Nitrates are prodrugs that release nitric oxide (NO) in the body. Common nitrate drugs include nitroglycerin and isosorbide mononitrate. Nitrates were first synthesized in the 1840s and are used to treat conditions like angina by relaxing smooth muscle and dilating blood vessels. They reduce blood pressure and myocardial oxygen demand. However, tolerance to nitrates develops rapidly due to desensitization of vascular smooth muscle. Providing a daily nitrate-free period can help overcome tolerance. Nitrates are also found naturally in soil and water and excess nitrates can cause methemoglobinemia or be linked to cancer.
This document provides information on the pharmacology of diuretics. It begins by explaining that diuretics cause a net loss of sodium and water in urine but sodium balance is restored through homeostatic mechanisms. It then classifies diuretics and describes various classes in detail, including their mechanisms and sites of action, uses, and adverse effects. The classes discussed include high efficacy loop diuretics like furosemide, medium efficacy thiazides, weak carbonic anhydrase inhibitors, potassium sparing aldosterone antagonists, and renal sodium channel inhibitors.
A power point presentation on "Drugs affecting coagulation and anticoagulants" suitable for undergraduate medical students. Also suitable for Post Graduate students of Pharmacology and Pharmaceutical Sciences.
in this presentation i have tried to briefly discuss about diuretics (water pills), their classification, mechanism of action, pharmacokinetics and pharmacodynamics of these drugs
Mucolytic drugs like Mucomyst work by breaking bonds in mucus to decrease its viscosity, making it easier to clear. It is used for abnormal thick mucus and to prevent acetaminophen toxicity. Expectorants also make mucus easier to clear by reducing adhesiveness. Decongestants constrict blood vessels to reduce nasal congestion from infections or allergies. Antitussives suppress coughing. Antihistamines block histamine receptors to relieve allergy symptoms. Bronchodilators relax airways to relieve asthma symptoms. Corticosteroids reduce inflammation for asthma or COPD.
This document discusses adrenergic antagonists (sympatholytics) which inhibit the sympathetic nervous system by blocking adrenergic receptors or neurons. It describes various types of adrenergic blocking drugs that are selective for α and β receptors. Non-selective α-blockers like phenoxybenzamine cause irreversible blockade while phentolamine is competitive. Selective α1-blockers lower blood pressure with minimal effects on cardiac output. Orthostatic hypotension is a common side effect of α-blockers due to inhibition of venous vasoconstriction.
The document discusses different classes of diuretic drugs, including their mechanisms and effects. It describes loop diuretics like furosemide that inhibit sodium chloride reabsorption in the thick ascending limb of Henle's loop, increasing excretion of sodium and chloride in urine. It also discusses thiazide diuretics that act in the early distal tubule by inhibiting carbonic anhydrase and enhancing excretion of magnesium and potassium while inhibiting calcium and uric acid excretion. Finally, it mentions osmotic diuretics like mannitol that cause water retention in the proximal tubule through osmotic effects, resulting in water diuresis.
This document discusses angiotensin receptor blockers (ARBs) which are used to treat hypertension and other cardiovascular conditions. It notes that ARBs work by competitively blocking the angiotensin receptor type 1, leading to vasodilation and other effects. Some examples of individual ARB drugs are provided like losartan, candesartan, and valsartan. The document compares ARBs to ACE inhibitors, noting that ARBs do not cause cough like ACE inhibitors. It concludes by discussing the theoretical rationale and benefits of combining ARBs with ACE inhibitors to more completely suppress the renin-angiotensin system.
Nitrates are prodrugs that release nitric oxide (NO) in the body. Common nitrate drugs include nitroglycerin and isosorbide mononitrate. Nitrates were first synthesized in the 1840s and are used to treat conditions like angina by relaxing smooth muscle and dilating blood vessels. They reduce blood pressure and myocardial oxygen demand. However, tolerance to nitrates develops rapidly due to desensitization of vascular smooth muscle. Providing a daily nitrate-free period can help overcome tolerance. Nitrates are also found naturally in soil and water and excess nitrates can cause methemoglobinemia or be linked to cancer.
This document provides information on the pharmacology of diuretics. It begins by explaining that diuretics cause a net loss of sodium and water in urine but sodium balance is restored through homeostatic mechanisms. It then classifies diuretics and describes various classes in detail, including their mechanisms and sites of action, uses, and adverse effects. The classes discussed include high efficacy loop diuretics like furosemide, medium efficacy thiazides, weak carbonic anhydrase inhibitors, potassium sparing aldosterone antagonists, and renal sodium channel inhibitors.
A power point presentation on "Drugs affecting coagulation and anticoagulants" suitable for undergraduate medical students. Also suitable for Post Graduate students of Pharmacology and Pharmaceutical Sciences.
in this presentation i have tried to briefly discuss about diuretics (water pills), their classification, mechanism of action, pharmacokinetics and pharmacodynamics of these drugs
Mucolytic drugs like Mucomyst work by breaking bonds in mucus to decrease its viscosity, making it easier to clear. It is used for abnormal thick mucus and to prevent acetaminophen toxicity. Expectorants also make mucus easier to clear by reducing adhesiveness. Decongestants constrict blood vessels to reduce nasal congestion from infections or allergies. Antitussives suppress coughing. Antihistamines block histamine receptors to relieve allergy symptoms. Bronchodilators relax airways to relieve asthma symptoms. Corticosteroids reduce inflammation for asthma or COPD.
This document discusses adrenergic antagonists (sympatholytics) which inhibit the sympathetic nervous system by blocking adrenergic receptors or neurons. It describes various types of adrenergic blocking drugs that are selective for α and β receptors. Non-selective α-blockers like phenoxybenzamine cause irreversible blockade while phentolamine is competitive. Selective α1-blockers lower blood pressure with minimal effects on cardiac output. Orthostatic hypotension is a common side effect of α-blockers due to inhibition of venous vasoconstriction.
The document discusses different classes of diuretic drugs, including their mechanisms and effects. It describes loop diuretics like furosemide that inhibit sodium chloride reabsorption in the thick ascending limb of Henle's loop, increasing excretion of sodium and chloride in urine. It also discusses thiazide diuretics that act in the early distal tubule by inhibiting carbonic anhydrase and enhancing excretion of magnesium and potassium while inhibiting calcium and uric acid excretion. Finally, it mentions osmotic diuretics like mannitol that cause water retention in the proximal tubule through osmotic effects, resulting in water diuresis.
This document discusses angiotensin receptor blockers (ARBs) which are used to treat hypertension and other cardiovascular conditions. It notes that ARBs work by competitively blocking the angiotensin receptor type 1, leading to vasodilation and other effects. Some examples of individual ARB drugs are provided like losartan, candesartan, and valsartan. The document compares ARBs to ACE inhibitors, noting that ARBs do not cause cough like ACE inhibitors. It concludes by discussing the theoretical rationale and benefits of combining ARBs with ACE inhibitors to more completely suppress the renin-angiotensin system.
Pharmacological management of heart failureNaser Tadvi
Heart failure is caused by decreased cardiac output and increased sympathetic discharge. Drugs used to treat heart failure include diuretics to reduce preload, ACE inhibitors to reduce afterload, beta blockers to attenuate sympathetic activation, and digitalis for its inotropic effects. Newer drugs target vasodilation and myosin activation to further increase cardiac efficiency while reducing energy demands. Combination therapy following an assessment of cardiac function and volume status provides the best approach for management of heart failure.
The document discusses adrenergic drugs, which act on the adrenergic nervous system to produce effects similar to the sympathetic nervous system. It defines adrenergic receptors and classifies adrenergic drugs according to their mode of action, receptor selectivity, and chemical nature. Key adrenergic drugs discussed include adrenaline, noradrenaline, clonidine, and their mechanisms of action, pharmacological effects, indications, and adverse effects.
This document discusses various drug therapies for treating cough, including antitussives that act peripherally like demulcents and local anesthetics, and those that act centrally like opioids and non-opioids. It also covers expectorants that work as mucolytics or bronchial secretion enhancers, as well as nasal decongestants, cold remedies, and other supportive treatments. The target is to provide relief from cough symptoms by acting on sites of action in the peripheral nervous system or central nervous system. A multifaceted approach is often used to manage cough associated with colds through various combinations of drugs.
This document discusses antiepileptic drugs, including their mechanisms of action, classifications, pharmacokinetics, indications, and adverse effects. It classifies antiepileptic drugs based on their actions on ion channels and neurotransmitter systems. The main mechanisms of action are enhancement of GABA transmission, inhibition of sodium channels, and inhibition of calcium channels. Common antiepileptic drugs like phenytoin, carbamazepine, valproic acid, lamotrigine, ethosuximide, gabapentin, vigabatrin, and tiagabine are described in terms of their pharmacological properties and clinical uses.
This document discusses lipoproteins and drugs that lower lipid levels. It begins by defining lipoproteins and how they transport lipids in blood, classifying them into six groups. It then discusses the functions of different lipoproteins and causes of hyperlipoproteinemias. The document focuses on statins, how they work by inhibiting HMG-CoA reductase, and their effects on cholesterol, LDL, HDL, and triglyceride levels. It covers the pharmacokinetics of statins, their adverse effects and uses. Other drug classes discussed include bile acid sequestrants, fibrates, nicotinic acid and their mechanisms and uses for treating different lipid abnormalities.
Diuretics : Dr Renuka Joshi MD,DNB, (FNB )Renuka Buche
This document discusses different classes of diuretic drugs, including their mechanisms of action, examples, effects, dosages, and interactions. It covers loop diuretics like furosemide and bumetanide that act in the thick ascending loop of Henle; thiazide diuretics like hydrochlorothiazide that act in the distal convoluted tubule; and potassium-sparing diuretics like spironolactone and amiloride that act in the collecting duct. It provides recommendations for diuretic use and combinations in the treatment of heart failure and fluid overload.
role of diuretics in the management of congestive heart failurePriyatham Kasaraneni
Diuretics are used to treat congestive heart failure (CHF) by reducing preload and removing edema. They work by increasing urination and fluid loss. Loop diuretics like furosemide are most effective for rapid fluid removal in moderate to severe CHF. Thiazide diuretics are used for mild to moderate cases. Both can cause side effects like hypokalemia and hyponatremia. K+ sparing diuretics and aldosterone inhibitors are also used alone or combined with other diuretics to prevent electrolyte loss. Diuretics relieve symptoms of CHF but do not cure its underlying causes.
6.0 drugs used in Cardio Vascular SystemSaroj Suwal
The document discusses various drugs used for cardiovascular conditions. It covers antihypertensive drugs like diuretics, calcium channel blockers, ACE inhibitors, ARBs, and adrenergic blockers. It defines hypertension and describes the mechanisms and side effects of different classes of antihypertensive drugs. These include thiazide, loop, and potassium sparing diuretics, calcium channel blockers like nifedipine, ACE inhibitors, ARBs, alpha blockers, beta blockers, and centrally acting drugs like clonidine and methyldopa. Cardiotonic drugs are also briefly mentioned.
This document provides information about antidiuretic drugs. It begins by defining antidiuretics as drugs that inhibit water excretion without affecting salt excretion. It then lists common antidiuretic drugs including antidiuretic hormone, desmopressin, thiazide diuretics, and others. The document discusses the mechanism of action of antidiuretic hormone, its effects on various organs like the kidneys and blood vessels, and conditions it can be used to treat like diabetes insipidus. It also covers antidiuretic hormone receptors, interactions with other drugs, and potential adverse effects.
This document discusses drugs used to treat congestive heart failure (CHF). CHF occurs when the heart cannot pump enough blood to meet the body's needs. Key drugs mentioned include digitalis glycosides like digoxin, which increase the force of heart contractions; diuretics like furosemide that reduce fluid buildup; ACE inhibitors and ARBs that lower blood pressure and prevent further heart damage; and inotropic drugs like dobutamine that strengthen heart contractions. Adverse effects, mechanisms of action, and guidelines for use are provided for several common CHF medications.
This document discusses different types of volume expanders used to increase blood volume, including crystalloids like normal saline and Ringer's lactate, as well as colloids like albumin, dextrans, gelatin polymers, and hydroxyethyl starch. It provides details on the composition and uses of various fluids, as well as their advantages and disadvantages. The ideal properties of volume expanders are described. Crystalloids expand extracellular volume while colloids are better at expanding plasma volume due to their larger size, though some colloids can interfere with coagulation or cause allergic reactions.
Congestive heart failure (CHF) is a condition where the heart cannot pump enough blood to meet the body's needs. It can be caused by systolic or diastolic dysfunction. Common symptoms include fatigue, weight gain, cough, and shortness of breath. Treatment includes drugs that increase cardiac contractility, reduce fluid retention, block the renin-angiotensin system, dilate blood vessels, and reduce heart rate. New drugs like ivabradine and sacubitril/valsartan may also help lower hospitalization rates.
1) Diuretics are drugs that cause net loss of sodium and water in urine. They are classified as loop diuretics, thiazide diuretics, potassium-sparing diuretics, carbonic anhydrase inhibitors, and osmotic diuretics.
2) Loop diuretics like furosemide work by inhibiting sodium-potassium-chloride reabsorption in the loop of Henle, while thiazide diuretics inhibit sodium-chloride reabsorption in the distal tubule.
3) Diuretics are used to treat conditions like edema, hypertension, heart failure, nephrotic syndrome, and cerebral edema. Common side effects include
Antiarrhythmic drugs are used to treat and prevent cardiac arrhythmias by blocking ion channels involved in cardiac impulse generation and conduction. Class I drugs like quinidine and procainamide block sodium channels to prolong the action potential duration, while Class IB drugs like lignocaine shorten repolarization. Class III drugs like amiodarone block potassium channels to prolong the action potential. Calcium channel blockers like verapamil inhibit calcium influx. Other drugs include adenosine for paroxysmal supraventricular tachycardia, beta blockers for supraventricular arrhythmias, and atropine for bradycardias. Adverse effects vary between drugs but include arrhythmias, heart block and QT prolong
This document discusses various classes of antihypertensive drugs used to treat high blood pressure. It describes 7 classes: diuretics, beta blockers, calcium channel blockers, ACE inhibitors, angiotensin receptor blockers, sympatholytic and alpha adrenergic blockers, and direct arterial vasodilators. For each class, it provides examples of drugs, their mechanisms of action, advantages, indications, side effects and other relevant information. Diuretics are further broken down into their types, mechanisms, effects and side effects.
This document discusses beta-blockers, including their discovery, mechanism of action, uses, side effects, and current research. Beta-blockers were discovered in 1962 and work by blocking beta-1 and beta-2 adrenoceptors. They are used to treat various cardiovascular conditions like hypertension, angina, and arrhythmias. While generally effective, they can cause side effects like bradycardia, bronchospasm, and hypoglycemia. Current research is exploring their potential roles in cancer treatment and fracture prevention.
This document provides an overview of the autonomic nervous system (ANS). It describes the ANS as having sympathetic and parasympathetic divisions that work to regulate involuntary body functions like heart rate and digestion. The sympathetic nervous system uses norepinephrine as a neurotransmitter and prepares the body for "fight or flight" while the parasympathetic uses acetylcholine and allows the body to "rest and digest". The document discusses how drugs can mimic or block these neurotransmitters to stimulate or inhibit the ANS.
The nervous system controls all major body functions and is divided into central and peripheral systems. The peripheral system includes the somatic and autonomic systems. The autonomic nervous system (ANS) controls involuntary functions like circulation, respiration, digestion and temperature regulation. It is divided into the sympathetic and parasympathetic systems which use norepinephrine and acetylcholine as neurotransmitters respectively. Adrenergic drugs mimic sympathetic effects by stimulating adrenergic receptors, while anticholinergic drugs block parasympathetic effects by blocking cholinergic receptors. These receptor systems allow drugs to selectively target specific organ systems.
Pharmacological management of heart failureNaser Tadvi
Heart failure is caused by decreased cardiac output and increased sympathetic discharge. Drugs used to treat heart failure include diuretics to reduce preload, ACE inhibitors to reduce afterload, beta blockers to attenuate sympathetic activation, and digitalis for its inotropic effects. Newer drugs target vasodilation and myosin activation to further increase cardiac efficiency while reducing energy demands. Combination therapy following an assessment of cardiac function and volume status provides the best approach for management of heart failure.
The document discusses adrenergic drugs, which act on the adrenergic nervous system to produce effects similar to the sympathetic nervous system. It defines adrenergic receptors and classifies adrenergic drugs according to their mode of action, receptor selectivity, and chemical nature. Key adrenergic drugs discussed include adrenaline, noradrenaline, clonidine, and their mechanisms of action, pharmacological effects, indications, and adverse effects.
This document discusses various drug therapies for treating cough, including antitussives that act peripherally like demulcents and local anesthetics, and those that act centrally like opioids and non-opioids. It also covers expectorants that work as mucolytics or bronchial secretion enhancers, as well as nasal decongestants, cold remedies, and other supportive treatments. The target is to provide relief from cough symptoms by acting on sites of action in the peripheral nervous system or central nervous system. A multifaceted approach is often used to manage cough associated with colds through various combinations of drugs.
This document discusses antiepileptic drugs, including their mechanisms of action, classifications, pharmacokinetics, indications, and adverse effects. It classifies antiepileptic drugs based on their actions on ion channels and neurotransmitter systems. The main mechanisms of action are enhancement of GABA transmission, inhibition of sodium channels, and inhibition of calcium channels. Common antiepileptic drugs like phenytoin, carbamazepine, valproic acid, lamotrigine, ethosuximide, gabapentin, vigabatrin, and tiagabine are described in terms of their pharmacological properties and clinical uses.
This document discusses lipoproteins and drugs that lower lipid levels. It begins by defining lipoproteins and how they transport lipids in blood, classifying them into six groups. It then discusses the functions of different lipoproteins and causes of hyperlipoproteinemias. The document focuses on statins, how they work by inhibiting HMG-CoA reductase, and their effects on cholesterol, LDL, HDL, and triglyceride levels. It covers the pharmacokinetics of statins, their adverse effects and uses. Other drug classes discussed include bile acid sequestrants, fibrates, nicotinic acid and their mechanisms and uses for treating different lipid abnormalities.
Diuretics : Dr Renuka Joshi MD,DNB, (FNB )Renuka Buche
This document discusses different classes of diuretic drugs, including their mechanisms of action, examples, effects, dosages, and interactions. It covers loop diuretics like furosemide and bumetanide that act in the thick ascending loop of Henle; thiazide diuretics like hydrochlorothiazide that act in the distal convoluted tubule; and potassium-sparing diuretics like spironolactone and amiloride that act in the collecting duct. It provides recommendations for diuretic use and combinations in the treatment of heart failure and fluid overload.
role of diuretics in the management of congestive heart failurePriyatham Kasaraneni
Diuretics are used to treat congestive heart failure (CHF) by reducing preload and removing edema. They work by increasing urination and fluid loss. Loop diuretics like furosemide are most effective for rapid fluid removal in moderate to severe CHF. Thiazide diuretics are used for mild to moderate cases. Both can cause side effects like hypokalemia and hyponatremia. K+ sparing diuretics and aldosterone inhibitors are also used alone or combined with other diuretics to prevent electrolyte loss. Diuretics relieve symptoms of CHF but do not cure its underlying causes.
6.0 drugs used in Cardio Vascular SystemSaroj Suwal
The document discusses various drugs used for cardiovascular conditions. It covers antihypertensive drugs like diuretics, calcium channel blockers, ACE inhibitors, ARBs, and adrenergic blockers. It defines hypertension and describes the mechanisms and side effects of different classes of antihypertensive drugs. These include thiazide, loop, and potassium sparing diuretics, calcium channel blockers like nifedipine, ACE inhibitors, ARBs, alpha blockers, beta blockers, and centrally acting drugs like clonidine and methyldopa. Cardiotonic drugs are also briefly mentioned.
This document provides information about antidiuretic drugs. It begins by defining antidiuretics as drugs that inhibit water excretion without affecting salt excretion. It then lists common antidiuretic drugs including antidiuretic hormone, desmopressin, thiazide diuretics, and others. The document discusses the mechanism of action of antidiuretic hormone, its effects on various organs like the kidneys and blood vessels, and conditions it can be used to treat like diabetes insipidus. It also covers antidiuretic hormone receptors, interactions with other drugs, and potential adverse effects.
This document discusses drugs used to treat congestive heart failure (CHF). CHF occurs when the heart cannot pump enough blood to meet the body's needs. Key drugs mentioned include digitalis glycosides like digoxin, which increase the force of heart contractions; diuretics like furosemide that reduce fluid buildup; ACE inhibitors and ARBs that lower blood pressure and prevent further heart damage; and inotropic drugs like dobutamine that strengthen heart contractions. Adverse effects, mechanisms of action, and guidelines for use are provided for several common CHF medications.
This document discusses different types of volume expanders used to increase blood volume, including crystalloids like normal saline and Ringer's lactate, as well as colloids like albumin, dextrans, gelatin polymers, and hydroxyethyl starch. It provides details on the composition and uses of various fluids, as well as their advantages and disadvantages. The ideal properties of volume expanders are described. Crystalloids expand extracellular volume while colloids are better at expanding plasma volume due to their larger size, though some colloids can interfere with coagulation or cause allergic reactions.
Congestive heart failure (CHF) is a condition where the heart cannot pump enough blood to meet the body's needs. It can be caused by systolic or diastolic dysfunction. Common symptoms include fatigue, weight gain, cough, and shortness of breath. Treatment includes drugs that increase cardiac contractility, reduce fluid retention, block the renin-angiotensin system, dilate blood vessels, and reduce heart rate. New drugs like ivabradine and sacubitril/valsartan may also help lower hospitalization rates.
1) Diuretics are drugs that cause net loss of sodium and water in urine. They are classified as loop diuretics, thiazide diuretics, potassium-sparing diuretics, carbonic anhydrase inhibitors, and osmotic diuretics.
2) Loop diuretics like furosemide work by inhibiting sodium-potassium-chloride reabsorption in the loop of Henle, while thiazide diuretics inhibit sodium-chloride reabsorption in the distal tubule.
3) Diuretics are used to treat conditions like edema, hypertension, heart failure, nephrotic syndrome, and cerebral edema. Common side effects include
Antiarrhythmic drugs are used to treat and prevent cardiac arrhythmias by blocking ion channels involved in cardiac impulse generation and conduction. Class I drugs like quinidine and procainamide block sodium channels to prolong the action potential duration, while Class IB drugs like lignocaine shorten repolarization. Class III drugs like amiodarone block potassium channels to prolong the action potential. Calcium channel blockers like verapamil inhibit calcium influx. Other drugs include adenosine for paroxysmal supraventricular tachycardia, beta blockers for supraventricular arrhythmias, and atropine for bradycardias. Adverse effects vary between drugs but include arrhythmias, heart block and QT prolong
This document discusses various classes of antihypertensive drugs used to treat high blood pressure. It describes 7 classes: diuretics, beta blockers, calcium channel blockers, ACE inhibitors, angiotensin receptor blockers, sympatholytic and alpha adrenergic blockers, and direct arterial vasodilators. For each class, it provides examples of drugs, their mechanisms of action, advantages, indications, side effects and other relevant information. Diuretics are further broken down into their types, mechanisms, effects and side effects.
This document discusses beta-blockers, including their discovery, mechanism of action, uses, side effects, and current research. Beta-blockers were discovered in 1962 and work by blocking beta-1 and beta-2 adrenoceptors. They are used to treat various cardiovascular conditions like hypertension, angina, and arrhythmias. While generally effective, they can cause side effects like bradycardia, bronchospasm, and hypoglycemia. Current research is exploring their potential roles in cancer treatment and fracture prevention.
This document provides an overview of the autonomic nervous system (ANS). It describes the ANS as having sympathetic and parasympathetic divisions that work to regulate involuntary body functions like heart rate and digestion. The sympathetic nervous system uses norepinephrine as a neurotransmitter and prepares the body for "fight or flight" while the parasympathetic uses acetylcholine and allows the body to "rest and digest". The document discusses how drugs can mimic or block these neurotransmitters to stimulate or inhibit the ANS.
The nervous system controls all major body functions and is divided into central and peripheral systems. The peripheral system includes the somatic and autonomic systems. The autonomic nervous system (ANS) controls involuntary functions like circulation, respiration, digestion and temperature regulation. It is divided into the sympathetic and parasympathetic systems which use norepinephrine and acetylcholine as neurotransmitters respectively. Adrenergic drugs mimic sympathetic effects by stimulating adrenergic receptors, while anticholinergic drugs block parasympathetic effects by blocking cholinergic receptors. These receptor systems allow drugs to selectively target specific organ systems.
Autonomic Nervous System Pharmacology and Cholinergics (updated 2016) - drdhr...http://neigrihms.gov.in/
The document discusses autonomic drugs and the autonomic nervous system. It notes that autonomic drugs are clinically relevant and used to treat conditions like angina, heart failure, and high blood pressure. The autonomic nervous system maintains homeostasis through the sympathetic and parasympathetic nervous systems. Cholinergic transmission occurs through the release and binding of acetylcholine to nicotinic and muscarinic receptors.
drugs that affect the autonomic nervous system.ppt [autosaved] [autosaved]Sujit Karpe
This document provides an overview of the autonomic nervous system and discusses various adrenergic and cholinergic drugs. It defines the sympathetic and parasympathetic nervous systems and describes how adrenergic drugs stimulate the sympathetic system while cholinergic drugs stimulate the parasympathetic system. It then discusses the classification, mechanisms of action, effects and uses of various adrenergic and cholinergic drugs including catecholamines, alpha and beta receptor agonists and antagonists, anticholinesterases and direct acting cholinergic drugs. It also touches on myasthenia gravis and organophosphorus poisoning.
The document discusses drugs that act on the autonomic nervous system, including:
- Adrenergic drugs that stimulate the sympathetic nervous system by mimicking norepinephrine and epinephrine. This includes both catecholamines and non-catecholamines.
- Adrenergic blockers that block the actions of norepinephrine and epinephrine at adrenergic receptor sites. This includes both alpha-blockers and beta-blockers.
- Cholinergic drugs that stimulate the parasympathetic nervous system by mimicking acetylcholine, and anticholinergic drugs that block acetylcholine's actions. Cholinergic drugs can be direct-acting or indirect-
The document provides information about the autonomic nervous system (ANS). It describes that the ANS acts involuntarily to control organs like the heart, lungs, intestines and glands. The ANS has two divisions - the sympathetic and parasympathetic nervous systems which generally work in opposition. The sympathetic system prepares the body for "fight or flight" while the parasympathetic system helps with "rest and digest" functions. Key neurotransmitters that are discussed are norepinephrine for the sympathetic system and acetylcholine for the parasympathetic system. Drugs can mimic or block these neurotransmitters to affect ANS functions.
The autonomic nervous system (ANS) controls involuntary body functions through two divisions - the sympathetic and parasympathetic systems. The sympathetic division uses the neurotransmitter norepinephrine to activate the fight or flight response. The parasympathetic division uses acetylcholine primarily to restore and maintain bodily functions at rest. Both systems work in opposition through receptors to precisely control organs like the heart, lungs, and digestive system. Diseases like Horner's syndrome involving the ANS can impact functions like sweating and eye movement. Tests of the ANS evaluate responses like heart rate and blood pressure with activities like breathing and standing.
The document provides an overview of the autonomic nervous system (ANS), including its distribution and differences between the sympathetic and parasympathetic nervous systems. It discusses neurohumoral transmission in the ANS and the main neurotransmitters for each division. The sympathetic nervous system uses norepinephrine and epinephrine as neurotransmitters, while the parasympathetic nervous system uses acetylcholine. It also briefly describes the synthesis of acetylcholine and catecholamines.
Introduction to Autonomic Nervous systemNaser Tadvi
The document provides an overview of the autonomic nervous system (ANS), including its distribution and differences between the sympathetic and parasympathetic nervous systems. It discusses that the ANS is divided into the sympathetic and parasympathetic nervous systems. The sympathetic nervous system uses norepinephrine as its neurotransmitter and is involved in the body's fight or flight response. The parasympathetic nervous system uses acetylcholine as its neurotransmitter and is involved in rest and digest functions. Neurotransmission in the ANS occurs through the release and binding of neurotransmitters to receptors on target organs.
This document provides an overview of the autonomic nervous system (ANS) and autonomic drugs. It begins by outlining the objectives and reviewing the physiology of the ANS, distinguishing the sympathetic and parasympathetic nervous systems. It then discusses the major neurotransmitters of the ANS (acetylcholine, epinephrine, norepinephrine) and how different classes of autonomic drugs (sympathomimetics, parasympathomimetics) act on the sympathetic and parasympathetic systems. Specific examples are provided of cholinergic drugs and their clinical uses and effects in various organ systems.
General anesthetics are drugs that produce reversible loss of sensation and consciousness to facilitate surgery. They act primarily by enhancing the action of the inhibitory neurotransmitter GABA at GABAA receptors, causing chloride channels to open. This hyperpolarizes neurons and reduces neuronal excitability. The main stages of general anesthesia include induction, maintenance, and recovery. Drugs are administered via inhalation or intravenous routes to induce unconsciousness, analgesia, muscle relaxation, and amnesia in a safe and controlled manner.
The document discusses central nervous system (CNS) stimulants. It defines stimulants as substances that increase behavioral activity when administered. CNS stimulants can elevate mood, increase motor activity and alertness, and decrease need for sleep. The mechanisms of action of stimulants include blocking neurotransmitter reuptake, promoting neurotransmitter release, and blocking metabolism or antagonizing inhibitory neurotransmitters. Specific stimulants discussed include amphetamine, picrotoxin, and strychnine, along with their mechanisms and effects on mice.
The autonomic nervous system (ANS) modulates the activity of involuntary organs like the heart, lungs, and gastrointestinal tract. It has sympathetic and parasympathetic divisions. The sympathetic division prepares the body for emergencies through effects like increased heart rate and dilation of bronchioles. The parasympathetic division has opposite relaxing effects and prepares the body for rest. The ANS uses acetylcholine and norepinephrine as neurotransmitters and targets organs through muscarinic, nicotinic, and adrenergic receptors. Drugs can mimic or block the effects of the ANS. Diseases and toxins can also impact the ANS.
Serotonin is a monoamine neurotransmitter synthesized from tryptophan. It is found extensively in the gastrointestinal tract and in serotonergic neurons in the central nervous system. Serotonin receptors include 5-HT1-7 and are involved in various physiological functions like mood, appetite, sleep, and pain perception. Imbalances in the serotonergic system are associated with disorders like depression, anxiety, schizophrenia, and impulse control disorders. Drugs that affect the serotonergic system include SSRIs, SNRIs, triptans, 5-HT3 antagonists, buspirone, and MAOIs.
The document discusses the autonomic and somatic nervous systems. It begins by defining the autonomic nervous system as the subdivision of the peripheral nervous system that regulates involuntary body functions like smooth muscle contraction and gland secretion. It then describes the two divisions of the autonomic nervous system - the sympathetic and parasympathetic nervous systems - and their opposing roles in mobilization versus rest and digestion. The document also discusses the somatic nervous system and how it differs from the autonomic system in having a single motor neuron that directly innervates skeletal muscle.
3 ANS PHARMACOLOGY FOR PHARMACY 01 Midwife 2015(1).pptxwakogeleta
This document discusses autonomic drugs and their classification. It begins by outlining the objectives of understanding different classes of autonomic drugs and their effects. It then provides details on the autonomic nervous system, including its divisions and neurotransmitters. The main classes of autonomic drugs discussed are cholinergic agents, anticholinergic agents, adrenergic agents, and ganglionic blockers. Specific drugs within each class are defined along with their mechanisms of action, therapeutic uses, side effects, and contraindications. Neuromuscular blocking agents are also briefly covered.
The autonomic nervous system (ANS) controls involuntary body functions through the sympathetic and parasympathetic divisions. The sympathetic division uses norepinephrine as its neurotransmitter and is active during fight or flight responses. The parasympathetic division uses acetylcholine and is active during rest. Both have preganglionic and postganglionic neurons connected by autonomic ganglia. The ANS regulates functions of organs like the heart, blood vessels, lungs, GI tract and more to maintain homeostasis.
This document provides an overview of the autonomic nervous system (ANS). It discusses the divisions of the ANS including the sympathetic and parasympathetic nervous systems. Key points covered include the anatomical organization of the ANS from the central nervous system to peripheral ganglia. The roles and effects of the sympathetic and parasympathetic systems on various organs are described. Neurotransmitters, receptors, and reflexes of the ANS are also summarized.
This document provides tips for creating successful content on TikTok. It discusses that raw, authentic content focused on providing value works best on TikTok rather than overly produced content. It recommends creating video series rather than focusing on trends. It also provides tips for using hashtags, posting regularly, engaging with your audience, and using hooks and titles to capture viewers' attention. The key takeaway is that TikTok rewards content that provides genuine value to viewers.
This document provides guidelines for preparing an investment proposal (PIN) to present to the Management Investment Committee (MIC) for evaluation. The PIN should address: 1) the profitability of the investment based on internal rate of return estimates, 2) available competitive strategies and the recommended strategy, 3) what must be done well to succeed, and 4) risks and opportunities and their potential impacts. If approved, the assumptions in the PIN will become the objectives for the business. Actual performance will later be compared to targets in a post-audit review at exit. Overhead and depreciation estimates are provided to aid financial evaluations.
The document outlines the key elements that make up a good project funding proposal, including an introduction describing the project aim and qualifications, a need statement, measurable objectives and goals, an evaluation plan, a budget summary and detailed budget, and plans for follow-up funding. A good proposal provides all necessary information on these elements to convince the funding agency to support the project.
The document discusses principles of oral surgery including access, visibility, and flap design. It states that adequate access requires wide mouth opening and retraction of tissues away from the surgical field. Improved access can be gained by creating surgical flaps using incisions. Key principles of incisions and flap design are outlined such as using a sharp blade, firm strokes, avoiding vital structures, and designing flaps to ensure adequate blood supply and healing. Common flap types including triangular, trapezoidal, envelope, and semilunar flaps are described. Careful handling of tissues is also emphasized to minimize damage.
Lecture 3 Facial cosmetic surgery
Maxillofacial Surgery
Dental Students Fifth Year second semester
Al Azhar University Gaza Palestine
Dr. Lama El Banna
https://twitter.com/lama_k_banna
Lecture 1 Facial cosmetic surgery
Maxillofacial Surgery
Dental Students Fifth Year second semester
Al Azhar University Gaza Palestine
Dr. Lama El Banna
https://twitter.com/lama_k_banna
Facial neuropathology Maxillofacial SurgeryLama K Banna
Lecture 4 facial neuropathology
Maxillofacial Surgery
Dental Students Fifth Year second semester
Al Azhar University Gaza Palestine
Dr. Lama El Banna
https://twitter.com/lama_k_banna
Lecture 2 Facial cosmetic surgery
Maxillofacial Surgery
Dental Students Fifth Year second semester
Al Azhar University Gaza Palestine
Dr. Lama El Banna
https://twitter.com/lama_k_banna
Lecture 12 general considerations in treatment of tmdLama K Banna
Maxillofacial Surgery
Dental Students Fifth Year First semester
Lecture Name 12 general considerations in the treatment of TMJ
Al Azhar University Gaza Palestine
Dr. Lama El Banna
Maxillofacial Surgery
Dental Students Fifth Year First semester
Lecture Name TMJ temporomandibular joint
Lecture 10
Al Azhar University Gaza Palestine
Dr. Lama El Banna
https://twitter.com/lama_k_banna
Lecture 11 temporomandibular joint Part 3Lama K Banna
Maxillofacial Surgery
Dental Students Fifth Year First semester
Lecture Name TMJ temporomandibular joint Part 3
Lecture 11
Al Azhar University Gaza Palestine
Dr. Lama El Banna
Maxillofacial Surgery
Dental Students Fifth Year First semester
Lecture Name TMJ anatomy examination 2
Lecture 9
Al Azhar University Gaza Palestine
Dr. Lama El Banna
Lecture 7 correction of dentofacial deformities Part 2Lama K Banna
Maxillofacial Surgery
Dental Students Fifth Year First semester
Lecture Name Correction of dentofacial deformities Part 2
Lecture 7
Al Azhar University Gaza Palestine
Dr. Lama El Banna
Lecture 8 management of patients with orofacial cleftsLama K Banna
Maxillofacial Surgery
Dental Students Fifth Year First semester
Lecture Name management of patients with orofacial clefts
Lecture 8
Al Azhar University Gaza Palestine
Dr. Lama El Banna
Lecture 5 Diagnosis and management of salivary gland disorders Part 2Lama K Banna
Maxillofacial Surgery
Dental Students Fifth Year First semester
Lecture Name Salivary gland 2
Diagnosis and management of salivary gland disorders Part 2
Al Azhar University Gaza Palestine
Dr. Lama El Banna
Lecture 6 correction of dentofacial deformitiesLama K Banna
The document discusses epidemiological studies that estimate the prevalence of malocclusion and dentofacial deformities in the United States population. The National Health and Nutrition Examination Survey found that approximately 2% of the US population has severe mandibular deficiency or vertical maxillary excess, while other abnormalities such as mandibular excess or open bite affect about 0.3-0.1% of the population. Overall, about 2.7% of Americans may have dentofacial deformities severe enough to require surgical treatment along with orthodontics.
lecture 4 Diagnosis and management of salivary gland disordersLama K Banna
Maxillofacial Surgery
Dental Students Fifth Year First semester
Lecture Name Salivary gland
Diagnosis and management of salivary gland disorders
Al Azhar University Gaza Palestine
Dr. Lama El Banna
This document discusses principles of managing panfacial fractures, including anatomic considerations of the craniofacial skeleton and buttresses. It describes two main theories for management: bottom up/inside out and top down/outside in. Reduction, fixation, immobilization and early return of function are discussed. Closed reduction uses manipulation without visualization, while open reduction allows visualization but requires surgery. Various fixation methods are outlined, including arch bars, wiring techniques, and maxillomandibular fixation.
Maxillofacial Surgery
Dental Students Fifth Year First semester
Lecture Name maxillofacial trauma part 2
Al Azhar University Gaza Palestine
Dr. Lama El Banna
These lecture slides, by Dr Sidra Arshad, offer a simplified look into the mechanisms involved in the regulation of respiration:
Learning objectives:
1. Describe the organisation of respiratory center
2. Describe the nervous control of inspiration and respiratory rhythm
3. Describe the functions of the dorsal and respiratory groups of neurons
4. Describe the influences of the Pneumotaxic and Apneustic centers
5. Explain the role of Hering-Breur inflation reflex in regulation of inspiration
6. Explain the role of central chemoreceptors in regulation of respiration
7. Explain the role of peripheral chemoreceptors in regulation of respiration
8. Explain the regulation of respiration during exercise
9. Integrate the respiratory regulatory mechanisms
10. Describe the Cheyne-Stokes breathing
Study Resources:
1. Chapter 42, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 36, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 13, Human Physiology by Lauralee Sherwood, 9th edition
Histololgy of Female Reproductive System.pptxAyeshaZaid1
Dive into an in-depth exploration of the histological structure of female reproductive system with this comprehensive lecture. Presented by Dr. Ayesha Irfan, Assistant Professor of Anatomy, this presentation covers the Gross anatomy and functional histology of the female reproductive organs. Ideal for students, educators, and anyone interested in medical science, this lecture provides clear explanations, detailed diagrams, and valuable insights into female reproductive system. Enhance your knowledge and understanding of this essential aspect of human biology.
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We’re talking about Vedic Meditation, a form of meditation that has been around for at least 5,000 years. Back then, the people who lived in the Indus Valley, now known as India and Pakistan, practised meditation as a fundamental part of daily life. This knowledge that has given us yoga and Ayurveda, was known as Veda, hence the name Vedic. And though there are some written records, the practice has been passed down verbally from generation to generation.
DECLARATION OF HELSINKI - History and principlesanaghabharat01
This SlideShare presentation provides a comprehensive overview of the Declaration of Helsinki, a foundational document outlining ethical guidelines for conducting medical research involving human subjects.
Promoting Wellbeing - Applied Social Psychology - Psychology SuperNotesPsychoTech Services
A proprietary approach developed by bringing together the best of learning theories from Psychology, design principles from the world of visualization, and pedagogical methods from over a decade of training experience, that enables you to: Learn better, faster!
Adhd Medication Shortage Uk - trinexpharmacy.comreignlana06
The UK is currently facing a Adhd Medication Shortage Uk, which has left many patients and their families grappling with uncertainty and frustration. ADHD, or Attention Deficit Hyperactivity Disorder, is a chronic condition that requires consistent medication to manage effectively. This shortage has highlighted the critical role these medications play in the daily lives of those affected by ADHD. Contact : +1 (747) 209 – 3649 E-mail : sales@trinexpharmacy.com
1. Nervous System
Dr. Mahmoud H. Taleb
Assistant Professor of Pharmacology and Toxicology
Head of Pharmacology and Medical sciences Department
Faculty of Pharmacy- Al azhar University
2. Central Nervous System (CNS) - Brain and
spinal cord
Peripheral Nervous System (PNS) - Located
outside the brain & spinal cord
* Autonomic Nervous System (ANS) &
the somatic
The PNS receives stimuli from the CNS &
initiates responses to the stimuli after it’s
interpreted by the brain
3. General organization of NSGeneral organization of NS
1.1. Central Nervous SystemCentral Nervous System
► The brain + the spinal cordThe brain + the spinal cord
• The center of integration and controlThe center of integration and control
1.1. Peripheral Nervous SystemPeripheral Nervous System
► The nervous system outside of the brain andThe nervous system outside of the brain and
spinal cordspinal cord
► Consists of:Consists of:
• 31 Spinal nerves31 Spinal nerves
► Carry info to and from the spinal cordCarry info to and from the spinal cord
• 12 Cranial nerves12 Cranial nerves
► Carry info to and from the brainCarry info to and from the brain
Dr. Mahmoud H. 3
4. ► Responsible for communication btwn theResponsible for communication btwn the
CNS and the rest of the body.CNS and the rest of the body.
► Can be divided into:Can be divided into:
• Sensory DivisionSensory Division
►Afferent divisionAfferent division
• Conducts impulses from receptors to the CNSConducts impulses from receptors to the CNS
• Informs the CNS of the state of the body interior and exteriorInforms the CNS of the state of the body interior and exterior
• Sensory nerve fibers can beSensory nerve fibers can be somaticsomatic (from skin, skeletal(from skin, skeletal
muscles or joints) ormuscles or joints) or visceralvisceral (from organs w/i the ventral(from organs w/i the ventral
body cavity)body cavity)
• Motor DivisionMotor Division
►Efferent divisionEfferent division
• Conducts impulses from CNS to effectors (muscles/glands)Conducts impulses from CNS to effectors (muscles/glands)
• Motor nerve fibersMotor nerve fibers
Dr. Mahmoud H. 4
Peripheral Nervous System
5. Motor Efferent DivisionMotor Efferent Division
► Can be divided further:Can be divided further:
• Somatic nervous systemSomatic nervous system
►VOLUNTARY (generally)VOLUNTARY (generally)
►Somatic nerve fibers that conduct impulses fromSomatic nerve fibers that conduct impulses from
the CNS to skeletal musclesthe CNS to skeletal muscles
• Autonomic nervous systemAutonomic nervous system
►INVOLUNTARY (generally)INVOLUNTARY (generally)
►Conducts impulses from the CNS to smoothConducts impulses from the CNS to smooth
muscle, cardiac muscle, and glands.muscle, cardiac muscle, and glands.
5
6. Autonomic Nervous SystemAutonomic Nervous System
Can be divided into:Can be divided into:
• Sympathetic NervousSympathetic Nervous SystemSystem
• ““Fight or Flight”Fight or Flight”
• ParasympatheticNervousParasympatheticNervous
SystemSystem
• ““Rest and Digest”Rest and Digest”
6
These 2 systems are antagonistic.These 2 systems are antagonistic.
Typically, we balance these 2 to keepTypically, we balance these 2 to keep
ourselves in a state of dynamic balance.ourselves in a state of dynamic balance.
7. Divisions of human nervous systemDivisions of human nervous system
7Dr. Mahmoud H. Taleb
9. Summary of some neurotransmitters of the central nervousSummary of some neurotransmitters of the central nervous
system. GABA = λ-aminobutyric acidsystem. GABA = λ-aminobutyric acid
Dr. Mahmoud H. 9
13. Is the neurotransmitter of the parasympatheticIs the neurotransmitter of the parasympathetic
N.S and cholinergic nerves, it is therapeuticallyN.S and cholinergic nerves, it is therapeutically
of no importance due to:of no importance due to:
1. Multiplicity of actions.1. Multiplicity of actions.
2. Rapid inactivation by acetyl-cholinesterase.2. Rapid inactivation by acetyl-cholinesterase.
3. Has both muscarinic and nicotinic activity.3. Has both muscarinic and nicotinic activity.
ACHACH
Dr. Mahmoud H. Taleb 13
23. Neurotransmission in adrenergic neurons closelyNeurotransmission in adrenergic neurons closely
resembles that already described for the cholinergicresembles that already described for the cholinergic
neurons except that norepinephrine is theneurons except that norepinephrine is the
neurotransmitter instead of acetylcholine.neurotransmitter instead of acetylcholine.
Neurotransmission takes place at numerous bead-likeNeurotransmission takes place at numerous bead-like
enlargements called varicosities. The process involvesenlargements called varicosities. The process involves
five steps:synthesis, storage, release, and receptorfive steps:synthesis, storage, release, and receptor
binding of norepinephrine, followed by removal of thebinding of norepinephrine, followed by removal of the
neurotransmitter from the synaptic gapneurotransmitter from the synaptic gap
A. NeurotrANsmissioN AtA. NeurotrANsmissioN At
AdreNergic NeuroNsAdreNergic NeuroNs
Dr. Mahmoud H. Taleb 23
24. : Adrenergics and Adrenergic: Adrenergics and Adrenergic
BlockersBlockers
Drugs that Stimulate the sympathetic Nervous
System (adrenergics, adrenergic agonists,
sypathomimetics, or adrenomimetics)
Mimic the sympathetic neruotransmitters
norepinephrine and epinephrine
Act on one or more adrenergic receptor sites
located on the cells of smooth muscles -
heart, bronchioles, GI tract, bladder, eye
4 main receptors (alpha-1, alpha-2, beta-1,
beta-2)
26. Sympathomimetics/Sympathomimetics/
AdrenomimeticsAdrenomimetics
Stimulate adrenergic receptors: 3 categories
1. Direct-acting = directly stimulates receptors
(epinephrine or norepinephrine)
2. Indirect-acting = stimulates release of norep.
from terminal nerve endings (amphetamine)
3. Mixed-acting (indirect & direct) = stimulates
receptor sites & release of norep. from nerve
endings (Ephedrine)
27. Sympathomimetic Agents/Sympathomimetic Agents/
AdrenergicsAdrenergics
Action - Many of the adrenergic drugs
stimulate more than one of the adrenergic
receptor sites (alpha & Beta)
Response = Inc. BP, pupil dilation, inc. HR, &
bronchodilation
Use = Cardiac stimulation, bronchodilator,
decongestant
Side effects = Hyperness in body
28. Sympathomimetics/AdrenergicsSympathomimetics/Adrenergics
Albuterol - Beta-2 agonist (bronchodilation)
Use - bronchospasm, asthma, bronchitis
SE - nervousness, restlessness
CI - severe cardiac disease, HTN
Epinephrine - stimulates alpha & beta
Use - allergic reaction, cardiac arrest
SE - nervousness, agitation
CI - cardiac dysrhythmias
29. Adrenergic AgentsAdrenergic Agents
Dopamine - alpha-1 & beta-1
stimulation
Use - Hypotension, shock, inc. cardiac
output, improve perfusion to vital
organs
SE - N & V, headache
CI - V. Tach
31. Nonselective vs Selective BetaNonselective vs Selective Beta
blockersblockers
Nonselective have an equal inhibitory effect
on B1 & B2 receptors -
- Drugs have lots of interactions due to lots of
alpha/beta receptor sites throughout body
- use with caution on clients with cardiac
failure or asthma
Selective B1 helpful in asthma clients
32. Adrenergic Blocking AgentsAdrenergic Blocking Agents
Inderal (Propranolol) - Nonselective
Use - angina, dysrhythmias, HTN, migraines
SE - Many d/t nonselective
CI - asthma, heart block > 1st degree
Minipress (Prazosin) - A blocker
Use - mild to mod. HTN
SE - orthostatic hypotension
Tenormin (Atenolol), Lopressor (Metoprolol)
B1 (cardio) selective
Use - mild to mod HTN, angina
33. Cholinergics andCholinergics and
AnticholinergicsAnticholinergics
Cholinergics stimulate the parasympathetic
nervous system
Mimic the neurotransmitter acetylcholine
2 types of cholinergic receptors
1. muscarinic - stimulates smooth muscle &
slows HR
2. nicotinic - affect skeletal muscle
Many = nonselective & affect both receptors
Some affect only the muscarinic receptors
and not the nicotinic receptors
35. Cholinergic AgentsCholinergic Agents
Direct acting - act on the receptors to
activate a tissue response
Indirect acting - inhibit the action of the
enzyme cholinesterase
(acetylcholinesterase - ACH)
Major uses = Stimulate bladder & GI
tone, constrict pupils (miosis), neuro-
muscular transmission
37. Cholinergic AgentCholinergic Agent
(Parasympathomimetics)(Parasympathomimetics)
Bethanechol (Urecholine) selective to
muscarinic receptors, mimic action of
acetylcholine
Use - For urinary retention
* Take on an empty stomach d/t inc. peristalsis
* Alert- Never give IM or IV – circulatory
collapse, hypotension, shock & cardiac arrest
poss.
Pilocarpine (Pilocar) - Ophthalmic - direct
acting
38. Cholinergic Blocking AgentsCholinergic Blocking Agents
Anticholinergics/ParasympatholyticsAnticholinergics/Parasympatholytics
Drugs that inhibit action of acetylcholine
(ACH) receptors
Affects the heart, resp. tract, GI tract, bladder,
eye, & exocrine glands.
Allows the sympathetic nervous system to
dominate
Anticholinergic & cholinergic drugs have
opposite effects
Major responses = dec. in GI motility, dec. in
salivation, dilation of pupil (mydriasis), inc.
pulse rate
39. AnticholinergicsAnticholinergics
Uses: Pre-op meds,bradycardia, GI/urinary
antispasmodic
SE: Dry mouth/mucus membranes
Atropine Sulfate - Inhibits ACH blocks
vagal effects on SA & AV nodes inc.
conduction & inc. HR
Use = Bradycardia, pre-up to dec. secretions,
peptic ulcer disease
SE = Many. Most frequent = dry mouth,
blurred vision, urine retention, constipation