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New Readers: Welcome, and please see page tabs above for introductory information.

I can't promise a regular posting schedule right now, but I am trying to keep to an "every other day" schedule, I may go back to MWF with optional weekend material if needed.

Posts from "The Lab Rats' Guide to the Brain" will have the heading "The GUIDE". Other content: Science and Lab Humor, etc. (heading: FUNNY); Commentary on science in the news (heading: NEWS), Interesting science pages and neat links (heading: NEAT STUFF); book reviews of fiction and nonfinction works I've read (heading: REVIEWS); original short and serialized stories (heading: FICTION).


Monday, February 27, 2012

The GUIDE: "Three M's" - Part 1 Multiple Sclerosis

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Image Copyright Alila Sao Mai, 2012
Used under license from Shutterstock.com
Today we start with the three M's of neuromuscular diseases with Multiple Sclerosis.  The name "sclerosis" means "scar" and one of the characteristics signs of MS in autopsy is the scar-like appearance of the long neurons in "multiple" locations throughout the body, spinal cord and brain.

Way back in the dim mists of this blog (just over a year ago), I described the basic mechanism of neurons, the building blocks of the brain and nervous system.  The blog is here (http://teddysratlab.blogspot.com/2011/02/piece-of-action-potential.html) if you need to refresh your memory on the subject.  One of the key features of neurons are their long axons which conduct an electrochemical signal over long distances - many meters in some cases.  One of the means of speeding up the transmission is to insulate most of the axon, leaving periodic gaps for the chemical channels required to propagate the action potential.

That insulation is illustrated on a neuron in the figure abovet.  The left neuron is normal and has intact myelin insulating its axon.  The right neuron has damaged myelin, which slows and even stops the signal, due to the fact that once an axon is wrapped with myelin, it doesn't have ion channels under the insulation.  Without ion channels covered the whole length of the (exposed) axon, an action potenial cannot keep occurring in sequence down the length of the axon.  Without an action potential, the neuron cannot transfer information from brain to muscle or from sensory organs to the brain.  Even inside the brain, axons that cover "long distances" (more than a few millimeters) are also insulated, thus MS can affect the normal function of information processing in the brain.

So - three questions come up: What is myelin?  How does the degeneration of MS occur?  How can it be treated?

Myelin is actually a special type of cell - called a "Schwann Cell" - that wraps itself around an axon many times.  The normal cell membrane is supplemented with thick lipid (fat or oil) deposit within the layers of cell 
surrounding the neuron, forming an electrical insulator - much the way non-conducting grease or transformer oil is used in high-voltage electrical installations.  The insulation serves two purposes - it prevents the "leakage" of electrical charge from axons, and the thick blanket of Schwann Cell surrounding the axon prevents any of the fluid surrounding the neuron from making contact with the membrane (and any ion channels located there).  The neuron adapts to the insulation by moving it's ion channels to the gaps between Schwann Cells.  These gaps have the name "Nodes of Ranvier" and are a key component of the signal speed increase caused by myelination.  With ion channels concentrated at the Nodes, the action potentials are actively generated only at the nodes, then passively conducted through the now very efficiently insulated spaces between the nodes.  The speed of action potential propagation is at least ten times faster in myelinated vs. unmyelinated axons, which is very important for sending signals to distant muscles.

MS is an "autoimmune" disease, meaning that the bodies own antibodies attack the Schwann Cells and cause the damage to the myelin that is characteristic of MS.  The location and extent of myelin damage controls the severity and type of symptom, which can range from dizziness, unusual sensations and muscle tremors at it's mildest, to muscle spasms, paralysis, blindness, at worst.  All of the causative factors are not clear, but MS affects more women than men, runs in families and also is also more frequent in certain parts of the world.

Symptoms of MS can occur in multiple parts of the muscle and nervous system - hence its designation as a neuromuscular disease.  Muscle symptoms include loss of balance, weakness, spasms, problems with coordination and/or tremor.  MS can cause vision problems including double vision, sudden eye movement and blindness; it can cause hearing loss, speech problems, dizziness, depression, memory loss, decreased attention, difficulty reasoning and making decisions. MS is also associated with many internal issues as well, constipation, trouble swallowing, incontinence, erectile dysfunction.  The most notable symptoms with the most difficult treatment are a burning/tingling/crawling sensation of the skin, painful spasms, facial pain and fatigue.  MS is diagnosed via tests of nerve and muscle conduction speed, an MRI, spinal tap to look for inflammation proteins in the cerebrospinal fluid, and physical examination for changes in vision, hearing, sense of touch, pain sensation, balance, muscle coordination, etc.  [As usual, the PubMed Health site on MS: http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001747/ is an excellent place to start for more information.]

Since MS is an autoimmune disease, one course of treatment is to suppress inflammation and immune function using chemotherapy, interferon or antibodies to immunoglobin E (IgE) - the primary immune system
protein responsible for autoimmune reactions.  However, these drugs will only slow the course of the disease, they cannot restore lost function.  Given that damaged neurons will not regrow, it is possible to supplement the normal neuron function by replacing or reinforcing the action of certain neurotransmitters - such as GABA-like medicines for muscle spasms, acetylcholine for urinary problems or antidepressants for the mental changes.

This will seem a bit strange for those who know my stand on medical marijuana, but cannabinoids have been shown to reduce spasms, reduce pain and alleviate mood changes.  I still maintain that these effects would be better served by a true medicinal cannabinoid with controlled formulation and dosing, but in the case of MS and cancer pain, smoked marijuana appears to be quite effective.

Patients with MS can live quite a long time (20+ years) with minimal symptoms, or may have periodic attacks with severe symptoms, but be symptom-free for months or even years in between.  Keeping in mind that I am writing about neurological and neuromuscular disorders at fictional plot devices, MS is the sort of disorder that a person can have and show no overt symptoms, while the disease continues to affect neurons until a tipping point is reached in which the patient experiences loss of both voluntary and involuntary muscle control and requires assistance caring for themselves.

I highly recommend that anyone desiring more information visit the PubMed Health site and start there.

We will continue with the "Three M's" next time, with Myasthenia Gravis, a disease that can have many overlapping symptoms with MS, but with a totally different causative source.





Sunday, February 26, 2012

Updated NEWS: Stellarcon 2012, March 2-4, High Point, NC.

http://teddysratlab.blogspot.com [Full link to blog for email clients.][FT:C44]


Finding Baen folks at Stellarcon, Mar. 2-4.


Bar Fly Central, Suite 215.

UPDATED, with panelist changes and moderators now indicated by "(M)".
Also note my science talk "I Remember When" on Saturday at 3 PM.


---------------
Friday 4 PM, Programming 3, "Con Health", Speaker to Lab Animals, Chris Ross

Friday 5 PM, Programming 1, "Hard Science Fiction", Paula Jordan, Gray Rinehart, Speaker to Lab
Animals (M), Michael A. Stackpole, Toni Weisskopf

Friday 5 PM, Programming 3, "The Pirate Panel", Danny Birt (M), James Fulbright, Laura Haywood-Cory

Friday, 6 PM, Main Programming, “Stellarcon Opening Ceremonies”, James Fulbright, Tera Fulbright, Albin Johnson,John Kovalic, Mark Poole, Patrick Rothfuss, Brad Sappington, Michael A. Stackpole, Chris Weed, Michael Z. Williamson

Friday, 7 PM, Programming 1, “Writing Action Scenes”, Chris Berman, Podcasting's Rich Sigfrit (M), Michael Z. Williamson

Friday, 8 PM, Programming 1, "Research for the Writer", Theresa Bane (M), Paula Jordan, Karen McCullough, Speaker to Lab Animals, Amy H. Sturgis

Friday, 8 PM, Programming 2, "Short Stories and Publication", Barbara Friend Ish (M), Stuart Jaffe, Andi
Newton, Gray Rinehart

Friday, 8 PM, Programming 3, "Shooting First: Moral Ambiguity and Star Wars", Davey Beauchamp (M),
James Fulbright, Jim Minz, Podcasting's Rich Sigfrit, Michael A. Stackpole

Friday, 9 PM, Programming 3, “Surviving the Zombie Apocalypse”, Brad Sappington, Speaker to Lab Animals (M), Chris Weed, Michael Z. Williamson

Friday, 9 PM, Workshops/Reading, "Filk Circle", Danny Birt, Gray Rinehart, Blibberering Humdingers

---------------

Saturday, 9 AM, Offsite, “Bar Fly Range Trip to Proshots Range in Winston-Salem” (Exit 118 off of US. 52 North, about 40 minutes from Stellarcon)

Saturday, 12 PM, Programming 1, "Character Building Workshop", Barbara Friend Ish, Steve Long (M), Gray Rinehart, Patrick Rothfuss

Saturday, 1 PM, Main Programming, “Interview with Michael Z. Williamson”, Speaker to Lab Animals (M), Toni Weisskopf(M), Michael Z. Williamson

Saturday, 2 PM, Programming 1, "The Role of the Publisher in Today’s Market", Barbara Friend Ish, John G. Hartness, J.L. Hilton (M), Misty Massey, Toni Weisskopf

Saturday, 3 PM, Programming 2, "SONAR 2012: Symposium On Nerdy Academic Research", Dr. Tedd Roberts, "I Remember When…"

Saturday 3 PM, Programming 3, "The Art of Revision", Marilynn Byerly, Tony Daniel, Laura Haywood-
Cory, Stuart Jaffe (M)

Saturday 4 PM, Main Programming, “Baen Travelling Roadshow”, Tony Daniel, Laura Haywood-Cory, Jim
Minz, Gray Rinehart, Toni Weisskopf, Michael Z. Williamson

Saturday, 6 PM, Programming 3, "I'd Rather Be _________", Danny Birt (M), Jim Minz, Janine K. Spendlove, Michael A. Stackpole, Allen Wold

Saturday, 9 PM, Programming 3, “Dystopian Literature: how political philosophy can influence depictions of dystopia”, Nicole Givens Kurtz, J.L. Hilton, Speaker to Lab Animals (M), Michael Z. Williamson

Saturday, 9 PM, Workshops/Reading, "Filk Circle", Danny Birt, Gray Rinehart, Blibberering Humdingers

Saturday, 10 PM, Programming 3, “Messiest Way to Kill a Zombie”, Dan Johnson, Stephen Mark Rainey, Brad Sappington, Chris Weed, Michael Z. Williamson (M)

---------------

Sunday 10 AM, Programming 3, “Strong Female Characters”, Diana Bastine, Chris Berman, Teresa Frohock (M), Michael Z. Williamson

Sunday 11:30 AM, Workshops/Reading, “Reading”, Michael Z. Williamson

Sunday 12 PM, Dealer Room, “Signing”, Michael Z. Williamson

Wednesday, February 22, 2012

The GUIDE: Neuromuscular Diseases

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I am running into some commitments on the Day Job that have derailed my ability to get the next series of blogs written, so instead of launching right into the blogs on the "Three-M's" of Multiple Sclerosis (MS), Myasthenia Gravis (MG) and Muscular Dystrophy (MD), I am writing this brief introduction to the topic.

Neuromuscular diseases are basically those disorders in which the majority of damage is to the nerves that carry signals from the brain/spinal cord to the muscles.  Essentially, the breakdown in communication can be in the brain (but we have covered those syndromes elsewhere), in the spinal cord, in the nerves as they leave the spinal cord, at the junction between nerve and muscle, or in the muscle itself.

Technically, the catch-all term "muscular dystrophy" refers to the latter category - those diseases or disorders in which theproblem is with the muscles themselves.  However, common use includes amyotrophic lateral sclerosis (ALS - Lou Gehrig's Disease, which we'll cover later), MS and MG - particularly when mentioned in a fundraising telethon.

Several significant differences exist with respect to the MD-category of diseases.  Again, MD is a catch-all term, but the implication is a disorder of the muscles.  MS is a disorder of the nerves, both in the brain & spinal cord and between spinal cord and muscle.  The "insulation" that allows nerves to conduct electrical activity very fast over long distances begins to break down in MS.  This results in muscle spasm and weakness, but also pain and distorted sensation.  MG is specifically a disease of the chemical neurotransmitter receptors at the junction between nerve and muscle.  The bodies own immune system attacks the proteins at the junction, preventing the neurotransmitter from being recognized by the muscle, weakening the signals from brain to muscle.  ALS is a disease in which the nerve axons themselves begin to die.  Each of these disease disconnects the brain from the muscles, and in some cases, the brain from the sensory receptors for touch and position of the body.  Muscle weakness, tremors, spasms and pain are the result.

We'll resume the next blog with a look at Multiple Sclerosis, causes, and treatments, followed by Myasthenia Gravis, Muscular Dystrophy, then ALS. 

Monday, February 20, 2012

COMMENT: The Big Lie

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For years, a prominent animal rights activist group - whom I shall NOT name, because I don't want to give them the search boost - has been telling Americans and the world that animal researchers are heartless sadists who enjoy torturing animals in the name of worthless science.

Lies.

In the first place, scientists quite frequently have pets and care for animals in many ways.  Some of the research done on animals in the name of human medicine really does benefit animals.  For example, I had a dog that required two knee surgeries.  I have known people whose pets and even farm animals have had cataract operations, treatment for heart disease, diabetes, leukemia, lymphoma.

Second, bad health makes bad data.  Results obtained from mistreated or sick animals is worthless to scientific research.  The guiding principle of the experimental method is control of variables.  That is difficult with living tissues, more so with behaving animals.  Why would anyone think a scientist would complicate matters by working with sick, abused, distressed animals?  Under such circumstances, there would be totally different results with each trial, each animal. 

Third, the accusation of worthless repetitive science shows a fundamental lack of understanding of the scientific method.  Experiments must be repeated under controlled, identical conditions to ensure that the outcome is in fact due to the drug or treatment being tested.  Then experiments should be repeated under different conditions to ensure that the treatment will work each time.  You have certainly all seen this - a friend tells you about a great new drug, diet or exercise, it worked wonders for them.  You try it and it doesn't work, was it that you did it wrong?  Was your friend mistaken as to what actually produced the results?  Or did the diet just not work for *you*?

Frankly, animal rights activists betray a fundamental lack of education in science, and a profound selfishness. 

Selfishness?  Yes - the philosophy that "A rat, is a pig, is a dog, is a boy" does not mean that the speaker values animal life as much as human, but that they have *devalued* *other* human lives much less than their own.  Basically, *they* must be important, or else they would eagerly sacrifice their own lives for the cause.  No, they'd rather sacrifice *your* life by denying scientific and medical advances.  The animal rights organization does not believe in rights, but in control.

Animal rights activism is a Big Lie.  

Today my lab lost a valuable lab animal.  I have spent all day in a surgical and autopsy suite trying first to save it, then to figure out why this happened.  Preliminary findings suggest that it was an infection unrelated to our experimental procedures. This animal had been involved in many studies, and helped provide data that may one day be used to counter drug addiction, alleviate sleep deprivation or result in prosthetic devices for the brain.  I feel the loss much the same as when my family lost our dog to lymphoma a few years ago.  

But then, it was just an animal - and I'm just a cruel, heartless scientist.

The Big Lie.  Will you believe it?  Or reject it as just another means of manipulation and control. 

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This event has altered my posting schedule.  The start of the blogs on dystrophies and neuromuscular diseases are postponed until Wednesday.