Category Medical World

How do MRNA vaccines work?

A shot in the arm!

Vaccines have helped control many infectious diseases. But developing them is not easy and also takes years. With researchers working tirelessly for months together, what seemed like an endless wait for a vaccine against COMD-19 has given way to hope with the UK approving the Pfizer/ BioNTech vaccine for the coronavirus. COVID-19 has claimed over 1.5 million lives worldwide

Pfizer’s BNT162b2, which took only 10 months from conception to approval is an MRNA vaccine approved for use in humans for the first time. The vaccine has been shown to be 95% effective in preventing COMD-19. It needs to be stored in bones containing dry ice that are capable of staying at -70 degrees Celsius, the frigid temperature needed to preserve the drug. Besides the U.K., other countries such as Bahrain Canada, Saudi Arabia, Mexico, Israel and the U.S. have approved the emergency use of the Pfizer vaccine.

What is an MRNA vaccine?           

Vaccines work by priming the body to recognise and fight the proteins produced by disease-causing organisms. Instead of using an inactivated coronavirus or viral proteins in a vaccine, an MRNA vaccine uses a messenger RNA, or MRNA, to prompt an immune response in the body. An MRNA is a synthetic genetic material, a copy of a natural component of living cells. An mRNA vaccine carries genetic instructions, which direct cells in the body to make viral proteins that prime the immune system to produce protective antibodies. If these antibodies adhere to a virus, it cannot enter the cells to replicate.

Are they safe?

MRNA vaccines are said to be safer than live vaccines, as there is a risk of the virus reverting to a dangerous form with the latter. MRNA vaccines are not likely to produce unwanted reactions. Besides, they can be made much faster than the traditional vaccines.

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How do hearing aids work?

A hearing aid, which consists of a microphone, amplifier, and speaker, makes sound louder for the user.

A hearing aid is a small electronic or digital medical device designed to help people who are hard of hearing. It makes sound louder for the user.

A hearing aid basically consists of three parts- a microphone, amplifier, and speaker. The microphone collects the sounds from the user’s environment and converts the sound waves into electrical (or digital) signals. The amplifier magnifies the power of the signals and then sends them to the inner ear through a speaker.

Those with a hearing disability have damaged hair cells in the inner ear. The surviving hair cells detect the sound vibrations magnified by the hearing aid and transmit them to the brain. However, if the hair cells are too damaged, then a hearing aid may be ineffective.

Hearing aids are available in various styles. The most common ones known as behind-the-ear (BTE) aids, consist of plastic cases worn behind the ear, which contain the electronic parts. The cases are connected with a narrow tube to the earmold which is inserted inside the ear. Smaller hearing aids in the form of earmolds that fit in snugly inside the ear are almost invisible to others like in-the-ear (ITE), in-the-canal (ITC) and completely-in-canal (CIC) aids.

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What are the achievements of T Govindaraju?

T Govindaraju has made significant contributions in the medical field. He is a professor in the Bioorganic Chemistry Laboratory at the Jawaharlal Nehru Centre for Advanced Scientific Research (JNCAR), Bengaluru. Bioorganic Chemistry uses chemical methods in the study of biological processes.

Prof. Govindaraju is from a remote village in Karnataka. As a school boy, he saw that mentally ill patients were treated cruelly. This image guided him to choose his area of research. He completed his PhD from CSIR-NCL. He then did post-doctoral research in the U.S and Germany. His research was on neuro degenerative diseases and cancer. Neuro degenerative diseases occur when cells in the central nervous system stop working.

You must have also heard about Alzheimer’s disease. This occurs when the brain becomes small and the brain cells die. Prof. Govindaraju and his team discovered a new molecule -TGR63 which could be the future drug to treat Alzheimer’s. A Delhi based pharma company has obtained the rights to do its trial runs.

Prof. Govindaraju found the similarities between Alzheimer’s disease and cancer and this led to the discovery of TGP 18, another molecule-based drug. This could be used to treat lung cancer.

He was a Humboldt research fellow in Germany and a visiting faculty at the University of Paris, France. He is also keen on raising the standards of rural schools and has been a part of outreach initiatives. He is also into bringing awareness about mental illness among school children in Karnataka and other states.

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How did Wilson Greatbatch invented the pacemaker?

Quite by accident, American engineer Wilson Greatbatch invented the implantable cardiac pacemaker in the year 1958. Read on to know how….

An artificial pacemaker is a small battery-operated electronic device that’s placed under the skin in the chest to help control the heartbeat. The first successful implantable pacemaker was invented in 1958 by an American electrical engineer, Wilson Greatbatch. He was making a heart rhythm recorder when, by mistake, he added a wrong electronic component. He was shocked when the device, instead of simply recording the sound of the heartbeat, produced electronic pulses quite similar to the sounds made by a healthy heart.

It struck him then that the device could make an unhealthy heart beat in rhythm by delivering electrical pulses to make the heart muscles contract and pump blood. For two years he worked on modifying the device. He miniaturised it, coated it with a kind of resin to prevent it from getting damaged by body fluids, and powered it with a mercury-zinc battery.

Greatbatch discussed his invention with surgeon William Chardack, whom he met in a chance encounter. In 1960, the Chardack-Greatbatch pacemaker was implanted in an elderly man with an irregular heartbeat. The patient’s life was extended by 18 months.

Pacemakers today are about the size of a bullet. They are encased in titanium and keep the heart ticking with regular beats through computer-guided electrical pulses. They are inserted through the leg up into the right ventricle. Their batteries can last from 5 to 15 years.

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Scientists create first ‘synthetic embryo’

In a research breakthrough, scientists have created world’s first synthetic embryo with a brain and a beating heart. The scientists used only stem cells to create synthetic mouse embryo models. Replete with a beating heart, and a brain, the embryo was created sans sperm, eggs and fertilisation.

The feat was achieved by researchers from the University of Cambridge. The team was led by Professor Magdalena Zernicka-Goetz. The result was the creation of a beating heart and brain. The work is the result of decades-long research.

The new findings will aid in reaching a better understanding about how tissues are formed during the natural course of development, that is in the case of natural embryos.

The breakthrough is key because it opens new frontiers for learning how the stem cells form into organs in the embryo. In the future, this could help grow organs and tissues using synthetic embryo models. They are called synthetic embryos as they are made without fertilised eggs. This will be a game-changer for human organ transplantation as transplantable tissues can be created thus.

“Our mouse embryo model not only develops a brain but also a beating heart, all the components that go on to make up the body,” said Zemicka-Goetz, Professor in Mammalian Development and Stem Cell Biology in Cambridge’s Department of Physiology, Development and Neuroscience in a release issued by the university.

“The stem cell embryo model is important because it gives us accessibility to the developing structure at a stage that is normally hidden from us due to the implantation of the tiny embryo into the mother’s womb. This accessibility allows us to manipulate genes to understand their developmental roles in a model experimental system.” Zernicka-Goetz added in the release.

For the development of the synthetic embryo, cultured stem cells representing the types of tissues were put together in a suitable environment that aided in their growth. One of the major achievements of the study is the growth of the entire brain, especially the anterior part of the brain.

The present research was being carried out in mouse models and the researchers plan to develop human models. This will aid in studying those aspects of the organs that would not be possible in real embryos.

The researchers are also developing an analogous model of the human embryo to further their studies. This is crucial as all these findings can help understand why some human pregnancies fail.  The understanding at the embryo level is crucial as the majority of human pregnancies fail at the developmental stage.

WHAT ARE STEM CELLS?

Our body is home to hundreds of types of cells. A majority of them begin as stem cells. They carry within them instructions to develop into specialised cells such as muscle, blood or brain cell. In short, stem cells are human cells that grow into different cell types ranging from brain cells to nerve cells. They can be used to treat damaged tissues. Stem cell-based therapies are being carried out for serious medical conditions such as Alzheimer’s, Parkinsons’ and other genetic disorders.

MAJOR BREAKTHROUGHS IN STEM CELL RESEARCH

1981:  Embryonic stem cells identified in mice for the first time by Martin Evans of Cardiff University, UK.

1997:  The first artificial animal clone, Dolly the sheep, created. It was a turning point in stem cell research.

1998:  Human embryonic stem cells were isolated and grown in the lab. 2007 The Nobel Prize in Medicine, 2007, was given to Mario R. Capecchi, Sir Martin J. Evans and Oliver Smithies “for their discoveries of principles for introducing specific gene modifications in mice by the use of embryonic stem cells.”

2012:  Human embryonic stem cells used in two patients. It helped improve their vision.

2022:  The Ogawa-Yamanaka Stem Cell Prize was awarded to Juan Carlos Izpisua Belmonte for his work on cellular rejuvenation programming aimed at improving age-associated diseases.

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WHAT IS A BILDUNGSROMAN?

A bildungsroman is a testament to how literature deals with the souls of individuals. It highlights how our lives are a multi-dimensional confluence of revenge, tragedy, comedy, and satire, seasoned with age and made amicable by experience.

A bildungsroman is a jargonic term used for a coming-of-age story. It is a literary genre that focusses on the protagonist’s spiritual journey from a point in his or her childhood to adulthood. Coined in 1819 by Karl Morgenstern a philologist, this term is a combination of two German words ‘Bildung’ meaning education, and Roman’ which means “novel.” The first book to ascribe to this genre was Wilhelm Meister’s Apprenticeship by Johann Wolfgang Goethe. Published in 1796, this German classic records the titular character Wilhelm Meisters journey to self-discovery through the medium of theatre and art.

The Shift

Literary works of this genre are character-centric and lay special emphasis on the shifts in prespective that accompany life-altering experiences and help mould a more realistic worldview of the character.

A bildungsroman is a testament to how literature deals with the souls of individuals. It highlights how our lives are a multi-dimensional confluence of revenge, tragedy, comedy, and satire, seasoned with age and made amicable by experience. Some popular literary works of this genre include To Kill a Mockingbird by Harper Lee. The Diary of a Young Girl by Anne Frank, David Copperfield by Charles Dickens, The Harry Potter series by J. K. Rowling, and The Lord of the Ring” series by J. R. R. Tolkien.

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THE CURIOUS CASE OF EMM NEGATIVE

India has reported its first case of EMM negative blood. What is unique about the type? Why does it not find a place in the existing blood groups?

IN SCHOOL DESK

One of the first things that schools ask when students enroll is their blood group. This crucial information is added to the identity card and student files so that, in case of a medical emergency, the information is available at hand. But can you imagine a scenario when a lab is unable to identify your blood group because it is extremely rare? That’s what happened when a 65-year-old man in Gujarat who had gone for cardiac treatment, tried to find out his blood group.

Even specialists were left puzzled as his blood sample did not seem to match others. The patient needed to know his blood group in order to have a compatible donor who could give him blood for a heart surgery. Only after a long ordeal ending with his blood sample being sent to the United States for testing, did the man find out that he had EMM negative blood. He is the first recorded case in India to have such a blood type and the tenth in the world. The blood group has been assigned with the symbol ISBT042.

What are blood types?

Blood is characterised into types to prevent adverse reactions during blood transfusions. In general, we know of the blood types A, B, O or AB. Further, these groups take on a negative or positive factor.

However, there are 42 different types of blood systems, including A, B, O, Rh, and Duffy. The names come from the ABO antigens, which are basically protein molecules that are found on our red blood cells. In most blood groups, EMM is present. But there are rare cases where EMM is negative.

In the case of the Gujarat man, even his children’s blood samples were not a perfect match and he could have had a reaction if their blood was given to him.

Why is the ISBT042 blood type so rare?

Understanding the Emm antigen has been a struggle even for scientists. But by studying those with the blood type and comparing their samples with those of relatives, scientists have found that a deletion in a gene could be responsible for the blood type. People with EMM negative blood group can’t donate blood to anyone or accept blood from anyone.

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What is ASMR (AUTONOMOUS SENSORY MERIDIAN RESPONSE)?

It refers to the tingling sensation one experiences due to various kinds of feel-good sounds.

Autonomous sensory meridian response (ASMR) is a term that describes a spontaneous, enjoyable, and relaxing tingling sensation that begins in the scalp and radiates down the spine to your upper back shoulders, and legs. The sensation is triggered by various stimuli such as gentle whispering, brushing hair, soft finger tapping, crumpling or folding of paper, etc. The term was coined by Jennifer Allen in 2010 when she formed a Facebook group dedicated to ASMR. It is colloquially known as ‘brain massage, head tingle, brain tingle’, or ‘spine tingle. ASMR is being currently studied by scientists and psychologists.

According to an ongoing online survey, ASMR is experienced by people of all ages across the globe irrespective of race or culture, suggesting it is a sa biological response. So far scientists can’t explain why it works for many people or why it doesn’t affect some people. ASMR has, of late, become a YouTube phenomenon with millions of ASMR videos flooding the Internet. They feature someone talking softly, making soothing sounds, gently scratching various surfaces with fingernails, etc. People watch these videos to induce sleep or relaxation. However, professionals caution against depending much on ASMR, as its drawbacks, if any are yet to be fully ascertained.

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WHAT IS RED LIST INDEX?

Put together by the International Union for the Conservation of Nature (IUCN), the IUCN Red List tells us how likely it is for a species to go extinct (such as EN – endangered, VU vulnerable, etc.). But the list does not offer insights into meaningful trends in the status of biodiversity. To address this, the Red List Index (RLI) has been created to show trends in the status of groups of species based only on genuine improvement or deterioration. Right now, RLI is available for birds, mammals, amphibians, cycads (vascular plants), and corals.

Sampled approach

Producing indices of change in extinction risk by comprehensively assessing whole species groups, while feasible for well studied groups with relatively few species, is not suitable for all taxonomic groups. Assessing every species in the larger and lesser known groups which comprise the majority of the world’s biodiversity, such as fungi, invertebrates (particularly insects) and plants, is not practical.

The Red List Index (sampled approach) (SRLI) has been developed in order to determine the threat status and also trends of lesser-known and less charismatic species groups. It is a collaboration between IUCN members and is coordinated through the Institute of Zoology (IoZ), the research division of the Zoological Society of London (ZSL). The SRLI is based on a representative sample of species selected from taxonomic groups within animals (invertebrates and vertebrates), fungi and plants.

Assessment of the selected species will provide baseline information on the current status of biodiversity. Reassessment at regular intervals will identify changes in threat status over time to provide a more broadly representative picture of biodiversity change.

Applications

The aim is that the SRLI will aid in the production of a global biodiversity indicator capable of measuring whether the rate of biodiversity loss has been reduced. In addition, it will help to develop a better understanding of which taxonomic groups, realms or ecosystems are deteriorating the most rapidly, why species are threatened, where they are threatened, what conservation actions exist and which actions are needed. The aim is to provide policy makers, resource managers, scientists, educators, conservation practitioners and the general public with more thorough knowledge of biodiversity change and further tools with which to make informed decisions.

In April 2002 at the Convention on Biological Diversity (CBD), 188 Nations committed themselves to actions to: “… achieve, by 2010, a significant reduction of the current rate of biodiversity loss at the global, regional and national levels…” The RLI has been adopted by the CBD as one of the indicators to measure progress towards this important target, and specifically to monitor changes in threat status of species.

Credit : Wikipedia

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HOW DOCTORS STARTED USING STETHOSCOPES TO DIAGNOSE PROBLEMS WITH THE CHEST?

The practice of using stethoscopes started in a hospital in Paris, in the early 19th Century.

The Necker-Enfants Malades Hospital in Paris provided specialised medical care. Rene Laennec, one of the doctors there, was trained to use sound to diagnose diseases of the chest.

One day in 1816, a young woman who had a heart problem came to consult Dr. Laennec. Ordinarily, the physician would have put his ear to the woman’s chest and listened to her heartbeats to detect if there was any aberration. But the woman who came to see Dr. Laennec was rather plump. Uncomfortable with the idea of putting his ear to her chest, the doctor’s eyes fell on a newspaper lying there…and he got a brainwave!

He rolled the newspaper into a cylinder and applied one end of it to the region of the woman’s heart and the other to his ear. And then his own heart thumped in joy and excitement! He could hear her heartbeats more clearly than if he had put his ear directly to her chest. It was a landmark moment in medical science.

Laennec fashioned a hollow, wooden cylinder and catalogued the various sounds he could hear through it when applied to a patient’s chest, and what the sounds indicated about the health of the patient. He sent his findings to the Academy of Science, in Paris.

It was not long before his invention began to be used by physicians all over Europe.

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WHAT IS CRYOGENIC ELECTRON MICROSCOPY?

Did you know scientists hope to develop targeted drugs for hard-to-treat diseace using the technique?

Ultra high-definition 3D videos of cells inside the body taken by an advanced microscope are creating a revolution in modern biology. Previously, transmission electron microscope (TEM) images of living cells (called biomolecules) were indistinct blobs. This was because the high-energy electron beams would dry out the water surrounding the molecules and burn them.

In cryogenic electron microscopy (cryo-EM), biomolecules are cooled to extremely low temperatures and embedded in vitrified water (ice that has no crystals). This ensures that they are preserved intact. The three scientists who developed the cryo-EM technique won the 2017 Nobel Prize in Chemistry.

The current level of sophistication in the cryo-EM technique is largely due to advances in camera technology, image processing and computer software. The biomolecules are photographed from thousands of different angles and at different stages. The images are put together to create a video, allowing researchers to see the structure of the molecules in live action within the cell.

Using this technique, scientists hope to develop targeted drugs for hard-to-treat diseases such as dementia and Parkinson’s.

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WHAT TYPE OF VACCINE IS R21?

Scientists behind the Oxford-AstraZeneca coronavirus shot have produced the vaccine. “This was by far a much more difficult vaccine to make work.” Adrian Hill, the Jenner Institute’s director, said in northern Tanzania on a visit to field trials of the R21/Matrix-M malaria vaccine.

While the coronavirus responsible for Covid-19 has 12 genes, Plasmodium-the parasite that causes malaria – has more than 5,000 genes. It’s an organism that infects the liver and bloodstream, infecting red blood cells.  Hill explains that R21/Matrix-M combines the R21 vaccine with a vaccine booster or adjuvant Matrix-M, which stimulates the human immune system to attack the parasite.  When an infectious mosquito feeds on a human being, it injects parasites in a form called sporozoites into the bloodstream, where they travel directly to the liver. The sporozoites divide rapidly, producing around 20,000 merozoites that rupture the liver cells and invade red blood cells.  R21 targets a circumsporozoite protein (CSP) present on the parasite’s surface during the sporozoite stage. CSP rarely mutates among the four strains of malaria parasites that infect humans. The human body does not readily react with a complete immune response to foreign proteins. The R21 focus on CSP boosted by the proprietary Novavax adjuvant- produces a more robust, better-targeted antibody response.  Clinical trials are now moving to the third phase in four countries across Africa – Mali, Tanzania, Kenya, and Burkina Faso.

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How surgeons smooth away the wrinkles?

As the skin ages, some of the subcutaneous or underlying fat which supports and pads it dissolves away. And one of the skin-s main constituents, called collagen, loses its ability to retain moisture, making the skin less elastic and drier. The result is sagging skin and wrinkles.

Most people accept wrinkles as part of growing older. For others, particularly those in the public eye like entertainers and politicians, ageing skin can be a problem. The only answer is cosmetic surgery.

There is more to cosmetic surgery than a face-lift — which, as its names suggests, means pulling the skin up over the face. Its cosmetic effects are, for the most part, restricted mostly to the chin and neck. Wrinkles around the eyes the side of the, nose, and across the forehead have to be dealt with in separate operations, such as an eyebrow or forehead lift, or a nasal fold removal. In blepharoplasty, excess loose skin is removed from the upper and lower eyelids.

Minor nips and tucks arc clone under local anaesthetic, bat a face-lift is a major

operation, and is usually done under general anaesthetic. The surgeon first makes an incision into the skin around each ear. He starts the cut well within the hairline above the ear, and continues it around the bottom of the ear and then up behind it. The cut is then taken horizontally towards the back of the head. Most of the cut is within the area covered by hair, so that the scars will be hidden.

Once the cuts are made, the surgeon carefully separates the skin below the line of the cut from the underlying fatty layer. He then pulls the loose skin towards the back of the head. The thin layer of muscle tissue in the neck is lifted and tightened. The excess skin is cut off and the incision sewn up.

 It often takes two to three weeks to recover from the slight inflammation of the face caused by the operation. The scars, which can be camouflaged by make-up a week after the operation, fade in time.

No face-lift retards ageing permanently. The ageing process continues from the time of the operation at the normal rate. More face-lifts can be performed on the same person but there is always a limit, because each time the surgeon removes more skin. When the skin is stretched to its tightest limit without hindering normal functions, such as smiling, there is no excess available and further operations become impossible. Not all operations are a success and some people have been left with badly scarred faces.

 

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What happens in a heart transplant?

When a heart becomes available, a suitable recipient is quickly located and told to get to the hospital immediately. At the same time, a combination of police, ambulance and helicopters race the donated organ to the hospital. A heart may travel hundreds of kilometres from donor to recipient, sometimes across international boundaries. But to save time, the European computerized system, Euro transplant, tries to locate recipients who live as close to the donor as possible.

To prepare a patient for a heart transplant, the surgeon cuts into the chest and ties off the blood vessels leading to and from the recipient’s heart. The recipient’s blood supply is then redirected through the heart-lung machine, which replaces the function of the patient’s own heart and lungs. The faulty heart is taken out, and the new organ is placed in the space. The new heart is then connected to the major veins and arteries before the recipient’s blood is diverted through the new organ. The surgeon then sews up the chest and the operation is complete.

 

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How a pacemaker helps a heart patient to lead a normal life?

The human heart beats 3000 million times in an average lifetime, pumping the equivalent of 48 million gallons (218 million litres) of blood around the body.

The regular rhythm — on average, 72 beats each minute — is controlled by the sino-atrial node, a tiny rounded organ located in the top left corner inside the heart. This is the heart’s natural pacemaker, which sends electrical impulses to the tissues. The heart contracts and heart’s expands in response to these impulses, producing the heartbeat.

Occasionally, the heart’s electrical con-ducting system can be disturbed by illness, such as angina or a heart attack. Sometimes it just fails completely. If this happens, the heart can be stimulated electrically to continue beating regularly.

If the heart stops it can sometimes be restarted with an electrical shock from a machine called a defibrillator. If the normal beat does not resume immediately, some-times a temporary pacemaker can be fitted outside the body — it is usually strapped to the waist. For those suffering from other irregularities of the heart beat a pacemaker is surgically placed inside the body, implanted in the chest.

 All pacemakers, inside and outside the body, work in the same way. An electrode on wire, called the end of a pacing lead, is attached to the wall of the heart’s right ventricle (chamber), either directly through the chest, or threaded through a vein. The electrode is powered by the pacing box, a miniature generator operated by lithium batteries. Modern pacemaker batteries last at least five years, and some last up to 12 years.

 Powered by the pacing box, the electrode produces electrical impulses which stimulate the sino-atrial node and make the heart beat. The pacing box is set to maintain the intervals of the impulses at a given rate, usually one beat per second, which is a little slower than the average heart rate. However, the box functions only when the heart is not producing its own electrical impulses at the correct intervals. It is sensitive enough to detect these delays and by filling in the gaps, maintains a normal rhythm. Some models include a radio transmitter and receiver, which means that a doctor can adjust the rate of the pacemaker from outside the patient’s body.

The first successful pacemakers were used by Dr Walter Lillehei, a cardiac specialist at the University of Minnesota, USA, in the late 1950s. They consisted of an electrode on a wire fed to the heart through the chest and attached to a battery pack strapped around the waist. The pack was about the size of a cigarette packet. Although the system was convenient because no surgery was needed to replace the batteries, the opening in the chest for the wire repeatedly became infected. External pacemakers are now used for temporary heart problems only, or until an internal pacemaker can be fitted.

The pacing box of the most commonly used internal pacemaker is about the size of a matchbox and weighs no more than 25g. It is usually made of lightweight titanium.

The box is implanted in the body, usually just inside the skin of the chest wall. It must be in the best position for threading the tube through the large vein to the heart and attaching the electrode, which is the size of a match head, to the heart wall. The body does not reject it because it is not living material.

The implanting operation is done while the patient is under general anaesthetic, but surgery to replace the batteries can usually be done with only a local anaesthetic.

 A person wearing a pacemaker needs to be examined by a doctor frequently to make sure that it is functioning properly. Also, some wearers have to take care that their pacemakers are not affected by certain electrical circuits, such as magnetic detectors in airports or libraries.

New electronic technology may produce even smaller pacemakers which can be attached to the heart wall, eliminating, wires and large battery packs, although!they are still powered by batteries.

 Another development is the rate-responsive pacemaker, which is sensitive to the patient’s activity. Instead of providing at impulse once a second, it will increase the impulses when he is active and slow them down when he is resting — like the heart, natural pacemaker.

Since the First successful pacemaker developed, more than 5 million people with serious heart disease have been helped to live more comfortable and active lives.

 

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How do anaesthetics numb pain?

Less than 150 years ago, surgery was performed without any anaesthetic. A patient was held down by strong men as he battled to escape from the pain of the surgeon’s knife. Surgeons even resorted to stupefying their patients with alcohol, knocking them unconscious, or freezing the part to be operated on with ice.

The first time an anaesthetic was used was on March 30, 1842, in Jefferson, Georgia, USA, when Dr Crawford Long removed a tumour from the neck of James Venable, who first inhaled ether. But it was only following William Morton’s public demonstration in Boston of the extraction of a tooth under ether, in 1846, that ether became widely adopted as an anaesthetic.

At around the same time in the United States, nitrous oxide, also known as laughing gas and used as a music hail entertainment, was being inhaled as an anaesthetic for dental surgery. In Britain. Research was being done on the uses of chloroform, particularly to relieve the pain of childbirth. Without these early attempts at the use of anaesthetics, many of today’s surgical procedures would not be possible. Now, major operations, such as heart trans; plants, cosmetic surgery and removal,01 cancer, are possible without pain. But just, how do anaesthetics allow people to slip off into a world where pain does not exist?

Anaesthesia derives from the Greek word for ‘lack of feeling’. All anaesthetics induce this condition by blocking the of pain signals to the brain. However, how they actually work is not yet fully understood.

Anaesthetics take two forms — general, which put the patient ‘to sleep’, and local, which affect only part of the body.

Loss of sensation, ox or analgesia may be provided by nitrous oxide, not put the patient to sleep. It may cause mental or physical excitement. Sleep is usually induced by an injected barbiturate. The muscles are then relaxed with a neuroblocker, or muscle relaxant, such as curare.

During surgery, the patient is watched so that any changes in circulation; so that any changes in circulation, breathing or kidney function which may result from the anaesthetic can be regulated.

Local anaesthetics are given as an injection to remove all sensation from and a localised area. The patient is conscious can cooperate with the surgeon.

There are three principal uses of local anaesthetic. Topical anaesthetics remove the sensation from nerve endings in mucous membranes such as those in the eye, the nose and the mouth. They are used, for example, to remove a foreign object from the eye. Nerve-block anaesthetics are injected into a nerve to anaesthetise a small area, for example, to enable a tooth to be extracted. Other anaesthetics are injected into a large nerve group to numb a larger part of the body, such as an arm.

Atoms that transmit pain

A clue to the way general anaesthetics work comes from research into local anaesthetics. These are known to interfere with the way nerve impulses are transmitted a along the nerve fibres. Sodium and potassium atoms play an important pa sending these impulses to the brain. If you stub your toe, for example, the sodium and potassium atoms pass in opposite directions across the membrane of the nerve cell causing the next cell to do the same and so on until the signal reaches the brain, when you feel pain. But local anaesthetics stop the atoms from passing in and out of the nerve cell, so no pain signal reaches the spinal cord.

 Scientists think that general anaesthetics may cause unconsciousness by suppressing the activity of certain enzyme in the nerve cells, or changing the prop of the nerve-cell membranes, or even by interacting with water molecules in the brain to form small crystals which affect the path of a signal along a nerve cell. Research. Continues into the exact -mechanism, but what is certain is that without anaesthetics a great deal of surgery could never he performed.

 

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How surgeons do bloodless operations with just a beam of light?

Until laser surgery was invented in 1963, someone with a growth, a cancer or a cataract, needed a major operation to have it removed. Now, laser beams can be used in ‘bloodless’ operations to remove growths and even repair tissues, without cutting, less painfully and more safely.

 In laser surgery to remove a growth from the throat, for example, a small tube, or endoscope, is passed down the patient’s throat, under local anaesthetic. A laser beam is directed down the tube along an optical fibre and is focused on the growth. All laser surgery works on this principle of passing light down an optical fibre. The beam is a form of light which carries a great deal of energy. The energy is absorbed by the tissues of the growth, or the skin tissues to be removed, which become hot. By controlling the heat intensity, doctors can burn off — literally vaporise — unwanted cells.

In this way, laser beams are used to cut away cancers, vaporise the dyes in tattoos or get rid of birthmarks.

Another use of laser beams is to heat tissues sufficiently to `weld’ them together — to stop blood vessels bleeding, for example. The operation might be per-formed on a patient who is bleeding from a stomach ulcer.

 The wavelength of the laser beam affects the way in which tissues respond to it. Lasers that use carbon dioxide produce beams of light which are absorbed by tissues at a depth of only 0.1mm. This means that they can be used to make fine cuts in tissue, as a sort of ‘laser scalpel’. Such precision cutting might be used when making incisions in the cornea of the eye to correct defects in sight, or in removing throat tumours.

 Lasers using a metal-based chemical called neodymium produce light which is absorbed by a greater depth of tissue, making it useful to destroy cancers.

Those lasers that use the gas argon produce a distinctive blue-green light, which is absorbed by haemoglobin — the chemical in the blood that gives it its red colouring. Argon beams can therefore be used where haemoglobin levels are high,, in birthmarks.

A further benefit of laser beams is that they allow doctors to reach areas of the body previously hard to get at with a scalpel and to perform operations that were impossible before: to rid arteries of block. Ages of fatty deposits; to sew back detached retinas; to cut a hole through a cataract in a lens and so restore vision; and to cure cancer of the cervix.

 

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How do doctors perform microsurgery?

On Christmas Eve in 1980, Beatrice Ramos threw herself and her 13-month-old son, Vladimir, under a subway train in New York. Both were badly hurt. Vladimir’s right foot and left leg were injured beyond repair. But to spare him from having two false limbs, surgeons at Bellevue Hospital performed a pioneering operation in which they attached his left foot to his right leg.

Only ten years earlier, such an operation would have been thought impossible. Now, operations to save limbs are much more common.

Microsurgery involves working on the tiniest structures in the human body, such as nerve fibres, veins and fine arteries. When sewing back a severed part of the body, it is not sufficient simply to sew it on. Without connecting blood vessels the part would die from lack of oxygen, and if the nerves were not connected, it would have no nervous stimulation and would be useless.

Since the structures involved are so fine — an artery in a finger is about I/16in (1-2mm) wide and a nerve fibre varies from .002mm to .02mm — microsurgery is possible only with high-powered microscopes. These instruments have a magnification from x 6 to x 40, allowing surgeons to see the tiny structures that need joining up. Micro-scopes with two or three heads have been developed, which allow more than one surgeon to work at the same time.

 When stitching nerves, surgeons have to make sure that they join matching bundles. They are usually identified before surgery.

The surgeon works with a needle which is only 50 microns (.05mm) thick, with 18 micron (nearly .02mm) nylon thread.

When stitching two blood vessels together. A surgeon normally uses a method known as triangulation. Three stitches are made 120 degrees apart at the end of the blood vessels, and then the surgeon sews all the way around their circumference, a third at a time.

It can take 15 to 30 minutes to stitch one vein to another. Stitching back a hand can take 19 hours.

Sometimes blood vessels can be joined together without intricate sewing. By using electrical probes to heat up the severed ends the surgeons can literally weld them together.

After surgery, physiotherapy is essential to restore the replanted limb to working order. For a replanted hand it takes about 200 days for the nerve and blood vessel tissues to regenerate. It takes longer. However, for the part to function normally.

 Apart from repairing injuries, micro-surgical techniques can be used for a host of other problems. Eye operations, for example, involve microsurgery. An eye operation called ‘radial keratotomy’, which was pioneered by Russian surgeons, can sometimes cure short sight. The surgeon makes a number of slits radiating from the centre of the cornea, the surface of the eye. The cuts change the shape of the cornea, which alters the distance between the front of the eye and the retina, bringing objects into focus which previously was not.

Brain surgeons use operating micro-scopes to place their instruments with much greater precision, so improving the chances of success in removing tumors. The microscopes enable surgeons to re-move the tumor without cutting away any normal brain tissue.

 

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Why carbohydrates are important for athletes?

There is one dietary regime which has been shown to boost athletes’ energy levels significantly. Known as carbohydrate loading, it increases the level of glycogen in the muscles. Glycogen is a form of glucose which is broken down to release energy. By building up the amount of glycogen they contain, the muscles can work hard for longer.

 The programme usually starts a week before a competition. On the seventh day before the event, preferably in the evening, the athlete performs a strenuous training routine to deplete the glycogen stored in his muscles, and eats a low-carbohydrate meal. During the following three days he trains less and continues with low-carbohydrate meals.

On days three and two the athlete eats a high-carbohydrate diet and eases the training further.

On day one the carbohydrate intake is increased again, and the athlete rests, in preparation for the event the following day.

The principle behind this programme is that when a high level of carbohydrates is introduced to muscles low on glycogen, the muscles overcompensate and take in a higher than normal level of glycogen over a short period. It is these surplus stores that the athlete draws on during his event, which keep him going longer.

 Following this dietary routine, some top-ranking marathon runners have found that their performances have improved significantly.

 

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How do you remember?

In Rangoon, Burma, in 1974, a man called Bhandanta, Vicitsara recited 16,000 pages of Buddhist text from memory. That sort of memory is phenomenal, but almost everyone is able to remember surprisingly large amounts of information. Despite this, you forget a new telephone number almost immediately after you dial it.

This apparent contradiction occurs because people have two types of memory. Short-term memory can retain only six or seven items for up to a minute. Long-term memory can retain much more complex information for years and even decades.

Scientists have discovered that short and long-term memory are located in different parts of the brain. Short-term memory is found in the middle of the brain, but long-term memory is located all over the outer part. This is why, when a disease or stroke affects the inner part of the brain, and results in memory loss, the victim can remember events leading up to his memory loss, because they are part of his long-term memory, but cannot store new memories.

Psychologists know that memory is linked to the five senses. During the leading phase, child who has reached the age of six has a vocabulary of 6000 words. Throughout the rest of his life he average person will acquire only another 14,000. Yet the foundations are laid before he can read, so he has learned these sounds by their meaning, rhythm and tone, and by association.

When information is held in the long-term memory, it is probably translated into some kind of picture and stored in the nerve cells in the outer part of the brain. There are more than 100,000 million such cells, each of which has 10,000 connections to other cells, making the network unbelievably complex.

The information in the cells is probably stored by chemicals which after the way the cells work and the way they are connected to each other.

Something in a person’s short-term memory can be transferred to his long-term memory by repetition and learning. The information is actually transferred by chemical messengers. These messengers are molecules which travel from one brain cell to another. Each molecule causes a specific action, and so ‘transmits’  message.

So even though you may forget a telephone number you have just dialed, you can eventually store it in your long-term memory if you are going to read it in the future.

 

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How glasses sharpen your vision?

If you have perfect vision, the light rays entering the pupils of your eyes will converge exactly on the retina at the back, and the sharply focused picture will be relayed to the brain.

Most people’s vision is at its sharpest at about the age of one year. Problems often develop at around puberty. The eyeball grows too long from front to back, or not long enough or it becomes misshapen. These are the three most common reasons why pepole need to wear glasses to correct the eye’s focal length.

In early life, a person’s potential sight problems may be compensated for by the strong action of the ciliary muscles attached to the iris of the eye’s lens. These muscles increase or decrease the curvature of the lens so that it is possible to focus on things up or far away.

But if the ciliary muscles weaken as often happens in middle age, the lens can no longer be made thick enough to focus on close-up objects, such as small type on a printed page. A person who at the age of ten could focus on the tip of his own nose may suddenly find that he cannot read a book unless he holds it at arm’s length.

The three main causes of blurred vision are long-sightedness, short-sightedness and astigmatism, and glasses of different types are used to correct them. Tinted lenses help wearers whose eyes are sensitive to light or reflections from clear lenses. An anti-reflection substance can also be used to coat lenses and help to make vision sharper.

Spectacle lenses are made of either glass or plastic. Glass is heavier but it also more resistant to scratching.

 

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