which is true of the process of digestion

ATI TEAS 7

ATI TEAS Science Test

1. Which statement is true regarding the process of digestion?

A. Digestion of starch begins in the mouth.
B. Amylase is produced by the stomach to help break down food in the upper intestine.
C. The di- and tri-saccharides produced in early digestion are absorbed through the intestinal wall.
D. Proteases are responsible for breaking down starches.

Correct answer: A

Rationale: The statement 'Digestion of starch begins in the mouth' is correct. Salivary amylase, an enzyme produced in the salivary glands, initiates the breakdown of starch into simpler sugars like maltose in the mouth before further digestion in the stomach. This initial breakdown of starch is crucial in the digestion of carbohydrates, marking the beginning of the digestive process. Choice B is incorrect because amylase is produced in the salivary glands, not the stomach. Choice C is incorrect because di- and tri-saccharides are further broken down into monosaccharides before absorption. Choice D is incorrect because proteases are enzymes that break down proteins, not starches.

2. Which neurotransmitter is associated with mood regulation, sleep, and appetite?

A. Acetylcholine
B. Dopamine
C. Serotonin
D. GABA (Gamma-aminobutyric acid)

Correct answer: C

Rationale: The correct answer is C: Serotonin. Serotonin is a neurotransmitter that plays a crucial role in mood regulation, sleep, and appetite. It helps regulate emotions, mood, and behavior. Imbalances in serotonin levels have been associated with conditions such as depression, anxiety, and eating disorders. Choice A, Acetylcholine, is primarily involved in muscle control and memory functions. Choice B, Dopamine, is associated with reward, motivation, and motor control. Choice D, GABA (Gamma-aminobutyric acid), is an inhibitory neurotransmitter that helps reduce neuronal excitability and is not directly linked to mood regulation, sleep, or appetite.

3. What is the cellular function of cilia and flagella?

A. Cilia and flagella are responsible for cell movement.
B. Cilia and flagella synthesize proteins.
C. Cilia and flagella help protect the cell from its environment.
D. Cilia and flagella have enzymes that help with digestion.

Correct answer: A

Rationale: The correct answer is A: Cilia and flagella are responsible for cell movement. Cilia and flagella are specialized structures found on the surface of many types of cells. They are involved in the movement of the cell itself or in moving substances around the cell. This movement helps in various functions such as propulsion, moving fluids, and sensing the environment. Choices B, C, and D are incorrect. Cilia and flagella are not involved in synthesizing proteins, protecting the cell from its environment, or aiding in digestion. Their primary function is related to cell movement and cellular transport.

4. Which of the following is NOT one of the major types of bones in the human body?

A. Dense bone
B. Long bone
C. Short bone
D. Irregular bone

Correct answer: A

Rationale: The correct answer is A: 'Dense bone'. Dense bone is not a classification of bone types in the human body. The major types of bones include long, short, flat, and irregular bones. Long bones, like the femur, are characterized by being longer than they are wide. Short bones, such as those in the wrist (carpals) and ankle (tarsals), are generally cube-shaped. Flat bones, like the skull or scapula, are thin and provide protection. Irregular bones, such as the vertebrae, have complex shapes that do not fit into the other categories.

5. What is the term for a genetic disorder caused by a mutation in a mitochondrial gene?

A. Autosomal dominant disorder
B. Autosomal recessive disorder
C. Sex-linked disorder
D. Mitochondrial disorder

Correct answer: D

Rationale: A) Autosomal dominant disorder: This type of genetic disorder is caused by a mutation in one copy of an autosomal gene. It is not related to mitochondrial gene mutations. B) Autosomal recessive disorder: This type of genetic disorder is caused by mutations in both copies of an autosomal gene. It is not related to mitochondrial gene mutations. C) Sex-linked disorder: This type of genetic disorder is caused by mutations in genes located on the sex chromosomes (X or Y). It is not related to mitochondrial gene mutations. D) Mitochondrial disorder: Mitochondrial disorders are genetic disorders caused by mutations in genes located in the mitochondria, the energy-producing structures within cells. These disorders are inherited maternally and can affect various organs and systems in the body due to the role of mitochondria in energy production.