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The respiratory system Respiration is controlled by spontaneous rhythmic discharges from R.C. Many factors can affect the respiratory center including : Partial pressure of carbon dioxide Partial pressure of oxygen A moderate degree of voluntary control can be superimposed on the automatic regulation of breathing Regulation of airway muscle, blood vessels and glands Efferent pathway Afferent pathway Efferent pathway The parasympathetic nerves which mediates bronchial constriction and mucus secretion through its action on M3 receptors. The sympathetic nerves which innervate blood vessels (causing constriction) and glands (causing inhibition of its secretion), with no sympathetic innervations of bronchial smooth muscle. Circulating adrenaline acts on β2-receptors in the alveoli (relaxation), mast cells (inhibition of inflammatory mediators release) and increase mucocilliary clearance. The main neurotransmitter causing relaxation of airway smooth muscles is the NANC inhibitory transmitter, though to be NO. NANC excitatory transmitters are released from sensory fibers when stimulated by inflammatory mediators and irritant chemicals as substance P (which increase permeability and mucus secretion) and neurokinin A (a potent spasmogen). Afferent pathway Irritant receptors (on vagal fibers in the upper airway) and sensory nerve fibers (in the lower airway) respond to exogenous chemicals( e.g. ammonia, sulfur dioxide and cigarette smoke), endogenous inflammatory mediators and physical stimuli (e.g. cold air) causing constriction of the bronchi and mucus secretion through A.Ch. release in the upper airway and release of excitatory transmitters in the lower airway. DISORDERS OF THE RESPIRATORY STSTEM Bronchial asthma It is a condition of recurrent reversible bronchial obstruction leading to: coughing shortness of breath chest tightness wheezing inflammation rapid respiration Etiology of bronchial asthma Externsic factors (mainly in children -Allergic asthma ): Pollen grains ,house dust, cockroach detritus and mites Cigarette smoke by the parents. Industrial chemicals Food allergy Internsic factors (mainly in adults): Emotional stress Viral infection in respiratory tract epithelial damage and mucosal inflammation Exercise (water and heat lose from airway inflammatory mediators release). Drug induced (e.g.) NSAID especially aspirin. The development of allergic asthma Upon exposure of genetically sensitive individuals to allergens, this will cause an Immediate phase of inflammation: Stimulation of Th2-lymphocytes cytokines that promote: -differentiation and activation of eosinophiles. -IgE production and release. -expression of IgE receptors on mast cells and eosinophils. The allergen interact with mast cell-fixed IgE release of several spasmogen as :histamine, leukotrienes, prostaglandin and TNF-α Bronchospasm. Also mast cells release many chemotaxins and chemokines which attract more WBCs. The role of T lymphocytes in asthma The late phase of inflammation This response occurs at a variable time after exposure to the stimulus and includes: Vasodilatation Edema Hypersecretion of mucus Bronchospasm by the released inflammatory mediators Different phases of asthmatic attack Diagnosis of bronchial asthma Patient usually suffers from cough with difficulty in breathing out (dyspnoea) and wheezing. Full history of the patient (genetic susceptibility). Lung function tests (after allergen challenge) e.g. forced expiratory volume (FEV ) 1 Drugs used in treatment of asthma Bronchodilators These medications relieve the symptoms of asthma by relaxing the muscle bands that tighten around the airways. This action rapidly opens the airways, letting more air come in and out of the lungs. As a result, breathing improves. Bronchodilators also help clear mucus from the lungs. As the airways open, the mucus moves more freely and can be coughed out more easily. Anti-inflammatory This is the most important type of therapy for most people with asthma because these drugs prevent asthma attacks on an ongoing basis. These drugs reduce swelling and mucus production in the airways. As a result, airways are less sensitive and less likely to react to antigen. Bronchodilators 2 β -agonists Xanthines Leukotriene-receptor antagonist Muscarinic-receptor antagonists β2-agonists They are first line drugs in treatment of asthma , they are used by inhalation or IV( in status asthmaticus). – mechanism: -Dilate the bronchi by direct action on β2-receptors. -They inhibit mediators release from mast cells. -They may increase mucus clearance by an action on cilia. Short-acting beta 2-agonists : are also called "quick acting," "reliever," or "rescue" medications because they relieve asthma symptoms very quickly by opening the airways. These inhalers are the best for treating sudden and severe or new asthma symptoms. They work within 30 minutes and last four to six hours. They are also the medications to use 15-20 minutes before exercise to prevent exercise-induced asthma symptoms. E.g.:salbutamol and terbutaline bambuterol (pro-drug of terbutaline). Long-acting forms of beta 2-agonist : are used to provide control -- NOT QUICK RELIEF -- of asthma. These drugs take longer to begin to work, but their benefits last longer, even up to 12 hours. They are used twice a day in conjunction with anti-inflammatory inhalers to maintain open airways for long term-control. E.g.salmeterol, formoterol, reprotelol (long- acting). Side effects of β2-agonists Side effects of beta 2-agonists include: Nervous or shaky feeling Overexcitement or hyperactivity Increased heart rate Trouble sleeping (rare) Xanthenes They are second line drugs, they are used orally or intravenously. Theophylline It is a bronchodilator that is used to control asthma. It is available as an oral (pill and liquid) or intravenous (slow IV loading dose followed by infusion in acute attack) form. Mechanisms of action: -Inhibition of phosphodiestrase enzyme increase cAMP -Competitive antagonism with adenosine at adenosine receptors. -Improve diaphragmatic contraction. Side effects of theophyline Side effects include: Nausea and/or vomiting Diarrhea Headache Muscle cramps Nervous feeling, alertness ,tremor and interfere with sleep (CNS stimulant) Hyperactivity Dysrhythmia (fatal) Hypotension As it has narrow therapeutic index, regular blood analysis should be don (especially if taken in high oral dose or when used IV in status asthmaticus) These symptoms may be a sign of having taken too much medication,or due to other certain medications, such as antibiotics containing erythromycin, oral contraceptives and ulcer medicine (inhibitors of P450). Seizure medicine as phenytoin,carbamazepine, Phenobarbital, antibiotics as rifampicin and smoking can also interfere with the way theophylline works (inducers of P450). Also, other medical conditions as some diseases and illnesses can change how the body responds to theophylline. Muscarinic receptor antagonist (Anticholinergic Drugs) Ipratrpium It is used to control asthma and is not a rescue or quickrelief drug. It is available in both a metered-dose inhaler and a nebulizer solution. For asthma it works best when used with a short-acting beta 2-agonist inhaler. It is a not a quick-relief medication. It isn't commonly used alone to treat asthma. Side effects are minor; dry throat is the most common. If the medication gets in the eyes, it may cause blurred vision for a short period of time. It is not recommended for elderly patients and glaucoma patients Leukotriene-receptors antagonists - They are used orally -These drugs competitively block leukotriene receptors. -They are useful in aspirin- and exercise-induced asthma. -They have a bronchodilator effect that is additive with β2-agonist ,so used as add-on therapy for mild and moderate asthma. -E.g.: zafirlukast and montelukast. -Side effects include: GIT- disturbances (Nausea and/or vomiting). Headache Anti-inflammatory drugs Anti-inflammatory drugs are some of the most important treatment options for people with asthma. They prevent asthma attacks and work by reducing swelling and mucus production in the airway. Inhaled Corticosteroids Inhaled corticosteroids are the most effective medications to reduce airway inflammation and mucus production. The use of these medicines leads to: Better asthma control Fewer symptoms Reduced need for hospitalization Inhaled steroids prevent symptoms, they do not relieve symptoms. E.g.: fluticasone propionate budesonide Mechanism of action of corticosteroid - Decrease the formation of Th2 cytokines. - Inhibit the generation of both LTs and PGs by inhibiting phospholipase enzyme (decrease mediators formation). - Decrease the formation of LTB (chemotaxin) and platelet-activating factor reduce antigen-induced influx of eosinophils into lung). - Upregulate β -receptors. - Vasoconstricting effect( edema). - Decrease the release of inflammatory mediators from mast cells. 2 side effects Inhaled corticosteroids have very few side effects, especially at lower doses. It is rare, but if you are taking higher doses, candidiasis (fungal infection in the mouth) may occur. Rinsing the mouth, gargling after each use will help prevent such side effects. It is also easily treated with an anti-fungal (e.g. nystatin) mouthwash. Inhaled steroids are safe to give to both adults and children. Oral (and Intravenous) Corticosteroids (Systemic Corticosteroids) Systemic corticosteroids are used to treat severe asthma episodes. These drugs are used with other medications to either control sudden and severe asthma attacks or to treat long-term, hard-tocontrol asthma. Systemic steroids include: Deltasone (prednisone) Prednisolone Beclomethasone Side effects of systemic steroids tend to occur after years of use and include: acne, weight gain, mood or behavior changes, upset stomach, bone loss, eye changes, and slowing of growth. These side effects rarely occur with short-term use, as is used for an acute asthma episode . Mast Cell Stabilizers Cromoglycate Mechanism of action This is inhaled asthma medication that work by preventing the release of irritating and inflammatory substances from immune cells called mast cells. They effectively prevent asthma symptoms, especially in children with allergies and asthma and in exercise-induced asthma. It also depress the exaggerated neuronal reflexes which are caused by stimulation of irritant receptors or sensory fibers. This drug need to be taken two to four times a day, and take three to four weeks to start working (prophylacting drug). side effects This medication is very safe and have few side effects. Upper airway irritation is the main S.E. Also, hypersensitivity reactions as urticaria may occur. Quick-Relief Medications: Stopping the Asthma Attack These medicines are used to provide prompt relief of asthma attack symptoms (cough, chest tightness and wheezing -- all signs of airway bronchoconstriction). They include: Short acting beta-agonists (bronchodilators that are the drug of choice to relieve asthma attacks and prevent exercise-induced asthma symptoms) . Anticholinergics (bronchodilators used in addition to short-acting beta-agonists when needed). Systemic corticosteroids (an anti-inflammatory drug used in an emergency to get rapid control of the disease while initiating other treatments and to speed recovery) Long Term Control Medications: Treating the Inflammation Research has shown that reducing and preventing further inflammation is the key to prevent asthma attacks, hospitalizations and death from asthma. Long-term control medications are taken daily over an extended period of time to achieve and maintain control of persistent asthma (asthma that causes symptoms more than twice a week and frequent attacks that affect activity). The most effective long-term control medications are those that stop airway inflammation (antiinflammatory drugs), but there are others that are often used along with anti-inflammatory drugs to enhance their effect. Long Term Control Medications: Treating the Inflammation Long-term control medications include: Corticosteroids (The inhaled form is the antiinflammatory drug of choice for persistent asthma). Mast cell stabilizers (anti-inflammatory drugs). Long acting beta-agonists (bronchodilators often used along with an anti-inflammatory drug) . Theophylline (a bronchodilator used along with an anti-inflammatory drug to prevent nighttime symptoms) Chronic obstructive pulmonary disease Definition COPD is a group of lung diseases that reduce the ability of the lungs to oxygenate the blood. Emphysema and chronic bronchitis are the main diseases that make up COPD. What is chronic bronchitis? Chronic bronchitis is inflammation and irritation of the airways of the bronchial tubes ,which is characterized by thickening of the muscular wall of the large airways and an increase in size and activity of mucous glands. This leads to airway narrowing and blockage by thick, tenacious secretions result in productive cough that is present for a period of 3 months in each of 2 consecutive years . Chronic bronchitis The symptoms include: -Chronic cough -Mucus production (sputum) -Shortness of breath -fever due to infection) -mild wheezing -and chest pain. Pathogenesis of Bronchitis 1-Susceptible individual exposed to trigger (e.g. cigarette smoke) initiate an inflammatory processes and several mediators are released as well as increased mucus secretion. 2-Risk of infection increase. 3-In sever cases ,mucus plug the lung difficulty in expiration air entrapment elasticity of alveoli decrease (+infection) destruction of alveoli walls emphysema Emphysema Emphysema develops over many years. It is an inflammation (edema) which is usually induced by cigarette smoke. The tiny air sacs within the lungs (alveoli) are gradually destroyed. As a result, the alveoli are not able to pick up enough oxygen (more and more short of breath). Pathogenesis of emphysema The exposure of a susceptible individual to noxious particles and gases (Cigarette smoke as well as other gases and particles) an inflammatory process. The predominant inflammatory cell is the neutrophil ,macrophages and Tlymphocytes are increased in the various parts of the lungs, and several mediators are released, including leukotriene B4, interleukin 8, and TNF α leading to sever inflammatory process and edema. Altered protease/antiprotease balance, at least in individuals with severe deficiency of alpha1-antitrypsin, has been shown to predispose to emphysema. Individuals with severe deficiency of alpha1-antitrypsin may develop emphysema at an early age (fourth decade), in contrast to the "usual" emphysema, which typically begins in the sixth decade. Pathogenesis of emphysema What does the alpha1 antitrypsin do in the body? Alpha-1 antitrypsin is a major protein in the blood. It is produced mainly in the liver cells. It protects the lung by blocking the effects of a powerful enzyme called elastase. Elastase is normally carried in white blood cells and protects the delicate tissue of the lung by killing bacteria and neutralizing tiny particles inhaled into the lung. Alpha-1 antitrypsin inactivates elastase once it has finished its job. Without alpha1 antitrypsin, elastase can destroy the air sacs of the lung. Symptoms of emphysema Initial symptoms include: - Chronic coughing, which may be worse upon awakening. - Increased production of mucus (which is actually a symptom of chronic bronchitis). - Shortness of breath. - Fatigue easily even with little physical exercise (stair climbing, walking). As the disease progresses: -Shortness of breath may be present at rest. -Some people with emphysema develop body changes; their chest begins to take on a "barrel-like" appearance as the lungs compensate for the loss of functioning tissue by expanding. -Others develop a bluish color of the lips and nail beds, resulting from chronically low levels of oxygen in the blood. -Some people with emphysema will develop heart failure that may lead to swelling in the lower extremities and increased fluid in the lungs. Etiology of COPD : 1-The most important cause is tobacco smoke. 2- It can also develop after exposure to chemicals or air pollution. 3-Deficiency of alpha1-antitrypsin, has been shown to predispose to emphysema. 4-Bronchitis is also can be caused by infection with a virus (less commonly with a bacteria or fungus). Diagnosis To diagnose COPD : Detailed medical history including family history of lung disease Physical exam Breathing tests and X-rays Special blood tests used for diagnosis of inherited emphysema. The test measures the concentration of alpha-1 antitrypsin in the blood. Medication Therapy Bronchodilators: Bronchodilators include ß-adrenergic agonists, anticholinergics, and methylxanthines. Corticosteroids: used along with bronchodilators. Immunizations Prophylactic immunization with the influenza vaccine yearly and with the 23-polyvalent pneumococcal vaccine every 5-10 years is recommended. Mucolytics Mucolytic drugs (eg, ambroxol, erdosteine, carbocysteine, iodinated glycerol, etc) are beneficial and are recommended. In the specific case of alpha 1-antitrypsin deficiency, intravenous augmentation therapy with pooled human plasma antiprotease can raise serum levels of alpha 1-antitrypsin above a protective threshold value . Non-pharmacologic treatments Behavior Modification In addition to medicines, the management of COPD includes: Exercise and a healthy lifestyle Adequate nutrition. Avoidance of infection Oxygen therapy Giving Up Smoking Giving up smoking and avoiding secondhand smoke is very important. Smoking can accelerate or speed the development of the disease and shorten the lifespan. Surgery Lung transplants may be an option for people severely affected by the disorder. Cough Coughing is the body's way of removing foreign material or mucus from the lungs and upper airway passages or of reacting to an irritated airway.. A cough is only a symptom, not a disease, and often the importance of your cough can be determined only when other symptoms are evaluated. There are many causes of a productive cough, such as: Viral illnesses: It is normal to have a productive cough when you have a common cold. An infection :of the lungs or upper airway passages can cause a cough. A productive cough may be a symptom of pneumonia, bronchitis, sinusitis, or tuberculosis. Chronic lung disease: A productive cough could be a sign that a disease such as chronic obstructive pulmonary disease (COPD) is getting worse. Stomach acid backing up into the esophagus : This type of coughing may be a symptom of gastroesophageal reflux disease (GERD) and may awaken you from sleep. Nasal discharge: draining down the back of the throat (postnasal drip syndrome). Smoking: or other tobacco use. Here, productive coughs is often a sign of lung damage or irritation Drugs used for treatment of cough Codeine: -Less addiction liability -Effective cough suppressant -Decrease secretions in the bronchioles -S.E.: Constipating effect & cilliary clearance Dextromethorphan: -It is a synthetic narcotic analgesic -Its antitussive effect = that of codeine -Less Constipating effect & less inhibition on cilliary clearance