Altklausur Flashcards
Which of the following statements is false?
A) The toxic effects of drug A may be due to a drug interaction when co-administered drug B induces CYP3A4 that degrades drug A into its inactive metabolite
B) The toxic effects of drug A may be due to a drug interaction when co-administered drug B blocks CYP3A4 that degrades drug A into its inactive metabolite
C) Drug A may be ineffective due to a drug interaction when co-administered drug B induces CYP2D6 that degrades drug A into its inactive metabolite
D) CYP2D6 is a prominent example for a polymorphic CYP enzyme
E) Grapefruit juice can block CYP3A4
A) The toxic effects of drug A may be due to a drug interaction when co-administered drug B induces CYP3A4 that degrades drug A into its inactive metabolite
Which of the following statements regarding the bioavailability of a drug is false?
A) is the fraction of the administered dose reaching the systemic circulation
B) is calculated by the ratio of the area under the curves (AUC) following oral drug application and the maximal plasma concentration following intravenous drug application
C) is dependent of first pass metabolism
D) ranges from 0 to 100 % after oral application
E) indicates the concentration at the drug target (e.g. receptor, enzyme)
D) ranges from 0 to 100 % after oral application
Which of the following statements regarding drugs interacting with the RAAS is false?
A) Candesartan Cilexetil is a prodrug
B) Captopril is an inhibitor of ACE2
C) Renin can be inhibited by aliskiren
D) Sacubitril induces an increase of BNP
E) Icatibant is an antagonist at B2 receptors
A) Candesartan Cilexetil is a prodrug
Which of the following statements regarding telmisartan is true?
A) Compared to its affinity at AT2 receptor, the ki value of telmisartan at AT1 receptors is >10,000 fold higher
B) Cough is a typical side effect of temisartan
C) Telmisartan delays the onset of type 2 diabetes
D) Telmisartan lowers the ventricular ejection fraction
E) Telmisartan reduces the plasma levels of angiotensinII
A) Compared to its affinity at AT2 receptor, the ki value of telmisartan at AT1 receptors is >10,000 fold higher
Which of the following statements is true?
The typical mechanisms of action of antiepileptic drugs include the
A) agonism at NMDA receptors
B) modulation of voltage dependent Ca2+ channels
C) permanent and irreversible setting of voltage gated Na+ channels to resting closed state
D) activation of GABA transaminase
E) inactivation of GABA decarboxylase
B) modulation of voltage dependent Ca2+ channels
Which of the following statements regarding anti epileptic drugs is FALSE?
A) The alpha1-subunit of the GABAA receptor mediates the anti epileptic action of benzodiazepines
B) Up to now, no anti epileptic drug has been found to be effective in the prevention of epileptogenesis
C) Many anti epileptic drugs are effective by reducing GABA degradation
D) Benzodiazepines are regarded as the agents of first choice for anti epileptic treatment
E) Many anti epileptic drugs are blockers of voltage dependent Na+ channels
D) Benzodiazepines are regarded as the agents of first choice for anti epileptic treatment -> sedative side effects!!!
Which of the following statements is FALSE?
A) The thyroid hormone receptors TRalpha and TRbeta are encoded by 2 different agents
B) The thyroid hormone receptors isoforms TRbeta1 and TRbeta2 are generated by alternative splicing
C) TR only increases but dies nit inhibit the expression of target genes
D) TRalpha1, TRbeta1 and TRbeta2 display extensive structural similarities, with the exception of an N-terminal extension, which is absent in TRalpha1
E) TRs act mainly as heterodimers with the retinoid acid nuclear receptor
C) TR only increases but does not inhibit the expression of target genes
Which of the filling statements concerning the main mode of action of methimazole is correct?
A) Inhibition of iodine uptake in the thyroid gland
B) Inhibition of TRH secretion
C) Inhibition of TRH secretion
D) Inhibition of thyroid peroxidase
E) Increase metabolism of T3
D) Inhibition of thyroid peroxidase
Which of the following statements is FALSE?
Liraglutid
A) has more than 90 % homology to human GLP-1
B) typically increases the body weight
C) lowers cardiovascular mortality
D) enhances the release of insulin from pancreatic beta cells
E) has an elimination half-life of approximately 24 h
B) typically increases the body weight
Which of the following statements addressing the mechanism on oral anti diabetic agents is FALSE?
A) Metformin inhibits the mitochondrion specific isoform of glycerophosphate dehydrogenase
B) Empagliflozin specifically blocks SGLT2
C) Sitagliptine inhibits DPP4
D) Acerbose is a glucosidase inhibitor
E) Pioglitazone is a PPAR gamma inhibitor
D) Acerbose is a glucosidase inhibitor
Which of the following statements is true?
Acetylsalicylic acid (Aspirin) is
A) a thrombolytic agent
B) an antihypertensive agent
C) a lipid lowering drug
D) an anti diabetic drug
E) a platelet aggregation inhibitor
E) a platelet aggregation inhibitor
Which of the following statements is FALSE?
A risk factor for hemorrhagic stroke is
A) the use of ACE inhibitors
B) cerebral amyloid antipathy
C) acetylsalicylic acid (Aspirin) use
D) tissue plasminogen activator treatment
E) old age
A) the use of ACE inhibitors
Which of the following statements is FALSE?
A) Competitive antagonists increase the ED50 value of the corresponding agonist
B) Competitive antagonists do not alter the maximal effect of the corresponding agonist
C) non competitive antagonists bind allosterically to the corresponding receptor
D) non competitive antagonists lead to a right shift of the dose-response curve of the corresponding agonist
E) non competitive antagonists reduce the Emax of the corresponding agonist
D) non competitive antagonists lead to a right shift of the dose-response curve of the corresponding agonist
Which of the following statements is FALSE?
A) The EC50 of different agonists at a given receptor can vary
B) The potency pD2 of an agonist is calculated from its EC50 value
C) The maximal response (Emax) of different agonists at a given receptor can vary
D) The intrinsic activity alpha of an agonist determines its Emax
E) The potency pD2 of an agonist is determined by its intrinsic activity alpha
E) The potency pD2 of an agonist is determined by its intrinsic activity alpha
Which of the following statements is FALSE?
A) FLIPR stands for “Fluorometric Imaging Plate Reader”
B) Receptor antagonists cannot be identified with the FLIPR technology
C) The FLIPR technology allows the measurement of intracellular Ca2+ concentrations
D) With FLIPR technology, it is not possible to observe Ca2+ concentrations in single cells (ca2+ imaging)
E) With FLIPR technology, new specific ligands of receptors can be identified
B) Receptor antagonists cannot be identified with the FLIPR technology
Which of the following statements is FALSE?
A) Orexin are peptides for the potential treatment of narcolepsy
B) All orexin receptor antagonists are peptides
C) Orexin receptor antagonists are being developed for the treatment of sleep disorders
D) [Ala11, D-Leu15] Orexin-B is an orexin type 2 (OX2) receptor selective agonist
E) Orexins affect food intake and metabolism
B) All orexin receptor antagonists are peptides
Which of the following statements regarding benzodiazepines (BZDs) is FALSE?
A) the sedative effect of BZD relies crucially on the alpha1 subunit of the GABAA receptor
B) An active metabolite is produced and accumulates in the chronic administration of diazepam
C) BZDs as positive allosteric modulators of the GABAA receptor enhance the chloride conductance of the channel
D) A short action of a BZD dispute its possible long elimination half-life is explained by its redistribution from the gray matter into peripheral fat tissue
E) BZDs have a narrower therapeutic range than barbiturates
B) An active metabolite is produced and accumulates in the chronic administration of diazepam
Which of the following statements regarding viral vectors is FALSE?
A) Recombinant vectors based on Adeno-associated viruses (AAV) mostly persist as episcopal DNA
B) All approved in vivo gene therapy approaches utilize retroviral vectors
C) Retroviral vectors integrate into the genome
D) AAV can transduce hepatocytes and various other cell types
E) The capsid of AAV can be modified to redirect the tropism towards different target tissues
B) All approved in vivo gene therapy approaches utilize retroviral vectors
Which of the following statements regarding alipogene tiparvovec is true?
A) Alipogene tiparvovec has been approved for the treatment of severe combined immunodeficiency due ti adenosine deaminase deficiency (ADA SCID)
B) Alipogene tiparvovec is based on a gammarettoviral vector
C) Alipogene tiparvovec has been approved already several years ago in the EU
D) An estimated half a million potential patients in the EU may benefit from a treatment with Alipogene tiparvovec
E) Alipogene tiparvovec is the only gene therapy to be administered orally
B) Alipogene tiparvovec is based on a gammarettoviral vector
Which of the following statements is FALSE?
A) The effect of most drugs is mediated by a receptor
B) The number of receptors that are known to play a role in modern drug therapy come close to the number of human genes (about 22,000)
C) some of the drug receptors are found in microbial pathogens
D) G protein coupled receptors have been one of the most successful classes of drug targets
E) Pharmacologically used drugs can bind to more than one receptor
B) The number of receptors that are known to play a role in modern drug therapy come close to the number of human genes (about 22,000)
Which of the following statements is FALSE?
A) Phytotherapy is still used nowadays
B) The use of morphine, which was discovered as an ingredient of Palaver somniferous (poppy), is an example of phytotherapy
C) Phytotherapy has led to the discovery of numerous pharmacologically active compounds that are still used in modern medicine
D) In phytotherapy, plant extracts are used instead of purified compounds
E) A key problem of phytotherapy is the standardization of drugs
B) The use of morphine, which was discovered as an ingredient of Palaver somniferous (poppy), is an example of phytotherapy
Which of the following physiological effects is caused by an increased release of substance P?
A) Analgesia
B) Vasoconstriction
C) Vasodilation
D) Substance P counteracts inflammation
E) None of the above
A) Analgesia
Naloxon and Naltrexone belong toe which of the following drug classes?
A) Mixed agonists/antagonists
B) Opioid receptor antagonists
C) Opioid receptor agonists
D) Non-steroidal anti-inflammatory drugs
B) Opioid receptor antagonists
Which of the following statements is FALSE?
The blood-brain barrier restricts the blood-to-brain extravasation of
A) leukocytes
B) proteins
C) gaseous molecules, e.g. CO2
D) small hydrophilic molecules
E) pathogens
C) gaseous molecules, e.g. CO2
Which of the following properties or mechanisms leads to the permutation of L-DOPA into the brain?
L-DOPA
A) is transported by LAT1 (large amino acid transporter) into the brain
B) is highly lipophilic
C) is highly hydrophilic
D) is transported by P-gp (P-glycoprotein) into the brain
E) gets into the brain by transcytosis
A) is transported by LAT1 (large amino acid transporter) into the brain
Which of the following statements on hypnotics and sleep is FALSE?
A) Barbiturates can induce chloride currents within the GABAA channel without the presence of GABA
B) The hypnotic effect of benzodiazepines (BZDs) relies on facilitating the GABAergic inhibition of the ventrolateral prophetic area (VLPOA) on the arousal system(s) of the brain stem and forebrain
C) Zopiclon with an elimination half-life of about 5th facilitates sleep maintenance
D) Adenosine, which accumulates during wakefulness, is an endogenous sleep factor
E) Barbiturates, benzodiazepines and zolpidem always increase the amount of time spent in slow-wave sleep
E) Barbiturates, benzodiazepines and zolpidem always increase the amount of time spent in slow-wave sleep
Which of the following statements is FALSE?
Patients with the Allan Herndon Dudley Syndrome are characterized by
A) a peripheral hyperthyroidism
B) a central hyperthyroidism
C) a deficit in the thyroid hormone transport by the monocarboxylate transporter 8
E) motor deficits
B) a central hyperthyroidism
Which of the following statements is false?
A) The thyroid hormone 3,3’5,5’ tetraiodothyronine (T4) is transported by specialised transporters (e.g. monocarboxylate transporter 8) into cells
B) 3,3’,5 triiodothyronine (T3) binds to a nuclear receptor
C) T4 is more potent than the metabolite T3
D) T3 is produced in the thyroid gland
E) T3 is inactivated by the typ-III deiodinase
C) T4 is more potent than the metabolite T3
Which of the following strategies could NOT be used to increase the availably of a drug in the brain?
A) inducing temporary damage to the blood-brain barrier
B) coupling of the drug to a transferrin receptor antibody
C) inhibition of P-glycoprotein
D) using a transportable drug precursor
E) increasing the hydrophilicity of the drug
E) increasing the hydrophilicity of the drug
Which of the following statements is true
Na+ channel blocker’s used for antiepileptic treatment (e.g. Carbamazepine, Valproate, Phenytoin are effective by
A) stabilizing the inactivated state of voltage-gated Na+ channels
B) allosteric binding to alpha-subunits of Na+ channels
C) permanently and irreversibly setting voltage-gated Na+ channels to resting (closed) state
D) changing direction of ion flux through the channel
E) permanently removing the activation gate of voltage-gated Na+ channels
A) stabilizing the inactivated state of voltage-gated Na+ channels
Which of the following statements as treatment for epilepsies is true?
Barbiturates
A) are regarded as agents of first choice for antiepileptic treatment, as side-effects are rare
B) are only used to treat focal seizures
C) have an effect by binding to the gamma1-binding site at the GABAB receptor
D) are only used to treat absence seizures
E) are effective by allosteric binding at the GABAA receptor
E) are effective by allosteric binding at the GABAA receptor