This document provides an overview of opioids including their pharmacology, mechanisms of action, classifications, and clinical uses. It discusses how opioids bind to receptors in the central and peripheral nervous systems to produce analgesic and other effects. Opioids are classified based on their receptor activities and include pure agonists, partial agonists, mixed agonist-antagonists, and pure antagonists. The document reviews the central and peripheral effects of opioids as well as their indications, contraindications, and interactions. It also discusses opioid tolerance, dependence, overdose, and withdrawal.
Sedatives are drugs that reduce excitement and calm a person, while hypnotics produce sleep resembling normal sleep. The document discusses several classes of sedatives and hypnotics including barbiturates, benzodiazepines, and newer nonbenzodiazepine hypnotics like zolpidem and zaleplon. It provides details on their mechanisms of action, pharmacokinetics, therapeutic uses, and adverse effects.
This document provides information on anti-epileptic drugs (AEDs) including their mechanisms of action, uses, and side effects. It discusses the classification, treatment, and management of epilepsy and seizures. Some key points include:
- AEDs work by enhancing GABA inhibition, blocking sodium channels, or inhibiting calcium currents to suppress neuronal firing and seizures.
- Common AEDs include phenytoin, carbamazepine, valproic acid, lamotrigine, levetiracetam, and topiramate.
- AEDs are used to treat generalized tonic-clonic, absence, myoclonic and partial seizures. Some are also used for neuropathic
This document discusses antianxiety agents used to treat anxiety disorders. It notes that anxiety is an unpleasant state of tension that can be part of other disorders or found in normal situations. The major anxiety disorders include panic disorder, generalized anxiety disorder, phobic disorders, stress disorders, and obsessive-compulsive disorder. Benzodiazepines like diazepam, chlordiazepoxide, oxazepam, lorazepam, and alprazolam are commonly prescribed antianxiety agents, along with azapirone drugs like buspirone, sedative antihistamines like hydroxyzine, beta blockers like propranolol, and SSRIs or TCA
Parkinson's disease is a progressive nervous system disorder that causes a loss of dopamine-producing brain cells, leading to motor symptoms like tremors and rigidity. It occurs due to degeneration of the substantia nigra, decreasing dopamine levels in the basal ganglia. The document discusses the causes, symptoms, diagnosis, treatment and management of Parkinson's disease with a focus on increasing dopamine levels through drugs like L-DOPA, COMT inhibitors, and dopamine receptor agonists.
This document discusses opioids, including their uses, types, mechanisms of action, indications, contraindications, and adverse effects. It defines pain and analgesics, describes the different types of pain (acute, chronic, nociceptive, neuropathic), and classifies analgesics as NSAIDs or opioids. Specific opioids discussed include morphine, codeine, heroin, hydrocodone, oxycodone, pethidine, fentanyl, and tramadol. Nursing responsibilities for opioid administration and monitoring are also outlined.
This document provides an overview of opioids including their pharmacology, mechanisms of action, classifications, and clinical uses. It discusses how opioids bind to receptors in the central and peripheral nervous systems to produce analgesic and other effects. Opioids are classified based on their receptor activities and include pure agonists, partial agonists, mixed agonist-antagonists, and pure antagonists. The document reviews the central and peripheral effects of opioids as well as their indications, contraindications, and interactions. It also discusses opioid tolerance, dependence, overdose, and withdrawal.
Sedatives are drugs that reduce excitement and calm a person, while hypnotics produce sleep resembling normal sleep. The document discusses several classes of sedatives and hypnotics including barbiturates, benzodiazepines, and newer nonbenzodiazepine hypnotics like zolpidem and zaleplon. It provides details on their mechanisms of action, pharmacokinetics, therapeutic uses, and adverse effects.
This document provides information on anti-epileptic drugs (AEDs) including their mechanisms of action, uses, and side effects. It discusses the classification, treatment, and management of epilepsy and seizures. Some key points include:
- AEDs work by enhancing GABA inhibition, blocking sodium channels, or inhibiting calcium currents to suppress neuronal firing and seizures.
- Common AEDs include phenytoin, carbamazepine, valproic acid, lamotrigine, levetiracetam, and topiramate.
- AEDs are used to treat generalized tonic-clonic, absence, myoclonic and partial seizures. Some are also used for neuropathic
This document discusses antianxiety agents used to treat anxiety disorders. It notes that anxiety is an unpleasant state of tension that can be part of other disorders or found in normal situations. The major anxiety disorders include panic disorder, generalized anxiety disorder, phobic disorders, stress disorders, and obsessive-compulsive disorder. Benzodiazepines like diazepam, chlordiazepoxide, oxazepam, lorazepam, and alprazolam are commonly prescribed antianxiety agents, along with azapirone drugs like buspirone, sedative antihistamines like hydroxyzine, beta blockers like propranolol, and SSRIs or TCA
Parkinson's disease is a progressive nervous system disorder that causes a loss of dopamine-producing brain cells, leading to motor symptoms like tremors and rigidity. It occurs due to degeneration of the substantia nigra, decreasing dopamine levels in the basal ganglia. The document discusses the causes, symptoms, diagnosis, treatment and management of Parkinson's disease with a focus on increasing dopamine levels through drugs like L-DOPA, COMT inhibitors, and dopamine receptor agonists.
This document discusses opioids, including their uses, types, mechanisms of action, indications, contraindications, and adverse effects. It defines pain and analgesics, describes the different types of pain (acute, chronic, nociceptive, neuropathic), and classifies analgesics as NSAIDs or opioids. Specific opioids discussed include morphine, codeine, heroin, hydrocodone, oxycodone, pethidine, fentanyl, and tramadol. Nursing responsibilities for opioid administration and monitoring are also outlined.
1. A 64-year-old architect presents with signs and symptoms consistent with Parkinson's disease, including a resting tremor, stooped posture, dragging of the left leg when walking, and slight unsteadiness. He remains independent in daily activities.
2. The clinical features suggest degeneration of dopaminergic neurons in the substantia nigra, resulting in dopamine deficiency in the basal ganglia and associated motor symptoms.
3. Pharmacological treatment options aim to restore dopamine levels or balance cholinergic and dopaminergic activity in the basal ganglia.
This document discusses central nervous system stimulants and nootropics. It describes various classes of CNS stimulants like amphetamines and analeptics. Amphetamines produce euphoria and wakefulness but can have side effects like rapid heart rate and high blood pressure. Caffeine is discussed in depth, with its mechanisms of action and effects on exercise performance. Other cognitive enhancers mentioned include racetams, citicoline, and herbs. The document also covers potential adverse effects of CNS stimulants like restlessness, convulsions, and cardiac issues.
The document discusses various types of analgesics, including opioids and non-opioid analgesics. It provides details on morphine, including its mechanism of action, uses, side effects, and toxicity. It also covers non-steroidal anti-inflammatory drugs (NSAIDs) like aspirin and acetaminophen. NSAIDs work by inhibiting prostaglandin synthesis and reducing inflammation. The document outlines their mechanisms, classifications, uses, and potential side effects.
This document discusses antiepileptic drugs, including their mechanisms of action, uses, and side effects. It covers common antiepileptics like phenobarbital, phenytoin, carbamazepine, ethosuximide, valproic acid, diazepam, gabapentin, vigabatrin, and tiagabine. It also describes the classification and types of seizures as well as the treatment of status epilepticus.
This document discusses various central nervous system stimulants and hallucinogens. It describes how stimulants like amphetamines and cocaine work by increasing levels of dopamine and norepinephrine in the brain. It also covers hallucinogens like LSD, THC, and PCP, noting their mechanisms of action involve serotonin receptors for LSD and cannabinoid receptors for THC. The document provides information on therapeutic uses and adverse effects of these substances.
Opioid analgesics work by binding to opioid receptors in the brain and spinal cord to reduce pain. There are several types of opioid receptors that endogenous opioid peptides and exogenous opioids can bind to, including mu, delta, and kappa receptors. Opioids are well absorbed orally or parenterally and distributed widely throughout the body. They are metabolized in the liver mainly by conjugation with glucuronic acid and excreted in urine. Opioids produce analgesia, sedation, respiratory depression, nausea, vomiting, and constipation by acting on central and peripheral opioid receptors. Tolerance and physical dependence may develop with repeated use.
This document summarizes key information about opioid analgesics including:
1. It classifies opioids based on their strength from strong to weak and lists examples in each category.
2. It outlines several clinical uses of opioids such as for analgesia, cough suppression, and treatment of opioid dependence.
3. It describes the pharmacokinetics of opioids including absorption, metabolism, and ability to cross the placental barrier and affect fetuses.
4. It explains the mechanism of action of opioids including their binding to μ, δ, and κ receptors in the brain and spinal cord to produce effects like analgesia and respiratory depression.
The document provides an overview of the nervous system and cholinergic transmission. It discusses the organization and functions of the sympathetic and parasympathetic nervous systems. It describes the cholinergic receptors (muscarinic and nicotinic), cholinergic transmission, and the actions of cholinergic drugs including choline esters, alkaloids, anti-cholinesterases, and their therapeutic uses and side effects. In summary, it provides a comprehensive review of the cholinergic nervous system, receptors, transmission, and pharmacology of drugs that act on this system.
Sedatives and hypnotics drugs ppt by kashikant yadavKashikant Yadav
Sedatives and hypnotics are central nervous system depressants that are used to induce sleep or reduce anxiety. Barbiturates were previously commonly used but have largely been replaced by benzodiazepines due to lower risks of dependence and overdose. Both classes of drugs work by enhancing the effects of the inhibitory neurotransmitter GABA. Sedatives primarily reduce anxiety and excitement while hypnotics are used to induce sleep. Common side effects include drowsiness, dizziness, and impaired coordination. Tolerance can develop with repeated use of both barbiturates and benzodiazepines.
This document provides information about antiepileptic drugs. It discusses the history and classification of epilepsy. It then describes several classes of antiepileptic drugs including barbiturates, benzodiazepines, succinimides, and hydentoins. For each drug class, it summarizes the mechanism of action, pharmacokinetics, adverse effects, and therapeutic uses for treating epilepsy. The document aims to educate about different treatment options for controlling seizures.
Anti depressant and its classificationsNatasha Puri
This document discusses anti-depressant drugs and their classification. It defines depression as a serious mood disorder that can affect people of all ages and backgrounds. The main types of depression are described as uni-polar, bi-polar, and endogenous. Causes include family history, life events, medications, alcohol use, and chemical imbalances in the brain. Common symptoms are loss of interest and sadness/irritability. The document then covers various theories of depression before discussing treatment options like psychotherapy, ECT, natural alternatives, and medications. Anti-depressant drugs are classified as tricyclic antidepressants, selective serotonin reuptake inhibitors, serotonin-norepinephrine reuptake inhibitors, atypical antidepressants,
This document discusses anti-convulsant drugs used to treat epilepsy. It describes different types of seizures including partial, generalized tonic-clonic, absence and myoclonic seizures. Common anti-convulsants like carbamazepine, phenytoin, valproic acid, ethosuximide work by blocking sodium channels, calcium channels, or enhancing GABA effects. Adverse effects include dizziness, rashes, and gastrointestinal issues. Status epilepticus requires initial treatment with benzodiazepines then phenytoin or fosphenytoin for long-term control.
This document discusses CNS stimulants and nootropic agents. It begins by classifying various CNS stimulants such as psychostimulants, respiratory stimulants, convulsants, and listing examples like amphetamines, caffeine, nicotine. It then describes the mechanisms, effects and uses of specific stimulants - amphetamines, cocaine, caffeine, strychnine. Next, it covers nootropic agents like cholinergic activators rivastigmine, donepezil, memantine, piracetam and their mechanisms in improving cognition. The learning objectives are also stated.
This document summarizes a presentation about ganglions and ganglion stimulants and blockers. It defines a ganglion as a cluster of nerve cell bodies in the autonomic nervous system. It describes how ganglion stimulants like nicotine activate nicotinic receptors on postganglionic neurons. These stimulants are used to help people quit smoking by reducing nicotine cravings and withdrawal symptoms. Ganglion blockers inhibit transmission between preganglionic and postganglionic neurons by antagonizing nicotinic receptors. They were previously used to treat hypertension but caused intolerable side effects. The document outlines the mechanisms, effects, uses and side effects of both ganglion stimulants and blockers
This document discusses drugs used to treat gout, including colchicine, NSAIDs, corticosteroids, uricosuric agents like probenecid and sulfinpyrazone, and the uric acid synthesis inhibitor allopurinol. It provides details on the pathophysiology of gout, mechanisms of action, pharmacokinetics, indications, dosages and adverse effects of these drugs for both acute gout attacks and long-term treatment of chronic gout and hyperuricemia.
This document discusses opioids, including their classification, mechanisms of action, effects and side effects. It notes that opioids act on three receptor families in the central nervous system to produce analgesic and other effects. It describes the pharmacokinetics of opioids like morphine, including their metabolism and potential drug interactions. The document also discusses the use of opioid antagonists like naloxone to reverse overdose effects.
This document discusses anxiolytics and hypnotics, specifically focusing on barbiturates and benzodiazepines. It covers their history, classifications, mechanisms of action, pharmacokinetics, therapeutic uses, adverse effects, and treatment of overdoses. Barbiturates were originally used as sedatives but were replaced by benzodiazepines in the 1990s due to benzodiazepines having a better safety profile with less dependence and abuse potential. Both classes of drugs work by enhancing the effects of the neurotransmitter GABA.
This document discusses sedative-hypnotic drugs and classifies them as barbiturates or benzodiazepines. It explains that both act on GABA receptors, with barbiturates having both GABA facilitatory and direct effects while benzodiazepines only have GABA facilitatory effects. The document outlines the mechanism of action, pharmacokinetics, clinical effects, adverse effects and conclusions about each class. It emphasizes that while both can cause tolerance and dependence, benzodiazepines have fewer adverse effects and drug interactions than barbiturates.
1) The document provides definitions and explanations of key concepts related to drugs of abuse including drug abuse, drug dependence, drug addiction, drug tolerance, cross-dependence, and cross-tolerance.
2) It discusses the different types of drug dependence including psychological dependence and physiological dependence.
3) The document also covers topics like drug toxicity, co-administration of drugs, and provides additional learning resources on neurotransmission and mental disorders.
Este documento descreve os serviços de treinamento, palestras e consultorias oferecidos pela empresa BRgestão em Educação Executiva. A empresa oferece soluções em vendas, gestão, liderança e outdoor training para melhorar o desempenho e resultados de equipes comerciais, principalmente no setor do agronegócio. O documento também apresenta o facilitador dos treinamentos, Alessandro Lunardon, e alguns dos clientes atendidos pela empresa.
Este documento resume los cambios en las esferas (biosfera, litosfera, atmósfera) que ocurren cuando se construye una ciudad. Explica que antes de la construcción de la ciudad, los ecosistemas se encuentran poco intervenidos y hay una gran biodiversidad, pero la construcción elimina gran parte de la vegetación nativa. También altera la litosfera al perforarla para servicios y remodelar el terreno, y cambia la atmósfera volviéndola más contaminada con ráfagas de viento entre edificios.
1. A 64-year-old architect presents with signs and symptoms consistent with Parkinson's disease, including a resting tremor, stooped posture, dragging of the left leg when walking, and slight unsteadiness. He remains independent in daily activities.
2. The clinical features suggest degeneration of dopaminergic neurons in the substantia nigra, resulting in dopamine deficiency in the basal ganglia and associated motor symptoms.
3. Pharmacological treatment options aim to restore dopamine levels or balance cholinergic and dopaminergic activity in the basal ganglia.
This document discusses central nervous system stimulants and nootropics. It describes various classes of CNS stimulants like amphetamines and analeptics. Amphetamines produce euphoria and wakefulness but can have side effects like rapid heart rate and high blood pressure. Caffeine is discussed in depth, with its mechanisms of action and effects on exercise performance. Other cognitive enhancers mentioned include racetams, citicoline, and herbs. The document also covers potential adverse effects of CNS stimulants like restlessness, convulsions, and cardiac issues.
The document discusses various types of analgesics, including opioids and non-opioid analgesics. It provides details on morphine, including its mechanism of action, uses, side effects, and toxicity. It also covers non-steroidal anti-inflammatory drugs (NSAIDs) like aspirin and acetaminophen. NSAIDs work by inhibiting prostaglandin synthesis and reducing inflammation. The document outlines their mechanisms, classifications, uses, and potential side effects.
This document discusses antiepileptic drugs, including their mechanisms of action, uses, and side effects. It covers common antiepileptics like phenobarbital, phenytoin, carbamazepine, ethosuximide, valproic acid, diazepam, gabapentin, vigabatrin, and tiagabine. It also describes the classification and types of seizures as well as the treatment of status epilepticus.
This document discusses various central nervous system stimulants and hallucinogens. It describes how stimulants like amphetamines and cocaine work by increasing levels of dopamine and norepinephrine in the brain. It also covers hallucinogens like LSD, THC, and PCP, noting their mechanisms of action involve serotonin receptors for LSD and cannabinoid receptors for THC. The document provides information on therapeutic uses and adverse effects of these substances.
Opioid analgesics work by binding to opioid receptors in the brain and spinal cord to reduce pain. There are several types of opioid receptors that endogenous opioid peptides and exogenous opioids can bind to, including mu, delta, and kappa receptors. Opioids are well absorbed orally or parenterally and distributed widely throughout the body. They are metabolized in the liver mainly by conjugation with glucuronic acid and excreted in urine. Opioids produce analgesia, sedation, respiratory depression, nausea, vomiting, and constipation by acting on central and peripheral opioid receptors. Tolerance and physical dependence may develop with repeated use.
This document summarizes key information about opioid analgesics including:
1. It classifies opioids based on their strength from strong to weak and lists examples in each category.
2. It outlines several clinical uses of opioids such as for analgesia, cough suppression, and treatment of opioid dependence.
3. It describes the pharmacokinetics of opioids including absorption, metabolism, and ability to cross the placental barrier and affect fetuses.
4. It explains the mechanism of action of opioids including their binding to μ, δ, and κ receptors in the brain and spinal cord to produce effects like analgesia and respiratory depression.
The document provides an overview of the nervous system and cholinergic transmission. It discusses the organization and functions of the sympathetic and parasympathetic nervous systems. It describes the cholinergic receptors (muscarinic and nicotinic), cholinergic transmission, and the actions of cholinergic drugs including choline esters, alkaloids, anti-cholinesterases, and their therapeutic uses and side effects. In summary, it provides a comprehensive review of the cholinergic nervous system, receptors, transmission, and pharmacology of drugs that act on this system.
Sedatives and hypnotics drugs ppt by kashikant yadavKashikant Yadav
Sedatives and hypnotics are central nervous system depressants that are used to induce sleep or reduce anxiety. Barbiturates were previously commonly used but have largely been replaced by benzodiazepines due to lower risks of dependence and overdose. Both classes of drugs work by enhancing the effects of the inhibitory neurotransmitter GABA. Sedatives primarily reduce anxiety and excitement while hypnotics are used to induce sleep. Common side effects include drowsiness, dizziness, and impaired coordination. Tolerance can develop with repeated use of both barbiturates and benzodiazepines.
This document provides information about antiepileptic drugs. It discusses the history and classification of epilepsy. It then describes several classes of antiepileptic drugs including barbiturates, benzodiazepines, succinimides, and hydentoins. For each drug class, it summarizes the mechanism of action, pharmacokinetics, adverse effects, and therapeutic uses for treating epilepsy. The document aims to educate about different treatment options for controlling seizures.
Anti depressant and its classificationsNatasha Puri
This document discusses anti-depressant drugs and their classification. It defines depression as a serious mood disorder that can affect people of all ages and backgrounds. The main types of depression are described as uni-polar, bi-polar, and endogenous. Causes include family history, life events, medications, alcohol use, and chemical imbalances in the brain. Common symptoms are loss of interest and sadness/irritability. The document then covers various theories of depression before discussing treatment options like psychotherapy, ECT, natural alternatives, and medications. Anti-depressant drugs are classified as tricyclic antidepressants, selective serotonin reuptake inhibitors, serotonin-norepinephrine reuptake inhibitors, atypical antidepressants,
This document discusses anti-convulsant drugs used to treat epilepsy. It describes different types of seizures including partial, generalized tonic-clonic, absence and myoclonic seizures. Common anti-convulsants like carbamazepine, phenytoin, valproic acid, ethosuximide work by blocking sodium channels, calcium channels, or enhancing GABA effects. Adverse effects include dizziness, rashes, and gastrointestinal issues. Status epilepticus requires initial treatment with benzodiazepines then phenytoin or fosphenytoin for long-term control.
This document discusses CNS stimulants and nootropic agents. It begins by classifying various CNS stimulants such as psychostimulants, respiratory stimulants, convulsants, and listing examples like amphetamines, caffeine, nicotine. It then describes the mechanisms, effects and uses of specific stimulants - amphetamines, cocaine, caffeine, strychnine. Next, it covers nootropic agents like cholinergic activators rivastigmine, donepezil, memantine, piracetam and their mechanisms in improving cognition. The learning objectives are also stated.
This document summarizes a presentation about ganglions and ganglion stimulants and blockers. It defines a ganglion as a cluster of nerve cell bodies in the autonomic nervous system. It describes how ganglion stimulants like nicotine activate nicotinic receptors on postganglionic neurons. These stimulants are used to help people quit smoking by reducing nicotine cravings and withdrawal symptoms. Ganglion blockers inhibit transmission between preganglionic and postganglionic neurons by antagonizing nicotinic receptors. They were previously used to treat hypertension but caused intolerable side effects. The document outlines the mechanisms, effects, uses and side effects of both ganglion stimulants and blockers
This document discusses drugs used to treat gout, including colchicine, NSAIDs, corticosteroids, uricosuric agents like probenecid and sulfinpyrazone, and the uric acid synthesis inhibitor allopurinol. It provides details on the pathophysiology of gout, mechanisms of action, pharmacokinetics, indications, dosages and adverse effects of these drugs for both acute gout attacks and long-term treatment of chronic gout and hyperuricemia.
This document discusses opioids, including their classification, mechanisms of action, effects and side effects. It notes that opioids act on three receptor families in the central nervous system to produce analgesic and other effects. It describes the pharmacokinetics of opioids like morphine, including their metabolism and potential drug interactions. The document also discusses the use of opioid antagonists like naloxone to reverse overdose effects.
This document discusses anxiolytics and hypnotics, specifically focusing on barbiturates and benzodiazepines. It covers their history, classifications, mechanisms of action, pharmacokinetics, therapeutic uses, adverse effects, and treatment of overdoses. Barbiturates were originally used as sedatives but were replaced by benzodiazepines in the 1990s due to benzodiazepines having a better safety profile with less dependence and abuse potential. Both classes of drugs work by enhancing the effects of the neurotransmitter GABA.
This document discusses sedative-hypnotic drugs and classifies them as barbiturates or benzodiazepines. It explains that both act on GABA receptors, with barbiturates having both GABA facilitatory and direct effects while benzodiazepines only have GABA facilitatory effects. The document outlines the mechanism of action, pharmacokinetics, clinical effects, adverse effects and conclusions about each class. It emphasizes that while both can cause tolerance and dependence, benzodiazepines have fewer adverse effects and drug interactions than barbiturates.
1) The document provides definitions and explanations of key concepts related to drugs of abuse including drug abuse, drug dependence, drug addiction, drug tolerance, cross-dependence, and cross-tolerance.
2) It discusses the different types of drug dependence including psychological dependence and physiological dependence.
3) The document also covers topics like drug toxicity, co-administration of drugs, and provides additional learning resources on neurotransmission and mental disorders.
Este documento descreve os serviços de treinamento, palestras e consultorias oferecidos pela empresa BRgestão em Educação Executiva. A empresa oferece soluções em vendas, gestão, liderança e outdoor training para melhorar o desempenho e resultados de equipes comerciais, principalmente no setor do agronegócio. O documento também apresenta o facilitador dos treinamentos, Alessandro Lunardon, e alguns dos clientes atendidos pela empresa.
Este documento resume los cambios en las esferas (biosfera, litosfera, atmósfera) que ocurren cuando se construye una ciudad. Explica que antes de la construcción de la ciudad, los ecosistemas se encuentran poco intervenidos y hay una gran biodiversidad, pero la construcción elimina gran parte de la vegetación nativa. También altera la litosfera al perforarla para servicios y remodelar el terreno, y cambia la atmósfera volviéndola más contaminada con ráfagas de viento entre edificios.
Este documento descreve vários locais religiosos no município de Gondomar que apresentam características do estilo barroco, incluindo igrejas, capelas e mosteiros do século XVIII. Detalha elementos arquitetônicos como altares, tribunas, frontões e portais decorados com volutas, conchas e talha dourada.
El documento clasifica los árboles en tres categorías: árboles de hoja caduca que pierden sus hojas estacionalmente, árboles de hoja perenne que mantienen sus hojas agujas o escamas todo el año, y palmeras cuyas hojas son palmeadas o pinnadas y cuyos troncos son esbeltos y robustos.
El documento describe las propiedades fundamentales de la materia. Define materia como todo lo que tiene masa y ocupa un espacio. Explica que la masa es la cantidad de materia de un cuerpo y el volumen es el espacio que ocupa. Además, detalla algunas propiedades físicas como el estado físico, la densidad, el punto de fusión y ebullición. Finalmente, menciona propiedades intrínsecas como el color, olor, sabor y algunas propiedades mecánicas como la dureza, elasticidad y ductilidad
Este documento presenta el Manual de documentos electrónicos elaborado por el Comité de archivos de gestión en entorno electrónico del Consejo Internacional de Archivos (ICA). El manual ofrece enfoques prácticos para la gestión de documentos electrónicos a lo largo de su ciclo de vida, con el objetivo de ampliar la Guía para la gestión archivística de documentos electrónicos publicada por el ICA en 1997. El manual aborda temas como la definición de conceptos, la influencia de las tecnologías de la información, la implementación
Este documento presenta información sobre oscilaciones y movimiento armónico simple. Explica conceptos clave como periodo, frecuencia, amplitud, elongación y constante elástica. Incluye ecuaciones que describen la posición, velocidad y aceleración de un objeto en movimiento armónico. También presenta ejemplos numéricos para calcular valores relacionados con oscilaciones.
Este documento presenta los conceptos e importancia de los proyectos de inversión. Explica que un proyecto es un conjunto de actividades coordinadas para cumplir un objetivo específico. Los proyectos surgen de la necesidad de resolver problemas o aprovechar oportunidades. Se componen generalmente de cuatro estudios: mercado, técnico, financiero y organizacional. Los proyectos se pueden clasificar por el tipo de bienes o servicios que generan, por sector o por su evolución privada o pública. Siguen etapas como identificación, factibilidad
Arquitectura de la información diseño e implementaciónnatalymoreno08
Este documento trata sobre la arquitectura de la información y describe su importancia en el diseño e implementación de sistemas de información. La arquitectura de la información involucra la organización, navegación y rotulado de contenido para mejorar la experiencia del usuario. Un buen diseño reduce los costos y mejora la búsqueda y uso de información.
The term video editing can refer to: The process of manipulating video images. Once the province of expensive machines called video editors, video editing software is now available for personal computers and workstations.
O documento discute os perigos da influência excessiva da mídia, especialmente da televisão, no desenvolvimento e educação das crianças. Afirma que a permissividade da mídia está contribuindo para a puberdade precoce e sexualização precoce das crianças. Defende que os pais devem assumir o papel de educar seus filhos e filtrar o conteúdo da mídia a que eles têm acesso, em vez de deixar a educação deles nas mãos de estranhos.
A empresa de tecnologia anunciou um novo smartphone com câmera aprimorada, tela maior e bateria de longa duração por um preço acessível. O dispositivo tem como objetivo atrair mais consumidores em mercados emergentes com suas especificações equilibradas e preço baixo. Analistas esperam que as melhorias e o preço baixo impulsionem as vendas do novo aparelho.
O documento lista os manuais escolares e livros de leitura usados pelo autor no 1o e 2o ano da Escola Preparatória Júlio Dinis, incluindo manuais de Francês, História, Geografia, Português, Ciências da Natureza e um livro de leitura chamado "Gente Ousada".
A empresa de tecnologia anunciou um novo smartphone com câmera aprimorada, maior tela e bateria de longa duração. O dispositivo também possui processador mais rápido e armazenamento expansível. O novo modelo será lançado em outubro por um preço inicial de US$799.
Uma apresentação para expressar gratidão por uma amizade valiosa e prometer apoio incondicional. O autor diz que escolheu o amigo como família e que sua amizade ultrapassará os desafios que enfrentarão juntos no futuro.
A autora descreve como a contemplação da beleza da natureza, especialmente os pôr-do-sols, a ajudou a se curar da depressão. Hoje ela procura ensinar seu filho a valorizar as pequenas coisas da vida, como tirar uma foto de um pôr-do-sol, para que ele possa ser feliz. Ela incentiva o leitor a fazer passeios com a família para apreciar a natureza e acreditar que Deus os ama.
O documento descreve a evolução histórica dos sistemas operacionais, desde os primeiros computadores da década de 1940 até os dias atuais. A primeira geração utilizava válvulas e painéis de programação. A segunda geração introduziu os transistores e sistemas em lote. A terceira geração trouxe circuitos integrados e a multiprogramação com o sistema operacional OS/360. A quarta geração se baseia em circuitos integrados de larga escala que permitiram o desenvolvimento dos computadores pessoais.
The document discusses opioid analgesics, which are derived from the opium seed and relieve deep seated pain without causing loss of consciousness. It describes the endogenous opioid peptides and their receptors in the brain and spinal cord that regulate pain responsiveness. It provides details on the classification, mechanisms of action, effects and therapeutic uses of various opioid analgesics, including morphine, codeine, heroin, pethidine, fentanyl, and tramadol. It also discusses the treatment of opioid dependence and the use of opioid antagonists like naloxone and naltrexone.
The document discusses drug treatment of pain, outlining the goals of understanding pain pathways and classifications of analgesics like narcotic and non-narcotic drugs. It covers topics like peripheral and central pain mechanisms in the body, the role of the brain in pain perception, types of acute and chronic pain, and mechanisms of pain relief through drugs that act on opioid receptors in the nervous system. The document provides details on classification and examples of opioid analgesics, including their actions on mu, delta, and kappa opioid receptors in the body.
This document discusses opioid analgesics, including their classification, mechanisms of action, and examples. It covers natural, semisynthetic, and synthetic opioids that act as agonists or antagonists at opioid receptors in the body. Key opioids discussed include morphine, codeine, pethidine, naloxone, and pentazocine. The document details the pharmacological effects, uses, adverse effects and management of addiction for some of these opioids.
This document provides an overview of non-narcotic analgesics and anti-inflammatory agents. It begins by classifying analgesics as either opioid or non-opioid. It then discusses the mechanisms of action of various opioid analgesics like morphine, codeine, and meperidine. It provides details on their uses, pharmacology, and mechanisms of binding to opioid receptors in the central nervous system. The document also covers opioid antagonists like nalorphine and levallorphane that are used to reverse the effects of opioid overdose.
1. The document discusses pain and the various drugs used to treat it, including opioids (narcotic analgesics) which act in the central nervous system, and non-narcotic analgesics which act peripherally.
2. It describes the four major aspects of pain - nociception, pain perception, suffering, and pain behavior - and notes that opioids may relieve acute pain but are generally avoided for chronic pain where other therapies are often needed.
3. The history of opioids is reviewed, including the isolation of morphine from opium in the early 1800s, and various receptor mechanisms and classifications of opioid agonists and antagonists are presented.
The document discusses opioids and their use in pain management. It provides an overview of opioids, describing them as natural, semisynthetic, or synthetic drugs that bind to opioid receptors in the central nervous system. It then discusses several specific opioids like morphine, codeine, oxycodone, fentanyl, and methadone, outlining their classifications, mechanisms of action, indications, and side effects. The document also covers topics like opioid receptors, partial agonists and mixed agonist-antagonists, and the physiological effects of stimulating opioid receptors.
Analgesics are drugs that relieve pain without causing unconsciousness. Opiates are obtained from the opium poppy and act on opioid receptors in the central nervous system and tissues. There are three main types of opioid receptors that are involved in analgesia, respiratory depression, and euphoria. Opioid analgesics include natural, semisynthetic, and synthetic drugs and can be classified as agonists, antagonists, or mixed agonist-antagonists. Morphine is a potent agonist that binds to opioid receptors, decreasing substances involved in pain transmission and producing analgesia, euphoria, respiratory depression, constipation and other effects. It is metabolized in the liver and excreted in urine.
Narcotic analgesics can cause several side effects by interacting with receptors in the central nervous system. Respiratory depression occurs as narcotics bind to mu-opioid receptors in the brainstem respiratory center, suppressing neuronal activity and reducing breathing rate. Drowsiness and sedation result from CNS depression and effects on neurotransmitters like GABA. Narcotics may also cause nausea and vomiting by directly stimulating the chemoreceptor trigger zone in the brain or affecting gastrointestinal motility. Close monitoring is needed when using narcotics due to risks of respiratory depression and other side effects.
This document summarizes a presentation on drug abuse given by 5 students from the Department of Pharmacy at Jessore University of Science and Technology. It defines drug abuse and outlines the causes, routes of administration, signs and symptoms. It discusses how drug addiction occurs and categories of commonly abused drugs like marijuana, cocaine, heroin and alcohol. The presentation covers the physical and mental effects of dependence, prevention and control of drug abuse.
This document discusses different types of pain medications, including opioids. It describes various opioid drugs like morphine, codeine, heroin, methadone, fentanyl, and others. It explains how opioids work by binding to mu, delta, and kappa receptors in the central nervous system and periphery. Tolerance and dependence are noted as issues with long-term opioid use. Guidelines are provided for using different opioids to treat mild, moderate, and severe acute and chronic pain according to the World Health Organization.
The document discusses opioid analgesics and their mechanisms of action, receptors, endogenous opioids, and examples like morphine, codeine, pethidine. It summarizes their pharmacokinetics, pharmacodynamics, uses, adverse effects, interactions, and contraindications. The three major classes of opioid receptors are mu, kappa, and delta, which are G-protein coupled receptors located in the CNS and peripheral nerves. Opioids can act as agonists, antagonists, or mixed agonist-antagonists at these receptors. Tolerance and dependence develop with repeated use of opioids.
I am sharing this ppt on topic Narcotic Analgesia and it's antagonist. In that we include the Narcotic Receptors, Narcotic Analgesic introduction and mechanism of Action also i was explained about Narcotic Antagonist.
This document discusses the use of opioids to treat pain and inflammation. It begins by explaining pain physiology, including the pathways and fibers involved in pain signaling and processing. It describes the endogenous opioid system and different types of opioid receptors. It then classifies and describes various opioid analgesics, including strong agonists like morphine, mild-to-moderate agonists like codeine, mixed agonist-antagonists, and antagonists like naloxone. The document also discusses a case study of a patient taking meperidine after shoulder surgery and manipulation, highlighting the need to time physical therapy sessions around the drug's peak effects and monitor for side effects like respiratory depression.
This document provides an overview of opioids and opioid analgesics. It discusses how opioids act in the central nervous system and peripheral tissues to relieve pain. It describes the endogenous opioid system and three families of opioid peptides: endorphins, enkephalins, and dynorphins. It also discusses the three main types of opioid receptors: mu, kappa, and delta. The rest of the document details specific opioid analgesics including natural alkaloids like morphine and codeine, semi-synthetic opioids like heroin and oxycodone, and synthetic opioids like methadone and tramadol. It provides information on their mechanisms of action, therapeutic uses, and adverse effects.
Opioids are narcotic analgesics that bind to opioid receptors in the central and peripheral nervous systems to relieve pain. The major opioid receptors are mu, kappa, and sigma. Opioids produce analgesia by inhibiting neurotransmitter release presynaptically and by hyperpolarizing neurons postynaptically. Opioids are classified as agonist, agonist-antagonist, partial agonist, or antagonist depending on their receptor activity. Common opioids include morphine, codeine, hydromorphone, oxymorphone, pethidine, tramadol, methadone, fentanyl, remifentanil, buprenorphine, and naltrexone.
This document provides an overview of analgesics, including both opioid and non-opioid analgesics. It discusses various opioid analgesics like morphine, codeine, fentanyl and pentazocin. It describes their mechanisms of action, indications, routes of administration, side effects and contraindications. It also discusses non-opioid analgesics like paracetamol, acetylsalicylic acid and analgin, and describes their mechanisms of action as inhibitors of prostaglandin synthesis. The document classifies different types of pain and summarizes the history and development of commonly used opioid analgesics.
Narcotics are opioid drugs derived from opium poppy that are addictive and affect mood. They work by acting on receptors in the brain and nervous system to reduce pain and slow breathing. Common routes of administration include oral, intravenous, and inhalation. While narcotics have medical uses for pain relief, side effects include addiction, sedation, and trouble breathing. Treatment for narcotic addiction involves medication, counseling, and rehabilitation to support abstinence and prevent relapse.
Opioids are natural, semi-synthetic, and synthetic compounds that mimic the action of morphine. They act on opioid receptors both endogenously and exogenously. The physiological effects of opioids include analgesia through raising pain threshold and tolerance, respiratory depression by decreasing sensitivity to carbon dioxide, and euphoria producing a relaxed state. Opioids also cause sedation, gastrointestinal effects like nausea and constipation, and cardiovascular effects such as mild bradycardia and hypotension.
This document discusses narcotic analgesics and their classification, mechanisms of action, effects, and side effects. It notes that narcotics are potent analgesics that relieve severe pain and produce tolerance, dependence, and addiction upon administration. The document categorizes narcotics and discusses their receptors and effects. It specifically examines morphine, its analgesic, sedative, and respiratory effects as well as side effects like addiction, constipation, and respiratory depression. It also discusses non-narcotic analgesics that provide milder pain relief without loss of consciousness.
This document discusses opioid receptors and opioid analgesics. It begins by introducing opioids and their interaction with opioid receptors in the central nervous system and gastrointestinal tract. It then describes the three main types of opioid receptors - mu, kappa, and delta - and their locations in the brain and spinal cord. The document outlines various classes of opioid analgesics and antagonists based on their receptor interactions. It explains the mechanisms of action of opioids like morphine at opioid receptors, including their analgesic, sedative, and other effects. The pharmacokinetics, uses, and adverse effects of representative opioids like morphine and semi-synthetic derivatives are summarized. Finally, the mechanisms and applications of opioid antagonists such as naloxone and naltrexone
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
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2. Narcotics agents are potent analgesics which are
effective for the relief of severe pain.
Two phrases:-
Narcotic:-The term narcotic ( from ancient Greek "to make
numb") originally referred medically to any psychoactive
compound with any sleep-inducing properties .
Commonly morphine and heroin and their derivatives, such
as hydrocodone.
Analgesics:-These are selective CNS depressants which
are used for the relief of pain
3. Narcotic agents are classified into four major
groups:-
1.Morphine and Codeine:-natural alkaloids (mainly
resins of poppy Plant, fam. (papaver somniferum)
2.Synthetic derivatives of morphine such as heroin
3.Synthetic agents which resembles the morphine
structure. e.g. Pethidine,Methadone,Tramadol.
4.Narcotics antagonists which are used for overdose of
narcotic analgesics.
E.g.Naloxone,Dapsone
5. Works by two process
1.By opening Na+channel causing Hyperpolarization
Mainly three different types of receptors (mew,delta,kappa)
G-protein linked
Works by binding to opoid receptors present in
Central Nervous System Peripheral Nervous System
6. Overall
Reduces neuronal activity in pain carrying pathways
In turn
Inhibits release of all excitatory neurotransmitters
OR
By inhibiting Ca++ channel opening
7. Mu, delta and kappa receptors.
Mu agonists:- produce analgesia
affect numerous body systems
influence mood & behavior.
Delta agonists:- produce analgesia. Its not
frequently used
Kappa agonists:- produce analgesia
may cause less respiratory
depression and miosis.
psych effects, can produce dysphoria
8.
9. Pharmacokinetic properties of an opioid can dictate
the circumstance which they are appropriate in:
E. g- Lipid-soluble drug such as fentanyl, which diffuse
rapidly across the BBB, are preferable if analgesia is
required immediately before a short, painful procedure.
Elimination half life very short:
So, steady state reached in a day or less!
◦ Thus, you can adjust the dose daily knowing we are
seeing it’s effect.
10. Morphine sold under many trade names, is a pain
medication of the opiate type.
It acts directly on the central nervous system (CNS)
to decrease the feeling of pain.
It can be used for both acute pain and chronic pain.
Morphine is also frequently used for pain
from myocardial infarction and during labour.
11. 1.CNS:- Morphine has site specific depressant and
stimulant actions in the CNS by interacting primarily with
the mew opoid receptors as full agonist.
Analgesia, sedation, mood and subjective effects,
respiratory center depresses, cough center depresses,
temperature control center depresses.
2.CVS:-Morphine causes vasodilatation due to
A) Histamine release
B)Depression of the vasomotor center.
C)Direct action by decreasing the tone of blood vessel.
12. 3)SMOOTH MUSCLES GIT:-Constipation is the
common effect feature by morphine.
Reduce all gastrointestinal secretions
Tone of duodenum and colon may be increase.
Actions directly on intestine and in CNS increases
tone but decreases propulsive movement.
4)ANS:-Morphine causes mild hyperglycemia due
to central sympathetic stimulation.
14. When people use narcotics only to control pain, they are
unlikely to become addicted to the drugs. However,
opioids provide an intoxicating high when injected or
taken orally in high doses. Opioids are also
powerful anxiety relievers.
Narcotic rehab centers are widely available to individuals
who have become dependent on the drug
Reduce abuse of Drugs.
Proper prescribing and administration
15. REFERENCES
1.Sakchainanont, B, Ruangkanchanasetr, S, Chantarojanasiri, T, et al (1990)
Effectiveness of narcotic analgesics in siesure. J Med Assoc Thai 73, 96-101
2.Principle of Experimental Pharmacology . Rage and Dale
3.Pathophysioloy of Disease. Robins. H