Tick the antimalarial drug belonging to pyrimidine derivatives:

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Pharmacology Across the Lifespan ATI Questions

Question 1 of 5

Tick the antimalarial drug belonging to pyrimidine derivatives:

Correct Answer: B

Rationale: The correct answer to the question is B) Pyrimethamine. Pyrimethamine is an antimalarial drug that belongs to the class of pyrimidine derivatives. This drug works by inhibiting the enzyme dihydrofolate reductase in Plasmodium species, thereby disrupting the parasite's ability to synthesize DNA and RNA. Option A) Mefloquine is an antimalarial drug belonging to the class of quinolines, not pyrimidine derivatives. Mefloquine works by interfering with parasite's ability to break down hemoglobin in red blood cells. Option C) Quinidine is an antiarrhythmic medication, not an antimalarial drug. Option D) Chloroquine is an antimalarial drug, but it belongs to the class of aminoquinolines, not pyrimidine derivatives. Chloroquine exerts its antimalarial activity by accumulating in the acidic food vacuoles of the parasite and inhibiting heme polymerase activity. Understanding the classification of antimalarial drugs based on their chemical structure is crucial for pharmacology students. This knowledge helps in selecting the appropriate drug for specific types of malaria infections and understanding their mechanisms of action, pharmacokinetics, and potential side effects. Additionally, knowing the differences between various classes of antimalarial drugs is essential for effective patient care and management of malaria cases across different age groups.

Question 2 of 5

Tick the drug for echinococcosis treatment:

Correct Answer: B

Rationale: In the context of treating echinococcosis, the correct answer is B) Mebendazole or Albendazole. These drugs belong to the class of anthelmintics and are commonly used for the treatment of parasitic infections such as echinococcosis. Mebendazole and Albendazole work by inhibiting the parasites' ability to uptake glucose, leading to their eventual death. Option A) Suramin is used to treat African sleeping sickness caused by trypanosomes and is not effective against echinococcosis. Option C) Piperazine is used to treat roundworm infections and is not effective against echinococcosis. Option D) Iodoquinol is used to treat parasitic infections such as amoebiasis and is not a first-line treatment for echinococcosis. Understanding the correct medication for treating echinococcosis is crucial for healthcare providers, especially in regions where parasitic infections are prevalent. Mebendazole and Albendazole are considered safe and effective treatments for echinococcosis, and having this knowledge ensures appropriate management and care for patients with parasitic infections.

Question 3 of 5

Tick the antiviral drug which belongs to endogenous proteins:

Correct Answer: C

Rationale: The correct answer is C) Interferon alfa because it belongs to endogenous proteins. Interferons are proteins produced naturally by the body in response to viral infections. They play a crucial role in the body's immune response to viruses by inhibiting viral replication and spread. A) Amantadine is an antiviral medication used to treat influenza A, but it is not an endogenous protein. It works by blocking the viral ion channel protein. B) Saquinavir is a protease inhibitor used in the treatment of HIV infection. It is a synthetic drug and not an endogenous protein. D) Pencyclovir is an antiviral medication used to treat herpes virus infections. It is a synthetic nucleoside analog and not an endogenous protein. Educational Context: Understanding the classification of antiviral drugs based on their mechanism of action and origin (endogenous vs. synthetic) is crucial in pharmacology. Knowing that interferon alfa is an endogenous protein helps students differentiate it from other antiviral drugs and understand its unique role in the body's immune response to viral infections. This knowledge is essential for safe and effective medication administration and patient care.

Question 4 of 5

Tick the group of hormonal drugs used for cancer treatment:

Correct Answer: B

Rationale: The correct group of hormonal drugs used for cancer treatment is option B) Glucocorticoids and gonadal hormones. Glucocorticoids, such as prednisone and dexamethasone, are commonly used in cancer treatment to reduce inflammation and suppress the immune system. They can help manage side effects of chemotherapy and radiation therapy. Gonadal hormones, such as estrogen and testosterone, are also used in cancer treatment. For example, hormone therapy is a common approach for hormone receptor-positive breast and prostate cancers. These hormones can either stimulate or inhibit the growth of certain types of cancer cells. Mineralocorticoids (Option A) are not typically used in cancer treatment. They primarily regulate electrolyte and fluid balance in the body. Gonadal hormones and somatotropin (Option C) are not commonly used for cancer treatment. Somatotropin is growth hormone, which is not a standard treatment for cancer. Insulin (Option D) is a hormone used to regulate blood sugar levels in conditions like diabetes and is not a primary treatment for cancer. Educationally, understanding the role of different hormonal drugs in cancer treatment is crucial for healthcare professionals to provide optimal care to cancer patients. Knowing which hormones are involved in cancer growth and how certain drugs can target these hormones is essential for effective treatment planning and patient management.

Question 5 of 5

Enzyme drug used for acute leukemia treatment:

Correct Answer: B

Rationale: In the treatment of acute leukemia, the enzyme drug used is Asparaginase. Asparaginase works by depleting levels of asparagine in the blood, which is essential for leukemia cells to grow and survive. By depriving the cancer cells of this vital amino acid, their growth is inhibited, leading to cell death. Option A, Dihydrofolate reductase, is not the correct answer because it is an enzyme targeted by drugs like methotrexate for the treatment of various cancers and autoimmune diseases, not specifically acute leukemia. Option C, Aromatase, is an enzyme targeted in hormone-positive breast cancer treatment to inhibit estrogen production, and it is not used in acute leukemia therapy. Option D, DNA gyrase, is an enzyme targeted by antibiotics like fluoroquinolones to inhibit bacterial DNA replication, and it is not relevant to the treatment of acute leukemia. Understanding the mechanism of action of each drug is crucial for healthcare professionals to make informed decisions in patient care. In the context of pharmacology across the lifespan, knowing the appropriate enzyme drug for specific conditions is essential for providing safe and effective treatment, especially in vulnerable populations like pediatric patients with acute leukemia.

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