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Mechanism of action

A Wisdom Archive on Mechanism of action

Mechanism of action

A selection of articles related to Mechanism of action

We recommend this article: Mechanism of action - 1, and also this: Mechanism of action - 2.
Mechanism of action

ARTICLES RELATED TO Mechanism of action

Mechanism of action: Encyclopedia II - Teriparatide - Mechanism of action

Teriparatide is the portion of human parathyroid hormone (PTH),amino acid sequence 1 through 34 of the complete molecule which contains amino acid sequence 1 to 84. Endogenous PTH is the primary regulator of calcium and phosphate metabolism in bone and kidney. Daily injections of teriparatide stimulate new bone formation leading to increased bone mineral density. Teriparatide is the first FDA approved agent for the treatment ...

See also:

Teriparatide, Teriparatide - Administration, Teriparatide - Uses, Teriparatide - Mechanism of action, Teriparatide - FDA approval, Teriparatide - External links

Read more here: » Teriparatide: Encyclopedia II - Teriparatide - Mechanism of action

Mechanism of action: Encyclopedia II - Phentermine - Mechanism of action

Phentermine, as many other prescription drugs, works with neurotransmitters in the brain. It is a centrally-acting stimulant chemically related to the amphetamines. It stimulates neuron bundles to release a particular group of neurotransmitters known as catecholamines; these include dopamine, epinephrine (also known as adrenalin), and norepinephrine (noradrenaline). This is the same mechanism of action as other stimulant appetite suppresants such as ...

See also:

Phentermine, Phentermine - History, Phentermine - Mechanism of action, Phentermine - Clinical use, Phentermine - Side effects, Phentermine - Contraindications

Read more here: » Phentermine: Encyclopedia II - Phentermine - Mechanism of action

Mechanism of action: Encyclopedia II - Ketorolac - Mechanism of action

The primary mechanism of action responsible for Ketorolac's anti-inflammatory/antipyretic/analgesic effects is the inhibition of prostaglandin synthesis by competitive blocking of the the enzyme cyclooxygenase (COX). Like most NSAIDs, Ketorolac is a non-selective cyclooxygenase inhibitor. As with other NSAIDs, the mechanism of the drug is associated with the chiral S form. Conversion of the R enantiomer into the S enantiomer has been shown to occur in the metabolism of ibuprofen; it is unknown ...

See also:

Ketorolac, Ketorolac - Chemistry, Ketorolac - Mechanism of action, Ketorolac - Indications, Ketorolac - Contraindications, Ketorolac - Adverse effects, Ketorolac - Warnings and precautions, Ketorolac - Notes, Ketorolac - Dosage availability and price

Read more here: » Ketorolac: Encyclopedia II - Ketorolac - Mechanism of action

Mechanism of action: Encyclopedia II - Paracetamol - Mechanism of action

Paracetamol has long been suspected of having a similar mechanism of action to aspirin because of the similarity in structure. That is, it has been assumed that paracetamol acts by reducing production of prostaglandins, which are involved in the pain and fever processes, by inhibiting the cyclooxygenase (COX) enzyme. However, there are important differences between the effects of aspirin and those of paracetamol. Prostaglandins participate in the inflammatory response, but paracetamol has no appreciable anti-inflammatory action. Furth ...

See also:

Paracetamol, Paracetamol - History, Paracetamol - Available forms, Paracetamol - Mechanism of action, Paracetamol - Metabolism, Paracetamol - Toxicity, Paracetamol - Overview, Paracetamol - Mechanism of toxicity, Paracetamol - Risk factors for toxicity, Paracetamol - Natural history, Paracetamol - Diagnosis, Paracetamol - Treatment

Read more here: » Paracetamol: Encyclopedia II - Paracetamol - Mechanism of action

Mechanism of action: Encyclopedia II - Neurotransmitter - Mechanism of action

Within the cells, small-molecule neurotransmitter molecules are usually packaged in vesicles. When an action potential travels to the synapse, the rapid depolarization causes calcium ion channels to open. Calcium then stimulates the transport of vesicles to the synaptic membrane; the vesicle and cell membrane fuse, leading to the release of the packaged neurotransmitter, a mechanism called exocytosis. The neurotransmitters then diffuse across the synaptic cleft to bind to receptors. The receptors are broadly classified into ionotropic ...

See also:

Neurotransmitter, Neurotransmitter - Types of neurotransmitters, Neurotransmitter - Mechanism of action, Neurotransmitter - Post-synaptic effect, Neurotransmitter - Specific actions, Neurotransmitter - Common neurotransmitters, Neurotransmitter - Amino acids, Neurotransmitter - Biogenic amines, Neurotransmitter - Monoamines, Neurotransmitter - Polypeptides neuropeptides

Read more here: » Neurotransmitter: Encyclopedia II - Neurotransmitter - Mechanism of action

Mechanism of action: Encyclopedia II - Alprazolam - Mechanism of action

Alprazolam is a triazolobenzodiazepine, that is, a benzodiazepine with a triazolo-ring attached to its structure. Alprazolam binds to the GABAA subtype of the GABA receptor, increasing inhibitory effects of GABA within the central nervous system. The binding site for benzodiazepines is distinct from the binding site for GABA on the GABA receptor. Unlike other benzodiazepines, alprazolam may also have some antidepressant activi ...

See also:

Alprazolam, Alprazolam - Indications, Alprazolam - Narcotic regulations, Alprazolam - Mechanism of action, Alprazolam - Pharmacokinetics, Alprazolam - Recreational use

Read more here: » Alprazolam: Encyclopedia II - Alprazolam - Mechanism of action

Mechanism of action: Encyclopedia II - Diclofenac - Mechanism of action

The exact mechanism of action is not entirely known, but it is thought that the primary mechanism responsible for its anti-inflammatory/antipyretic/analgesic action is inhibition of prostaglandin synthesis by inhibition of cyclooxygenase (COX). Diclofenac, it seems, may also be a unique member of the NSAIDs. There is some evidence that diclofenac inhibits the lipooxygenase pathways, thus reducing formation of the leukotrienes (also pro-inflammatory autacoids). There is also speculation that diclofenac may inhibit phospholipase A2 ...

See also:

Diclofenac, Diclofenac - Mechanism of action, Diclofenac - Common uses, Diclofenac - Off label/investigational uses, Diclofenac - Contraindications, Diclofenac - Side effects, Diclofenac - Veterinary information, Diclofenac - Interactions, Diclofenac - Dosage, Diclofenac - Animal toxicity and human overdose, Diclofenac - Environmental problems, Diclofenac - Reference

Read more here: » Diclofenac: Encyclopedia II - Diclofenac - Mechanism of action

Mechanism of action: Encyclopedia II - Heparin - Mechanism of action

Heparin works by potentiating the action of antithrombin III, as it is similar to the heparan sulfate proteoglycans which are naturally present on the cell membrane of the endothelium. Because antithrombin III inactivates many coagulation proteins, the process of coagulation will slow down. The effects of heparin are measured in the lab by the partial thromboplastin time (aPTT), (the time it takes the blood plasma to clot). ...

See also:

Heparin, Heparin - History, Heparin - Mechanism of action, Heparin - Administration, Heparin - Medical use, Heparin - Other uses, Heparin - Treatment of overdose, Heparin - Adverse reactions

Read more here: » Heparin: Encyclopedia II - Heparin - Mechanism of action

Mechanism of action: Encyclopedia II - Nadolol - Mechanism of action

Nadolol non-selectively blocks beta-1 adrenergic receptors mainly in the heart, inhibiting the effects of the catecholamines epinephrine and norepinephrine and decreasing heart rate and blood pressure. It also blocks beta-2 adrenergic receptors located in bronchiole smooth muscle, causing vasoconstriction. By binding beta-2 receptors in the juxtaglomerular apparatus, nadolol inhibits the production of renin, thereby inhibiting angiotensin II and aldosterone production. Nadolol therefore inhibits the vasoconstriction and water retention due to angiotensin II and aldosterone, respectively. The drug impai ...

See also:

Nadolol, Nadolol - Chemistry and pharmacokinetics, Nadolol - Mechanism of action, Nadolol - Indications, Nadolol - Contraindications, Nadolol - Side effects

Read more here: » Nadolol: Encyclopedia II - Nadolol - Mechanism of action

Mechanism of action: Encyclopedia II - Gefitinib - Mechanism of action

Gefitinib is the first selective inhibitor of epidermal growth factor receptor (EGFR) tyrosine kinase. The target protein (tyrosine kinase) is also sometimes referred to as Her1 or ErbB-1 depending on the literature source. EGFR is overexpressed in the cells of certain types of human carcinomas - for example in lung and breast cancers. This leads to inappropriate activation of the apoptotic Ras signal transduction cascade, eventually leading to uncontrolled cell proliferation. Research on gefitinib-sensitive non-small cell lung cancer ...

See also:

Gefitinib, Gefitinib - Mechanism of action, Gefitinib - Clinical uses, Gefitinib - Genzyme test, Gefitinib - Adverse effects, Gefitinib - Common, Gefitinib - Infrequent

Read more here: » Gefitinib: Encyclopedia II - Gefitinib - Mechanism of action

Mechanism of action: Encyclopedia II - Flecainide - Mechanism of action

Flecainide works by blocking the Nav1.5 sodium channel in the heart, causing prolongation of the cardiac action potential.6 This thereby slows conduction of the electrical impulse within the heart. The greatest effect is on the His-Purkinje system and ventricular myocardium. The effect of flecainide on the ventricular myocardium causes decreased contractility of the muscle, which leads to a decrease in the ejection fraction. The effect of flecainide on the sodium channels of the heart increases as the heart rate increases.< ...

See also:

Flecainide, Flecainide - Uses, Flecainide - Dosing, Flecainide - Mechanism of action, Flecainide - Metabolism and drug interactions, Flecainide - Serious adverse reactions, Flecainide - Toxicity, Flecainide - Long term effects

Read more here: » Flecainide: Encyclopedia II - Flecainide - Mechanism of action

Mechanism of action: Encyclopedia II - Ibuprofen - Mechanism of action

Ibuprofen is an NSAID which is believed to work through inhibition of cyclooxygenase (COX); thus inhibiting prostaglandin synthesis. As with other NSAIDs, ibuprofen inhibits platelet aggregation, but is not used therapeutically for this action since it is a minor and reversible effect. Main article: Non-steroidal anti-inflammatory drug ...

See also:

Ibuprofen, Ibuprofen - Clinical use, Ibuprofen - Indications, Ibuprofen - Off-Label and investigational use, Ibuprofen - Ibuprofen lysine, Ibuprofen - Mechanism of action, Ibuprofen - Adverse effects, Ibuprofen - Reported ADRs, Ibuprofen - Photosensitivity, Ibuprofen - Cardiovascular risk, Ibuprofen - Stereochemistry, Ibuprofen - Human toxicology, Ibuprofen - Availability

Read more here: » Ibuprofen: Encyclopedia II - Ibuprofen - Mechanism of action

Mechanism of action: Encyclopedia II - Chlorpromazine - Mechanism of action

Chlorpromazine - Central. Chlorpromazine acts as an antagonist (blocking agent) on different postsysnaptic receptors -on dopaminergic-receptors (subtypes D1, D2, D3 and D4 - different antipsychotic properties on productive and unproductive symptoms), on serotonergic-receptors (5-HT1 and 5-HT2, with anxiolytic, antidepressive and antiaggressive properties as well as an attenuation of extrapypramidal side-effects, but also leading to weight gain, fall in blood pressure, sedation and ejaculation difficulties), on hi ...

See also:

Chlorpromazine, Chlorpromazine - Chemistry, Chlorpromazine - Mechanism of action, Chlorpromazine - Central, Chlorpromazine - Peripheral, Chlorpromazine - History, Chlorpromazine - Side effects, Chlorpromazine - Interactions, Chlorpromazine - Uses, Chlorpromazine - Common uses, Chlorpromazine - Off-label and controversial uses, Chlorpromazine - Veterinary uses, Chlorpromazine - Dosage, Chlorpromazine - Necessary examinations and laboratory checks during treatment, Chlorpromazine - Discontinuation of treatment, Chlorpromazine - Sources

Read more here: » Chlorpromazine: Encyclopedia II - Chlorpromazine - Mechanism of action

Mechanism of action: Encyclopedia II - Sildenafil - Mechanism of action

Part of the physiological process of erection involves the release of nitric oxide (NO) in the corpus cavernosum. This then activates the enzyme guanylate cyclase which results in increased levels of cyclic guanosine monophosphate (cGMP), leading to smooth muscle relaxation in the corpus cavernosum, resulting in increased inflow of blood and an erection. Sildenafil is a potent and selective inhibitor of cGMP specific phosphodiesterase type 5 (PDE5) which is responsible for degradation of cGMP in the corpus cavernosum. This means that, ...

See also:

Sildenafil, Sildenafil - History, Sildenafil - Mechanism of action, Sildenafil - Dosage and price, Sildenafil - Contraindications and side effects, Sildenafil - Uses outside of erectile dysfunction, Sildenafil - Pulmonary hypertension, Sildenafil - Raynaud's phenomenon

Read more here: » Sildenafil: Encyclopedia II - Sildenafil - Mechanism of action

Mechanism of action: Encyclopedia II - Indomethacin - Mechanism of action

Indomethacin is a nonselective inhibitor of cyclooxygenase (COX) 1 and 2, enzymes that participate in prostaglandin synthesis from arachidonic acid. Prostaglandins are hormone-like molecules normally found in the body, where they have a wide variety of effects, some of which lead to pain, fever, and inflammation. Prostaglandins also cause uterine contractions in pregnant women. Indomethacin is an effective tocolytic agent, able to delay premature labor by reducing uterine contractions through inhibition of PG synthesis in the uterus a ...

See also:

Indomethacin, Indomethacin - Chemical properties, Indomethacin - Indications, Indomethacin - Contraindications, Indomethacin - Mechanism of action, Indomethacin - Adverse effects, Indomethacin - Necessary Examinations during Longterm Treatment, Indomethacin - Animal Toxicity and Human Overdose, Indomethacin - Usual Dosage Forms, Indomethacin - History

Read more here: » Indomethacin: Encyclopedia II - Indomethacin - Mechanism of action

Mechanism of action: Encyclopedia II - General anaesthetic - Mechanism of action

Researchers agree that ion channels are the ultimate site of action of general anaesthetics, and are now determining the exact molecular mechanisms. However, the sites of action of general anaesthetics proved difficult to identify until the last decade. The wide variation in structure, ranging from complex steroids to the inert monatomic gas xenon, led to several now outdated theories of anaesthetic action. It is now known that general anaesthetics act on the central nervous system by modifying the electrical activity of neurons at a ...

See also:

General anaesthetic, General anaesthetic - Mechanism of action

Read more here: » General anaesthetic: Encyclopedia II - General anaesthetic - Mechanism of action

Mechanism of action: Encyclopedia II - Capsaicin - Mechanism of action

The burning and painful sensations associated with capsaicin result from capsaicin's chemical interaction with sensory neurons. Capsaicin, as a member of the vanilloid family, binds to a receptor called the vanilloid receptor subtype 1 (VR1). First cloned in 1997, VR1 is an ion channel-type receptor. VR1, which can also be stimulated with heat and physical abrasion, permits positively-charged ions (i.e. cations) to pass through the cell membrane and into the cell from outside when activated. The resulting "depolarization" of the neuron stimu ...

See also:

Capsaicin, Capsaicin - Capsaicinoids, Capsaicin - Uses, Capsaicin - Food, Capsaicin - Medical, Capsaicin - Non-lethal force, Capsaicin - Pest deterrent, Capsaicin - Mechanism of action, Capsaicin - Capsaicin high

Read more here: » Capsaicin: Encyclopedia II - Capsaicin - Mechanism of action

Mechanism of action: Encyclopedia II - Chlorpromazine - Mechanism of action

Chlorpromazine - Central. Chlorpromazine acts as an antagonist (blocking agent) on different postsysnaptic receptors -on dopaminergic-receptors (subtypes D1, D2, D3 and D4 - different antipsychotic properties on productive and unproductive symptoms), on serotonergic-receptors (5-HT1 and 5-HT2, with anxiolytic, antidepressive and antiaggressive properties as well as an attenuation of extrapypramidal side-effects, but also leading to weight gain, fall in blood pressure, sedation and ejaculation difficulties), on hi ...

See also:

Chlorpromazine, Chlorpromazine - Chemistry, Chlorpromazine - Mechanism of action, Chlorpromazine - Central, Chlorpromazine - Peripheral, Chlorpromazine - History, Chlorpromazine - Side effects, Chlorpromazine - Interactions, Chlorpromazine - Cancer risk carcinogenecity, Chlorpromazine - Uses, Chlorpromazine - Common uses, Chlorpromazine - Off-label and controversial uses, Chlorpromazine - Veterinary uses, Chlorpromazine - Dosage, Chlorpromazine - Necessary examinations and laboratory checks during treatment, Chlorpromazine - Discontinuation of treatment, Chlorpromazine - Sources

Read more here: » Chlorpromazine: Encyclopedia II - Chlorpromazine - Mechanism of action

Mechanism of action: Encyclopedia II - Amiodarone - Mechanism of action

Amiodarone is categorized as a class III antiarrhythmic agent, and prolongs phase 3 of the cardiac action potential. It has numerous other effects however, including actions that are similar to those of antiarrhythmic classes Ia, II, and IV. Amiodarone shows beta blocker-like and calcium channel blocker-like actions on the SA and AV nodes, increases the refractory period via sodium- and potassium-channel effects, and slows intra-cardiac conduction of the car ...

See also:

Amiodarone, Amiodarone - History, Amiodarone - Dosing, Amiodarone - Mechanism of action, Amiodarone - Indications for use, Amiodarone - Ventricular fibrillation, Amiodarone - Ventricular tachycardia, Amiodarone - Atrial fibrillation, Amiodarone - Contraindications, Amiodarone - Metabolism, Amiodarone - Interactions with other drugs, Amiodarone - Excretion, Amiodarone - Side effects, Amiodarone - Thyroid, Amiodarone - Eye, Amiodarone - Gastrointestinal system, Amiodarone - Skin, Amiodarone - Lung, Amiodarone - Related topics

Read more here: » Amiodarone: Encyclopedia II - Amiodarone - Mechanism of action

Mechanism of action: Encyclopedia II - Folinic acid - Mechanism of action

Folinic acid is a 5-formyl-derivative of tetrahydrofolic acid. It is readily converted to other reduced folic acid derivatives (e.g. tetrahydrofolate). Since it does not require the action of dihydrofolate reductase for its conversion, it will be unaffected by inhibition of this enzyme by drugs such as methotrexate. This, therefore, allows for purine/pyrimidine synthesis to occur; so normal DNA repl ...

See also:

Folinic acid, Folinic acid - Mechanism of action, Folinic acid - Therapeutic use

Read more here: » Folinic acid: Encyclopedia II - Folinic acid - Mechanism of action

Mechanism of action: Encyclopedia II - HT-0712 - Mechanism of action

HT-0712 appears to work by blocking phosphodiesterase 4, thereby increasing cAMP levels. When cAMP levels are increased in neurons, this may trigger activation of cAMP response element-binding proteins (CREB). CREBs are transcription factors involved in the formation of long-term memory. The side effects of the drug are not yet fully known. ...

See also:

HT-0712, HT-0712 - Mechanism of action, HT-0712 - Medical Use, HT-0712 - Performance Enhancing Use

Read more here: » HT-0712: Encyclopedia II - HT-0712 - Mechanism of action




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