COPD & Emphysema Support Group
COPD is a progressive disease characterized by airflow obstruction or limitation. Emphysema is characterized by loss of elasticity of the lung tissue, destruction of structures supporting the alveoli and of capillaries feeding the alveoli. Both have symptoms that include shortness of breath, among other respiratory troubles. If you are a COPD or Emphysema sufferer, join...
ScienceDaily (Mar. 21, 2012) The third most deadly disease in the U.S., chronic obstructive pulmonary disease (COPD), appears to be partly driven by the action of immune cells circulating in the blood entering into the tissues of the lungs. UC Davis scientists have discovered that this key process begins in the blood vessels around the large airways in the center of the lung. The discovery helps clarify how smoking can bring about this severe respiratory condition.
The research also identifies a potential new target for directed drug therapy to counter the disease, which kills about 3 million people a year in the U.S. The study is published online March 22 in the PLoS One an open-access public science journal.
"Understanding how a disease begins is an important step to develop new therapies, and knowing the mechanism and location of white blood cell recruitment to the lung early on in the development of COPD in this model will allow us to more rapidly screen drugs and determine how they work," said Benjamin Davis, a researcher with the Center for Health and the Environment and the lead study author.
"We are currently testing whether statin drugs that may prevent the development of COPD in this model. The model appears to be ideal for screening drugs to treat early COPD, but the ultimate test comes when a treatment is transitioned from the lab to COPD patients," Davis said. "Our primary goal is to save lives."
Davis and his colleagues used a highly reproducible animal model of COPD to show, in effect, that the equivalent of approximately 10 years of one-pack-a-day cigarette smoking leads to a striking immune response in the lungs: Bronchial airways -- the air passages to the lungs -- are completely physically damaged and scarred, accelerating inflammation and cellular changes that in turn can obstruct airflow and reduce normal lung function.
In people who smoke for 30 to 40 years, inflammation destroys the delicate balance of cells lining the airways, increasing the respiratory system's vulnerability to infection and the ability to clear inhaled particles. This is full-blown COPD.
Researchers had not known if the immune cell-triggered inflammation started in the blood that feeds bronchial airways or if instead, it started in alveoli deep in the lungs where oxygen is transferred to blood vessels. The new finding resolves the question.
The research demonstrates tobacco-smoke exposure stimulates a specific type of white blood cell called a neutrophil to migrate out of bronchial blood vessels and accumulate in the lung tissues. Davis and colleagues found that these cells leave the circulation due to the production of "adhesion molecules" and immune proteins called chemokines in bronchial blood vessel cells. Although neutrophils aid in tissue repair, when present in excess numbers and activated, these white blood cells can release enzymes that kill cells and accelerate inflammation.
"Now that we have determined where the process starts, we hope that therapeutic drugs can be developed to target this inflammatory process in the bronchial airways to reduce severe lung damage," said Kent Pinkerton, a coauthor of the study, professor of pediatrics and director of the Center for Health and the Environment at UC Davis.
More than 80 percent of COPD is caused by smoking. Inhaling on a lit cigarette exposes smokers to some 4,000 different compounds present in vapors, particles and smoke. All of this material comes in contact with, and eventually kills, fragile airway epithelial cells that are lined with cilia and films of mucus to facilitate passage of air into the lungs.
The researchers studied rats that appear to have a genetic defect making them react to smoke exposure much like people who develop smoking-related diseases. The scientists showed that the animals develop all of the physiological and anatomical traits of COPD found in humans, making them ideal models to study the disease.
The rats experience these symptoms and conditions much faster than other laboratory animals that have been studied, and the development of the rat model is expected to be useful in future studies on COPD and ways to treat it.
In the research, a "smoking machine" automatically loads, lights and puffs on cigarettes. Rats are exposed to smoke proportional to a two-pack-a-day smoker. However, due to the sensitivity of these rats to tobacco smoke, exposures are only for six hours a day, three days per week.
The researchers found that 12 days of exposure over a period of four weeks led to physiological changes reflective of a 10- to 20-year smoker who develops respiratory complications of wheezing, coughing and reduced respiratory function. With 12 weeks of smoke exposure, the conditions in these rats approximate those found in a 30- to 40-year smoker who has developed severe limitations in breathing and COPD.
The scientists now plan to test a variety of potential drugs with the long-term aim of finding new ways to treat people with the disease.
Coauthors on the study include Yi-Hsin Shen, Vanessa Flores and Ryan P. Davis, all in the Center for Health and the Environment and Daniel J. Tancredi of the Department of Pediatrics in the UC Davis School of Medicine. The study was funded by the National Center for Research Resources of the National Institutes of Health and the Tobacco-Related Disease Research Program.
http://www.sciencedaily.com/releases/2012/03/120321172354.htm
I thought this was very interesting, and thought some of you might think so too.
Love
Holly
The research also identifies a potential new target for directed drug therapy to counter the disease, which kills about 3 million people a year in the U.S. The study is published online March 22 in the PLoS One an open-access public science journal.
"Understanding how a disease begins is an important step to develop new therapies, and knowing the mechanism and location of white blood cell recruitment to the lung early on in the development of COPD in this model will allow us to more rapidly screen drugs and determine how they work," said Benjamin Davis, a researcher with the Center for Health and the Environment and the lead study author.
"We are currently testing whether statin drugs that may prevent the development of COPD in this model. The model appears to be ideal for screening drugs to treat early COPD, but the ultimate test comes when a treatment is transitioned from the lab to COPD patients," Davis said. "Our primary goal is to save lives."
Davis and his colleagues used a highly reproducible animal model of COPD to show, in effect, that the equivalent of approximately 10 years of one-pack-a-day cigarette smoking leads to a striking immune response in the lungs: Bronchial airways -- the air passages to the lungs -- are completely physically damaged and scarred, accelerating inflammation and cellular changes that in turn can obstruct airflow and reduce normal lung function.
In people who smoke for 30 to 40 years, inflammation destroys the delicate balance of cells lining the airways, increasing the respiratory system's vulnerability to infection and the ability to clear inhaled particles. This is full-blown COPD.
Researchers had not known if the immune cell-triggered inflammation started in the blood that feeds bronchial airways or if instead, it started in alveoli deep in the lungs where oxygen is transferred to blood vessels. The new finding resolves the question.
The research demonstrates tobacco-smoke exposure stimulates a specific type of white blood cell called a neutrophil to migrate out of bronchial blood vessels and accumulate in the lung tissues. Davis and colleagues found that these cells leave the circulation due to the production of "adhesion molecules" and immune proteins called chemokines in bronchial blood vessel cells. Although neutrophils aid in tissue repair, when present in excess numbers and activated, these white blood cells can release enzymes that kill cells and accelerate inflammation.
"Now that we have determined where the process starts, we hope that therapeutic drugs can be developed to target this inflammatory process in the bronchial airways to reduce severe lung damage," said Kent Pinkerton, a coauthor of the study, professor of pediatrics and director of the Center for Health and the Environment at UC Davis.
More than 80 percent of COPD is caused by smoking. Inhaling on a lit cigarette exposes smokers to some 4,000 different compounds present in vapors, particles and smoke. All of this material comes in contact with, and eventually kills, fragile airway epithelial cells that are lined with cilia and films of mucus to facilitate passage of air into the lungs.
The researchers studied rats that appear to have a genetic defect making them react to smoke exposure much like people who develop smoking-related diseases. The scientists showed that the animals develop all of the physiological and anatomical traits of COPD found in humans, making them ideal models to study the disease.
The rats experience these symptoms and conditions much faster than other laboratory animals that have been studied, and the development of the rat model is expected to be useful in future studies on COPD and ways to treat it.
In the research, a "smoking machine" automatically loads, lights and puffs on cigarettes. Rats are exposed to smoke proportional to a two-pack-a-day smoker. However, due to the sensitivity of these rats to tobacco smoke, exposures are only for six hours a day, three days per week.
The researchers found that 12 days of exposure over a period of four weeks led to physiological changes reflective of a 10- to 20-year smoker who develops respiratory complications of wheezing, coughing and reduced respiratory function. With 12 weeks of smoke exposure, the conditions in these rats approximate those found in a 30- to 40-year smoker who has developed severe limitations in breathing and COPD.
The scientists now plan to test a variety of potential drugs with the long-term aim of finding new ways to treat people with the disease.
Coauthors on the study include Yi-Hsin Shen, Vanessa Flores and Ryan P. Davis, all in the Center for Health and the Environment and Daniel J. Tancredi of the Department of Pediatrics in the UC Davis School of Medicine. The study was funded by the National Center for Research Resources of the National Institutes of Health and the Tobacco-Related Disease Research Program.
http://www.sciencedaily.com/releases/2012/03/120321172354.htm
I thought this was very interesting, and thought some of you might think so too.
Love
Holly
I was a 55 year, 2 pk a day smoker and am now paying the price with end stage "E". I have a younger sister who has been dx'd for at least ten years, but isn't as bad as I am. Our mother died of lung caancer 7 years ago.
The other day my father and I were attending the funeral of my uncle, his brother in law. At the luncheon following the services, my dad asked me how I and my sister both have "E". Trying to keep my composure and reply with a civil answer, I replied: "It's your fault and moms' fault. We all were exposed to 2nd hand smoke from the day that we were born. You both smoked, thus starting us on the road of smoking when we were born. But, sure, the fact that both of us became smokers "added the nails to our coffin lids." He didn't say too much after that except to remind me that the anniv of my mothers' death is approaching!
Finding more meds to treat us is certainly a heroic endeavor, but for me that is far too late. What all must do is try to get cigarette smoking dangers embedded in the minds of the young people of this world.
Surely manufacturing processes play another contributing factor to our lung problems. In my case, I was a welder for forty years in chemical plants here in NJ. So, in addition to a deadly smoking addiction, I breathed in the fumes and smoke generated in the welding processs, plus, I have been exposed to the fumes of some of the harshest chemicals produced by mankind (probably why I've been fighting Parkinson Disease for the last 35 1/2 years too!).
All I can say now is that more emphasis should be directed towards eliminating cigarette smoking, especially in young people, the most vulnerable!
Just my unadulterated opinion!
Jim Evridge
PS: do ya think I'm mad? You betcha I am ... I'm pissed that educated people in this country let this scourge continue like it's not their concern!
Hugs Peta x