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Lab Attendance

Lab 1 --Z3415242 (talk) 12:45, 6 August 2014 (EST)

http://www.ncbi.nlm.nih.gov/pubmed

Pubmed

PMID2508416

<pubmed>25084016</pubmed>


Lab 2 attendance --Z3415242 (talk) 12:25, 13 August 2014 (EST)

Lab 3 attendance -- --Z3415242 (talk) 22:12, 2 September 2014 (EST)

Lab 4 attendance--Z3415242 (talk) 12:31, 27 August 2014 (EST)

Lab 5 attendance--Z3415242 (talk) 12:53, 3 September 2014 (EST)--Z3415242 (talk) 12:53, 3 September 2014 (EST)

Lab 6 attendance--Z3415242 (talk) 12:41, 10 September 2014 (EST)

Lab 7 attendance--Z3415242 (talk) 11:24, 17 September 2014 (EST)

Lab 8 attendance----Z3415242 (talk) 12:48, 24 September 2014 (EST)

Lab Assessment 1

Article 1

<pubmed>PMC3985938</pubmed>

The above article has suggested that vitamin D may have an impact on human reproduction. The aim of the investigation was to see if vitamin D levels can help predict rate of implantation and clinical pregnancy in infertile women after having IVF (in vitro fertilisation).

Method

The following method was used to perform the investigation. Vitamin D status as determined by serum 25(Oh) D levels were evaluated amongst a group of woman who went for IVF. 182 women were recruited and of that 172 were included for analysis. Woman who were aged 18-41 years, had FSH level 12 IU/L or lower and were able to provide informed consent were included in the study. Third party reproduction cycle, those with uterine abnormalities and language barriers were excluded. The participants underwent a normal IVF cycle. Standard agonist and antagonist protocols were used. Busrelin acetate was used in the agonist protocol and cetrolix acetate or ganirelix acetate was used in antagonist protocol. Controlled ovarian hyper-stimulation was achieved by recombinant or purified FSH with or without LH or human menopausal gonadotropin. The doses of the medication were determined on individual basis.

Ovarian response was examined by serial transvaginal ultrasonography as well as through serum lutenizing and estradiol assay. Serum25 (OH) D samples had been collected before oocytes were retrieved. Nuclear maturation was triggered with HcG.Oocytes were retrieved under ultrasound guidance transverginally 36-38 hours following injection of HCG. On day 3-5 after fertilisation, embryo was transferred and vaginal progesterone was used for luteal phase support.

Findings

Patients were classified into sufficient (greater than 75nmol/L of vitamin D) and insufficient levels(less than 75nmol/L). From results, those from sufficient group showed to be more likely to undergo embryo transfer on day 5( 71.8% as statistically analysed) compared to woman from insufficient group ( 58.9%). Higher clinical pregnancy rate per cycle was discovered amongst woman with sufficient level compare to woman with insufficient level. They also found higher clinical pregnancy per embryo transfer in the sufficient group of woman. Implantation rate was observed to be higher in sufficient group however this was not statistically significant. Multivariable analysis adjusted for age, BMI and day 5 verses day 3 embryo transfers showed that serum level was an independent predictor of clinical pregnancy. Woman in this study with sufficient vitamin D level had a higher rate of clinical pregnancy following IVF compare with woman with insufficient level. Vitamin D supplement could provide an easy and cost effective way of improving pregnancy rate in woman undergoing IVF.

Article 2

<pubmed>24834703</pubmed> Properties of Zona Pellucida are believed to be important for oocyte cytoplasmic maturation and meiotic spindle for chromosomal alignment and proper separation of maternal chromosome. This study aimed to find the possible effect of ZP birefringment properties and mitotic spindle visualisation and localisation as a predictor of IVF outcome.

Method

This was a perspective study performed over 16 months at Medical University of Bialystok Poland where 51 patients undergoing IVF-ET (In vitro fertilisation and embryo transfer), intracytoplasmic sperm injection (ICSI) were included. Of 51 couples 39 had unexplained infertility and 12 had mild male factor. Two different methods for controlled ovarian hyper stimulation were used.

1. Long protocol (n=32) – The drug used was GNRH agonist Diphereline SR. It is a recombinant form of FSH.

2. Antagonist protocol (n=19). FSH and GNRH antagonist was used.

Ovulation was induced with HCG (human chorionic gonadotropin) in all patients. Oocyte retrieved transvaginally under ultrasound guidance 36 hours after HCG injection. Oocyte denudation was performed using hyaluronidase. Before intracytoplasmic sperm injection (ICSI) non invasive measuring with Olympus X7 inverted microscope was performed. Through this 228 cumulus oophorus were selected to be examined. 31were excluded due to inadequate oocyte maturation. Examination was done in different ways. 1. ZP birefringence was evaluated in a scale of 0degree to 4degree, 2. ZP autoscoring was performed, 3. ZP numeral autoscoring was performed, 4.MS visualisation, 5.Spindle detection and localisation of MS in relation to polar body.

Detection was grouped as: 1. Oocyte with spindle forming at less than 30 degree 2. 30-45 degree 3. 45-120 degree and 4. More than 120 degree, to PB. Oocytes whose spindles were located to be in another position where rotated in such way that the injected needle did not penetrate it. After this, oocytes were able to be divided into 3 groups. Group1: Embryo selected for transfer and outcome- day 14 after ET positive pregnancy test. Group 2: Embryo selected-day 14 after ET negative pregnancy test, Group 3: Embryo was not selected for transfer.

FINDINGS

Autoscores obtained in all three groups were nearly identical and no statistically difference were found in study groups. MS localisation in relation to PB was very close ( <450) in 70.9% of oocytes. The rate of MS positive oocyte was highest in group with pregnancy but statistically not significant. Between oocyte selected and non-selected for ET, no statistically significant difference is numeral score of ZP was found. ZP manual evaluation indicated stronger bifringement when pregnancy was not achieved. The rate of MS positive oocyte was higher in group with pregnancy. None of this was statistically significant so it was concluded that polarisation microscopy imaging and rating of ZP and MS cannot be a direct predictor of IVF outcome.

Lab Online Assessment 2-IMAGE

Adriamycin treated mouse shows association of abnormal notochord branching and fore gut abnormality

A)Different angle of a control embryo showing endoderm, notochord and floor plate in white. (B-H)- Adriamycin treated embryos immunostained for HNF3β demonstrating morphological abnormalities. Abnormal notochord branching is indicated with red arrow while different fore gut abnormalities are indicated with green arrow.[1]


Copyright: © 2011 Hajduk et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.


Note - This image was originally uploaded as part of an undergraduate science student project and may contain inaccuracies in either description or acknowledgements. Students have been advised in writing concerning the reuse of content and may accidentally have misunderstood the original terms of use. If image reuse on this non-commercial educational site infringes your existing copyright, please contact the site editor for immediate removal.

Lab Online Assessment 3

Subheading:

Abnormalities that can occur in GIT system during fetal development

List of research/articles:

1.<pubmed>22777173</pubmed> 2.<pubmed>3832654</pubmed> 3.[1]

  1. ↑ Charles D. Bluestone M.D., Roy Kerry M.D. andWilliam K. Sieber M.D,2009,January,Congenital esophageal stenosis†‡,The Laryngoscope,volume79,issue 6,1095–1104,http://onlinelibrary.wiley.com.wwwproxy0.library.unsw.edu.au/doi/10.1288/00005537-196906000-00004/pdf}}


Lab Online Assessment 4

1. Identify a paper that uses cord stem cells therapeutically and write a brief (2-3 paragraph) description of the paper's findings.

Successful Stem Cell Therapy Using Umbilical Cord Blood-Derived Multipotent Stem Cells for Buerger's Disease and Ischemic Limb Disease Animal Model

The study found a possibility of treating Buerger’s disease patients by using MSC ( Mesenchymal stem cells) that came from human umbilical cord blood(UCB). Results supported the theory of angiogenesis as being a therapeutic mechanism used by UCB derived MSC in patients with Buerger’s disease.

Through Angiography, it was discovered that in affected lesion, there was an increase in capillary formation and decrease vascular resistance when UCB derived MSC was transplanted to patients with Buerger’s disease. Furthermore ischemic rest pain reduced more rapidly (within 2 weeks) than the formation of new capillaries which took 120 days after the Angiography.

Buerger’s disease is not common in animals so femoral artery ligation was performed to induce limb ischemia in animals. This was followed by medium control and un-injected control. Limb salvage was not observed in either medium control or uninjected control. 1 day after femoral artery ligation, extensive forefoot necrosis was observed and this lead to spontaneous amputation in 70% (7 out of 10) in both controls. Preserved limb was observed in 3 out of 7 of uninjected control while in contrast, 5 out of 8 mice with UCB derived MSC transplant was associated with successful limb salvage. Foot necrosis was limited in only 4 of 8 with necrotic lesions being healed within a month and only 38% with UCB derived MSC transplant showed spontaneous limb amputation. So there was statistical significance between UCB derived MSC treated mice and medium and uninjected controls therefore showing that UCB derived MSC blood stem cells can have therapeutic use for Buerger’s disease.

Reference:

<pubmed>16497946</pubmed>

2.There are a number of developmental vascular "shunts" present in the embryo, that are closed postnatally. Identify these shunts and their anatomical location.

Ductus Venosus: It is a temporary blood vessel (fetal vein) carrying oxygenated blood. It bypasses through the fetal liver, originating at the left umbilical vein (at the placenta) and going to the inferior vena cava to the heart of the fetus.

Ductus Arteriosus: is a blood vessel in the developing fetus which lies between the left pulmonary artery and the proximal descending aorta of the fetus and thus connecting them. It bypasses the lung to distribute oxygen which is received through the placenta from the mother’s blood.

Foramen Ovale: is an opening located between two atria which bypasses the lung to allow blood to be channelled in the systemic circulation. Blood enters the right atrium then through foramen ovale and into the left atrium.


Lab Online Assessment 5

Laryngeal Atresia

The larynx develops from endodermal lining and the adjacent mesenchyme of the foregut between 4th and 6th Branchial arches. The foregut is first identifiable at 20 days gestation and ventral laryngotracheal groove differentiates into primitive laryngeal sulcus by 22 days and right and left lung buds appear by 24 days.[1]The laryngotracheal groove continues to deepen until its lateral edges fuse.

The failure of recanalisation of the laryngotracheal tube and therefore the non-development of the 6th brachial arch during embryological development causes Laryngeal atresia, a type of congenital high airway obstruction syndrome which is usually fatal. This rare anomaly occurs during the 3rd month of gestation and the larynx remains blocked by cartilage and other tissue and therefore there is complete absence of lumen in a new born baby.[1] There have been reported of 50 reported cases of larynx atresia in world literature.

Laryngeal atresia may be associated with other genetic abnormalities such as left persistent superior vena cava, single umbilical artery, oesophageal atresia and renal agenesis. [2] Partial trisomy 9 and 16, chromosome 5p deletion and 22q11.2 were also suggested as associated causes of Laryngeal atresia. [2]

Reference:

[1].[1]

  1. ↑ Tewfik T.L.,Meyers A.D.,2013,July,Congenital Laryngeal Atresia, Cysts, and Lymphangioma, Medscape, [ONLINE] Available at:http://emedicine.medscape.com/article/837630-overview

[2]. <pubmed>3566610</pubmed>

LAB 7

Identify and write a brief description of the findings of a recent research paper on development of one of the endocrine organs covered in today's practical.

The study was to investigate the role of Hes1 in thyroid development. The Hes1 expression was measured during Thyroid differentiation. Thyroid development in mice lacking in Hes1 was also studied. During normal mice thyroid development, Hes1 was detected from E9.5 onwards. The findings revealed dual role of Hes1 during Thyroid development, first-control of number of both thyrocyte and C-cell progenitors (via p57-independent mechanism) and second-adequate differentiation and endocrine function of thyrocytes and C-cells. Mice with Hes1 mutation showed severe thyroid hypoplasia and also decreased production of T4 and calcitonin. Results also suggested Hes1 expression was required for the developing thyroid gland to reach its normal size and shape.


<pubmed>PMC3045378</pubmed>

Identify the embryonic layers and tissues that contribute to the developing teeth.

Two types of teeth develop. Deciduous teeth and permanent teeth. Teeth develop from oral ectoderm, mesenchyme and neural crest cells. The tooth enamel is derived from the ectoderm of the oral cavity while the rest of the tissues differentiate from neural crest cells and mesenchyme. Tooth development involves induction between neural crest mesenchyme and oral epithelium.