Test 2 Flashcards

1
Q

Inhibits Hydrogen potassium ATPase enzyme found in the parietal cells of the stomach lining which are responsible for secreting acid into the stomach, therefore decreasing the amount.

A

Protein Pump Inhibitor - Gastric Acid Suppressant

Omeprazole

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2
Q

Blocks H2 Histamine receptors in the parietal cells in the stomach, therefore preventing the release of stomach acid which Histamine triggers.

A

Antihistamine Gastric Acid Supressent

Famotidine

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3
Q

Blocks the D2 Dopamine receptors in the gut, this increases gut motility which in turn reduces nausea and vomiting

A

Dopamine Antagonist Antiemetic

Metoclopramide

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4
Q

Blocks the 5-HT3 receptor to prevent the cascade of events that can lead to nausea and vomiting.

A

Serotonin Antagonist Antiemetic

Ondansetron

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5
Q

Binds to the Histamine H1 receptor which affects gut motility amongst other things and can also help with sedation and anti cholinergic effects.

A

Antiemetic Antihistamine

Cyclizine

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6
Q

Blocks the binding of muscarinic receptors by acetylcholine which can otherwise lead to nausea, vomiting and smooth muscle contraction.

A

Antimuscarinic Antiemetic

Hyoscine

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7
Q

Draws water in to the colon

A

Laxative

Lactulose

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8
Q

Works by stimulating the nerve endings in the lining of the intestine, which leads to increased movement and contractions of the muscles in the intestinal wall.

A

Stimulant Laxative

Bisacodyl

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9
Q

Contains a stool softener that breaks up the surface tension of the stool to allow water and lipids to Penetrate the stool. Senna is a gut stimulant by increasing the contractions in the intestines

A

Laxative

Docusate + Senna

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10
Q

Inhibits prostaglandin (a neurotransmitter associated with pain) production in the CNS, reducing pain and fever

A

Analgesic

Paracetamol

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11
Q

COX inhibition but with variations of side effects and pharmacodynamic and pharmacokinetic profiles.

A

NSAIDs

Ibuprofen, Diclofenac, Naproxen

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12
Q

Mu-opioid receptor agonist. Mu opioid receptors inhibit transmission of pain signals. Activation of other opioid receptors leads to additional effects including sedation, mood and respiratory depressant effects.

A

Opioid Analgesics

Morphine, Oxycodone

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13
Q

Agonist for Mu opioid receptors which inhibit transmission of pain signals. Also agonist for delta opioid receptor which is believed to contribute to its effectiveness in treating opiate addiction.

A

Analgesic

Methadone

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14
Q

Same as Morphine but with a very high potency around 50-100 times greater than Morphine

A

Opioid Analgesic

Fentanyl

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15
Q

Same mechanism of action as Morphine, targeting Mu-opioid receptors but also good at suppressing coughing.

A

Opioid Analgesic

Codeine

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16
Q

Mu-opioid antagonist

A

Opioid Antidote

Naloxone

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17
Q

Precursor of the amino acid L-cysteine, which can be converted into glutathione, a powerful antioxidant that helps to protect cells from oxidative stress.

A

Paracetamol Antidote

Acetylcysteine

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18
Q

Enhances inhibitory neurotransmitters in the brain, specifically GABA. Binds on a subunit site or GABA receptors, not the main receptor itself.

A

Anaesthetic

Propofol

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19
Q

N-methyl-D-aspartate (NMDA) receptor, which is a type of glutamate receptor that plays a key role in the regulation of neuronal plasticity and synaptic transmission. Acts as an antagonist at the NMDA receptor and inhibits the transmission of excitatory signals in the brain.

A

Analgesic

Ketamine

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20
Q

Binds to and Inhibits voltage gated sodium channels which prevents the propagation of nerve fibre signals. Also affects Calcium and potassium channels which may explain it’s antiarrhythmic and Analgesic effect.

A

Anesthetic

Lignocaine

21
Q

Benzodiazepine which Enhances the action of GABA by binding to sites on an ancillary section of the receptor.

A

Premedication - Benzodiazepine

Midazolam

22
Q

Blocks Adrenaline and Noradrenaline at Beta-1 adrenergic receptors therefore reducing the sympathetic response. As targets beta-1 receptors more specifically, it has less side effects than Propranolol

A

Beta Blockers

Metoprolol, Atenolol

23
Q

Binds to and blocks both beta-1 and beta-2 adrenergic receptors non selectively, resulting in decreased heart rate, blood pressure, and cardiac output

A

Non Selective Beta Blocker

Propranolol

24
Q

Blocks Beta-1, beta-2 and alpha-1 receptor. The alpha-blocking activity may have beneficial effects on improving blood flow to the heart and reducing peripheral vascular resistance.

A

Beta Blocker

Carvedilol

25
Blocks Calcium channels located in the smooth muscle cells of blood vessels and cardiac myocytes, preventing calcium ions from entering the cells, which results in relaxation of the smooth muscle cells and vasodilation of the blood vessels alongside reduction of available calcium to cardiac myocytes which results in decreased oxygen demand by the heart, good for treatment of angina.
Ca Channel Blockers Amlodipine, Diltiazem, Verapamil
26
Acts on the kidneys by inhibiting the reabsorption of sodium and chloride ions from the tubules, which increases the excretion of these ions in the urine. This results in an increase in urine output and a decrease in blood volume, which lowers blood pressure.
Thiazide Diuretic Bendroflumethiazide
27
Acts on the kidneys by inhibiting the reabsorption of sodium and chloride ions from the loop of Henle, which increases the excretion of these ions in the urine. This results in an increase in urine output and a decrease in blood volume, which lowers blood pressure.
Loop Diuretic Furosemide
28
Aldosterone Antagonist, increases Sodium and water excretion
K+ sparing aldosterone antagonist diuretic Spironolactone
29
Alpha-2 adrenergic agonist, reduces noradrenaline production which reduces sympathetic activity in the body reduces HR, BP and peripheral vascular resistance
centrally acting alpha-agonist hypotensive agents Clonidine, Methyldopa
30
Target is the Sodium-potassium ATPase enzyme located in the cell membranes of cardiac myocytes, binding to the extracellular domain of the enzyme, inhibiting its function.
Cardiac Glycoside Digoxin
31
Receptor targets are thought to be multiple ion channels, including the sodium (Na+), potassium (K+), and calcium (Ca2+) ion channels in cardiac myocytes with complex effects on these ion channels, leading to a decrease in the automaticity of the SA node, a prolongation of the action potential duration and refractory period, and a reduction in the conduction velocity in the atria and ventricles.
K+ Channel Blocker Amiodarone
32
Inhibits ACE located in the lungs and blood vessels. ACE converts angiotensin I to angiotensin II, which is a potent vasoconstrictor that increases blood pressure.
ACE Inhibitor Cilazapril
33
Acts in a similar manner to other ACE Inhibitors but also increases the levels of bradykinin, a vasodilator, which may contribute to its BP lowering effects.
ACE Inhibitors Enalapril, Quinapril
34
Converts to nitric oxide in the body which targets the soluble guanylate cyclase (sGC) enzyme located in vascular smooth muscle cells. This starts a multi step process which results in a relaxation of vascular smooth muscle cells, dilation of blood vessels, and a decrease in BP
Nitrates GTN, Isosorbide Mononitrate
35
Inhibits the enzyme CPT-1, which leads to a decrease in fatty acid oxidation and an increase in glucose oxidation in the heart, resulting in a reduction in oxygen demand.
Anti-Anginals Perhexiline
36
Agonist for muscarinic acetylcholine receptors, blocks parasympathetic activity and can raise heart rate in Bradycardia.
Muscarinic Receptor Agonist Atropine
37
Inhibits HMG-CoA reductase, an enzyme that produces Cholesterol
Statin Atorvastatin
38
An agonist of the receptor PPAR-alpha, leading to an increase in the expression of genes that control lipid metabolism
Fibrate Bezafibrate
39
Targets the beta-2 adrenergic receptors in the lungs, this relaxes smooth muscle resulting in bronchodilation. Short Acting.
Short Acting Beta 2 agonist Salbutamol
40
Targets the beta-2 adrenergic receptors in the lungs, this relaxes smooth muscle resulting in bronchodilation. Long Acting.
Long Acting Beta 2 agonist Salmeterol
41
Targets and blocks acetylcholine action at the M3 muscarinic acetylcholine receptors in the smooth muscle of the airways. This causes relaxation of the smooth muscle and improves airflow in the lungs, leading to bronchodilation.
Muscarinic Antagonist Ipratropium
42
Inhibits Adenosine receptors in the lungs, leading to relaxation of smooth muscle and bronchodilation
Xanthine Theophylline
43
Blocks Leukotriene receptors from binding with Leukotriene which is an inflammatory mediator, therefore reducing inflammation and bronchospasm resulting in improved airway function. Useful in the treatment of Asthma, exercise-induced bronchoconstriction, and allergic rhinitis
Leukotriene Receptor Antagonist Montelukast
44
Synthetic version of cortisol, targets intracellular glucocorticoid receptors throughout the body, activating genes that trigger suppression of inflammation and the immune system.
Corticosteroids Fluticasone, Prednisone
45
Synthetic version of aldosterone, the receptor target is the mineralocorticoid receptor, found primarily in the kidneys, increasing the reabsorption of sodium and water, increases BP, good for orthostatic hypotension or adrenal insufficiency.
Corticosteroids Fludrocortisone
46
Activates adrenergic receptors all throughout the body, stimulating the sympathetic nervous system, this increases heart rate, blood pressure and bronchodilation.
Sympathomimetic Vasoconstrictor Adrenaline
47
Acts by modifying the intracellular calcium concentration, which is an essential regulator of cardiac muscle contractility as well as vasodilation.
Sympathomimetic Inotropic Dopamine
48
Inhaled Steroid that suppresses the actions of inflammatory cells, such as mast cells, eosinophils, basophils, lymphocytes, macrophages, and neutrophils.
Steroid Inhaler Beclomethasone
49
Binds to mu-opioid receptors in the CNS, also Kappa & Delta. Much less potent than Morphine. Additional action as an SNRI.
Opioid Painkiller Tramadol