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UnselfishAlgorithm1170

Uploaded by UnselfishAlgorithm1170

MD2009-3

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pharmacology questions drug action medicine medical science

Summary

This document is a collection of multiple-choice questions (MCQs) on pharmacology. It covers various aspects of drug action and effects, including mechanisms of action, side effects, and clinical applications. Pharmacology and medicine are covered in the questions.

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## MD2009-3 ### Page 7 of 14 43. The sodium/potassium ATPase is: - Activated by digoxin - Activated by levosimendan - Inhibited by digoxin - Inhibited by levosimendan 44. An important side effect of amiodarone (Class III antiarrhythmic drug) is: - Hyperthyroidism - Photosensitivity - Pulmonary fi...

## MD2009-3 ### Page 7 of 14 43. The sodium/potassium ATPase is: - Activated by digoxin - Activated by levosimendan - Inhibited by digoxin - Inhibited by levosimendan 44. An important side effect of amiodarone (Class III antiarrhythmic drug) is: - Hyperthyroidism - Photosensitivity - Pulmonary fibrosis - Visual disturbances 45. Which drug when used topically in the treatment of chronic open-angle glaucoma reduces intraocular pressure by decreasing formation of the aqueous humour? - Pilocarpine - Lanaprost - Timolol - Verteporfin 46. A young patient with asthma has "aspirin sensitivity" and experiences severe bronchospasm to even small doses. What is the most likely explanation of this? - Induces formation of antibodies directed against the salicylate on airway mast cells - Induces hypersensitivity of airway smooth muscle to H1 receptors - Induces hypersensitivity of airway smooth muscle to muscarinic receptors - Shunting of arachidonic acid towards synthesis of leukotrienes 47. The mechanism of action of allopurinol is through - Binding to tubulin which prevents formation of microtubules and cell division - Enhanced metabolism of uric acid - Increased uric acid secretion as a consequence of inhibiting its reabsorption - Inhibition of xanthine oxidase 48. The mechanism of action for the pharmacological effect of metronidazole is: - Activation of glutamate-gated chloride channels - **Conversion to a cytotoxic compound by pyruvate:ferredoxin oxidoreductase** - Inhibition of dihydrofolate reductase - Inhibition of ẞ-tubulin polymerisation 49. What is the pharmacological target of erlotinib - EGFR (epidermal growth factor receptor) - PDGFR (platelet derived growth factor receptor) - Proteasome - VEGF (vascular endothelial growth factor) ### Page 6 of 14 34. Which of the following mediators derived from arachidonic acid is best described as anti-inflammatory - Prostaglandins - Isoprostanes - Leukotrienes - Lipoxins 35. Desmopressin is used to reduce bleeding in mild haemophilia A because of which of the following effects - Increases in vWF release - Inhibits vitamin K epoxide reductase - Inhibits factor Xa - Increases in tissue plasminogen activator (t-PA) release 36. You prescribe a bronchodilator which is known to have adrenergic side effects on the heart. Which clinical sign should you look out for in your patient ? - Bradypnea - Tachypnea - Bradycardia - Tachycardia 37. How does cocaine act as a peripheral sympathomimetic ? - Blockade of uptake 1 - Displacement of noradrenaline from storage vesicles - Inhibition of catechol-O-methyl transferase - Inhibition of vesicular monoamine transport 38. Volume of distribution equals - Dose given/plasma concentration - Total amount of drug in the body/plasma concentration - Urine drug concentration/plasma concentration - Dose given/urine concentration 39. The pharmacological target of ritonavir is: - HIV protease - HIV reverse transcriptase - HIV viral integration - Neuraminidase 40. Sucralfate is effective in peptic ulcer disease because it: - Binds to glycoproteins forming a protective cap over the ulcer - Decreases prostaglandin synthesis - Is toxic to Helicobacter pylori - Reduces gastric acid secretion from parietal cells 41. Which histamine receptor mediates dilation of post-capillary venules? - H1 - H2 - H3 - H4 42. What is the mechanism of action of Ondansetron ? - Block of 5-HT3 receptors in the chemoreceptor trigger zone - Block of D2 receptors in the chemoreceptor trigger zone - Block of H1 receptors in vestibular nuclei - Blockade of muscarinic receptors in the cerebellum ### Page 5 of 14 26. A phosphodiesterase 5 inhibitor has which of the following effects - Increases breakdown of cGMP - Increases blood pressure - Increases vasodilation - Increases vasoconstriction 27. Insulin-like growth factor 1 (IGF-1) mediates the peripheral action of which anterior pituitary hormone - Thyroid stimulating hormone - Growth hormone - Prolactin - Adrenocorticotropin hormone 28. Which of the following agents is most likely to exacerbate hypothyroidism in a patient - Levothyroxine - Liothyronine - Adrenaline - Carbimazole 29. Denosumab is best described as a - Parathyroid hormone analogue - Pyrophosphate analogue - RANK ligand inhibitor - Selective oestrogen receptor modulator 30. Prolonged systemic use of synthetic glucocorticoids can result in which of the following effects - Increased cortisol production - Increased risk opportunistic infections - Protection from osteoporosis - Weight loss 31. Aspirin inhibits the production of which platelet activator - ADP - Thromboxane - Prostacyclin - Fibrinogen 32. Which of the following antidotes can reverse the effects of warfarin - Flumazenil - Naloxone - Vitamin K - Glucagon 33. A competitive inhibitor of HMG-CoA reductase best describes the action for which of the following lipid lowering agents - Simvastatin - Gemfibrozil - Niacin - Ezetimibe ### Page 4 of 14 18. A mosquito when it feeds on human blood - Injects sporozoites into the blood stream thus starting the malaria cycle in the human host - Injects merozoites into the blood stream thus starting the malaria cycle in the human host - Results in some injected sporozoites developing into male and female forms called gametocytes - Allows the merozoites in the salivary glands to be injected into a human host 19. In general, when a drug becomes ionized - The Log P increases - The Log P remains unchanged - The Log P decreases - The Log P can either increase or decrease 20. The time-concentration plot for a drug - Is a straight line - Can only be drawn for acidic drugs - Provides useful data such as the elimination half life - Cannot be drawn for a drug given orally 21. An adverse drug reaction - Only occurs when the medicine is used at the wrong dose - Always has serious consequences for the patients - Can be traced back to the pharmacological profile of the medicine in the majority of cases - Rarely occurs in patients less than 65 years of age 22. The Health Products Regulatory Authority - Is the national medicines regulatory authority in Ireland - Is responsible for licensing all drugs currently on the market in Ireland - Evaluates medicines for human consumption only - Undertakes animal testing as part of its remit in licensing new medicines 23. Lisinopril inhibits which one of the following enzymes - Angiotensin converting enzyme - Renin enzyme - Carbonic anhydrase II - Carbonic anhydrase IV 24. Thiazide diuretics work by inhibiting which of the following transporters in the nephron - Na+/K+/2Cl - Na+/Cl - Na+/K+ ATPase - Na+/Ca²+ exchanger 25. Which one of the following best describes the mechanism of action of Verapamil - Calcium channel blocker - Potassium channel blocker - Endothelin receptor antagonist - Alpha 1 - adrenergic antagonist ### Page 3 of 14 10. Slow metabolisers of isoniazid are more likely to experience - Increased hepatotoxicity and neurotoxicity - Increased hepatotoxicity and decreased neurotoxicity - Decreased hepatotoxicity and increased neurotoxicity - Decreased hepatotoxicity and neurotoxicity 11. Metabolism by CYP2D6 - Activates codeine - Inactivates codeine - Activates warfarin - Inactivates warfarin 12. The enantiomer selectivity of a drug is least likely to be affected by - Receptor structure - Drug structure Drug lipid solubility - Drug transporter 13. Oestrogens, after the onset of menstruation - Require sustained low concentration for about 36 hours for FSH/LH surge to release ovum - During the follicular phase require a low concentration in order to stimulate Gn/GnRH release [from pituitary/hypothalamus] - Do not influence mucus secretion - Are not involved in preparing the uterus for implantation 14. Testosterone is synthesised mainly by - The interstitial cells of the testes - Dihydrotestosterone modifying gene transcription by interacting with extracellular receptors - Working through tetrahydrotestosterone - decreasing aggressiveness in males 15. Quinine - Is the chief alkaloid of willow bark - Is a potent blood schizonticidal with ability to kill all four species of the parasite - Has a strong effect on sporozoites in the host - Is very useful for prophylaxis and radical cure 16. Dihydrotestosterone modifies gene transcription by - Stimulating ovulation at mid-cycle - Interacting with intracellular receptors - Interacting strongly with oestrogen receptors - Increasing levels of gonadotropins 17. Tibolone is a synthetic steroid - That has no androgenic properties - That has no progestogenic properties - That has oestrogenic properties - That is used in the therapy of some aplastic anaemias ### Page 2 of 14 **Section A** 1. Peptide co-transmitters include - **Substance P** - Bradykinin - Angiotensin II - Dopamine 2. The lethal effect of anticholinesterase overdose is mainly due to - Excessive cardiac slowing - Excessive tissue oedema - Impaired breathing - **Impaired central nervous system function** 3. Acetylcholine - Promotes acetylcholine release via muscarinic M2 receptors - Inhibits acetylcholine release via muscarinic M2 receptors - **Promotes acetylcholine release via nicotinic muscle receptors** - Inhibits acetylcholine release via nicotinic muscle receptors 4. Anticholinesterases - Increase depolarising neuromuscular blockade - **Increase non-depolarising neuromuscular blockade** - Do not affect depolarising neuromuscular blockade - Do not affect non-depolarizing neuromuscular blockade 5. Tubocurare acts via - The acetylcholine binding site on nicotinic receptors - The ion channel part of nicotinic receptors - **Both (a) and (b)** - Neither (a) nor (b) 6. TD50 refers to the dose that causes - A therapeutic effect in 50% of people - **A toxic effect in 50% of people** - 50% maximum therapeutic response - 50% maximum toxic response 7. Ergotamine triggers - Vasodilation via 5-HT2 receptors - Vasodilation via a-adrenergic receptors - **Vasoconstriction via 5-HT2 receptors** - Vasoconstriction via a-adrenergic receptors 8. The effector domain of a drug receptor determines the drug's - Safety - **Receptor efficacy** - Receptor affinity - Metabolism 9. The maximum effect of an agonist is reduced by - Chemical antagonism - **Down-regulation of its receptor** - Competitive antagonists - Increasing its metabolism

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