Kleine Levin Syndrome “Sleeping Beauty Syndrome”

Kleine Levin Syndrome “Sleeping Beauty Syndrome”

Kleine Levin Syndrome also called “Sleeping Beauty Syndrome” is a very rare disorder. The disorder is common in young adolescents, especially in males. The disorder is said to be a malfunction occurring in the hypothalamus. The hypothalamus is in the brain that controls many of the body functions such as appetite, thirst, sleep and also a role in controlling emotions. The National Institute of Neurological Disorders and Stroke have done much research on trying to understand the disorder an come up with treatment plans.

Kleine Levin Syndrome is rare sleeping disorder that effects approximately 70 percent of male adolescents. With this disorder one will need excessive amounts of sleep up to 20 hours a day, have excessive food intake and behavioral changes such as abnormally uninhibited sexual drive. Those effected by this condition usually have very childlike behavior. The episode of sleep may last for days or even weeks. A person will awake an may have no reelection of what occurred during the episode. A person with this disorder may see a decrease in episode after about 8 to 12 years. There is no cure for this rare condition yet. There was a report on ABC News that did coverage on this rare condition. ABC News reported that there had only been 1,000 reported case in the whole world.

The National Institute of Neurological Disorders and Stroke are still trying to find a treatment for those effected by the condition of Kleine Levin Syndrome. WIth the syndrome being so rare there is not a big testing group. This condition would be horrible to live with knowing there is no treatment out there yet for it and no way of controlling when an episode will occur. Those effected by this loose a great deal of time in their life  spending most of it sleeping an in a trance like state.

Kethanne K. Colich

Tortora, Gerard J and Derrickson, Bryan. Principles of Anatomy & Physiology. 13th. 2011.Print.

http://www.ninds.nih.gov/disorders/kleine_levin/kleine_levin.htm

Finding a New Route For Treatment

The blood-brain barrier is a major component in protecting our central nervous system from harmful substances.  It is composed a tight sealed junction of the capillaries in the brain along with a thick basement membrane. This barrier only allows certain substances through to the brain.  Some water-soluble substance pass through it very easily, and some substances cross through slowly.  On the other hand, substances such as antibiotics are not allowed to cross the blood-brain barrier (Tortora). This makes it difficult to treat central nervous disorders.  The medical community has been puzzled after many different attempts to get antibiotics across the barrier.  So, what is the best route to solve this problem?

Researchers from Harvard Medical School and Boston University have been working on a study to solve this difficult problem.  The researchers have realized the lining of the nasal cavity is the best way to get medication directly to the central nervous system. First, they constructed an animal model to evaluate their possible technique.  They realized that this method is able to send particles to the brain that are a thousand times larger than the particles that the blood-brain barrier lets through (Massachusetts Eye and Ear Infirmary).

The discovery that these researchers have made has a major impact on the medical community. The future, hopefully, holds a set of clinical trials for this method. This method could help many of the 20 million people who suffer from central nervous system diseases (Massachusetts Eye and Ear Infirmary).  The research of this method serves as a beacon of light for those surviving and their families.

 

 

 

Massachusetts Eye and Ear Infirmary (2013, April 24). Nasal lining used to breach blood/brain barrier. ScienceDaily. Retrieved November 30, 2013, from http://www.sciencedaily.com­ /releases/2013/04/130424185207.htm

 

Tortora G.J. and B. Derrickson. 2012. Principles of Anatomy and Physiology. 13th ed., John Wiley and Sons

Epilepsy, an Early Sign of Alzheimer’s Disease

          Epilepsy is characterized by short, recurrent attacks of motor, sensory, or psychological malfunction.  It affects about 1%of the entire world’s population.  Epilepsy is better known as seizures, or when the muscles of the body contract uncontrollably.  There are many causes, such as; brain damage, toxins, metabolic disturbances, and head injury.  A very common trigger for an epileptic episode is flashing lights.  There are medications available that can reduce or eliminate one’s epilepsy.

          While Epilepsy is a very serious disorder, it can be treated.  However, new studies suggest that the continuance of seizures late into life could be an early sign of Alzheimer’s Disease(AD).  The research suggests that patients with Epilepsy could endure much more severe effects from AD than patients without Epilepsy.  There is roughly a five to seven year difference in the occurrence of cognitive decline between epileptics and non-epileptics.  Epileptic patients can expect to see more neuronal damage, faster onset of symptoms, and a much faster rate of cognitive decline from AD.

           In conclusion, Epilepsy is a serious condition that can lead to even more harmful diseases.  The recent study has discovered a link between being epileptic and a faster development of AD.  Epilepsy in the earlier stages of life does not seem to affect the intelligence or normal functions of one’s brain.  However, over the period of sixty years, it has shown to cause more severe Alzheimer’s.  There will very likely be more research done into both disorders and possibly cures or treatments developed.  Neuronal-based sciences are still in a very early stage, and there are likely many discoveries ahead.

Tortora, Gerard J.  Bryan Derrickson.  A&P; principles of anatomy & physiology 13th edition.  John Wiley & Sons, inc.  2011.  Chapter 12.  Nervous Tissue.  Page 486.

The JAMA Network Journals. “Seizures late in life may be an early sign of Alzheimer’s disease.” ScienceDaily, 8 Jul. 2013. Web. 1 Dec. 2013.

Muscle Regeneration Improvements

Muscle Regeneration Improvements

            Muscular Atrophy is when muscles waste away usually because of disuse or malnourishment.  As myofibrils are lost, the muscle fibers shrink in size and capability.  Those with disuse atrophy experience a decrease in nerve impulses traveling to their muscles and also significantly less strength.  However, disuse atrophy is reversible with proper diet and exercise.  Denervation atrophy occurs when the connection from the nerves to the muscles is cut or disrupted.  With this disorder, the muscle, without connection to the nerves, shrinks to one-fourth of its original size within 6 months to 2 years.  Denervation atrophy is not a reversible disorder because the muscle fibers are replaced with fibrous connective tissue.

            However, there is some recent research that has the potential to cure or reverse many muscular disorders and diseases.  Researchers believe that stem cells are the answer.  In the past, the insertion of stem cells into those with muscular disorders has not had a high success rate.  Now, researchers are coupling the use of stem cells with tissue engineering.  This two-pronged process has been tested and results were seen.  The muscle cells began to regenerate and rebuild muscle cells in the body of one who has muscular dystrophy.

            This stem cell research and application can be used to change the lives of those who have been otherwise forced to live with muscular diseases and disorders.  Further testing and reviews are needed of course.  This revolutionary two-pronged idea has the potential to get rid of muscle deficiency altogether.  With more time and further research, perhaps more diseases could be treated or cured with this stem cell insertion and tissue engineering team.  It could free patients from bed, wheelchairs, and walkers!  It could possibly even lead to other tissue regenerations such as organ and limbs.

Sources:

Tortora, Gerard J.  Bryan Derrickson.  A&P; principles of anatomy & physiology 13th edition.  John Wiley & Sons, inc.  2011.  Chapter 10.2.  Skeletal Muscle Tissue.  Page 331.

BioMed Central Limited. “From degeneration to regeneration: Advances in skeletal muscle engineering.” ScienceDaily, 26 Nov. 2012. Web. 1 Nov. 2013.

Recovery After Strokes: Talking and the Left Brain

In the frontal lobe close to the lateral cerebral sulcus, you will find the Broca’s speech area. This area of the brain is localized in the left hemisphere for about 97% of the population. In the left frontal lobe is where planning and production of speech occur for most people (Tortora). We know that speech is localized in the left hemisphere of the brain for most individuals, but what happens when someone is affected by a stroke? How does the brain process speech if the Broca’s speech area was affected?

Kiel University scientists simulated a dysfunction in the brain, which was comparable to a stroke. They used a magnetic coil that transmitted a current pulse that interrupted the functioning area of the brain that is responsible for producing speech, the Broca’s area. The scientists insure that this process is harmless for volunteers and only influence speech, or the lack of speech for about 30 to 45 minutes (Christian).

Once this test was carried out, the scientists compared it to previous research, which indicated that speech was localized in the left hemisphere. They used several tests to show brain activity. One of which was a fMRI- functional magnetic resonance imaging test and a TMS- transcranial magnetic stimulation test. During the 30 to 45 minutes that speech was influenced, they asked volunteers to listen to pseudo words and repeat them. During this test they observed suppressed activity in the left hemisphere (due to the magnetic coil) and it took volunteers longer to repeat the words. They also saw a surprising display of activities on the right hemisphere of the brain (Christian).

This research is a sign of hope for the scientific and medical community. It shows us that although strokes could suppress speech activity in the left hemisphere, the right hemisphere could facilitate speech production for the injured or weakened left hemisphere (Christian). This gives the medical community hope for helping stroke patients recover their speech. This research gives us insight on what could possibly be done to prevent total speech loss and to help recover it. It gives hopes to medical professionals and families just alike, who equally want to help the patient recover to the best of their functional abilities.

 

Christian-Albrechts-Universitaet zu Kiel. “Speech recovery after stroke.” ScienceDaily, 27 Nov. 2013. Web. 29 Nov. 2013.

 

Tortora G.J. and B. Derrickson. 2012. Principles of Anatomy and Physiology. 13th ed., John Wiley and Sons

 

The Effects of Childhood Poverty on Brain Development

There are many aspects in the human body that are affected by childhood poverty, and brain development happens to be one of the many. Jama Pediatrics explains that learning disabilities, depression, and the inability to cope with stress are all results of childhood poverty. In fact, researchers from the University Of Washington School Of Medicine did a study on the effect that childhood poverty has on brain development and the results were shocking. The results that the researchers found were astonishing simply because of the huge effect that poverty withholds on the development of the brain.

According to Honor Whiteman in Medical News Today, Researchers located at the University Of Washington School Of Medicine researched the effects that childhood poverty has on brain development. They discovered not only fascinating results, but they also found a cure for the brain development deficiencies that childhood poverty brings about. Researchers at the University discovered that learning disabilities, depression, and the inability to cope with stress are all symptoms that may uncover from insufficient brain development. All of these cases are caused by the lack of nurturing that the parents or guardians perform on their children. In order to come up with each discovery, an MRI was performed on one hundred and forty-five children that happened to be a part of a Preschool Depression Study between the ages of six and twelve. Portions of the one hundred and forty-five children were healthy normal children, while others suffered from different illnesses such as depression and ADHD. The research study was done by placing children and their parents/guardians in a clinic. While in the designated waiting area in the office, the child was given a gift-wrapped box, and the parent/guardian was given paperwork to complete. The child was told that the gift could not be opened until their personal caregiver had completed the necessary paperwork. The true research was how well the caregiver coped with the whining child that is wanting so very badly to open up the gift the gift they had been given. The researchers claimed that the caregivers that seemed stressed and less able to nurture their whining child were the ones that showed signs of living in poverty. According to the research, children who were living in poverty with caregivers that could not properly nurture their child showed signs of having less white and grey matter than those who were not living in poverty. In addition, the MRI scans that were taken showed that parts of the brain such as the amygdala and the hypothalamus where exceptionally smaller in children living in poverty versus children who were far more better off.

It is evident that there are several things that effect brain development, and childhood poverty is one of them. It is important to know and understand all of the different ways of life that can affect human development, especially when it comes to the brain. It is especially important to know not only so that people can try to change it, but also so that people can be aware of the effects that childhood poverty has on the brain. Once there is a sense of awareness among people that is when change has the ability to take place.

“The Effects of Poverty on Childhood Brain Development.” Jama Pediatrics. 28 Oct. 2013. Web.

1 Dec. 2013.

Whiteman, Honor. “Childhood Poverty Affects Brain Development.” MNT. 29 Oct. 2013. Web.

Better Eyes Due to Vitamin D Intake

For many years vitamin D has been know as a bone builder.  It also helps prevent, osteoporosis and rickets in children.  All over the world, research is constantly being implemented to study the effects of Vitamin D but here recently research is being conducted to show how it help the eyes stay young even when your age.  These new studies have shown that Vitamin D is centered on fighting the effects of vision loss   as your eyes age.

The newest report from Neurobiology of Aging states that through a study at the Institute of Ophthalmology at University College London, they have found a favorable outcome to their research. Even though, the University is still in the process of working with animals they have created some encouraging results. They have found that vitamin D helps the aging process in your eyes in two main ways. The first area helps to reduce inflammation by lowering the amount of macrophages.  The second area helps to decrease the deposits of deadly molecules that would gather in your system as you age. This study was conducted on individuals around the age of fifty.

The findings from the university were encouraging because when the macrophages and toxic molecules mix they produce age related macular degeneration, which is the leading cause of blindness for individuals over fifty years of age. Vitamin D can be absorbed in many ways but your daily diet is a good way to start.  Such foods could include but are not limited to liver, salmon, tuna fish, and fortified milk. The main source of vitamin D we receive is by UV radiations from the sun.  These examples are ways of fighting the effects of aging eyes.

 

Green, Robert. “Vitamin D and the Effects on your Eyes.” Eye Specialists. 31, Jan. 2012.  30 Jan. 2014

< http://eyesfl.com/blog/vitamin-d-and-the-effects-on-your-eyes/ >

 

Pelino, J. Carlo, and Joseph J. Pizzimenti. “Vitamin D Comes to light.” Review of Optometry 15 Nov. 2013: 76-79

 

 

Osteoporosis: A New Possible Treatment

When we are young, our mothers always stress to us that we need to drink our milk so that our bones grow to be strong and healthy. What we don’t realize at the time is that our mom is right. When we are young, our bones grow and grow until we become an adult. What happens next is the question. According to Gerard Tortora and Bryan Derrickson, “osteoporosis affects 10 Million people a year in the United States” (Tortora and Derrickson 203). Osteoporosis is a bone disorder where your bones start to loose bone mass due to your body losing calcium. Osteoporosis primarily affects middle-aged and elderly women (Tortora and Derrickson  203).

Dr. Rhut believes he has found a way to use hormones in the body to help fight osteoporosis. In recent studies that Dr. Rhut has done, he has found that by using negative allosteric modulators to release parathyroid hormones into the bloodstream, this will stimulate new bone formation. When your concentration of calcium is too low, your body senses this. It will then release PTH. This will raise your calcium concentration until the calcium sensing receptors on the parathyroid cell are activated. Once activated, it reduces PTH release (arthritis foundation).

The negative allosteric modulators will take a quite a few more years before they will be passed to use on patients. If passed, this will definitely help cut down on the amount of people that have osteoporosis. This will reduce the risk of so many hip fractures, or fractures in general, in the elderly population. This will also help with bone shrinkage, height loss, hunched backs, and bone pain (Tortora and Derrickson).

 

 

Tortora, Gerard J., and Derrickson, Bryan. Principles of Anatomy & Phisiology .13th ed.  Hoboken:

John  Wiley & Sons, Inc., 2011. Print.

“Turning on Hormones to Fight Osteoporosis.” Research Alert. Arthritis Foundation, 2008. Web. 6 Oct.

2013.

Osteoporosis: A New Possible Treatment

When we are young, our mothers always stress to us that we need to drink our milk so that our bones grow to be strong and healthy. What we don’t realize at the time is that our mom is right. When we are young, our bones grow and grow until we become an adult. What happens next is the question. According to Gerard Tortora and Bryan Derrickson, “osteoporosis affects 10 Million people a year in the United States” (Tortora and Derrickson 203). Osteoporosis is a bone disorder where your bones start to loose bone mass due to your body losing calcium. Osteoporosis primarily affects middle-aged and elderly women (Tortora and Derrickson  203).

Dr. Rhut believes he has found a way to use hormones in the body to help fight osteoporosis. In recent studies that Dr. Rhut has done, he has found that by using negative allosteric modulators to release parathyroid hormones into the bloodstream, this will stimulate new bone formation. When your concentration of calcium is too low, your body senses this. It will then release PTH. This will raise your calcium concentration until the calcium sensing receptors on the parathyroid cell are activated. Once activated, it reduces PTH release (arthritis foundation).

The negative allosteric modulators will take a quite a few more years before they will be passed to use on patients. If passed, this will definitely help cut down on the amount of people that have osteoporosis. This will reduce the risk of so many hip fractures, or fractures in general, in the elderly population. This will also help with bone shrinkage, height loss, hunched backs, and bone pain (Tortora and Derrickson).

 

 

Tortora, Gerard J., and Derrickson, Bryan. Principles of Anatomy & Phisiology .13th ed.  Hoboken:

John  Wiley & Sons, Inc., 2011. Print.

“Turning on Hormones to Fight Osteoporosis.” Research Alert. Arthritis Foundation, 2008. Web. 6 Oct.

2013.

Fetal Bone Marrow Transplant

Bone marrow transplants are procedures that involve transplantation of hematopoietic stem cells. It is mainly done on people with bone marrow or blood cancer and even some diseases. Bone marrow transplants are very dangerous and have many complications; it is mainly for patients with life threatening diseases. The reason why this is very dangerous is because you really don’t have an immune system because of all the chemotherapy and radiation you have to go through. When you kill the immune system you are more vulnerable to viruses, but it also gives the new bone marrow a better chance to work. It is like that saying, a clean slate. If you try to do a transplant with cancer cells the transplant has a less chance of taking because it does not have any good cells to work with and the immune system would see the good marrow as bad marrow and attack it.  Now I am going to tell you why fetal bone marrow is the best source of stem cells for transplantation.

A study done by Maria Michejda, a Ph.D at Georgetown, found out that fetal bone marrow, from spontaneous abortions, is eight times more effective than umbilical cord blood, and twenty-three more times effective than adult bone marrow, for bone marrow transplantation. The reason for this is because fetal bone marrow contains the highest concentration of CD34+ cells, which is just the cells that are responsible for creating new blood cells, and it also contains the lowest concentration of CD-3. CD-3 cells are the cells that identify and reject foreign tissue. CD-3 cells are the main reasons transplants do not work.

Fetal bone marrow transplants will begin to change the way people do things. Before you start to think that fetal bone marrow comes from living babies think again. Fetal bone marrow does not put babies in pain or anything because it is not taken from them; it is taken from spontaneous abortions. Now when women have miscarriages they can take the bone marrow and save it for people that needs transplants. This will benefit the world in the long run because most bone marrow will accept FMB, instead of treating it like a foreign object. So this will cause more people to recover from bone marrow transplants instead of reject it and die

 

Bibliography

http://www.sciencedaily.com/articles/b/bone_marrow_transplant.htm

Bone Marrow Transplant.” ScienceDaily, 6 Jun. 1997. Web. 6 Oct. 2013.

 

http://en.wikipedia.org/wiki/Bone_marrow_transplant

Bone Marrow Transplant.”Wikipedia, 6 Jun. 1997. Web. 6 Oct. 2013.

 

http://www.sciencedaily.com/releases/1997/06/970606123807.htm

Transplantation.” ScienceDaily, 6 Jun. 1997. Web. 6 Oct. 2013.