This document discusses anthelmintic drugs used to treat helminth infections. It begins by describing common types of helminths including tapeworms, roundworms, and flukes. It then discusses the ideal properties of anthelmintic drugs and classifications based on mechanism of action, spectrum of activity, and type of helminth treated. Specific anthelmintic drugs are described for tapeworms (anticestodals), roundworms (antinematodals), and flukes (antitrematodals). Key drugs discussed include albendazole, mebendazole, praziquantel, pyrantel, and ivermectin. Clinical uses and mechanisms of action
Osmotic purgatives work by retaining water osmotically in the intestine, distending the bowel and indirectly increasing peristalsis. Common osmotic purgatives include magnesium and sodium salts like magnesium sulfate, magnesium hydroxide, sodium sulfate, and sodium phosphate. Lactulose is also an osmotic purgative, as the bacteria in the colon break it down into products that retain water osmotically. Osmotic purgatives differ in dose, palatability, and risk of systemic toxicity. Their main uses are in preparing the bowel before surgery or colonoscopy and in food/drug poisoning.
Histamine is a biogenic amine found in many tissues that is involved in allergic and inflammatory processes as well as gastric acid secretion and neurotransmission. It is synthesized and stored in mast cells and basophils and released during allergic reactions. Histamine exerts its effects through four receptor subtypes (H1-H4), with H1 and H2 receptors having drugs that target them clinically. H1 receptor antagonists are used to treat allergic rhinitis, chronic urticaria, and motion sickness, while H2 receptor antagonists suppress gastric acid secretion. New drugs targeting H3 and H4 receptors may provide treatments for neurological and inflammatory conditions, respectively.
Pharmacotherapy of Antihelminthic agentsManoj Kumar
1. Helminths, or worms, infect over 1/3 of the world's population and are most common in developing countries with poor sanitation. They are usually transmitted through feces and cause symptoms like anemia, diarrhea, abdominal pain, and organ damage.
2. The main drug classes used to treat helminth infections are benzimidazoles like mebendazole and albendazole, which inhibit polymerization of beta-tubulin in parasites. Other drugs include pyrantel pamoate, diethylcarbamazine, and ivermectin.
3. While effective, these drugs can cause side effects like nausea, vomiting, rash, and alopec
Sulfonamides and Sulfonamide Combinations Use in Animals.pptxOssama Motawae
This document discusses sulfonamides and sulfonamide combinations used in animals. It covers their introduction, therapeutic indications including treatment of various infections, mode of action by inhibiting bacterial folic acid synthesis, administration routes, pharmacokinetics of absorption, distribution, metabolism and excretion, adverse effects including hypersensitivity reactions, and drug interactions. The document provides details on various individual sulfonamides and potentiated sulfonamide combinations used in veterinary medicine.
This is the 4th webinar in a series of webinars on worms in sheep and goats. This presentation focuses on anthelmintics and other treatment options. The presentation was prepared by Susan Schoenian, University of Maryland Extension Sheep & Goat Specialist.
This document discusses serotonin (5-HT), an amine autacoid that acts as a local hormone. Some key points:
1. Serotonin is synthesized from the amino acid tryptophan and is widely distributed in the body, especially in the gastrointestinal tract and brain.
2. It has diverse physiological and pharmacological actions, including effects on mood, sleep, gastrointestinal motility, respiration, and cardiovascular function.
3. Serotonin signals through multiple receptor subtypes, and drugs that target specific receptors are used to treat conditions like anxiety, depression, migraine, and nausea/vomiting.
4. Dysregulation of serotonin signaling is implicated in diseases such as carcinoid syndrome and mood
1) Rheumatoid arthritis is an autoimmune disorder characterized by joint inflammation and cartilage destruction, causing pain, swelling, and loss of function. It affects around 1-2% of the population and is more common in women over age 55.
2) Disease-modifying antirheumatic drugs (DMARDs) like methotrexate, sulfasalazine, and hydroxychloroquine are used to suppress the rheumatoid process and bring remission, in addition to nonsteroidal anti-inflammatory drugs (NSAIDs) for symptom relief. Biologic response modifiers targeting tumor necrosis factor alpha are also used.
3) Methotrexate is one of the most effective and commonly used
Parasitic diseases remain a major constraint to livestock productivity across all agro ecological zones and production systems in Africa, and gastrointestinal nematodes remain a major economic importance in domesticated livestock throughout the world [1] being the chief parasitizes responsible for disease-related production losses arising from stock mortality, severe weight loss and poor production, especially in small ruminants. The World Health Organization estimates that a staggering 2 billion people harbour parasitic worm infections. Parasitic worms also infect livestock and crops, affecting food production with a resultant economic impact. Also of importance is the infection of domestic pets. Indeed, the companion animal market is a major economic consideration for animal health companies undertaking drug discovery programmes.
Osmotic purgatives work by retaining water osmotically in the intestine, distending the bowel and indirectly increasing peristalsis. Common osmotic purgatives include magnesium and sodium salts like magnesium sulfate, magnesium hydroxide, sodium sulfate, and sodium phosphate. Lactulose is also an osmotic purgative, as the bacteria in the colon break it down into products that retain water osmotically. Osmotic purgatives differ in dose, palatability, and risk of systemic toxicity. Their main uses are in preparing the bowel before surgery or colonoscopy and in food/drug poisoning.
Histamine is a biogenic amine found in many tissues that is involved in allergic and inflammatory processes as well as gastric acid secretion and neurotransmission. It is synthesized and stored in mast cells and basophils and released during allergic reactions. Histamine exerts its effects through four receptor subtypes (H1-H4), with H1 and H2 receptors having drugs that target them clinically. H1 receptor antagonists are used to treat allergic rhinitis, chronic urticaria, and motion sickness, while H2 receptor antagonists suppress gastric acid secretion. New drugs targeting H3 and H4 receptors may provide treatments for neurological and inflammatory conditions, respectively.
Pharmacotherapy of Antihelminthic agentsManoj Kumar
1. Helminths, or worms, infect over 1/3 of the world's population and are most common in developing countries with poor sanitation. They are usually transmitted through feces and cause symptoms like anemia, diarrhea, abdominal pain, and organ damage.
2. The main drug classes used to treat helminth infections are benzimidazoles like mebendazole and albendazole, which inhibit polymerization of beta-tubulin in parasites. Other drugs include pyrantel pamoate, diethylcarbamazine, and ivermectin.
3. While effective, these drugs can cause side effects like nausea, vomiting, rash, and alopec
Sulfonamides and Sulfonamide Combinations Use in Animals.pptxOssama Motawae
This document discusses sulfonamides and sulfonamide combinations used in animals. It covers their introduction, therapeutic indications including treatment of various infections, mode of action by inhibiting bacterial folic acid synthesis, administration routes, pharmacokinetics of absorption, distribution, metabolism and excretion, adverse effects including hypersensitivity reactions, and drug interactions. The document provides details on various individual sulfonamides and potentiated sulfonamide combinations used in veterinary medicine.
This is the 4th webinar in a series of webinars on worms in sheep and goats. This presentation focuses on anthelmintics and other treatment options. The presentation was prepared by Susan Schoenian, University of Maryland Extension Sheep & Goat Specialist.
This document discusses serotonin (5-HT), an amine autacoid that acts as a local hormone. Some key points:
1. Serotonin is synthesized from the amino acid tryptophan and is widely distributed in the body, especially in the gastrointestinal tract and brain.
2. It has diverse physiological and pharmacological actions, including effects on mood, sleep, gastrointestinal motility, respiration, and cardiovascular function.
3. Serotonin signals through multiple receptor subtypes, and drugs that target specific receptors are used to treat conditions like anxiety, depression, migraine, and nausea/vomiting.
4. Dysregulation of serotonin signaling is implicated in diseases such as carcinoid syndrome and mood
1) Rheumatoid arthritis is an autoimmune disorder characterized by joint inflammation and cartilage destruction, causing pain, swelling, and loss of function. It affects around 1-2% of the population and is more common in women over age 55.
2) Disease-modifying antirheumatic drugs (DMARDs) like methotrexate, sulfasalazine, and hydroxychloroquine are used to suppress the rheumatoid process and bring remission, in addition to nonsteroidal anti-inflammatory drugs (NSAIDs) for symptom relief. Biologic response modifiers targeting tumor necrosis factor alpha are also used.
3) Methotrexate is one of the most effective and commonly used
Parasitic diseases remain a major constraint to livestock productivity across all agro ecological zones and production systems in Africa, and gastrointestinal nematodes remain a major economic importance in domesticated livestock throughout the world [1] being the chief parasitizes responsible for disease-related production losses arising from stock mortality, severe weight loss and poor production, especially in small ruminants. The World Health Organization estimates that a staggering 2 billion people harbour parasitic worm infections. Parasitic worms also infect livestock and crops, affecting food production with a resultant economic impact. Also of importance is the infection of domestic pets. Indeed, the companion animal market is a major economic consideration for animal health companies undertaking drug discovery programmes.
This document provides information on antirheumatic drugs used to treat rheumatoid arthritis (RA). It describes the pathophysiology of RA involving inflammatory cytokines like TNF, IL-6, IL-1. NSAIDs provide initial symptomatic relief but DMARDs like methotrexate, hydroxychloroquine, leflunomide, and sulfasalazine suppress disease progression. Biological DMARDs targeting TNF or non-TNF pathways like abatacept are used when traditional DMARDs are ineffective. The goals of treatment are to reduce symptoms, prevent joint damage, and maintain function. Adverse effects of various drugs are also outlined.
This document provides information on various antihelmintic drugs used to treat helminth infections. It discusses the epidemiology of soil-transmitted helminth infections and mechanisms of action of different classes of antihelmintics. Key drugs discussed include mebendazole, albendazole, ivermectin, praziquantel, diethylcarbamazine, and piperazine. Each drug's indications, mechanisms of action, pharmacokinetics, clinical uses, and adverse effects are summarized.
The document discusses quinolones and fluoroquinolones, a class of synthetic antimicrobial drugs. It notes that early quinolones like nalidixic acid had limited usefulness due to low potency and high bacterial resistance. Fluoroquinolones were developed in the 1980s by adding fluorine substitutions, improving potency, spectrum of activity, and tissue penetration. Ciprofloxacin is a prototype fluoroquinolone with broad-spectrum bactericidal activity against both gram-positive and gram-negative bacteria. It is well-absorbed orally and concentrated in tissues, with mainly urinary excretion. Adverse effects are generally mild but include gastrointestinal issues, CNS effects, and
This document discusses antigout drugs used to treat gout. It begins by defining gout as a metabolic disease caused by increased uric acid levels in the blood. It then describes the mechanisms and classifications of various antigout drugs including allopurinol, probenecid, sulfinpyrazone, corticosteroids, NSAIDs, and colchicine. For each drug, it discusses their mechanisms of action, pharmacokinetics, uses, interactions, toxicity, and administration guidelines for treating both acute and chronic gout. The document provides an in-depth overview of different drug classes used to manage hyperuricemia and gouty arthritis.
This document summarizes various antiparasitic agents used to treat protozoal infections. It discusses the classification, mechanisms of action, administration, pharmacokinetics, side effects, drug interactions, and uses of different classes of drugs including nitroimidazoles, artemisinins, quinine, mefloquine, and halofantrine for treating diseases caused by protozoa such as Entamoeba histolytica, Plasmodium spp., Giardia lamblia, and Trypanosoma spp. The agents described target various protozoa that infect the intestinal tract, blood, and tissues.
1. The document discusses androgens and their role in male physiology and pharmacology. It describes hormones like testosterone and their effects on tissues like the testes, prostate, and muscles.
2. Various androgen therapies are mentioned for conditions like hypogonadism, breast cancer, and osteoporosis. Antiandrogen drugs are also summarized that block androgen receptors for prostate cancer.
3. Biosynthesis and metabolism of testosterone is outlined. Side effects of androgen therapies and indications for antiandrogens are provided. Erectile dysfunction treatments like sildenafil are also briefly described.
This document discusses peptic ulcers, including their causes, symptoms, and treatments. It notes that peptic ulcers are open sores in the upper digestive tract that can form in the stomach (gastric ulcer) or small intestine (duodenal ulcer). Common causes include H. pylori infection, NSAIDs, and stress. Symptoms may include abdominal pain, nausea, black stools, or weight loss. Treatments discussed include antibiotics to kill H. pylori, antacids to neutralize stomach acid, drugs that decrease acid secretion, ulcer protective drugs to coat the ulcer, and ulcer healing drugs.
This document discusses antimalarial drugs, including their classification, mechanisms of action, pharmacokinetics, clinical uses, and adverse effects. The main classes of antimalarial drugs are tissue schizonticides, blood schizonticides, and gametocides. Key drugs discussed include chloroquine, mefloquine, quinine, proguanil, pyrimethamine, primaquine, and artemisinin derivatives. The document also covers antimalarial drug combinations such as sulfadoxine-pyrimethamine and artemisinin-based combination therapies.
Expt. 7 Bioassay of acetylcholine using rat ileum by four point bioassayVISHALJADHAV100
Objective
Principle
Requirements
Experimental specifications (conditions)
Preparation of ACh stock and standard solutions
Preparation of frog ringer solution (PSS)
Procedure
Kymograph recording of contractions
Observation table
Calculation
Result and interpretation
The document discusses various aspects of helminths (parasitic worms) that infect humans including types of helminths, the diseases they cause, and drugs used to treat helminth infections. It describes the two main types of helminths - nematodes (roundworms) and platyhelminths (flatworms) which include trematodes (flukes) and cestodes (tapeworms). It then discusses various anthelmintic drugs, their mechanisms of action, clinical uses, and side effects. Key drugs mentioned include mebendazole, pyrantel pamoate, piperazine, ivermectin, praziquantel, niclosamide, and b
The document provides information on various aspects of helminths (worms) and anthelmintic drugs used to treat helminth infections. It defines helminths as macroscopic, multicellular parasites that are generally elongated or round. It describes the three main groups of helminths - cestodes, trematodes, and nematodes - and provides details on their lifecycles and morphology. The document then discusses common helminth infections and anthelmintic drug classes, mechanisms of action, specific drugs like piperazine, mebendazole, praziquantel, ivermectin, and pyrantel pamoate, along with their indications, pharmacokinetics
Asthma is characterized by airway hyperresponsiveness and inflammation. Common symptoms include wheezing, coughing, and shortness of breath. Treatment approaches include preventing antigen exposure, reducing inflammation, blocking mediators, and dilating airways. Main drug classes used are bronchodilators like beta-2 agonists, methylxanthines, anticholinergics; leukotriene antagonists; mast cell stabilizers; inhaled and systemic corticosteroids; and anti-IgE antibodies for severe cases. Medications work by various mechanisms like increasing cAMP, blocking receptors, or inhibiting inflammatory pathways. Choice of treatment depends on severity and goals of management.
Autacoids - pharmacological actions and drugs related to them. SIVASWAROOP YARASI
Autacoids or "autocoids" are biological factors which act like local hormones, have a brief duration, and act near the site of synthesis. The word autacoids comes from the Greek "autos" (self) and "acos" (relief, i.e. drug).
Introduction of Veterinary pharmacologyQaline Giigii
This document provides an introduction to veterinary pharmacology. It discusses how pharmacology can be defined as the study of substances that interact with living systems, and how veterinary pharmacology specifically focuses on preventing, diagnosing and treating disease in animals. The document then summarizes that veterinary pharmacology has two main subdivisions: pharmacokinetics, which is what the body does to a drug, and pharmacodynamics, which is what the drug does to the body. Several key pharmacokinetic and pharmacodynamic concepts are then defined, including absorption, distribution, metabolism, excretion, drug receptors, and drug effects.
Introduction to Anticoagulants
Coagulants, Local agents, Systemic agents, Anticoagulants, Heparin, Low molecular weight heparins, Heparinoids, Oral anticoagulants (Warfarin), Therapeutic uses
Presented by
N. Ramya
Department of Pharmacology
Physiological salt solutions, also known as Ringer's solution, are artificially prepared solutions used to maintain isolated animal tissues in an experimental setting. They are designed to mimic the composition of extracellular fluids and keep tissue alive outside the body. The main components of physiological salt solutions are sodium, potassium, calcium, chloride, magnesium, and glucose dissolved in distilled water. Each ingredient plays an important role like maintaining electrolyte and osmotic balance, nerve and muscle function. Care must be taken when preparing the solutions to maintain the proper pH and prevent bacterial growth. Different types of physiological salt solutions exist that are tailored to the specific needs of different tissue types.
Hypertension is a common cardiovascular condition caused by persistently high blood pressure that damages organs. Antihypertensive drugs work via different mechanisms like inhibiting the renin-angiotensin-aldosterone system, blocking calcium channels, promoting sodium excretion with diuretics, and reducing sympathetic nervous system activity. Common classes of antihypertensives include ACE inhibitors, angiotensin receptor blockers, calcium channel blockers, diuretics, sympatholytics, and vasodilators. Treatment involves beginning with certain drug classes based on patient characteristics and guidelines, and escalating treatment by adding other classes as needed to control blood pressure. Antihypertensive drug choice is also based on minimizing adverse effects and avoiding
Expt. 1 Introduction to in vitro pharmacology and physiological salt solutionsVISHALJADHAV100
This document provides an overview of in-vitro pharmacology experiments using isolated tissues and physiological salt solutions (PSS). It defines pharmacology and drugs, describes the aims of experimental pharmacology as finding therapeutic agents, studying toxicity and mechanisms of action. It also discusses types of experiments, equipment like organ baths and levers for recording tissue responses, and PSS compositions and roles. PSS are artificial solutions that maintain isolated tissues by resembling extracellular fluid composition. Selection of the appropriate PSS depends on the tissue being studied.
This document discusses anthelmintic drugs used to treat helminth infections. It begins by describing common types of helminths including tapeworms, roundworms, and flukes. It then discusses ideal properties of anthelmintic drugs and classifications based on mechanism of action, spectrum of activity, and type of helminth targeted. Specific drug classes and examples are provided, including benzimidazoles, tetrahydropyrimidines, piperazine, diethylcarbamazine, ivermectin, and others. Their mechanisms of action, clinical uses, safety profiles and pharmacokinetics are summarized for key anthelmintic drugs.
This document discusses common helminthic parasites and anthelmintic drugs. It describes the lifecycles and characteristics of tapeworms, roundworms, hookworms, pinworms, whipworms, flukes and schistosomes. It then profiles several classes of anthelmintic drugs including tetrahydropyrimidines, piperazine, levamisole, niclosamide and praziquantel. It explains their mechanisms of action, effectiveness against different parasite types, pharmacokinetics, safety and clinical uses in treating helminthic infections.
This document provides information on antirheumatic drugs used to treat rheumatoid arthritis (RA). It describes the pathophysiology of RA involving inflammatory cytokines like TNF, IL-6, IL-1. NSAIDs provide initial symptomatic relief but DMARDs like methotrexate, hydroxychloroquine, leflunomide, and sulfasalazine suppress disease progression. Biological DMARDs targeting TNF or non-TNF pathways like abatacept are used when traditional DMARDs are ineffective. The goals of treatment are to reduce symptoms, prevent joint damage, and maintain function. Adverse effects of various drugs are also outlined.
This document provides information on various antihelmintic drugs used to treat helminth infections. It discusses the epidemiology of soil-transmitted helminth infections and mechanisms of action of different classes of antihelmintics. Key drugs discussed include mebendazole, albendazole, ivermectin, praziquantel, diethylcarbamazine, and piperazine. Each drug's indications, mechanisms of action, pharmacokinetics, clinical uses, and adverse effects are summarized.
The document discusses quinolones and fluoroquinolones, a class of synthetic antimicrobial drugs. It notes that early quinolones like nalidixic acid had limited usefulness due to low potency and high bacterial resistance. Fluoroquinolones were developed in the 1980s by adding fluorine substitutions, improving potency, spectrum of activity, and tissue penetration. Ciprofloxacin is a prototype fluoroquinolone with broad-spectrum bactericidal activity against both gram-positive and gram-negative bacteria. It is well-absorbed orally and concentrated in tissues, with mainly urinary excretion. Adverse effects are generally mild but include gastrointestinal issues, CNS effects, and
This document discusses antigout drugs used to treat gout. It begins by defining gout as a metabolic disease caused by increased uric acid levels in the blood. It then describes the mechanisms and classifications of various antigout drugs including allopurinol, probenecid, sulfinpyrazone, corticosteroids, NSAIDs, and colchicine. For each drug, it discusses their mechanisms of action, pharmacokinetics, uses, interactions, toxicity, and administration guidelines for treating both acute and chronic gout. The document provides an in-depth overview of different drug classes used to manage hyperuricemia and gouty arthritis.
This document summarizes various antiparasitic agents used to treat protozoal infections. It discusses the classification, mechanisms of action, administration, pharmacokinetics, side effects, drug interactions, and uses of different classes of drugs including nitroimidazoles, artemisinins, quinine, mefloquine, and halofantrine for treating diseases caused by protozoa such as Entamoeba histolytica, Plasmodium spp., Giardia lamblia, and Trypanosoma spp. The agents described target various protozoa that infect the intestinal tract, blood, and tissues.
1. The document discusses androgens and their role in male physiology and pharmacology. It describes hormones like testosterone and their effects on tissues like the testes, prostate, and muscles.
2. Various androgen therapies are mentioned for conditions like hypogonadism, breast cancer, and osteoporosis. Antiandrogen drugs are also summarized that block androgen receptors for prostate cancer.
3. Biosynthesis and metabolism of testosterone is outlined. Side effects of androgen therapies and indications for antiandrogens are provided. Erectile dysfunction treatments like sildenafil are also briefly described.
This document discusses peptic ulcers, including their causes, symptoms, and treatments. It notes that peptic ulcers are open sores in the upper digestive tract that can form in the stomach (gastric ulcer) or small intestine (duodenal ulcer). Common causes include H. pylori infection, NSAIDs, and stress. Symptoms may include abdominal pain, nausea, black stools, or weight loss. Treatments discussed include antibiotics to kill H. pylori, antacids to neutralize stomach acid, drugs that decrease acid secretion, ulcer protective drugs to coat the ulcer, and ulcer healing drugs.
This document discusses antimalarial drugs, including their classification, mechanisms of action, pharmacokinetics, clinical uses, and adverse effects. The main classes of antimalarial drugs are tissue schizonticides, blood schizonticides, and gametocides. Key drugs discussed include chloroquine, mefloquine, quinine, proguanil, pyrimethamine, primaquine, and artemisinin derivatives. The document also covers antimalarial drug combinations such as sulfadoxine-pyrimethamine and artemisinin-based combination therapies.
Expt. 7 Bioassay of acetylcholine using rat ileum by four point bioassayVISHALJADHAV100
Objective
Principle
Requirements
Experimental specifications (conditions)
Preparation of ACh stock and standard solutions
Preparation of frog ringer solution (PSS)
Procedure
Kymograph recording of contractions
Observation table
Calculation
Result and interpretation
The document discusses various aspects of helminths (parasitic worms) that infect humans including types of helminths, the diseases they cause, and drugs used to treat helminth infections. It describes the two main types of helminths - nematodes (roundworms) and platyhelminths (flatworms) which include trematodes (flukes) and cestodes (tapeworms). It then discusses various anthelmintic drugs, their mechanisms of action, clinical uses, and side effects. Key drugs mentioned include mebendazole, pyrantel pamoate, piperazine, ivermectin, praziquantel, niclosamide, and b
The document provides information on various aspects of helminths (worms) and anthelmintic drugs used to treat helminth infections. It defines helminths as macroscopic, multicellular parasites that are generally elongated or round. It describes the three main groups of helminths - cestodes, trematodes, and nematodes - and provides details on their lifecycles and morphology. The document then discusses common helminth infections and anthelmintic drug classes, mechanisms of action, specific drugs like piperazine, mebendazole, praziquantel, ivermectin, and pyrantel pamoate, along with their indications, pharmacokinetics
Asthma is characterized by airway hyperresponsiveness and inflammation. Common symptoms include wheezing, coughing, and shortness of breath. Treatment approaches include preventing antigen exposure, reducing inflammation, blocking mediators, and dilating airways. Main drug classes used are bronchodilators like beta-2 agonists, methylxanthines, anticholinergics; leukotriene antagonists; mast cell stabilizers; inhaled and systemic corticosteroids; and anti-IgE antibodies for severe cases. Medications work by various mechanisms like increasing cAMP, blocking receptors, or inhibiting inflammatory pathways. Choice of treatment depends on severity and goals of management.
Autacoids - pharmacological actions and drugs related to them. SIVASWAROOP YARASI
Autacoids or "autocoids" are biological factors which act like local hormones, have a brief duration, and act near the site of synthesis. The word autacoids comes from the Greek "autos" (self) and "acos" (relief, i.e. drug).
Introduction of Veterinary pharmacologyQaline Giigii
This document provides an introduction to veterinary pharmacology. It discusses how pharmacology can be defined as the study of substances that interact with living systems, and how veterinary pharmacology specifically focuses on preventing, diagnosing and treating disease in animals. The document then summarizes that veterinary pharmacology has two main subdivisions: pharmacokinetics, which is what the body does to a drug, and pharmacodynamics, which is what the drug does to the body. Several key pharmacokinetic and pharmacodynamic concepts are then defined, including absorption, distribution, metabolism, excretion, drug receptors, and drug effects.
Introduction to Anticoagulants
Coagulants, Local agents, Systemic agents, Anticoagulants, Heparin, Low molecular weight heparins, Heparinoids, Oral anticoagulants (Warfarin), Therapeutic uses
Presented by
N. Ramya
Department of Pharmacology
Physiological salt solutions, also known as Ringer's solution, are artificially prepared solutions used to maintain isolated animal tissues in an experimental setting. They are designed to mimic the composition of extracellular fluids and keep tissue alive outside the body. The main components of physiological salt solutions are sodium, potassium, calcium, chloride, magnesium, and glucose dissolved in distilled water. Each ingredient plays an important role like maintaining electrolyte and osmotic balance, nerve and muscle function. Care must be taken when preparing the solutions to maintain the proper pH and prevent bacterial growth. Different types of physiological salt solutions exist that are tailored to the specific needs of different tissue types.
Hypertension is a common cardiovascular condition caused by persistently high blood pressure that damages organs. Antihypertensive drugs work via different mechanisms like inhibiting the renin-angiotensin-aldosterone system, blocking calcium channels, promoting sodium excretion with diuretics, and reducing sympathetic nervous system activity. Common classes of antihypertensives include ACE inhibitors, angiotensin receptor blockers, calcium channel blockers, diuretics, sympatholytics, and vasodilators. Treatment involves beginning with certain drug classes based on patient characteristics and guidelines, and escalating treatment by adding other classes as needed to control blood pressure. Antihypertensive drug choice is also based on minimizing adverse effects and avoiding
Expt. 1 Introduction to in vitro pharmacology and physiological salt solutionsVISHALJADHAV100
This document provides an overview of in-vitro pharmacology experiments using isolated tissues and physiological salt solutions (PSS). It defines pharmacology and drugs, describes the aims of experimental pharmacology as finding therapeutic agents, studying toxicity and mechanisms of action. It also discusses types of experiments, equipment like organ baths and levers for recording tissue responses, and PSS compositions and roles. PSS are artificial solutions that maintain isolated tissues by resembling extracellular fluid composition. Selection of the appropriate PSS depends on the tissue being studied.
This document discusses anthelmintic drugs used to treat helminth infections. It begins by describing common types of helminths including tapeworms, roundworms, and flukes. It then discusses ideal properties of anthelmintic drugs and classifications based on mechanism of action, spectrum of activity, and type of helminth targeted. Specific drug classes and examples are provided, including benzimidazoles, tetrahydropyrimidines, piperazine, diethylcarbamazine, ivermectin, and others. Their mechanisms of action, clinical uses, safety profiles and pharmacokinetics are summarized for key anthelmintic drugs.
This document discusses common helminthic parasites and anthelmintic drugs. It describes the lifecycles and characteristics of tapeworms, roundworms, hookworms, pinworms, whipworms, flukes and schistosomes. It then profiles several classes of anthelmintic drugs including tetrahydropyrimidines, piperazine, levamisole, niclosamide and praziquantel. It explains their mechanisms of action, effectiveness against different parasite types, pharmacokinetics, safety and clinical uses in treating helminthic infections.
1. The document discusses anti-helminthic drugs used to treat infections caused by parasitic worms in humans. It describes the common types of helminths including tapeworms, roundworms, and flukes.
2. Various anti-helminthic drugs are classified based on their mechanism of action, spectrum of activity, and source. Broad spectrum benzimidazoles like mebendazole and albendazole are effective against many worm types.
3. Individual drugs are discussed in more detail, including their mechanisms of action, uses for specific worm infections, dosages, and side effects. Commonly used drugs include albendazole, mebendazole, pyrantel
This presentation discusses anticestodes, which are drugs used to treat tapeworm infections. It outlines five common anticestodal drugs - albendazole, niclosamide, praziquantel, epsiprantel, and fenbendazole. For each drug, the summary discusses the mechanism of action, pharmacokinetics, and potential adverse effects. The presentation provides an overview of tapeworm lifecycles and diseases in humans and livestock.
This document discusses anthelmintic drugs used to treat parasitic worm infections. It classifies helminths into nematodes, which include roundworms and hookworms, and platyhelminths, which include flukes and tapeworms. Ideal anthelmintics are orally active, effective in a single dose, inexpensive, and have a wide safety margin between toxicity to worms and humans. Common anthelmintic drug classes discussed are benzimidazoles, piperazine derivatives, and imidazothiazoles. Specific drugs mentioned include mebendazole, albendazole, piperazine citrate, and levamisole. The document provides details on the mechanisms of
This document discusses anthelmintics, which are drugs used to kill or expel parasitic worms from the gastrointestinal tract and other tissues. It describes how anthelmintics can act as vermicides by killing parasites or vermifuges by removing parasites. The document outlines the characteristics of ideal anthelmintic drugs and discusses their various chemical classes and modes of action, such as affecting energy production or the neuromuscular system of parasites. Delivery forms, resistance, and strategies to prevent resistance are also covered.
The document discusses antimalarial, antiprotozoal, and antihelmintic agents used to treat parasitic infections. It describes the life cycles and transmission of malaria, protozoal infections like amebiasis, and helminth infections. It outlines the mechanisms of action and therapeutic uses of various antimalarial, antiprotozoal, and antihelmintic drugs, as well as their potential side effects. Nursing implications are monitoring for side effects and ensuring treatment compliance.
Protozoal infections and antiprotozoal drugs(therapy).Gagandeep Jaiswal
presentation comprising knowledge about various protozoal infections and therapy options available for the treatment of those infections. various different drugs used in the therapy with their proposed mechanism of action. Hope it will be useful for understanding the pharmacology of antiprotozoals.
Tetanus is caused by the bacteria Clostridium tetani entering the body through wounds and breaks in the skin. It produces a neurotoxin called tetanospasmin that causes painful muscle spasms and rigidity. The document outlines the history and identification of C. tetani as the causative agent. It describes the typical symptoms of tetanus including lockjaw, risus sardonicus, and opisthotonos. Treatment involves wound cleaning, antibiotics, immunoglobulins, and managing symptoms. The disease is preventable through active immunization with tetanus toxoid vaccines.
This document discusses strategies for minimizing drug use in small ruminant production. It begins by listing commonly used drugs like dewormers, vaccines, and antibiotics. It then discusses the risks of antibiotic resistance and regulatory changes around antibiotic use. For small ruminant producers, this means many antibiotics now require a prescription. The document provides alternatives to drug use like vaccinations, pasture management, genetic selection, and targeted selective treatment to control parasites. It emphasizes preventative healthcare through good nutrition, housing, and sanitation.
Revolution kills adult fleas and prevents flea eggs from hatching for one month and is indicated for the prevention and control of flea infestations (Ctenocephalides felis), prevention of heartworm disease caused by Dirofilaria immitis, and the treatment and control of ear mite (Otodectes cynotis) infestations.
Mushroom poisoning occurs when toxic substances in mushrooms are ingested. There are 70-80 poisonous mushroom species that contain toxic alkaloids. Symptoms vary based on toxin but include nausea, anxiety, and organ damage. Mushrooms are classified based on toxin, with Amanita species containing amatoxins that cause liver damage. Treatment focuses on supportive care, decontamination, and use of antidotes like benzyl penicillin for amatoxin poisoning.
This document provides definitions and information about pesticides. It begins with defining pesticides as substances intended to prevent, destroy or mitigate pests. It then discusses the history of pesticide use dating back to ancient civilizations, and provides examples of early pest control methods. The document categorizes common types of pesticides and discusses their classification, including organochlorines, organophosphates, carbamates, and pyrethroids. It also covers toxicity measures such as LD50, LC50 and MLD values.
Mebendazole, albendazole, and pyrantel pamoate are commonly used anthelmintic drugs. Mebendazole and albendazole are benzimidazole compounds that are poorly absorbed but have broad spectrum activity against intestinal nematodes. Pyrantel pamoate acts by stimulating acetylcholine release and inhibiting cholinesterase in helminths, causing paralysis. Diethylcarbamazine is effective against filarial nematodes and works by damaging the microfilariae membranes. Common side effects of these drugs include gastrointestinal issues.
Ivermectin is an anti-parasitic drug used widely in animals. It works by enhancing the release of the neurotransmitter GABA at the neuromuscular junction, causing paralysis in parasites. Ivermectin is used to control gastrointestinal roundworms, lungworms, cattle grubs, mites, and sucking lice in cattle. It is also used for heartworm prevention in dogs. While generally safe, ivermectin can be neurotoxic in some dog breeds and young animals due to their blood-brain barrier not being fully developed.
Anthelmintic.
According to the syllabus based on “PHARMACY COUNCIL OF INDIA”
“I Dedicate this work to all the
Students , Pharmacy Faculty & Family Members .”
Anthelmintic are the drugs that either KILL [vermicide] or Expel [vermifuge] infesting Helminths.
The choice of drug for each worm infestation is based not only on Efficacy, but also on Lack of Side effects/ Toxicity, Ease of administration [preferably single dose] & low cost.
Development of resistance has not been a problem in the clinical use of Anthelmintic.
Anthelmintics are used to kill or expel parasitic worms from the GI tract and other tissues. They work by either inhibiting the energy production pathways in helminths, like fumarate reductase, or by affecting their neuromuscular system and causing paralysis. The major classes of helminths are nematodes, cestodes, and trematodes. Resistance can develop with continuous use of anthelmintics, so proper rotation of drug classes with different mechanisms of action is important to delay resistance.
Antiworm 400mg Tablet is an oral antiparasitic medication used to treat infections caused by various parasitic worms. It works as an anthelmintic by killing or paralyzing the parasites. Common uses include treatment of hydatid disease, neurocysticercosis, pinworm infection, and others. Side effects can include headache, nausea, vomiting, hair loss, and liver enzyme elevation. Dosing instructions and warnings about drug interactions and allergic reactions are provided.
The document summarizes an assessment of the neuropharmacological activity of the methanolic extract of Lilium candidum. Preliminary tests found the extract contains flavonoids, tannins, steroids, terpenoids, and alkaloids. In hole cross and open field tests on mice, the extract at doses of 200 and 400 mg/kg showed significant suppression of movement from 30-90 minutes after administration, comparable to the drug diazepam. This indicates the extract has central nervous system depressant effects by decreasing exploratory behavior in a dose-dependent manner. The presence of flavonoids, alkaloids, terpenoids and tannins in the extract may account for its neuropharmacological
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This document discusses various classes of antiviral drugs, including those that target herpes viruses, influenza virus, hepatitis viruses, and HIV. It provides details on the mechanism of action, pharmacokinetics, uses, and adverse effects of representative drugs in each class, such as acyclovir for herpes, amantadine/rimantadine for influenza, lamivudine/adefovir for hepatitis B, ribavirin/interferon for hepatitis C, and zidovudine as the prototype nucleoside reverse transcriptase inhibitor for HIV. The goal of antiviral treatment is to inhibit virus-specific replication events while minimizing effects on host cell processes.
This document discusses anti-tubercular drugs. It begins by describing tuberculosis and its transmission. It then discusses the classification of anti-TB drugs into 1st line essential, 1st line supplemental, and 2nd line drugs. The individual drugs discussed in detail include isoniazid, rifampicin, ethambutol, pyrazinamide, and streptomycin. It covers their mechanisms of action, mechanisms of resistance, pharmacokinetics, dosages, adverse effects, and interactions. Treatment categories and regimens are also summarized.
Leprosy is a chronic infectious disease caused by Mycobacterium leprae. Antileprotics work by inhibiting the growth and multiplication of M. leprae. The main antileprotic drugs are dapsone, rifampicin, and clofazimine which act by interfering with bacterial metabolism or cell wall synthesis.
This document provides an overview of antifungal agents. It begins by describing the types of fungal organisms and differences between fungi and bacteria. It then classifies fungal infections and antifungal agents. The remainder of the document discusses the pharmacology of various antifungal classes, including polyenes like amphotericin B, azoles, allylamines, and echinocandins. It provides details on mechanisms of action, dosing, therapeutic uses and adverse effects of different antifungal drugs.
Sirturo (bedaquiline) is a new drug approved by the FDA in 2012 for the treatment of multi-drug resistant tuberculosis. It works by inhibiting mycobacterial ATP synthase, which is essential for energy generation in tuberculosis bacteria. Sirturo represents the first new class of tuberculosis drugs approved in over 40 years. It is meant to be used as part of a combination therapy for drug-resistant tuberculosis when alternative treatment options are limited.
Diuretics are drugs that promote increased production of urine. The lecture discusses the definition, objectives, kidney functions, nephron anatomy, physiology of urine formation, classification, mechanism of action, indications, side effects and uses of diuretics. Diuretics are classified as high efficacy loop diuretics which act on the ascending limb of loop of Henle, medium efficacy thiazide diuretics which act on the distal convoluted tubule, and weak efficacy carbonic anhydrase inhibitors and potassium sparing diuretics. The major mechanisms of action and side effects of each class are reviewed. Diuretics are used to treat conditions of fluid overload like edema, heart failure, hypertension and cirrhosis.
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Philippine Edukasyong Pantahanan at Pangkabuhayan (EPP) CurriculumMJDuyan
(𝐓𝐋𝐄 𝟏𝟎𝟎) (𝐋𝐞𝐬𝐬𝐨𝐧 𝟏)-𝐏𝐫𝐞𝐥𝐢𝐦𝐬
𝐃𝐢𝐬𝐜𝐮𝐬𝐬 𝐭𝐡𝐞 𝐄𝐏𝐏 𝐂𝐮𝐫𝐫𝐢𝐜𝐮𝐥𝐮𝐦 𝐢𝐧 𝐭𝐡𝐞 𝐏𝐡𝐢𝐥𝐢𝐩𝐩𝐢𝐧𝐞𝐬:
- Understand the goals and objectives of the Edukasyong Pantahanan at Pangkabuhayan (EPP) curriculum, recognizing its importance in fostering practical life skills and values among students. Students will also be able to identify the key components and subjects covered, such as agriculture, home economics, industrial arts, and information and communication technology.
𝐄𝐱𝐩𝐥𝐚𝐢𝐧 𝐭𝐡𝐞 𝐍𝐚𝐭𝐮𝐫𝐞 𝐚𝐧𝐝 𝐒𝐜𝐨𝐩𝐞 𝐨𝐟 𝐚𝐧 𝐄𝐧𝐭𝐫𝐞𝐩𝐫𝐞𝐧𝐞𝐮𝐫:
-Define entrepreneurship, distinguishing it from general business activities by emphasizing its focus on innovation, risk-taking, and value creation. Students will describe the characteristics and traits of successful entrepreneurs, including their roles and responsibilities, and discuss the broader economic and social impacts of entrepreneurial activities on both local and global scales.
Communicating effectively and consistently with students can help them feel at ease during their learning experience and provide the instructor with a communication trail to track the course's progress. This workshop will take you through constructing an engaging course container to facilitate effective communication.
3. Introduction:
Types of Common Helminthes
Taenia solium(Pork),
1. Gastrointestinal worms
A- TAPE WORMS (CESTODES)
⚫ Taenia saginata (Beef)
Diphylobothrium latum (Fish)
⚫ Humans infected by eating raw or under cooked meat containing
larvae or encysted in infected animal muscles.
3
1. Worms live in hosts GIT.
2.Worms or larvae live in other tissues of hostsꞌ body like muscles ,
viscera , meninges , lungs, subcutaneous tissues.
4. Tapeworm
1.Tapeworms (Cestodes)
T. saginata (Beef tapeworm)
T. solium (Pork tapeworm)
Diphylobothrium latum (fish tape
In case of D. latum infections
by eating raw or undercooked fish
In some conditions this larvae may
develop causing cysticercosis (i.e.
larvae gets encysted in muscle , or
more seriously in brain or eye)
CYSTICERCOSIS
4
5. 2/16/2015
Dr. Nehal Afifi 5
Table 1 : Tapeworms in Small Animals
Cestode Definitive
Host
Comments Approved
Treatments
Dipylidium caninum Dog,
cat
most common
tapeworm of dogs , cats
Epsiprantel,
Praziquantel
Taenia taeniaeformis
Cat
Common cestode of
cats, rare in dogs
Epsiprantel,
praziquantel,
fenbendazole
Taenia hydatigena Dog In farm dogs praziquantel,
fenbendazole
6. C. Hydatid tape worm
Echinococcus granulosus .
These are cestodes ,primary in canines (dogs) and sheep as
intermediate host.
Humans can act intermediate host
in which larvae develop to hydatid cyst
within the tissue.
HYDATEID CYCT
6
filariasis
12. Anthelmintic Drugs
12
Anti : against & helminthes : worms
Drugs kill or expel the internal parasitic worms infesting
GIT & other tissues of man and animals
Ideal Anthelmintic drug:
1.A wide therapeutic index; the ratio of the therapeutic dose to
the maximum tolerated dose. Wide safety margin of at least 1: 6
with highest toxicity to worms, but lesser toxic to the host
2- Broad spectrum of activity against mature & immature larval
worms of most types of parasites .
13. Ideal Anthelmintic drug
13
3- Easily administered to animal and have a pleasant taste.
4- Effective Orally .
5 Effective in a single dose
6Leave No or low tissue residues & have a short residence
time in Milk when used for treating food producing animals.
7 Economic (inexpensive) and compatible with other drugs.
8 inhibit reinfection for extended periods.
15. Classification of Anthelmintics
15
According to the type of action:
Vermicide: Drugs that kill worms( Bunamidine, Praziquante)
Vermifuge : Expel infesting worms alive (Piperazine ,Santonine)
According to the spectrum of activity:
Narrow spectrum Anthelmintics
Broad spectrum Anthelmintics
Endectocides
Narrow spectrum Anthelmintics such as: Nitroxynil( active
only against adult liver flukes) & Piperazine (against Ascarids Only)
16. 16
Broad spectrum Anthelmintics :
Active against GI nematodes , tape worms and / or flukes,such as
Benzimidazoles (Thiabenazole, Albendazole & Mebendazole)
Organophosphates (Dichlorvos & Trichlorphon ) .
Tetrahydropyrimidines (Morantel, Pyrantel & Oxantel )
Endectocides:
Drugs effective against both arthropodes & nematodes as both:
Avermectins ( Ivermectin, Abamectin, Doramectin) and
Milbemycins ( Moxidectin & Milbemycin D) .
According to the type of worms:
Anticestodals - Antinematodals - Antitrematodals
17. General MOA of Anthelmintics
17
⚫ Inhibiting energy production in the parasite by:
⚫ Inhibiting activity of fumarate reductase enz. in parasite(Albendazole,
⚫ Inhibiting mitochondrial phosphorylation process in parasite(Rafoxanide
⚫ Inhibiting process of glycolysis in parasite as Clorsulon, Phenothiazin
⚫ Causing muscular paralysis of the worm by:
⚫ Inhibiting cholinergic nerves of worm as nicotine sulphate.
⚫ Acting as GABA agonist so cause paralysis of worm as Piperazine.
⚫ Muscle hyperpolarization & paralysis of worm as Levamisole.
⚫ Other mechanism: Disruption of tegument (outer skin) as Bunamidine.
18. Anticestodal drugs
⚫ Drugs kill or expel tape worms (Cestodes) infesting man & animals.
⚫ Classification of Anticestodals:
⚫ I- Organic of plant origin:
Arecoline:
Alkaloid from Areca nut seeds given orally as vermifuge.
Effective against Taenia species infesting dogs and cats.
MOA: by inducing muscular paralysis of worms so lose their
attachment with intestinal mucosa & increase intestinal motility of
host ( as a neuromuscular purgative) → expel detached worms alive
Kamala powder:
A red powder act as vermifuge due to its irritant effect so expels
worms alive.
Given orally and effective against cestodes infesting poultry
19. II- Synthetic drugs:
Niclosamide (Mansonil®)
19
A salicylanilide derivative
Vermicide drug for treatment of tape worm infestation in dogs & cats ,
Beef tape worm, pork tape worm and fish tape worm.
has also activity against intestinal flukes as paramphistomes in ruminants
Not effective against cysticercosis or hydatic disease.
MOA: Adult worm killed by inhibiting the mitochondrial phosphorylation
process thus inhibiting energy production in worms.
Pharmacokinetic: Niclosamide poorly absorbed & very rapidly excreted
has a 5 to 7 folds safety margin
Given in a single dose on empty stomach & a purgative use after 2 hrs
20.
21. 2- Bunamidine:
⚫ Used as Effective remedy for tape worms infesting dogs & cats.
⚫ MOA: act as vermicide by disruption of the tegument (outer skin) of
worms and kill the worms.
⚫ Used for a long time as effective ttt for Echinococcus in pets
⚫ Adverse Effects: Diarrhea & vomition . sudden death in dogs may happen
as drug cause myocardial sensitization to catecholamine.
3- Dichlorophen:
A narrow spectrum anthelmintic against Taenia & Dipylidium speices in
dogs, but ineffective against Echinococcus.
MOA: as taenicide by inhibiting phosphorylation process in mitochondria
of worms so inhibit energy production.
22. 4- Prazequentel
22
A broad Spectrum ( Novel Anthelmintic)
Actives against Cestodes – Schistosomes -Trematodes
Effective against all adult Cestodes & their larval forms in dogs & cats
A potent schistosomicide with a high activity against Bl. flukes causing
bilharziasis in man.
Active on Trematodes as the lung and gut flukes in animals, but not
effective against liver flukes
MO A : Act as vermicide by 1- interfering with ionic balance due to
leakage of IC Ca. from membrane causing rapid muscular contraction
2. causing vacuolation → disruption of worm tegument & death. .
kinetics: Praziquantel given orally or (S/C) . Rapidly absorbed &
metabolized
its safety margin reaches 1:40 of the recommended dose.
23.
24. 2/16/2015
Dr. Nehal Afifi 24
5- Epsiprantel
⚫ A very potent, safe and novel tape worm remedy.
⚫ Given orally for treatment of cestodes of dogs & cats.
⚫ Safer than praziquantel as its safety margin is 1: 90
⚫ Not active against schistosomes.
⚫ MOA: anticestodal in a similar manner of praziquantel
6- Nitroscanate:
⚫ Like dichlorophen, but more safer ( safety margin 1: 40)
⚫ A broad spectrum anthelmintic against cestodes & nematodes of
dogs but not used for cats.
MOA: Taenicide by inhibiting phosphorylation process in mitochondr
of worms so inhibit energy production.
25. Antinematodal drugs
25
⚫ Drugs kill or expel round worms (nematodes) infesting man & animals
⚫ Classification of Antinematodals:
⚫ I- Organic of plant origin:
⚫ 1- Nicotine sulphate:
⚫ Alkaloid obtained from Nicotiana tobacco plant
⚫ Used orally as a drench as nicotine sulphate salt
⚫ Acts as a vermifuge for Ascaris &Trichostrongylus worms of ruminants.
⚫ MOA: By causing inhibition of the cholinergic nerves of worms leading
to muscular paralysis and expelling of worms.
26. 2- Santonine:
⚫ A pale yellow powder obtained from Artemisia plant
⚫ Santonine given orally to expel Ascarids worms of dogs & pigs .
⚫ Acts as a vermifuge due its irritant effect on worms .
⚫ A purgative given after it for rapid expelling of worms.
⚫3- Chenopodium oil:
⚫ A pale yellow volatile oil obtained from American wormseed plant.
⚫ Oil contain a mixture of volatile subs. & active principle (Ascaridol).
⚫ Ascaridol acts as a vermifuge by causing muscular paralysis of
worms and expel them outside
⚫ The oil active against Strongylus worms in horses & Ascardis
worms in pigs, dogs and cats.
⚫ Oil given orally in soft gelatinous capsules.
27. II- Synthetic drugs:
1- Benzimidazoles
Benzimidazoles ( Albendazloe, Thiabendazloe, Triclabendazole ,
Mebendazole, Oxfendazole , Fenbendazole & Flubendazole ).
⚫ A good activity against GIT nematodes & lung worms +their larvae.
⚫ The recent drugs Mebendazole & Oxfendazole are highly effective
against both nematodes & cestodes(broad spectrum ) .
⚫ Albendazole active against adult liver flukes, cestodes & GIT
nematodes larvae (broad spectrum ,vermicide, oral anthelmintic)
⚫ On contrast, Tricalbendazole is highly active against liver flukes
(fasciolicide), but has no activity against nematodes & cestodes
27
28. MOA:Benzimidazoles act as vermicide by inhibiting energy production
via inhibition of the activity of fumarate reductase enz.
Benzim. are very safe anthelmintics ; a wide safety margin from 1: 20
for albendazole to 1: 100 for fenbendazole (very safe).
Cambendazole ,Oxfendazole & Parbendazole have embryotoxic &
teratogenic effects → not given to pregnant animals.
Albendazole leave tissue residues therefore 10 days from the last
dosing of sheep and 14 days from the last dosing of cattle must be
elapsed before slaughtering animals.
Cows producing milk for human should Not treated with Albendazole.
Fenbendazole withdrawal time= 14 days for meat & 3 d. for milk
Triclab. withdrawal time = 28 days & Not use to animals providing milk.
29. Clinical uses of Albendazole
29
Albendazole is the drug of choice for treatment of intestinal round
worms as Ascaris , hook worm (Ankylostoma ) thread worm
(Strongyloids) , pin worms (Enterobius) & whip worm (Trichuris
trichuria) infestations, as a single dose repeated after 3 weeks .
Albendazole is the main drug for Hydatid disease (dog tapeworm)
twice / day for 1 month & repeat after 2-3wks if required up to 3
courses.
Used for treatment of tissue round worm (Trichnella spiralis)
for 3 days .
30. 2- Tetrahydropyrimidine derivatives
(Morantel, Pyrantel & Oxantel)
30
⚫ Morantel effective against GIT nematodes, but not against lung
worms in ruminants.
⚫ Used as a drench or "protect bolus" to provide prolonged
protection for 90 days ( slowly released).
⚫ Pyrantel pamoate:
⚫ A broad specturm anthelmintic , highly effective against adult &
larval nematodes of horse and dogs.
⚫ Not active against lung worms and whipworms.
⚫ Oxantel : Narrow spectrum ( only active against whipworm) dogs
⚫ MOA: Pyrantel is a depolrazing neuromuscular blocking agent
cause release of acetylcholine & inhibition of cholinesterase enz.
leading to muscular paralysis & death (Vermicide).
31.
32. Pyrantel Clinical uses :
32
Pyrantel is very safe remedy for horses and dogs
Pyrantel Given to pregnant or lactating animals.
Pyrantel given orally with or without food.
For Pin worm, Ascariasis & Hookworm as a single dose and
repeated after 2 wks.
Morantel is a very safe remedy and no withdrawal period is
required for the bolus, but a withdrawal period of 3 days is
required for the drench.
33. 3- Levamisole & Tetramisole
Levamisole: Effective against mature & immature larval GI round
and lung worms both orally & parenterally in ruminants & poultry.
Used with limited success against heartworm microfilaria in dogs.
Very rapid action & expel worms within 24 hrs.
Rapid absorbed from GIT- Metabolized by liver- Half life 3-4hr
Levamisole acts also as an immunostimulant drug
Neither embryotoxic nor teratogenic if given to pregnant animals
worms causing
⚫ MOA: NN agonist stimulate nicotinic ganglia in
muscular paralysis & death of the worms(vermicide).
⚫ Interfere with carbohydrate metabolism.
33
34. 4- Piperazine
34
⚫ Commonly used antinematodal drug against only Ascaris and
Oxyuris worms in man and animals.
⚫ Not recommended for other helminthes infestation.
⚫ Administered as citrate or phosphate salts and given orally as a
drench or added to drinking water for poultry.
⚫ MOA: act as vermifuge by its GABA agonist effect so it prevents
neural transmission in the worm causing muscular paralysis and
expelling of the worms alive.
⚫ A very safe drug for man and animals during pregnancy
⚫ Moderate oral absorption & excreted unchanged in urine.
35.
36. 5- Diethyl Carbamazine (DEC)
36
⚫ A highly soluble piperazine derivative → rapidly absorbed &
distributed throughout the body.
⚫ Drug of choice for treatment of Filariasis .
⚫ Highly selective effect on microfilaria.
⚫ Enhances cell mediated immunity
⚫ Used for control of heartworm larvae in dogs.
⚫ Safe for use in pregnant & young animals(Not teratogenic).
⚫ MOA: DEC disrupt the microtubules & inhibit microtubules
polymerization in microfilaria.
37. ⚫ MOA: 1- DEC Immobilize microfilaria & alter their membrane
structure displacing them from tissues & making them susceptible
to destruction by host defense mechanism.
⚫ 2.Alternation of microfilaria membrane → phagocytosed by fixed
tissue monocytes.
⚫ 3.Affect muscular activity and cause hyper polarization due to
piperazine moiety.
⚫ The drug should be given after meals.
38. 6- Ivermectin ( Ivomec® )
38
⚫ One of Avermectins that commonly used in vet. Med.
⚫ Highly effective against all nematodes in animals & arthropods as
mange mites, lice & ticks (endectocide).
⚫ has no activity against cestodes and flukes.
⚫ Given S/C at very low doses (o.2mg /kg for cattle, horse & sheep)
⚫ MOA: act as vermicide causing paralysis of worms by intensifying
the action of the inhibitory transmitter GABA at neuromuscular
junction → paralysis and death of the worms.
39. 2/16/2015
39
IVERMECTIN Pharmacokinetics
⚫ Rapidly absorbed & widely distributed .
⚫ Does not cross BBB
⚫ Half- life 2-3 days & Excretion mainly in feces.
⚫ Very safe remedy for ruminants, with withdrawal period = 28 days
⚫ Not used in dairy cows providing milk for human consumption.
⚫ Contraindication:
⚫ Pregnancy.
⚫ Concurrent use with other drugs that enhance GABA
e.g Barbiturates, valproaic acid & bnezodiazepines.
40. 7- Organophosphate compounds
40
⚫ Organophosphates as diclorvos, haloxon, & trichlorphon.
⚫ Effective against GI nematodes infesting animals.
⚫ MOA: Organophosphates inhibit the acetylcholinestrase of the
worms leading to their paralysis and death.
⚫ Nowadays, they are less commonly used because of their high
toxicity to the host.
41. III– Antitrematodal drugs (Antiflukes)
41
⚫ Drugs kill liver flukes (Fasciola hepatica & gigantica), rumen &
abomasums flukes (Paramphestomes) & Bl. flukes (Schistosomes)
infesting man and animals.
⚫ Classification:
⚫ I- Old fasciolicides:
⚫ 1-Carbon tetrachloride (Ccl 4):
⚫ Used for treating haemonchosis in ruminants, strongylosis in
horses, ancylostomiasis in dogs, fascioliasis in sheep & cattle.
⚫ Ccl 4 given either orally (as drench or in capsules) or (I/M).
⚫ Only kills adult flukes & not effective against immature flukes →
repeated after 3-4 weeks .
⚫ MOA: Ccl 4 acts as fasciolicide by inhibiting the metabolic enzyms
present in mature flukes.
42. ⚫ Toxic symptoms of Ccl4 : drowsiness, muscular incoordination
or convulsion, diarrhea and hypocalcaemia.
⚫ To reduce its toxic effects, premedication of animals with calcium
salts as calcium borogluconate (I/V) should be done.
⚫ 2- Hexachloroethane (C2cl 6):
⚫ Effective for treating liver fascioliasis in cattle, sheep & goats.
⚫ MOA: kills the mature flukes by inhibiting the metabolic enzymes
present in the mature worms only.
⚫ The dose of C2cl 6 should repeated after 3 weeks(immature not aff
⚫ C2cl 6 is less toxic than Ccl 4.
⚫ Toxic Symptomes in cattle loss of appetite & mild diarrhea.
43. II- Modern fasciolicides:
43
⚫ (A) Substituted phenols as:
⚫ 1- Nitroxynil:
⚫ Used for treating fascioliasis in cattle and sheep.
⚫ Nitroxynil only active by S/C injection & Not given orally due to rumen
microflora cause reduction of nitro group → loss anthelmintic activity
⚫ Effective against adult liver flukes & Bl. sucking nematodes.
⚫ A withdrawal period of 30 days before slaughtering the animal.
⚫ Should not dosed to cows producing milk for human consumption.
⚫ 2- Diamphenethide:
⚫ Active against mature & immature liver flukes in sheep, inactive in cattle.
⚫ MOA: fasciolicide by causing rupture of fluke tegument →muscular parals
⚫ Must not dosed to sheep producing milk for human consumption.
⚫ Has a 7 days withdrawal period for meat and its safety margin is 1:4.
44. (B) Salicylanilide derivatives:
1- Rafoxanide 3- Oxyclozanide
⚫1- Rafoxanide:
⚫ Active against mature & immature liver flukes in both cattle & sheep
as well as blood sucking nematodes.
⚫ MOA: Rafoxanide acts as fasciolicide by inhibiting the process of
phosphorylation in mitochondria of worms .
⚫ Given orally or by S/C injection & has a safety margin of 1: 6.
⚫ Rapidly absorbed, but slowly excreted →28 days withdrawal period
required for meat.
⚫ Rafoxanide not used for cows producing milk .
2- Closantel
44
45. ⚫ 2- Closantel:
⚫ A broad spectrum Anthelmintic active against mature & immature
flukes, Bl. sucking nematodes, and tape worms.
⚫ Closantel also active against external parast (mange, mites & ticks)
⚫ Closantel given orally or by S/C injection to sheep and cattle.
⚫ Has a six -fold safety margin.
⚫3- Oxyclozanide:
⚫ Effective oral fasciolicide in sheep and cattle,
⚫ Active against adult liver flukes only.
⚫ withdrawal time = 14 days for meat and zero for milk.
⚫ Dosed to lactating cows ( not excreted in milk)
46. (C) Sulphonamide derivatives:
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Dr. Nehal Afifi 2/16/2015
⚫Clorsulon:
⚫ Act as oral or injectable (S/C) fasciolicide in sheep and cattle.
⚫ Clorsulon active against mature and immature flukes.
⚫ MOA: by affecting the worm energy production via inhibiting two
enzymes (phosphoglycerate kinase & phosphoglycerate mutase)
which essential for glucose metabolism (glycolysis) in worms.
⚫ Its therapeutic index is 1: 25.
⚫ (D) Benzimidazole derivatives:
⚫ 1- Tricalbendalzole. 2- Albendazole.
⚫ Tricalbendazole has No antinematodal activity but active against
liver flukes ( Fasciola hepatica ) in sheep, goats and cattle .
47. ⚫ Tricalbendalzole very active against all stages (adult, immature
and larvae) of Fasciola hepatica from day 1 to adult worms.
⚫ Control & complete eradication of fascioliasis occur by breaking
L.C. liver flukes with triclabendazole once every 6-8 months .
⚫ A withdrawal time of 28 days for meat
⚫ Should not given to animals providing milk for human consumption
⚫ 2- Albendazole:
⚫ widely used for combating round worms & liver flukes in ruminants.
⚫ Available as intraruminal bolus for sustained release of Albendaz.
⚫ Active against all nematodes & their larvae, tapeworms & adult
liver flukes (broad spectrum anthemintic).
⚫ A withdrawal period of 10 days in sheep and 14 days in cattle.
⚫ Should not dosed in cows producing milk .
48. (E) Benzimidazole pro-drugs:
Netobimin
⚫ Netobimin is a pro-drug of albendazole.
⚫ When Netobimin dosed to sheep & cattle metabolized to Albendaz
then converted to albendazole sulphoxide → excreted
⚫ Netobimin active against GI nematodes & their larvae, tape
worms and flukes (broad spectrum anthemintic).
⚫ Given orally or by injection.
⚫ A withdrawal period for meat =5 days in sheep &10 days in cattle.
⚫ A withdrawal period for Milk= 3 days in sheep& 2 days in cattle.
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49. 49 Drugs
Table 3: Clinical uses of Vet. Anthelmintics
Principal use
Liver flukes in ruminants Rafoxanide – Nitroxynil- Clorsulon –
Closantel- Albendazole- Oxyclozanide –
Triclabendazol
Round worms in
ruminants
Phenothiazine- Morantel- Levamisole
Albendazole - Ivermectin- Febantel
Round worms in horse Ivermectin – Piperazine- Pyrantel-
Dichlorvos
Albendazole-Oxibendazole- Oxfendazole
Roundworms in dogs and cats Nitroscanate- Dichlorvos
Levamisole - Ivermectin- Piperazine
Tapeworms in dogs
and cats
Niclosamide- Bunamidine- Dichlorophen
Epsiprantel- Praziquantel
50. Anthelmintic combinations
50
⚫ Means finished formulated product has different anthemintics to
increase the spectrum of activity .
⚫ Drug mixtures are truly complementary ,e.g. ttt of round worms &
flukes in ruminants and round worms & tape worms in dogs.
⚫ the drug mixtures interact with each other e.g.combination of
piperazine and phenothiazine (both antinematodal)
⚫ The most Common anthelmintic combinations :
⚫ 1- For ruminants:
⚫ (a) Fasciolicide + antinematodal drug.
⚫ (b) Fasciolicide + trace element as cobalt or selenium.
⚫ 2- For horses:
⚫ Antinematodals with Anticestodal or Pesticide.