sperm</keyword>
	<keyword>Pure sperm</keyword>
	<keyword>Fish</keyword>
	</keywords>


	</record>
	<record>
	<language>per</language>
	<publisher>4</publisher>
	<journalTitle>Anatomical Sciences Journal</journalTitle>
	<issn>17286158</issn>
	<eissn>17286158</eissn>
	<publicationDate>2006-05</publicationDate>
	<volume>4</volume>
	<issue>1</issue>
	<startPage>11</startPage>
	<endPage>17</endPage>
	<documentType>article</documentType>
	<title language="eng">The Effect of Different Concentration of Human Recombinant of Leukemia Inhibitory Factor on Sperms of Asthenospermic Men</title>


	<authors>
	<author>
	<name>Ghasem Saki</name>
	<email></email>
	<affiliationId>1</affiliationId>
	 </author>
	<author>
	<name>Fakhrosadat Sajadian</name>
	<email></email>
	<affiliationId>2</affiliationId>
	 </author>
	<author>
	<name>Seyyed Rashidodin Kalantar Mahdavi</name>
	<email></email>
	<affiliationId>3</affiliationId>
	 </author>
	<author>
	<name>Ali Gholi Sobhani</name>
	<email></email>
	<affiliationId>4</affiliationId>
	 </author>
	</authors>
	 <affiliationsList>
	      <affiliationName affiliationId="1">
             Anatomy Department, Jondi Shapour University, Ahvaz, Iran.    
	      </affiliationName>
	      <affiliationName affiliationId="2">
                 
	      </affiliationName>
	      <affiliationName affiliationId="3">
                 
	      </affiliationName>
	      <affiliationName affiliationId="4">
                 
	      </affiliationName>
    </affiliationsList>


	<abstract language="eng">Introduction: Leukemia inhibitory factor is a secreted glycoprotein with a range of molecular weight forms, from 38-67kd, resulting from differential glycosylation of protein of approximately 20Kd. LIF has the four a helix cytokine structure that contains six cysteine residues, already known to occur in many hematopoietic factor. LIF is expressed at high constitutive in human fallopian tubal epithelium. Some studies has been done on the efect of LIF on normal sperm motility and shown that this factor could improve normal sperm motility. Objective: In this project y knowing that there is no report avout the effect of LIF on low motility sperms of asthenospermic men we decide to determine effect of this factor on low motility sperms.
Materials and Methods: In this investigation the sperm sample of 15 infertile men who have already referred to IVF department of Imam Khomeini hospital were collected and then preparing them by successive stages for culturing in Ham&#39;s F10+FCS 10% medium that contained various concentrations (0 ng/ml, 3 ng/ml, 5 ng/ml, 10 ng/ml, 50 ng/ml) of LIF at 37oC and under 5% of Co2 in air for up to 48 hours. Sperm motion characteristics were measured using Makler chamber. Sperm survival was determined by hyposmotic swelling test. Collected data with ANOVA method by means of SPSS software were analyzed.
Results: Sperm Motility and survival were not significantly enhance until 6 hours exposure to different concentration of LIF but sperm progressive. Motility were significantly higher after 24h exposure to 10 ng/ml of LIF. P&#60;0.05. The survival rate of sperm was significantly prolonged in that time exposure to 10 ng/ml of LIF P&#60;0.05. progressive motility of sperms and survival rate were signiicantly higher after 48h exposure to 50 ng/ml of LIF. P&#60;0.05.
Conclusion: It can be concluded that the effect of Leukemia Inhibitory Factor on sperm motility and survival were concentration dependent and LIF increased sperm motility and survival in vitro after at least 24 hours of hours of incubation and we could not find significantly differences in shorter incubation period.</abstract>
	<fullTextUrl format="pdf">http://anatomyjournal.ir/article-1-432-en.pdf</fullTextUrl>
	<keywords>
	<keyword>Motility</keyword>
	<keyword>Survival</keyword>
	<keyword>Lif</keyword>
	<keyword>Asthenospermia</keyword>
	</keywords>


	</record>
	<record>
	<language>per</language>
	<publisher>4</publisher>
	<journalTitle>Anatomical Sciences Journal</journalTitle>
	<issn>17286158</issn>
	<eissn>17286158</eissn>
	<publicationDate>2006-05</publicationDate>
	<volume>4</volume>
	<issue>1</issue>
	<startPage>29</startPage>
	<endPage>35</endPage>
	<documentType>article</documentType>
	<title language="eng">The Effects of Hypothyroidism on Wistar Rat Spermatogenesis</title>


	<authors>
	<author>
	<name>Mohammad Reza Nik Ravesh</name>
	<email></email>
	<affiliationId>1</affiliationId>
	 </author>
	<author>
	<name>Mahdi Jalali</name>
	<email></email>
	<affiliationId>2</affiliationId>
	 </author>
	</authors>
	 <affiliationsList>
	      <affiliationName affiliationId="1">
             Anatomy Department, Mashhad Medical Sciences University, Mashhad, Iran.    
	      </affiliationName>
	      <affiliationName affiliationId="2">
                 
	      </affiliationName>
    </affiliationsList>


	<abstract language="eng">Introduction: Previous studies have shown that thyroid hormones (T3 and T4) play importand role for postnatal development and maturation. In this study, the effect of hypothyroidism on spermatogenesis 2 month age Wistar rats were investigated.
Materials and Methods: The animals were divided into experimental and control groups. The experimental group were made hypothyroid by chemical thyroidectomy with propylthyourasil (PTU). The control were remind untreated. After 3 week, the animals were scarified and testes were fixed in formalin for histological studies.
Results: Our data indicated that, hypothyroidism resulted n significant reduction in seminiferous tubule and lumen diameter. Control ras showed active spermatogenesis whereas in hypothyroid rats, the proliferation and differentiation of germ cells were arrested and their number was decreased.
Conclusion: The present study clearly indicates that hypothyroidism adversely affects spermatogenesis; it also indicates that thyroid hormones are essential for normal spermatogenesis.</abstract>
	<fullTextUrl format="pdf">http://anatomyjournal.ir/article-1-435-en.pdf</fullTextUrl>
	<keywords>
	<keyword>Hypothyroidism</keyword>
	<keyword>Spermatogenesis</keyword>
	<keyword>Rat</keyword>
	</keywords>


	</record>
	<record>
	<language>per</language>
	<publisher>4</publisher>
	<journalTitle>Anatomical Sciences Journal</journalTitle>
	<issn>17286158</issn>
	<eissn>17286158</eissn>
	<publicationDate>2006-05</publicationDate>
	<volume>4</volume>
	<issue>1</issue>
	<startPage>81</startPage>
	<endPage>93</endPage>
	<documentType>article</documentType>
	<title language="eng">The Effects of Amiodarone of Rabbit Lung Alveolar Cells</title>


	<authors>
	<author>
	<name>Fereshte Mehr Aein</name>
	<email></email>
	<affiliationId>1</affiliationId>
	 </author>
	<author>
	<name>Ali Reza Shams</name>
	<email></email>
	<affiliationId>2</affiliationId>
	 </author>
	</authors>
	 <affiliationsList>
	      <affiliationName affiliationId="1">
             Anatomy Department, Iran Medical Sciences University, Tehran, Iran.    
	      </affiliationName>
	      <affiliationName affiliationId="2">
                 
	      </affiliationName>
    </affiliationsList>


	<abstract language="eng">Purpose: The effects of Amiodarone on lung tissue and morphologic changes of alveolar cells.
Materials and Methods: in this study, we used 21 mature male rabbits and they were divided into control and two experimental groups. Daily 80 mg/kg amiodarone was injected intra peritoneally to the experimental animals for one or two weeks. The control group received normal saline the same dose as amiodarone. Then the animals were anesthetized, perfused and the lung tissues were fixed in 2.5% glutaraldehyde and 4% paraformaldehyde. After the routine tissue processing was done, the specimens were blocked in paraffin and serial 8 mm sections was prepared. After staining with hematoxylin and eosin, the sections were studied by light microscope.
Results: The acute changes in lung tissue such as congestion of alveolar capillaries, hyperplasia of pneumocytes type II, death and pyknosis of alveolar cells, thickening of alveolar membrane and existance of fibrin like materials in the cells was seen. Furthermore the average of the nucleus diameter was decreased but the alveolar membranes increased statistically (P&#60;0.05).
Conclusion: These results indicate that i.p administration of amiodarone to rabbits can cause severe damages in their lung tissue.</abstract>
	<fullTextUrl format="pdf">http://anatomyjournal.ir/article-1-431-en.pdf</fullTextUrl>
	<keywords>
	<keyword>Amiodarone</keyword>
	<keyword>Lung</keyword>
	<keyword>Toxicity</keyword>
	</keywords>


	</record>
	<record>
	<language>per</language>
	<publisher>4</publisher>
	<journalTitle>Anatomical Sciences Journal</journalTitle>
	<issn>17286158</issn>
	<eissn>17286158</eissn>
	<publicationDate>2006-05</publicationDate>
	<volume>4</volume>
	<issue>1</issue>
	<startPage>95</startPage>
	<endPage>103</endPage>
	<documentType>article</documentType>
	<title language="eng">Differentiation Between the Effect of Protamine Deficiency and Failed Oocyte Activation on Fertilization Post ICSI</title>


	<authors>
	<author>
	<name>Mohammad Mardani</name>
	<email></email>
	<affiliationId>1</affiliationId>
	 </author>
	<author>
	<name>Mohammad Hosein Nasr Esfahani</name>
	<email></email>
	<affiliationId>2</affiliationId>
	 </author>
	<author>
	<name>Shahnaz Razavi</name>
	<email></email>
	<affiliationId>3</affiliationId>
	 </author>
	<author>
	<name>Reza Shiri</name>
	<email></email>
	<affiliationId>4</affiliationId>
	 </author>
	</authors>
	 <affiliationsList>
	      <affiliationName affiliationId="1">
                 
	      </affiliationName>
	      <affiliationName affiliationId="2">
             Department of Embryology, Royan Research Institute, Tehran, Iran.    
	      </affiliationName>
	      <affiliationName affiliationId="3">
                 
	      </affiliationName>
	      <affiliationName affiliationId="4">
                 
	      </affiliationName>
    </affiliationsList>


	<abstract language="eng">Sperm premature chromosomal condensaion (PCC) and failed oocyte activation are considered to result in failed fertilization post intracytoplasmic sperm injection (ICSI). Recent studies also suggested that sperm protamine deficiency may induce PCC. The ain of this study was to assess the effect of failed oocyte activation and protamine deficiency on failed ferilization post ICSI and to indicate whether these factors result fertilization failure, dependently or independently of each other.Materials and methods: This study consisted of 56 (first group) and 86 (second group) patients undergoing ICSI. After ICSI, the remaining processed samples were used for evaluation of protamine deficiency (Chromomycin A3 staining) and sperm morphology (Papanicolaou staining). 16-18 h post ICSI, oocytes were assessed for presence or absence of pronucleai in the both groups. In the second group te failed fertilized oocytes were chemically activated by ionomycin. Failed fertilized oocytes and chemically activated failed fertilized oocytes were fixed and stainde (Gimsa staining) for chromatin analysis.Reslts: Percentage of fertilization in the first and second groups of patients was 60.20% and 59.94%, respectively. In the second grop, percentage of fertilization rise to 83.72% following chemical activation. A significant negative correlation was observed between percentage of CMA3 positivity with ferilization rate in both groups of patients. A significant negative correlation was observed between percentage of PCC and fertilization rate in the first group while a significant posigive correlation was observed between percentage of PCC and CMA3 positivity in the second group.By subgrouping the patients into low and high CMA3 positivity in each group, the result reveal that ferilization rate, percentage of intact and PCC sperm were significantly different in the two subgroups in both groups of patients.Conclusion: the results of this study reveal that after failed oocyte activation, possibly due to sperm factors, protamine deficiency may induce failed fertilization by inducing PCC. However, mouse sperm lacking P2 protamine; have been shown to activate oocyte post ICSI, further emphasizaing these two factors may function independently of each ogher in failed fertilization.</abstract>
	<fullTextUrl format="pdf">http://anatomyjournal.ir/article-1-434-en.pdf</fullTextUrl>
	<keywords>
	<keyword>Failed oocyte activation</keyword>
	<keyword>Protamine deficiency</keyword>
	<keyword>ICSI</keyword>
	<keyword>Ionomycin</keyword>
	<keyword>PCC</keyword>
	</keywords>


	</record>
	<record>
	<language>per</language>
	<publisher>4</publisher>
	<journalTitle>Anatomical Sciences Journal</journalTitle>
	<issn>17286158</issn>
	<eissn>17286158</eissn>
	<publicationDate>2006-05</publicationDate>
	<volume>4</volume>
	<issue>1</issue>
	<startPage>105</startPage>
	<endPage>109</endPage>
	<documentType>article</documentType>
	<title language="eng">Serenomelia With Upper Limbs Abnormalities</title>


	<authors>
	<author>
	<name>Bahram Memar</name>
	<email></email>
	<affiliationId>1</affiliationId>
	 </author>
	<author>
	<name>Naser Tayebi Meybodi</name>
	<email></email>
	<affiliationId>2</affiliationId>
	 </author>
	<author>
	<name>Sakineh Amoueian</name>
	<email></email>
	<affiliationId>3</affiliationId>
	 </author>
	<author>
	<name>Mahdi Farzad Nia</name>
	<email></email>
	<affiliationId>4</affiliationId>
	 </author>
	<author>
	<name>Mahmoud Kalantari</name>
	<email></email>
	<affiliationId>5</affiliationId>
	 </author>
	<author>
	<name>Farzaneh Farhadi</name>
	<email></email>
	<affiliationId>6</affiliationId>
	 </author>
	</authors>
	 <affiliationsList>
	      <affiliationName affiliationId="1">
             Imam Reza Hospital, Mashhad University of Medical Sciences, Mashhad, Iran.    
	      </affiliationName>
	      <affiliationName affiliationId="2">
                 
	      </affiliationName>
	      <affiliationName affiliationId="3">
                 
	      </affiliationName>
	      <affiliationName affiliationId="4">
                 
	      </affiliationName>
	      <affiliationName affiliationId="5">
                 
	      </affiliationName>
	      <affiliationName affiliationId="6">
                 
	      </affiliationName>
    </affiliationsList>


	<abstract language="eng">Sirenomelia is a rare congenital anomaly that characterized by complete or incomplete fusion of lower lims and often associated with various malformations.In this report we describe one case of sirenomelia with multiple malformations including fibular agenesis, complete agenesis of anurectum, external genitalia and urinary tract, Inadditin, there was multiple anomaly upper limbs including agenosis of radius that is rarely seen in other reports.</abstract>
	<fullTextUrl format="pdf">http://anatomyjournal.ir/article-1-430-en.pdf</fullTextUrl>
	<keywords>
	<keyword>Sirenomelia</keyword>
	<keyword>Congenital anomaly</keyword>
	</keywords>


	</record>
 </records>
 
  
  
  
  
 