Acetylcholine is a neurotransmitter that functions in both the peripheral and central nervous systems. It is synthesized from choline and acetyl-CoA by the enzyme cholinesterase and is broken down by acetylcholinesterase. Acetylcholine is distributed throughout the body, including in muscles, nerves, the brain, and at neuromuscular junctions. It is stored in vesicles and released into the synaptic cleft upon arrival of an action potential.
The document discusses acetylcholine synthesis and degradation. Acetylcholine is synthesized from choline and acetyl-CoA by the enzyme choline acetyltransferase. It is degraded by acetylcholinesterase into inactive metabolites choline and acetate. Acetylcholinesterase is abundant in the synaptic cleft and clears acetylcholine, which is essential for proper muscle function. Deficiency of acetylcholinesterase can cause paralysis.
Neurotransmiters of ans synthesis and fateZulcaif Ahmad
Neurotransmitters of the autonomic nervous system are synthesized in presynaptic neurons and stored in vesicles. When an action potential reaches the presynaptic terminal, calcium influx causes vesicles to fuse with the membrane and release neurotransmitters into the synaptic cleft. Neurotransmitters then bind and activate receptors on the postsynaptic cell, eliciting a response. Acetylcholine is the main neurotransmitter of the parasympathetic nervous system and binds nicotinic and muscarinic receptors. Norepinephrine and epinephrine are the main neurotransmitters of the sympathetic nervous system and bind adrenergic receptors. Neurotransmitters are removed from the synaptic cleft primarily by reuptake or enzymatic breakdown to terminate their
This document discusses the adrenergic system. It describes the origins and divisions of the autonomic nervous system, including the sympathetic and parasympathetic systems. It then focuses on the adrenergic system, summarizing the neurotransmitters involved, including norepinephrine, epinephrine, and dopamine. It outlines the steps in catecholamine synthesis, storage, release, reuptake, and metabolism. It also describes the different types of adrenergic receptors, including alpha and beta receptors, and provides examples of agonists and antagonists for each. Finally, it categorizes different types of adrenergic drugs.
Adrenergic agonists and antagonists act on adrenergic receptors. Agonists like epinephrine and norepinephrine directly stimulate receptors, whereas antagonists like prazosin competitively block receptor activation. These drugs have widespread effects throughout the body due to the sympathetic nervous system's role in functions like heart rate, blood pressure, bronchodilation and uterine contraction. Care must be taken with certain drugs that can cause severe side effects like hypotension or bronchospasm.
Seretonin (5HT) and Its Antagonists PharmacologyPranatiChavan
Serotonin is a chemical that has a wide variety of functions in the human body. It is sometimes called the happy chemical, because it contributes to wellbeing and happiness.
The scientific name for serotonin is 5-hydroxytryptamine, or 5-HT. It is mainly found in the brain, bowels, and blood platelets.
Serotonin is used to transmit messages between nerve cells, it is thought to be active in constricting smooth muscles, and it contributes to wellbeing and happiness, among other things. As the precursor for melatonin, it helps regulate the body’s sleep-wake cycles and the internal clock.
It is thought to play a role in appetite, the emotions, and motor, cognitive, and autonomic functions. However, it is not known exactly if serotonin affects these directly, or if it has an overall role in co-ordinating the nervous system.
The document summarizes the structure and function of the nervous system. It describes how the nervous system is divided into the central nervous system (CNS) and peripheral nervous system. The peripheral nervous system is further divided into the efferent and afferent divisions. The efferent division carries signals from the CNS to peripheral tissues and is divided into the somatic and autonomic systems. The autonomic system regulates vital functions unconsciously through the neurotransmitters acetylcholine and norepinephrine. Acetylcholine and norepinephrine are synthesized, stored, released, and terminated through specific mechanisms to control organs and physiological processes.
The document summarizes key aspects of the nervous system, including the central nervous system (brain and spinal cord), peripheral nervous system, and autonomic nervous system. It describes the sympathetic and parasympathetic divisions of the autonomic nervous system which provide involuntary control of organs. It also outlines the basic structure and function of neurons, neurotransmission, and the roles of key neurotransmitters like acetylcholine and norepinephrine.
Acetylcholine is a neurotransmitter that functions in both the peripheral and central nervous systems. It is synthesized from choline and acetyl-CoA by the enzyme cholinesterase and is broken down by acetylcholinesterase. Acetylcholine is distributed throughout the body, including in muscles, nerves, the brain, and at neuromuscular junctions. It is stored in vesicles and released into the synaptic cleft upon arrival of an action potential.
The document discusses acetylcholine synthesis and degradation. Acetylcholine is synthesized from choline and acetyl-CoA by the enzyme choline acetyltransferase. It is degraded by acetylcholinesterase into inactive metabolites choline and acetate. Acetylcholinesterase is abundant in the synaptic cleft and clears acetylcholine, which is essential for proper muscle function. Deficiency of acetylcholinesterase can cause paralysis.
Neurotransmiters of ans synthesis and fateZulcaif Ahmad
Neurotransmitters of the autonomic nervous system are synthesized in presynaptic neurons and stored in vesicles. When an action potential reaches the presynaptic terminal, calcium influx causes vesicles to fuse with the membrane and release neurotransmitters into the synaptic cleft. Neurotransmitters then bind and activate receptors on the postsynaptic cell, eliciting a response. Acetylcholine is the main neurotransmitter of the parasympathetic nervous system and binds nicotinic and muscarinic receptors. Norepinephrine and epinephrine are the main neurotransmitters of the sympathetic nervous system and bind adrenergic receptors. Neurotransmitters are removed from the synaptic cleft primarily by reuptake or enzymatic breakdown to terminate their
This document discusses the adrenergic system. It describes the origins and divisions of the autonomic nervous system, including the sympathetic and parasympathetic systems. It then focuses on the adrenergic system, summarizing the neurotransmitters involved, including norepinephrine, epinephrine, and dopamine. It outlines the steps in catecholamine synthesis, storage, release, reuptake, and metabolism. It also describes the different types of adrenergic receptors, including alpha and beta receptors, and provides examples of agonists and antagonists for each. Finally, it categorizes different types of adrenergic drugs.
Adrenergic agonists and antagonists act on adrenergic receptors. Agonists like epinephrine and norepinephrine directly stimulate receptors, whereas antagonists like prazosin competitively block receptor activation. These drugs have widespread effects throughout the body due to the sympathetic nervous system's role in functions like heart rate, blood pressure, bronchodilation and uterine contraction. Care must be taken with certain drugs that can cause severe side effects like hypotension or bronchospasm.
Seretonin (5HT) and Its Antagonists PharmacologyPranatiChavan
Serotonin is a chemical that has a wide variety of functions in the human body. It is sometimes called the happy chemical, because it contributes to wellbeing and happiness.
The scientific name for serotonin is 5-hydroxytryptamine, or 5-HT. It is mainly found in the brain, bowels, and blood platelets.
Serotonin is used to transmit messages between nerve cells, it is thought to be active in constricting smooth muscles, and it contributes to wellbeing and happiness, among other things. As the precursor for melatonin, it helps regulate the body’s sleep-wake cycles and the internal clock.
It is thought to play a role in appetite, the emotions, and motor, cognitive, and autonomic functions. However, it is not known exactly if serotonin affects these directly, or if it has an overall role in co-ordinating the nervous system.
The document summarizes the structure and function of the nervous system. It describes how the nervous system is divided into the central nervous system (CNS) and peripheral nervous system. The peripheral nervous system is further divided into the efferent and afferent divisions. The efferent division carries signals from the CNS to peripheral tissues and is divided into the somatic and autonomic systems. The autonomic system regulates vital functions unconsciously through the neurotransmitters acetylcholine and norepinephrine. Acetylcholine and norepinephrine are synthesized, stored, released, and terminated through specific mechanisms to control organs and physiological processes.
The document summarizes key aspects of the nervous system, including the central nervous system (brain and spinal cord), peripheral nervous system, and autonomic nervous system. It describes the sympathetic and parasympathetic divisions of the autonomic nervous system which provide involuntary control of organs. It also outlines the basic structure and function of neurons, neurotransmission, and the roles of key neurotransmitters like acetylcholine and norepinephrine.
This document discusses drugs that act on the autonomic nervous system, specifically cholinergic and anticholinergic drugs. It begins by explaining that cholinergic drugs act on acetylcholine receptors, while anticholinergic drugs block these receptors. Acetylcholine is described as the neurotransmitter of the cholinergic system. Examples of direct and indirect acting cholinergic drugs are provided. Clinical uses and effects of specific cholinergic drugs like Bethanechol and Pilocarpine are summarized. Common anticholinergic drugs such as Atropine are also discussed in detail, outlining their mechanisms and therapeutic uses in conditions like peptic ulcer disease and asthma. Side effects of anticholinergic over
Androgens, anabolic steroids and antiandrogensAnkita Bist
1. The document discusses testosterone, the major androgen hormone. It is produced primarily by Leydig cells in testes and is responsible for male sexual development and maintenance of secondary sex characteristics. It acts through androgen receptors and is converted to the more potent dihydrotestosterone by 5-alpha reductase. Common uses include androgen replacement therapy and treatment of hypogonadism. Adverse effects may include acne, prostate issues, and virilization in women.
2. Synthetic anabolic steroids are discussed which have higher anabolic to androgenic ratios than testosterone. Common examples and uses are provided along with their similar adverse effect profiles to testosterone.
3. Antiand
The document discusses neurohumoral transmission via the autonomic nervous system. It describes how the ANS is comprised of the sympathetic and parasympathetic nervous systems which modulate involuntary functions via neurotransmitters. The two main divisions differ in their origins, neurotransmitters, and target organ effects. Neurotransmission occurs via the binding of neurotransmitters like acetylcholine and norepinephrine to receptors, producing excitatory or inhibitory post-synaptic potentials that mediate various physiological responses. Neurotransmitters are synthesized, stored in vesicles, released upon neuronal firing, and degraded or reabsorbed to terminate synaptic transmission.
This document discusses several classes of drugs that act on the autonomic nervous system and neuromuscular junction. It describes drugs that act as agonists or antagonists at adrenergic and cholinergic receptors in the sympathetic and parasympathetic nervous systems. It also discusses drugs that affect the release or reuptake of neurotransmitters, as well as ganglionic blocking drugs that inhibit transmission between pre- and postganglionic neurons. Finally, it summarizes drugs that enhance or block transmission at the neuromuscular junction.
This document summarizes opioids and their classification, mechanisms of action, pharmacokinetics and effects. It discusses both natural and synthetic opioids like morphine, codeine, heroin, fentanyl, hydromorphone, meperidine and methadone. It also covers opioid receptors, endogenous opioid peptides, and antagonists such as naloxone and naltrexone which are used to reverse opioid overdose and effects.
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.
This document discusses neurotransmitters and neuromodulators in the central nervous system. It describes how neurotransmitters transmit signals across synapses and provides examples of small molecule and large molecule transmitters. The major neurotransmitters discussed include amino acids like GABA, glycine, and glutamate, acetylcholine, and monoamines like dopamine, norepinephrine, epinephrine, histamine, and serotonin. It outlines the synthesis, storage, release, and termination of these neurotransmitters. Receptor types are also summarized.
The document discusses adrenergic drugs and their mechanisms of action. It notes that some adrenergic drugs act directly on adrenergic receptors to activate them, while others block receptor action. It provides tables listing examples of direct-acting, indirect-acting, and mixed-action adrenergic agonists. The document then discusses specific adrenergic drugs in more detail, including epinephrine, norepinephrine, isoproterenol, dopamine, dobutamine, oxymetazoline, phenylephrine, methoxamine, and clonidine. It explains their structures, receptor selectivities, and physiological effects.
General anaesthesia involves reversible loss of sensation and consciousness through administration of anaesthetic drugs. There are two main classifications of anaesthetics - inhalational and intravenous. Inhalational include gases like nitrous oxide and liquids like halothane. Intravenous include inducing agents like thiopentone sodium and propofol, and slower acting drugs like ketamine, benzodiazepines and opioids. Anaesthesia has four stages - from analgesia to medullary paralysis. Local anaesthetics work by blocking sodium channels to prevent nerve impulse conduction without affecting consciousness. Common local anaesthetics include lignocaine and bupivacaine.
The document discusses the glycine receptor, a ligand-gated chloride channel protein that is the major inhibitory neurotransmitter in the adult central nervous system. It exists as a pentameric protein composed of alpha and beta subunits that surround a central pore. Glycine binding activates the receptor, allowing chloride ion influx that hyperpolarizes the neuron. Disorders involving glycine receptor mutations can cause startle disease or non-ketotic hyperglycinemia. The receptor has many ligands but is antagonized primarily by strychnine.
This document discusses neurotransmitters, which are chemicals that neurons use to communicate with each other and target tissues. There are over 40 known neurotransmitters in the human nervous system. The document categorizes neurotransmitters as either excitatory or inhibitory based on whether they activate or inhibit target cells. It provides examples of major neurotransmitters like acetylcholine, norepinephrine, dopamine, GABA, glutamate, serotonin, and histamine. It describes the mechanisms of neurotransmission including synthesis, storage, release, binding to receptors, and termination of signaling. Neurotransmitters are further classified based on their chemical structure and functions in the nervous system.
This document discusses serotonin, its receptors, and drugs that affect the serotonin system. Serotonin is a neurotransmitter found in the gastrointestinal tract and central nervous system that regulates mood, sleep, and body temperature. It acts through various receptor subtypes (5-HT1-7) located on neurons and other cells. Drugs that affect serotonin include selective serotonin reuptake inhibitors for depression, triptans for migraine, cisapride for gastrointestinal issues, and antagonists for conditions like nausea. Serotonin receptors and their roles are important targets for psychotherapeutic drugs.
Introduction to the endocrine system
Growth hormone: Mechanism of Action, secretion, regulation.
Prolactin
Sex hormones
Oral contraceptives
Corticosteroids
Introduction to Physiological and pathological role of serotonin
Autocoids, Classification, synthesis ,Serotonergic receptors, Physiological actions, Pathophysiological role
Presented by
K.Firdous banu
Department of Pharmacology
The document discusses two catecholamine neurotransmitters, epinephrine and norepinephrine. Epinephrine, also known as adrenaline, is synthesized from phenylalanine and tyrosine and has a molecular weight of 183g. It is used to treat resuscitation, anaphylaxis, hypotension, shock, and asthma. Norepinephrine also acts as both a hormone and neurotransmitter and is involved in the stress response and fight-or-flight response by increasing heart rate, releasing glucose, and increasing blood flow to muscles. It has potent actions on both alpha-1 and beta-1 receptors.
Adrenoceptors are membrane bound receptors located throughout the body on neuronal and non-neuronal tissues where they mediate a diverse range of responses to the endogenous catecholamines- noradrenaline and adrenaline.
They are G protein coupled receptors.
Binding of catecholamine to the receptor is responsible for fight or flight response.
This document discusses drugs that act on the central nervous system. It begins by defining key terms like CNS pharmacology, neuropharmacology, and psychopharmacology. It then describes the major cell types in the CNS, including neurons and various types of neuroglia. The bulk of the document focuses on neurotransmission systems, describing the major neurotransmitters like acetylcholine, dopamine, GABA, norepinephrine, and serotonin. It provides details on how these neurotransmitter systems function and their roles in various brain functions and diseases. The document concludes by discussing general anesthetics and their mechanisms of action and phases of anesthesia.
This document discusses adrenergic transmission and adrenergic drugs. It begins by introducing adrenergic receptors and the endogenous catecholamines - epinephrine, norepinephrine, and dopamine. It then describes the synthesis, storage, release and metabolism of catecholamines. The effects of various adrenergic drugs are summarized, including their actions on organs like the heart, blood vessels, and metabolic effects. Specific adrenergic drugs are then discussed in more detail, including endogenous catecholamines, sympathomimetics like epinephrine, norepinephrine, dopamine, and isoproterenol. Classes of adrenergic drugs like alpha and beta agonists are also introduced
The autonomic nervous system (ANS) controls involuntary body functions through two divisions - the sympathetic and parasympathetic systems. The sympathetic system prepares the body for activity and stress while the parasympathetic system has opposite, restorative effects. The ANS acts through neurotransmitters like acetylcholine and norepinephrine to regulate organs. Higher brain centers such as the hypothalamus and medulla help control the ANS response.
This document discusses drugs that act on the autonomic nervous system, specifically cholinergic and anticholinergic drugs. It begins by explaining that cholinergic drugs act on acetylcholine receptors, while anticholinergic drugs block these receptors. Acetylcholine is described as the neurotransmitter of the cholinergic system. Examples of direct and indirect acting cholinergic drugs are provided. Clinical uses and effects of specific cholinergic drugs like Bethanechol and Pilocarpine are summarized. Common anticholinergic drugs such as Atropine are also discussed in detail, outlining their mechanisms and therapeutic uses in conditions like peptic ulcer disease and asthma. Side effects of anticholinergic over
Androgens, anabolic steroids and antiandrogensAnkita Bist
1. The document discusses testosterone, the major androgen hormone. It is produced primarily by Leydig cells in testes and is responsible for male sexual development and maintenance of secondary sex characteristics. It acts through androgen receptors and is converted to the more potent dihydrotestosterone by 5-alpha reductase. Common uses include androgen replacement therapy and treatment of hypogonadism. Adverse effects may include acne, prostate issues, and virilization in women.
2. Synthetic anabolic steroids are discussed which have higher anabolic to androgenic ratios than testosterone. Common examples and uses are provided along with their similar adverse effect profiles to testosterone.
3. Antiand
The document discusses neurohumoral transmission via the autonomic nervous system. It describes how the ANS is comprised of the sympathetic and parasympathetic nervous systems which modulate involuntary functions via neurotransmitters. The two main divisions differ in their origins, neurotransmitters, and target organ effects. Neurotransmission occurs via the binding of neurotransmitters like acetylcholine and norepinephrine to receptors, producing excitatory or inhibitory post-synaptic potentials that mediate various physiological responses. Neurotransmitters are synthesized, stored in vesicles, released upon neuronal firing, and degraded or reabsorbed to terminate synaptic transmission.
This document discusses several classes of drugs that act on the autonomic nervous system and neuromuscular junction. It describes drugs that act as agonists or antagonists at adrenergic and cholinergic receptors in the sympathetic and parasympathetic nervous systems. It also discusses drugs that affect the release or reuptake of neurotransmitters, as well as ganglionic blocking drugs that inhibit transmission between pre- and postganglionic neurons. Finally, it summarizes drugs that enhance or block transmission at the neuromuscular junction.
This document summarizes opioids and their classification, mechanisms of action, pharmacokinetics and effects. It discusses both natural and synthetic opioids like morphine, codeine, heroin, fentanyl, hydromorphone, meperidine and methadone. It also covers opioid receptors, endogenous opioid peptides, and antagonists such as naloxone and naltrexone which are used to reverse opioid overdose and effects.
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.
This document discusses neurotransmitters and neuromodulators in the central nervous system. It describes how neurotransmitters transmit signals across synapses and provides examples of small molecule and large molecule transmitters. The major neurotransmitters discussed include amino acids like GABA, glycine, and glutamate, acetylcholine, and monoamines like dopamine, norepinephrine, epinephrine, histamine, and serotonin. It outlines the synthesis, storage, release, and termination of these neurotransmitters. Receptor types are also summarized.
The document discusses adrenergic drugs and their mechanisms of action. It notes that some adrenergic drugs act directly on adrenergic receptors to activate them, while others block receptor action. It provides tables listing examples of direct-acting, indirect-acting, and mixed-action adrenergic agonists. The document then discusses specific adrenergic drugs in more detail, including epinephrine, norepinephrine, isoproterenol, dopamine, dobutamine, oxymetazoline, phenylephrine, methoxamine, and clonidine. It explains their structures, receptor selectivities, and physiological effects.
General anaesthesia involves reversible loss of sensation and consciousness through administration of anaesthetic drugs. There are two main classifications of anaesthetics - inhalational and intravenous. Inhalational include gases like nitrous oxide and liquids like halothane. Intravenous include inducing agents like thiopentone sodium and propofol, and slower acting drugs like ketamine, benzodiazepines and opioids. Anaesthesia has four stages - from analgesia to medullary paralysis. Local anaesthetics work by blocking sodium channels to prevent nerve impulse conduction without affecting consciousness. Common local anaesthetics include lignocaine and bupivacaine.
The document discusses the glycine receptor, a ligand-gated chloride channel protein that is the major inhibitory neurotransmitter in the adult central nervous system. It exists as a pentameric protein composed of alpha and beta subunits that surround a central pore. Glycine binding activates the receptor, allowing chloride ion influx that hyperpolarizes the neuron. Disorders involving glycine receptor mutations can cause startle disease or non-ketotic hyperglycinemia. The receptor has many ligands but is antagonized primarily by strychnine.
This document discusses neurotransmitters, which are chemicals that neurons use to communicate with each other and target tissues. There are over 40 known neurotransmitters in the human nervous system. The document categorizes neurotransmitters as either excitatory or inhibitory based on whether they activate or inhibit target cells. It provides examples of major neurotransmitters like acetylcholine, norepinephrine, dopamine, GABA, glutamate, serotonin, and histamine. It describes the mechanisms of neurotransmission including synthesis, storage, release, binding to receptors, and termination of signaling. Neurotransmitters are further classified based on their chemical structure and functions in the nervous system.
This document discusses serotonin, its receptors, and drugs that affect the serotonin system. Serotonin is a neurotransmitter found in the gastrointestinal tract and central nervous system that regulates mood, sleep, and body temperature. It acts through various receptor subtypes (5-HT1-7) located on neurons and other cells. Drugs that affect serotonin include selective serotonin reuptake inhibitors for depression, triptans for migraine, cisapride for gastrointestinal issues, and antagonists for conditions like nausea. Serotonin receptors and their roles are important targets for psychotherapeutic drugs.
Introduction to the endocrine system
Growth hormone: Mechanism of Action, secretion, regulation.
Prolactin
Sex hormones
Oral contraceptives
Corticosteroids
Introduction to Physiological and pathological role of serotonin
Autocoids, Classification, synthesis ,Serotonergic receptors, Physiological actions, Pathophysiological role
Presented by
K.Firdous banu
Department of Pharmacology
The document discusses two catecholamine neurotransmitters, epinephrine and norepinephrine. Epinephrine, also known as adrenaline, is synthesized from phenylalanine and tyrosine and has a molecular weight of 183g. It is used to treat resuscitation, anaphylaxis, hypotension, shock, and asthma. Norepinephrine also acts as both a hormone and neurotransmitter and is involved in the stress response and fight-or-flight response by increasing heart rate, releasing glucose, and increasing blood flow to muscles. It has potent actions on both alpha-1 and beta-1 receptors.
Adrenoceptors are membrane bound receptors located throughout the body on neuronal and non-neuronal tissues where they mediate a diverse range of responses to the endogenous catecholamines- noradrenaline and adrenaline.
They are G protein coupled receptors.
Binding of catecholamine to the receptor is responsible for fight or flight response.
This document discusses drugs that act on the central nervous system. It begins by defining key terms like CNS pharmacology, neuropharmacology, and psychopharmacology. It then describes the major cell types in the CNS, including neurons and various types of neuroglia. The bulk of the document focuses on neurotransmission systems, describing the major neurotransmitters like acetylcholine, dopamine, GABA, norepinephrine, and serotonin. It provides details on how these neurotransmitter systems function and their roles in various brain functions and diseases. The document concludes by discussing general anesthetics and their mechanisms of action and phases of anesthesia.
This document discusses adrenergic transmission and adrenergic drugs. It begins by introducing adrenergic receptors and the endogenous catecholamines - epinephrine, norepinephrine, and dopamine. It then describes the synthesis, storage, release and metabolism of catecholamines. The effects of various adrenergic drugs are summarized, including their actions on organs like the heart, blood vessels, and metabolic effects. Specific adrenergic drugs are then discussed in more detail, including endogenous catecholamines, sympathomimetics like epinephrine, norepinephrine, dopamine, and isoproterenol. Classes of adrenergic drugs like alpha and beta agonists are also introduced
The autonomic nervous system (ANS) controls involuntary body functions through two divisions - the sympathetic and parasympathetic systems. The sympathetic system prepares the body for activity and stress while the parasympathetic system has opposite, restorative effects. The ANS acts through neurotransmitters like acetylcholine and norepinephrine to regulate organs. Higher brain centers such as the hypothalamus and medulla help control the ANS response.
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.
The autonomic nervous system consists of the sympathetic and parasympathetic divisions. The sympathetic division uses norepinephrine as its neurotransmitter and is active during stress responses, while the parasympathetic division uses acetylcholine and is active at rest. Together they control functions like heart rate, digestion, and gland secretion through complementary actions on target organs like the heart and intestines. Pharmacological agents can either mimic or block the neurotransmitters of each division to modulate autonomic functions.
Pharmacology Lecture Slides on Autonomic Nervous System Introduction by Sanjaya Mani Dixit Assistant Professor of Pharmacology at Kathmandu Medical College
pharmacopeia, with
numerous new monoclonal antibodies and other biologic agents.
Case studies accompany most chapters, and answers to questions posed in the case studies appear at the end of each chapter.
The book is designed to provide a comprehensive, authoritative,
and readable pharmacology textbook for students in the health
sciences. Frequent revision is necessary to keep pace with the rapid
changes in pharmacology and therapeutics; the 2–3 year revision
cycle of this text is among the shortest in the field, and the availability of an online version provides even greater currency. The
book also offers special features that make it a useful reference for
house officers and practicing clinicians.
This edition continues the sequence used in many pharmacology courses and in integrated curricula: basic principles of drug
discovery, pharmacodynamics, pharmacokinetics, and pharmacogenomics; autonomic drugs; cardiovascular-renal drugs; drugs
with important actions on smooth muscle; central nervous system
drugs; drugs used to treat inflammation, gout, and diseases of
the blood; endocrine drugs; chemotherapeutic drugs; toxicology;
and special topics. This sequence builds new information on a
foundation of information already assimilated. For example, early
presentation of autonomic nervous system pharmacology allows
students to integrate the physiology and neuroscience they have
learned elsewhere with the pharmacology they are learning and
prepares them to understand the autonomic effects of other drugs.
This is especially important for the cardiovascular and central nervous system drug groups. However, chapters can be used equally
well in courses and curricula that present these topics in a different
sequence.
Within each chapter, emphasis is placed on discussion of drug
groups and prototypes rather than offering repetitive detail about
individual drugs. Selection of the subject matter and the order
of its presentation are based on the accumulated experience of
teaching this material to thousands of medical, pharmacy, dental,
podiatry, nursing, and other health science students.
Major features that make this book particularly useful in
integrated curricula include sections that specifically address the
clinical choice and use of drugs in patients and the monitoring of
their effects—in other words, clinical pharmacology is an integral
part of this text. Lists of the trade and generic names of commercial preparations available are provided at the end of each chapter
for easy reference by the house officer or practitioner evaluating a
patient’s drug list or writing a prescription.
Significant revisions in this edition include:
• Major revisions of the chapters on immunopharmacology,
antiseizure, antipsychotic, antidepressant, antidiabetic, antiinflammatory, and antiviral drugs, prostaglandins, and central
nervous system neurotransmitters.
• Continued expansion of the coverage of general concepts relating to newly dis
Development& Various Parts Of Peripheral Nervous Systemraj kumar
The autonomic nervous system innervates organs whose functions are not usually under voluntary control, such as the heart, smooth muscles, and glands. It has two divisions - the sympathetic and parasympathetic nervous systems. The sympathetic nervous system is activated during fight or flight responses and increases heart rate and blood glucose levels. The parasympathetic nervous system activates during rest and digestion and decreases heart rate and increases digestive activities. Both systems use acetylcholine and norepinephrine as neurotransmitters to regulate organs.
Development& Various Parts Of Peripheral Nervous Systemraj kumar
The autonomic nervous system innervates organs whose functions are not usually under voluntary control, such as the heart, smooth muscles, and glands. It has two divisions - the sympathetic and parasympathetic nervous systems. The sympathetic nervous system is activated during fight or flight responses and increases heart rate and blood glucose levels. The parasympathetic nervous system activates during rest and relaxation and decreases heart rate and increases digestive activities. Both systems use acetylcholine and norepinephrine as neurotransmitters to elicit different responses from target tissues and organs.
The document discusses the autonomic nervous system, describing the parasympathetic and sympathetic divisions. It explains that the parasympathetic nervous system uses acetylcholine as its neurotransmitter and targets muscarinic and nicotinic receptors, while the sympathetic nervous system uses norepinephrine and epinephrine as neurotransmitters. The actions of the sympathetic and parasympathetic systems are contrasted, with the sympathetic system preparing the body for "fight or flight" and the parasympathetic inducing "rest and digest".
1. The document discusses the autonomic nervous system and its sympathetic and parasympathetic divisions.
2. The sympathetic nervous system uses norepinephrine as a neurotransmitter and is involved in the "fight or flight" response. The parasympathetic nervous system uses acetylcholine and is involved in "rest and digest" functions.
3. Adrenergic drugs can stimulate sympathetic responses by directly or indirectly acting on adrenergic receptors, while anticholinergic drugs can block parasympathetic responses by antagonizing cholinergic receptors.
1. The document discusses the autonomic nervous system, which controls involuntary body functions. It has two divisions - the sympathetic and parasympathetic nervous systems.
2. The sympathetic nervous system uses norepinephrine as a neurotransmitter and prepares the body for "fight or flight" through processes like increased heart rate and dilation of airways.
3. The parasympathetic nervous system uses acetylcholine and activates "rest and digest" functions like slowed heart rate and constricted pupils.
The document discusses synapses and the autonomic nervous system. It describes two types of synapses - chemical and electrical. The autonomic nervous system consists of the sympathetic and parasympathetic systems which regulate organs through the release of neurotransmitters like acetylcholine and norepinephrine. The effects of these systems are described for various organs. Drugs can act as agonists or antagonists at cholinergic and adrenergic receptors to influence the autonomic nervous system.
Ans(organization , subdivision and innervations)Zulcaif Ahmad
The document discusses the organization and function of the autonomic nervous system (ANS). The ANS regulates organs automatically and unconsciously. It has two divisions - the sympathetic and parasympathetic nervous systems. The sympathetic system is active during fight or flight responses while the parasympathetic system acts during rest and digestion. Most organs receive input from both divisions, allowing for cooperative or opposing effects. The ANS maintains homeostasis through its control of various body systems.
The document discusses the autonomic nervous system and how drugs can affect it. It begins by explaining that the autonomic nervous system maintains homeostasis in the body by linking to target organs like the cardiovascular system and smooth muscles. It then describes how drugs can mimic or block neurotransmitters in the autonomic nervous system to decrease or increase the activity of organs. Specifically, it provides the examples of atropine blocking muscarinic receptors to decrease intestinal motility and propranolol blocking beta-adrenergic receptors to decrease blood pressure. In summary, the document outlines how the autonomic nervous system works to regulate the internal environment and how drugs are used to interact with its neurotransmitters to affect various organ systems.
The document discusses the nervous system and coordination. It describes how damage to the optic nerve can cause blindness from glaucoma as fluid buildup increases pressure in the eye. It outlines the central nervous system, peripheral nervous system, and different types of neurons. It explains how nerve impulses are transmitted via action potentials and the roles of myelin sheathing and neurotransmitters.
The document provides an overview of the autonomic nervous system (ANS), including its divisions (sympathetic and parasympathetic), neurons, neurotransmitters, receptors, and effects on target organs. It also discusses how drugs can influence ANS activity by stimulating or blocking its components. The sympathetic division activates the fight or flight response, while the parasympathetic division promotes rest and digestion. Both use two-neuron chains and acetylcholine as a neurotransmitter.
The peripheral nervous system (PNS) connects the central nervous system to the limbs and organs. It is divided into the afferent division, which brings sensory information to the CNS, and the efferent division, which carries signals from the CNS to peripheral tissues. The efferent division is further divided into the somatic and autonomic systems. The autonomic system regulates vital functions and is composed of the sympathetic and parasympathetic systems, which generally have opposing actions and work to balance each other. The sympathetic system activates the fight or flight response, while the parasympathetic system dominates during rest.
This document provides information on neurons and the nervous system. It discusses:
1) The three main types of neurons - afferent, efferent, and interneurons. It describes their functions in signal transmission.
2) The parts of neurons - cell body, dendrites, axons. It explains how axons conduct action potentials to different parts of the body.
3) How action potentials are initiated when the membrane potential reaches threshold. The influx of sodium ions causes rapid depolarization, and then repolarization occurs as potassium ions efflux.
4) Synaptic transmission and how calcium influx causes neurotransmitter release by exocytosis at the synaptic knob to continue the signaling process between neurons.
Functional Organization of Autonomic ActivityAkash Agnihotri
This slide including Functional Organization of Autonomic Activity
A little intro about ANS
Then Organization of the nervous system including
Afferent/Efferent: Transmission
Somatic and Autonomic Nervous system
Sympathetic and Parasympathetic nervous system
Enteric nervous system
Their functions, differences in between functions and organization with some tables and figures
Then, the Role of the CNS in the control of autonomic functions
with example
Then, presynaptic modulation and postsynaptic modulation
Also, Innervations by the ANS
And lastly Transmitters other than acetylcholine and noradrenaline
Similar to Pharmacology Of Autonomic Nervous System & Chemical Transmission ppt (20)
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3. Some Important Terms
ANS: The system of nerves and ganglia that
innervates the blood vessels,heart,smooth
muscle,viscera and glands
Controls their involuntary functions
Consisting of sympathetic and parasympathetic.
Neurones involved in the ANS pathway
Preganglionic
Postganglionic
• Ganglia
Sympathetic trunk ganglia
Preventral ganglia
Terminal ganglia
4. More Terms
Afferent neurons:- carry
nerve impulse from the organ to
the CNS.
Efferent neurons:- carry
impulses from CNS to the
organ
Neurotransmitters:-
chemicals substances made in
the neurons that are released
when an action potential comes
down the neurons.
Receptors:- structures
usually proteins that receive
neurotransmitters release from
the axonal terminals of the
neuron.
5. Sympathethic &
Parasympathetic
Nervous system
Two have opposite actions in many cases
One activates physiological response and
other inhibits it
Acc. to older simplifications one is
“excitory”(SNS) and other(PSNS) is
“inhibitory”.
But overturned due to many exceptions
Modern characterizations: SNS (quick
response mobilizing system) & PSNS(more
slowly activated dampening system)
7. Neurotransmiters
All preganglionic and postganglionic
parasympathetic neurons secret
acetylcholine
2% of postganglionic sympathetic
secret acetylcholine
These are termed as CHOLINERGIC
98% of postganglionic sympathetic
neurons secret norepinephrin
These neurons termed as
ADRENERGIC.
8. Receptors
Cholinergic : receptors which receive acetylcholine
Nicotinic
Location :skeletal muscle, dendrites of postganglionic neurons,adrenal
medulla
Mechanism of action direct.
Na+ ion influx produces depolarization of the membrane therefore excitation
Examples of action: skeletal muscle contraction, generation of action
potential on postganglionic neuron, stimulation of adrenal gland and
secretion of norepinephrin and epinephrine
Muscuranic
Location :effectors innervated by postganglionic parasympathetic neurons,
effectors innervated by postganglionic sympathetic neurons
Mechanism of action is indirect
Efflux of K+ ion is reduced ,depolarization results and the effect is excitation.
If Efflux of K+ ion is increased ,hyperpolarization results and the effect is
inhibition
Sympathetic examples:excitation –Eccrine Sweat Gland
inhibition-Blood vessels in skeletal muscles
Parasympathetic examples:excitation:G.I tract
inhibition: heart ,blood vessels supplying penis and
clitoris
9. Receptors
Adenergic: receptors which receive norepinephrin (NE)
Alpha 1:
Location:blood vessels serving skin,viscera,kidney,and
salivary gland
Most sympathetic target organ except heart
Mechanism of action is indirect
Mode of action:produce depolarization therefore they
are excitatory
Examples of action:
Constriction of blood vessels
Constricts visceral organ sphincters
Constriction of radial muscle of the iris,which causes
dilationof the pupil of the eye.
10. Receptors
Alpha 2
Location:blood platelets,exocrine glands
of pancreas,liver
Mecahnism of action is indirect
They produce hyperpolarization
therefore they are inhibitory
Examples of function:
Inhibition insulin and enzyme secretion
from the pancreas
Inhibit gall bladder contraction.
12. Sympathetic Nervous System
SNS general action is to mobilize body’s
nervous system flight or fight response.
Sympathetic nerves originate inside the
vertebral column, toward the middle of the
spinal cord in the intermediolateral cell column
(or lateral horn)
Beginning at the first thoracic segment of the
spinal cord & are thought to extend to the
second or third lumbar segments.
Because its cells begin in the thoracic & lumbar
regions of the spinal cord, the CNS is said to
have a thoracolumbar outflow.
SNS are composed of two-neuron systems
composed of pre- and post-ganglionic neurons.
13. SNS Divisions
Cell bodies of
preganglionic
neurons reside
within the CNS &
their axon extends
to specialized
sympathetic
ganglia outside of
the CNS where
they synapse on
postganglionic
neuron cell
bodies.
axons of these
postganglionic
neurons then