Nursing Elites

1. Where is oxygen exchanged between blood and tissues?

• A. capillaries
• B. veins
• C. ventricles
• D. arteries

Correct answer: A

Rationale: Oxygen is exchanged between blood and tissues primarily at the capillaries. Capillaries are the smallest blood vessels where the exchange of oxygen, nutrients, and waste products occurs between the blood and the tissues. This exchange process is crucial for delivering oxygen to the body's cells and eliminating carbon dioxide waste. Veins carry blood back to the heart, arteries carry blood away from the heart, and ventricles are the lower chambers of the heart responsible for pumping blood. Therefore, capillaries are the correct answer for where oxygen is exchanged between blood and tissues.

2. Which of the following best describes the function of the pericardium?

• A. Regulating blood flow through valves within the heart.
• B. Acting as a protective sac surrounding the heart.
• C. Generating the electrical impulses for heart contractions.
• D. Transmitting electrical signals between the atria and ventricles.

Correct answer: B

Rationale: The pericardium is a double-layered sac that surrounds and protects the heart. Its main functions include preventing overfilling of the heart, providing a physical barrier against infection and inflammation, and reducing friction between the heart and surrounding structures. Choices A, C, and D do not accurately describe the function of the pericardium. Option B is the correct answer as it aligns with the protective and supportive role of the pericardium, distinguishing it from the functions attributed to choices A, C, and D.

3. What is the process of converting ammonia, a byproduct of protein digestion, into a less toxic form?

• A. Deamination
• B. Transamination
• C. Decarboxylation
• D. Hydrolysis

Correct answer: A

Rationale: Deamination is the correct answer. It is the process of removing an amino group from a molecule, like converting ammonia (NH3) into a less toxic form such as urea. Ammonia, a byproduct of protein digestion, must be converted into a less toxic form for excretion. Deamination is a crucial step that mainly occurs in the liver through the urea cycle. Transamination involves transferring an amino group from one molecule to another, not removing it as in deamination. Decarboxylation is the removal of a carboxyl group from a molecule, and hydrolysis is the breakdown of a compound by adding water.

4. What is the structure of DNA?

• A. Single-stranded, linear
• B. Double-stranded, linear
• C. Double-stranded, helix
• D. Single-stranded, helix

Correct answer: C

Rationale: The correct answer is C: Double-stranded, helix. DNA is structured as a double helix formed by two strands of nucleotides. The nucleotides are paired with complementary bases (A-T and C-G) in the center, held together by hydrogen bonds. This double-stranded helical structure is a fundamental characteristic of DNA and essential for its function in storing genetic information. Choices A, B, and D are incorrect because DNA is not single-stranded; it consists of two strands that run antiparallel to each other and are connected via hydrogen bonds. Additionally, DNA does not have a linear structure but rather a helical one, providing stability and protection to the genetic information it carries.

5. How can a single gene mutation lead to multiple phenotypes depending on the organism?

• A. Pleiotropy describes the effect of one gene influencing multiple seemingly unrelated traits.
• B. Epigenetics involves environmental factors modifying gene expression without altering the DNA sequence.
• C. Genetic drift refers to random changes in allele frequencies within a population.
• D. Gene regulation controls the timing and level of gene expression within an organism.

Correct answer: A

Rationale: A single gene mutation can lead to multiple phenotypes through pleiotropy, where one gene influences diverse traits or functions in an organism. This phenomenon occurs when the mutated gene affects different biochemical pathways, developmental processes, or cellular functions, resulting in a cascade of downstream effects that manifest as a variety of phenotypic outcomes. Choice B, epigenetics, involves modifications in gene expression influenced by environmental factors without altering the DNA sequence, which is not directly related to the question about single gene mutations causing multiple phenotypes. Choice C, genetic drift, refers to random changes in allele frequencies within a population, which is unrelated to the impact of a single gene mutation on multiple phenotypes. Choice D, gene regulation, focuses on controlling the timing and level of gene expression within an organism, which is not directly addressing how a single gene mutation can lead to diverse phenotypes.

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