Welcome to The Visible Embryo
Home-- -History-- -Bibliography- -Pregnancy Timeline- --Prescription Drugs in Pregnancy- -- Pregnancy Calculator- --Female Reproductive System- -Contact
 

Welcome to The Visible Embryo, a comprehensive educational resource on human development from conception to birth.

The Visible Embryo provides visual references for changes in fetal development throughout pregnancy and can be navigated via fetal development or maternal changes.

The National Institutes of Child Health and Human Development awarded Phase I and Phase II Small Business Innovative Research Grants to develop The Visible Embryo. Initally designed to evaluate the internet as a teaching tool for first year medical students, The Visible Embryo is linked to over 600 educational institutions and is viewed by more than one million visitors each month.

Today, The Visible Embryo is linked to over 600 educational institutions and is viewed by more than 1 million visitors each month. The field of early embryology has grown to include the identification of the stem cell as not only critical to organogenesis in the embryo, but equally critical to organ function and repair in the adult human. The identification and understanding of genetic malfunction, inflammatory responses, and the progression in chronic disease, begins with a grounding in primary cellular and systemic functions manifested in the study of the early embryo.

WHO International Clinical Trials Registry Platform


The World Health Organization (WHO) has created a new Web site to help researchers, doctors and
patients obtain reliable information on high-quality clinical trials. Now you can go to one website and search all registers to identify clinical trial research underway around the world!



Home

History

Bibliography

Pregnancy Timeline

Prescription Drug Effects on Pregnancy

Pregnancy Calculator

Female Reproductive System

Contact The Visible Embryo

News Alerts Archive

Disclaimer: The Visible Embryo web site is provided for your general information only. The information contained on this site should not be treated as a substitute for medical, legal or other professional advice. Neither is The Visible Embryo responsible or liable for the contents of any websites of third parties which are listed on this site.
Content protected under a Creative Commons License.

No dirivative works may be made or used for commercial purposes.

 

Pregnancy Timeline by SemestersFetal liver is producing blood cellsHead may position into pelvisBrain convolutions beginFull TermWhite fat begins to be madeWhite fat begins to be madeHead may position into pelvisImmune system beginningImmune system beginningPeriod of rapid brain growthBrain convolutions beginLungs begin to produce surfactantSensory brain waves begin to activateSensory brain waves begin to activateInner Ear Bones HardenBone marrow starts making blood cellsBone marrow starts making blood cellsBrown fat surrounds lymphatic systemFetal sexual organs visibleFinger and toe prints appearFinger and toe prints appearHeartbeat can be detectedHeartbeat can be detectedBasic Brain Structure in PlaceThe Appearance of SomitesFirst Detectable Brain WavesA Four Chambered HeartBeginning Cerebral HemispheresFemale Reproductive SystemEnd of Embryonic PeriodEnd of Embryonic PeriodFirst Thin Layer of Skin AppearsThird TrimesterSecond TrimesterFirst TrimesterFertilizationDevelopmental Timeline
CLICK ON weeks 0 - 40 and follow along every 2 weeks of fetal development
Google Search artcles published since 2007
 
 

Home | Pregnancy Timeline | News Alerts |News Archive Oct 20, 2014

The citric acid cycle, also known as the Krebs cycle, is a series of chemical reactions, used by
all organisms requiring oxygen. The Krebs cycle generates energy by oxidating acetate from carbohydrates, changing fats and proteins into carbon dioxide, and making chemical energy
in the form of adenosine triphosphate (ATP).

 







CDC Growth Standards 0 to 2 Years of Age

 

Rett syndrome mice improve with diet

Study of rodents with Rett syndrome (an autism spectrum disorder) suggests a potential diet intervention. Mice on the special diet lived longer than mice on regular diets and their physical and behavioral symptoms were less severe.

Autism spectrum disorders (ASDs) affect an estimated one in 68 children in the United States. Rett syndrome is a rare ASD caused by mutations in the MECP2 gene. The syndrome includes autism-like signs including difficulty communicating, socializing and relating to others. Other hallmarks are seizures, decreased muscle tone, repetitive involuntary movements, with gastrointestinal and breathing problems. These symptoms are also seen in other ASD patients suggesting underlying similarities in their origins. While what causes most ASDs is unknown and thought to be complex, Rett syndrome is unique as it is the result of an error in a single gene.


When young mice with the rodent equivalent of Rett syndrome were fed a diet supplemented with the synthetic oil triheptanoin, the mice lived longer than mice on regular diets. Also, their physical and behavioral symptoms were less severe, according to results of new research from The Johns Hopkins University.


Triheptanoin is a triglyceride made of three 7-carbon fatty acids. These odd-numbered carbon fatty acids help replenish elements lost during the Tricarboxylic acid (TCA) Cycle (also called the Krebs or citric acid cycle). Triheptanoin is used in humans to treat inherited metabolic diseases, such as pyruvate carboxylase deficiency and carnitine palmitoyltransferase II deficiency.

Triheptanoin also appears to increase the effectiveness of a ketogenic (high-fat, adequate-protein, low-carbohydrate) diet as a treatment for epilepsy.


Scientists involved in the study think triheptanoin improves the function of mitochondria, the energy factories common to all cells. Since mitochondrial defects are seen in other autism spectrum disorders, these results offer hope that triheptanoin oil could help not just people with Rett syndrome, but patients with other, more common ASDs.


The research was published Oct. 9 in the journal PLOS ONE.

Researchers at the Johns Hopkins University School of Medicine, experimented with mice lacking the MeCP2 protein — leaving them with severe Rett syndrome. According to Gabriele Ronnett, MD, PhD, who led the research, the Rett mice weighed the same as healthy mice but carried large fat deposits along with lower amounts of muscle. This suggests that calories they ate were not being converted into normal tissue but instead being stored as fat.

This possibility led Ronnett and her team to consider mitochondrial errors. Mitochondria transform nutrient molecules into ATP — a high-energy molecule. ATP then drives muscle building and nerve cell growth using a series of biochemical reactions collectively called the TCA cycle.


"Rett syndrome becomes apparent in babies 6 to 18 months old, when the energy needs of the brain are particularly high and as new neural connections are being made. If the mitochondria are already defective, stressed or damaged, an increased demand for more would be too much for them."

Gabriele Ronnett, MD, PhD, research leader, Johns Hopkins University School of Medicine.


Previous small clinical trials in people with another metabolic disorder suggested that dietary intervention with triheptanoin could help. Triheptanoin is odorless, tasteless and a little thinner than olive oil. It is also easily processed to produce a component in the TCA cycle.

When Rett syndrome mice were weaned from their moms at 4 weeks of age, they were then fed a diet in which 30 percent of their calories came from triheptanoin, mixed in with their normal pellet food.


Though far from a cure, the results of triheptanoin treatment were impressive. Treated mice had healthier mitochondria, improved motor function, increased social interest in other mice and lived four weeks — or 30 percent — longer than mice who did not receive the oil. The team also found that the diet normalized their body fat, glucose and fat metabolism.


"You can think of the mitochondria of the Rett syndrome mice as damaged buckets full of holes that allowed TCA cycle components to leak out," says Aja. "We haven't figured out how to plug the holes, but we can keep the buckets full by providing triheptanoin to replenish the TCA cycle."

"It is still too early to assume that this oil will work in humans with ASDs, but these results give us hope," says Ronnett. "It's exciting to think that we might be able to improve many ASDs without having to identify each and every contributing gene."

The team would also like to conduct studies where they provide triheptanoin at earlier mouse pup ages, perhaps via the mothers' milk, to mimic developmental ages at which most children are diagnosed with Rett syndrome.


Triheptanoin is currently made for research purposes only and is not available as a medicine or dietary supplement for humans.


Abstract
Rett syndrome (RTT) is an autism spectrum disorder (ASD) caused by mutations in the X-linked MECP2 gene that encodes methyl-CpG binding protein 2 (MeCP2). Symptoms range in severity and include psychomotor disabilities, seizures, ataxia, and intellectual disability. Symptom onset is between 6-18 months of age, a critical period of brain development that is highly energy-dependent. Notably, patients with RTT have evidence of mitochondrial dysfunction, as well as abnormal levels of the adipokines leptin and adiponectin, suggesting overall metabolic imbalance. We hypothesized that one contributor to RTT symptoms is energy deficiency due to defective nutrient substrate utilization by the TCA cycle. This energy deficit would lead to a metabolic imbalance, but would be treatable by providing anaplerotic substrates to the TCA cycle to enhance energy production. We show that dietary therapy with triheptanoin significantly increased longevity and improved motor function and social interaction in male mice hemizygous for Mecp2 knockout. Anaplerotic therapy in Mecp2 knockout mice also improved indicators of impaired substrate utilization, decreased adiposity, increased glucose tolerance and insulin sensitivity, decreased serum leptin and insulin, and improved mitochondrial morphology in skeletal muscle. Untargeted metabolomics of liver and skeletal muscle revealed increases in levels of TCA cycle intermediates with triheptanoin diet, as well as normalizations of glucose and fatty acid biochemical pathways consistent with the improved metabolic phenotype in Mecp2 knockout mice on triheptanoin. These results suggest that an approach using dietary supplementation with anaplerotic substrate is effective in improving symptoms and metabolic health in RTT.

Other authors of the report include Min Jung Park, Qun Li, Alicia Degano, Judith Penati, Justin Zhuo and Charles Roe of the Johns Hopkins University School of Medicine.

On the Web
View article in PLOS ONE. http://dx.plos.org/10.1371/journal.pone.0109527
Learn more about The Center for Metabolism and Obesity Research. http://www.hopkinsmedicine.org/institute_basic_biomedical_sciences
/research_centers/metabolism_obesity_research/


This work was supported by research funds from Daegu Gyeongbuk Institute of Science and Technology Convergence Science Center, the National Institute of Neurological Disorders and Stroke (R01 NS041079), and Agilent Technologies.

Return to top of page