Showing posts with label Biology. Show all posts
Showing posts with label Biology. Show all posts

Saturday, March 26, 2011

Stem Cell Therapy in India


Stem Cells

  • Stem cells are the building blocks of our blood and immune systems.
  • They form the white cells (white blood corpuscles) that fight infection, red cells (red blood corpuscles) that carry oxygen and platelets that promote healing.
  • Stem cells are present in our bone marrow and they generate new cells throughout our lives.
  • Other than bone marrow, the blood in the umbilical cord also has stem cells (and this is why the reference to India’s childbirth).
  • It can be also used as a source of cells for transplants quite like the bone marrow stem cells.
  • The major advantage is that umbilical cord blood stem cells are easier to gather than stem cells from the bone marrow.
  • They have the unique ability to regenerate/reproduce into over 200 types of tissues. Above all, such stem cells, collected from the umbilical cord of your child, can be frozen and kept in a bank, which can be used later.

  • There are two types of stem cells in mammals
    • Embryonic stem cells
    • Adult stem cells
  • Stem cells are mainly found in blood from the umbilical cord and the bone marrow
  • Due to their self-renewing nature, stem cells are very important for treatment of diseases

Importance of stem cells
  • For a cell to be characterised as a stem cell, it must exhibit the following properties
    • Self renewal: the ability to go through numerous cycles of cell division while maintaining the undifferentiated state
    • Potency: the capacity to differentiate into specialised cell types
  • In developing embryos, stem cells can differentiate into all of the specialised embryonic tissues
  • In adult organisms, stem cells act as a repair system for the body, replenishing specialised cells
  • Stem cells also maintain the normal turnover of regenerative organs such as blood, skin or tissues
  • Stem cells can be grown and transformed into specialised cells of various tissues such as muscles and nerves using cell culture
  • Stem cell treatment holds the potential of transforming human medicine, wherein stem cells introduce new cells into damaged tissue in order to treat a disease or injury
  • The ability of stem cells to self renew and differentiate offers the potential to replace diseased and damaged tissue without the risk of rejection or side effects

  • What is special about stem cells compared to other cells in the body (the somatic cells)?
Somatic cells have become specialized for the jobs they have to perform to keep the “body machine” working properly. Stem cells have the ability to become a variety of cell types in a lineage with embryonic stem cells being able to become all cell types. New methods have led to re-programming of cells to be “stem-like” in their behavior, biomarkers, and their ability to become other cell types.

How are Stem Cells stored?

Stem cells, which hold the promise of new cell-based therapies to treat critical medical conditions, have to be effectively stored until it’s time to use them. The method is called cryopreservation: it freezes stem cells at temperatures below -150 o C, by immersing them in nitrogen vapour. But if the cells are to survive this process, they need to be frozen using a protective compound called a cryoprotectant, which is found to be toxic and can cause serious side-effects when administered. Research is on to find alternative, non-toxic compounds as protective agents of a technology which could rid the world of many diseases. In the past few years, it has become a norm to harvest the umbilical cord blood just after birth, as a guarantee of health for the child.

Current stem cell treatments
  • Currently, stem cell treatment is available to treat the side effects of chemotherapy on cancer patients, such as leukaemia or lymphoma
  • During chemotherapy most growing cells are killed by cytotoxic agents
  • These agents kill not only the leukaemia cells but also healthy haematopoietic stem cells in adjacent bone marrows.
  • Using stem cell therapy, healthy bone marrow stem cells are used to reintroduce healthy stem cells to replace those lost in the treatment
  • In Jan 2009, the US Food and Drug Administration (FDA) gave clearance to Geron Corporation for the first clinical trials of an embryonic stem cell therapy on humans. The trial will evaluate the efficacy of the drug GRNOPC1 on patients with spinal cord injury

Public stem cell bank
In Europe and in the United States many private stem cell banks like LifeCell operate as dual banks; that is as a private bank where individuals keep their stem cells by paying an amount, and also a public stem cell bank from where anybody can buy stem cells if they can.

LifeCell is India’s first such private stem cell bank, where you can store the umbilical cord of your child for a fee, for future use. They are planning for the first time in the country to have a public stem cell bank also.
K
Important milestones in stem cell research
  • 1963: Ernest McCullogh (Canada) and James Till (Canada) illustrate the presence of self renewing cells in the bone marrow
  • 1968: Bone marrow transplant between two siblings successfully treats Severe Combined Immunodeficiency (SCID)
  • 1978: haematopoietic stem cells discovered in human blood
  • 1998: James Thomson (USA) derives the first human embryonic stem cell line
  • 2001: Scientists at Advanced Cell Technology (USA) clone first early human embryos for the purpose of generating embryonic stem cells
  • 2006: Scientists at Newcastle University (England) create first every artificial liver cells using umbilical cord blood cells
  • 2008: Robert Lanza and colleagues at ACT create first human embryonic stem cells without destruction of the embryo

India is one of the most advanced nations in the world in terms of their aggressive research and implementation of stem cell therapy. The Indian parliament is debating their laws, but stem cell therapy is currently minimally regulated and is legal. There are numerous diseases that are treated with stem cell therapy in India, ranging from heart disease to cancer and spinal cord injuries.  

Overview of stemcell treatments in India

Is stemcell therapy legal in India?

According to the Indian Council of Medical Research, all stem cell therapy in India is considered to be experimental, with the exception of bone marrow transplants. However, the guidelines that were put into place in 2007 are largely non-enforceable. Regardless, stem cell therapy is legalized in India. 
Umbilical cord and adult stem cell treatment are considered permissible. 
Embryonic stem cell therapy and research is restricted.

Diseases being treated with stemcell therapy in India


The following is a partial list of diseases treated with stem cell therapy in India:
 
  • Spinal Cord Injury
  • Vitiligo
  • End Stage Liver Disease
  • Critical Limb Ischemia
  • Parkinson’s Disease
  • Psoriasis
  • Avascular Necrosis
  • Motor Neuron Disease (MND)
  • Alzheimer's
  • Cancer
  • Arthritis
  • Cerebral Palsy (CP)
  • Diabetes
  • Autism
  • Orthopedic degenerative disorders

Success rates of stemcell treatment in India

There is about a 60% to 80% overall success rate in the use of stem cell therapy in both India and around the world. However, success rates vary depending on the disease being treated, the institute conducting the procedures, and the condition of the patient. 
In order to receive complete information you will have to contact the medical institutes and ask specific questions concerning the patient's condition.

Monday, June 7, 2010

Wilson's Disease: Inherited Disease of Toxic Copper Accumulation

Due to a failure of copper excretion in the liver, toxic levels of copper build up and cause damage to the liver and central nervous system.

http://www.chemgapedia.de/vsengine/media/vsc/de/ch/4/cm/komplexe/bilder/kf2.jpg
Wilson's disease or Wilson disease or hepatolenticular degeneration is an inherited disorder involving toxic accumulation of copper in the liver and the central nervous system (CNS). Accumulation in the CNS usually occurs in the sites of the basal ganglia and globus pallidus. These symptoms are all due to a failure of copper excretion by the liver.

Genetics of Wilson Disease

The incidence of Wilson's disease is 3 in 100 000. It is an autosomal recessive disorder where there is a mutation on the ATP7B gene, an ATPase, which is a copper transporter on chromosome 13. There are many known mutations but the most common is HIS1069GLU which is most common in the European population.

Clinical Features of Wilson's Disease

Children can present with liver disease and this can be expressed as fulminant liver failure, hepatitis, or cirrhosis. In young adults, one can see CNS signs such as tremor, dysarthria, dysphagia, dyskinesias, dystonias, dementia, and parkinsonism. They can also develop affective features such as depression or mania, labile emotions, fluctuating libido and personality changes. With regards to their cognition, memory can decrease and problem solving can become increasingly difficult. A famous sign of Wilson disease is the presence of Kayser-Fleischer rings, which are copper deposits in the iris.

Tests and Diagnosis of Wilson Disease

In patients with Wilson's disease, serum copper and serum caeruoplasmin are usually decreased. One can test with a 24 hour urinary copper excretion. Molecular testing is available to look for mutations in the ATP7B gene and to make a definitive diagnosis. Magnetic resonance imaging (MRI) is often used to look for signs of basal ganglia degeneration.

Management and Treatment of Wilson's Disease

Patients with Wilson's disease are on lifelong penicillinamine.

Penicillinamine is a metabolite of peniciliin but it has no antibiotic properties. It is a chelating agent that binds to accumulated copper and is then eliminated through the urine. Some possible side effects of penicillinamine are nausea, rash, low white cell count, anemia, thrombocytopenia, and haematuria.
Reblog this post [with Zemanta]

Tuesday, December 1, 2009

Dose (Biologists)

  1. Louis Pasteur  was a French chemist and microbiologist best known for his remarkable breakthroughs in the causes and prevention of disease. His experiments supported the germ theory of disease, also reducing mortality from puerperal fever (childbed), and he created the first vaccine for rabies. He was best known to the general public for inventing a method to stop milk and wine from causing sickness - this process came to be called pasteurization. He is regarded as one of the three main founders of microbiology, together with Ferdinand Cohn and Robert Koch. He is also credited with dispelling the theory of spontaneous generation with his experiment employing chicken broth and a goose neck flask. He also made many discoveries in the field of chemistry, most notably the asymmetry of crystals. He is buried beneath the Institut Pasteur, an incredibly rare honor in France, where being buried in a cemetery is mandatory save for the fewer than 300 "Great Men" who are entombed in the Panthéon.
  2. Norman Ernest Borlaug is an American agricultural scientist, humanitarian, Nobel laureate, and has been called the father of the Green Revolution. Borlaug is one of five people in history to have won the Nobel Peace Prize, the Presidential Medal of Freedom and the Congressional Gold Medal.
  3. Alfred Russel Wallace, OM, FRS  was a British naturalist, explorer, geographer, anthropologist and biologist. He did extensive field work first in the Amazon River basin, and then in the Malay Archipelago, where he identified the Wallace line dividing the fauna of Australia from that of Asia.
  4. Johann Georg Adam Forster was a German naturalist, ethnologist, travel writer, journalist, and revolutionary. At an early age, he accompanied his father on several scientific expeditions, including James Cook's second voyage to the Pacific. His report from that journey, A Voyage Round the World, contributed significantly to the ethnology of the people of Polynesia and remains a respected work among both scientists and ordinary readers. As a result of the report Forster was admitted to the Royal Society at the early age of twenty-two and came to be considered one of the founders of modern scientific travel literature.
  5. Rosalind Elsie Franklin was a British physical chemist and crystallographer who made important contributions to the understanding of the fine structures of DNA, viruses, coal and graphite. Franklin is best known for her contribution to the discovery of the structure of DNA in 1953. In the years following, she led pioneering work on the tobacco mosaic and polio viruses. 
  6. Barbara McClintock was a pioneering American scientist and one of the world's most distinguished cytogeneticists. 
  7. Heinrich Hermann Robert Koch was a German physician. He became famous for the discovery of the anthrax bacillus (1877), the tuberculosis bacillus (1882) and the cholera bacillus (1883) and for his development of Koch's postulates. He was awarded the Nobel Prize in Physiology or Medicine for his tuberculosis findings in 1905. He is considered one of the founders of bacteriology.
  8. George Ledyard Stebbins, Jr. was an American botanist and geneticist who is widely regarded as one of the leading evolutionary biologists and botanists of the 20th century.
  9. Lynn Margulis is a biologist and University Professor at the University of Massachusetts Amherst. She is best-known for her theory on eukaryotic organelle genesis, the endosymbiotic theory, which is now accepted in the mainstream as the explanation for how certain organelles were formed.
  10. Gregor Mendel  was an Austrian monk who is often called the "father of genetics" for his study of the inheritance of traits in pea plants. Mendel showed that there was particular inheritance of traits according to his laws of inheritance. The significance of Mendel's work was not recognized until the turn of the 20th century.

Thursday, November 5, 2009

List of Tiger Reserves in India

State ↓Tiger Reserves ↓Year Estd. ↓Total Area (km2) ↓Management status ↓Remarks ↓
AssamKaziranga Tiger Reserve2006859goodGood tiger density
AssamManas Tiger Reserve1973-742840poorPoor tiger density, Recovering from prolonged disturbance due to Bodounrest
AssamNameri Tiger Reserve1999-2000344satisfactoryEncroachment and tree cutting by locals
Arunachal PradeshNamdapha Tiger Reserve1982-831985poorLow tiger density, Extremism , encroachment by Lisus
Arunachal PradeshPakhui Tiger Reserve1999-2000862goodGood tiger density
Andhra PradeshNagarjunsagar-Srisailam Tiger Reserve1982-833568poorLow tiger density Left wing extremism
BiharValmiki Tiger Reserve1989-90840PoorLow tiger density extremism
ChhattishgarhIndravati Tiger Reserve1982-832799poorSeverely affected by Naxalites, Out of bounds
JharkhandPalamau Tiger Reserve1973-741026PoorLow tiger density Left wing extremism
KarnatakaBandipur Tiger Reserve1973-74866goodGood tiger density
KarnatakaNagarhole (extension) Tiger Reserve1999-2000643goodGood tiger density
KarnatakaBhadra Tiger Reserve1998-99492satisfactoryLow tiger density
KeralaPeriyar Tiger Reserve1978-79777goodLow tiger density due to ecological reasons
Kerala/Tamil NaduAnnamalai-Parambikulam Tiger Reserve20081410goodModerate tiger density
Madhya PradeshBandhavgarh Tiger Reserve1993-941162goodGood tiger density
Madhya PradeshBori-Satpura Tiger Reserve1999-20001486satisfactoryPoor tiger density
Madhya PradeshKanha Tiger Reserve1973-741945goodGood tiger density
Madhya PradeshPanna Tiger Reserve1994-95542poorLocal extinction of tiger due to poaching, dacoit infestation
Madhya PradeshPench Tiger Reserve1992-93758goodGood tiger density
Madhya PradeshRatapani Tiger Reserve2008-09674
MaharashtraMelghat Tiger Reserve1973-741677poorLow tiger density
MaharashtraPench Tiger Reserve1992-93257satisfactoryModerate tiger density
MaharashtraTadoba-Andhari Tiger Reserve1993-94620satisfactoryModerate tiger density, High rate of man tiger conflicts
MaharashtraShahayadri Tiger Reserve2008-09569
MizoramDampa Tiger Reserve1994-95500poorLow tiger density due to ecological reasons
OrissaSimlipal Tiger Reserve1973-742750poorIow tiger density, Left wing extremism
OrissaSunabeda Tiger Reserve2008-09856
RajasthanRanthambhore Tiger Reserve1973-741334goodGood tiger density
RajasthanSariska Tiger Reserve1978-79866poorRecovering from local extinction of tiger due to poaching
Tamil NaduKalakad-Mundathurai Tiger Reserve1988-89800satisfactoryLow tiger density due to ecological reasons
Tamil NaduMudumalai National Park2008321satisfactoryModerate tiger density
Tamil Nadu/KeralaAnnamalai-Parambikulam Tiger Reserve20081410goodModerate tiger density
Uttar PradeshDudhwa Tiger Reserve1987-88811satisfactoryGood tiger density, Poaching along borders
Uttar PradeshPilibhit Tiger Reserve2008-091089
UttaranchalCorbett Tiger Reserve1973-741316goodGood tiger density
West BengalBuxa Tiger Reserve1982-83759poorLow tiger density offences by jobless tea plantation workers
West BengalSunderbans Tiger Reserve1973-742585goodGood tiger density
ChattisgarhUdanti & Sitanadi Tiger Reserve20081580poorLow tiger density
OrissaSatkosia Tiger Reserve2007988poorLow tiger density
ChattisgarhAchanakmar Tiger Reserve2008963poorLow tiger density
KarnatakaDandeli-Anashi Tiger Reserve2007875satisfactoryLow tiger density
Madhya PradeshSanjay National Park & Sanjay Dubri Wildlife Sanctuary Guru Ghasidas National Park2008831poorVery low tiger density
KarnatakaBanerghatta tiger and lion reserve1978104not a Project Tiger reserve