Pepsinogen is produced by __________ and is activated by _________ which is secreted by ________.
chief cells; carbonic anhydrase (CAH); parietal cells
chief cells; hydrochloric acid (HCI); parietal cells
parietal cells; hydrochloric acid (HCI): chief cells
parietal cells; carbonic anhydrase (CAH); chief cells
enteroendocrine cells; carbonic anhydrase (CAH); parietal cells
The Correct Answer is B
A. chief cells; carbonic anhydrase (CAH); parietal cells: Chief cells correctly synthesize the zymogen pepsinogen, but carbonic anhydrase is an enzyme, not a direct activator. CAH facilitates the formation of protons within cells but does not catalyze extracellular protein cleavage. Pepsinogen requires a low pH environment for activation.
B. chief cells; hydrochloric acid (HCl); parietal cells: Gastric chief cells secrete inactive pepsinogen into the stomach lumen. Hydrochloric acid, produced by parietal cells via proton pumps, lowers the luminal pH to approximately 2. This acidic environment triggers the autocatalytic conversion of pepsinogen into the active protease pepsin.
C. parietal cells; hydrochloric acid (HCl): chief cells: This selection incorrectly reverses the cellular origins of the enzyme and the acid. Parietal cells are responsible for secreting hydrochloric acid and intrinsic factor, not the zymogen pepsinogen. Chief cells provide the protein substrate but do not produce the acid required.
D. parietal cells; carbonic anhydrase (CAH); chief cells: Carbonic anhydrase is an intracellular enzyme that provides the hydrogen ions for acid production. It is not the molecule that directly interacts with pepsinogen in the gastric lumen. Furthermore, parietal cells do not produce the pepsinogen zymogen required for this reaction.
E. enteroendocrine cells; carbonic anhydrase (CAH); parietal cells: Enteroendocrine cells, specifically G cells, secrete hormones like gastrin into the bloodstream rather than digestive zymogens. Carbonic anhydrase remains an intracellular catalyst for ion formation. This combination fails to describe the luminal activation of proteases necessary for protein degradation.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is E
Explanation
A. squamous alveolar cells: These Type 1 cells are extremely thin to facilitate rapid gas exchange across the blood-air barrier. Their primary structural adaptation is for diffusion rather than secretion. They do not possess the intracellular machinery required to synthesize or release viscous mucus into the respiratory tract.
B. great alveolar cells: These Type 2 cells are responsible for the secretion of pulmonary surfactant, which reduces alveolar surface tension to prevent atelectasis. While they are secretory, their product is phospholipid-rich rather than mucin-based. They do not contribute to the mucus blanket found in the conducting zone.
C. the pleurae: The pleurae are serous membranes that produce a thin, watery serous fluid to lubricate the pleural cavity during lung expansion. This fluid remains external to the lung parenchyma and does not enter the airway lumen. It serves a mechanical purpose rather than a cleansing or trapping function.
D. ciliated cells: These cells possess apical projections that beat rhythmically to propel the mucus blanket toward the pharynx. While they are essential for the mucociliary escalator, they do not synthesize the mucus itself. Their role is the transport of trapped particulate matter rather than the production of secretions.
E. goblet cells: These specialized columnar epithelial cells synthesize and secrete mucins, which hydrate to form the protective mucus layer. This layer traps inhaled dust, pollen, and pathogens to protect the delicate lower respiratory tissues. They are found throughout the pseudostratified epithelium of the conducting airways.
Correct Answer is B
Explanation
A. C6H12O6 + 6 H2O -> 6 CO2 + 6 O2: This equation incorrectly lists water as a reactant instead of oxygen. Aerobic catabolism requires molecular oxygen as the terminal electron acceptor in the electron transport chain. Metabolism of glucose without oxygen input prevents oxidative phosphorylation.
B. C6H12O6 + 6 O2 -> 6 CO2 + 6 H2O: Hexose oxidation involves the complete breakdown of glucose in the presence of oxygen. This metabolic pathway yields carbon dioxide and water as primary byproducts while capturing chemical energy. It accurately reflects the stoichiometric balance of aerobic cellular respiration.
C. C6H12O6 + 6 CO2 -> 6 O2 + 6 H2O: Carbon dioxide functions as a metabolic waste product rather than a reactant in human cellular respiration. Glucose does not react with carbon dioxide to produce oxygen during heterotrophic metabolism. This chemical arrangement reverses the standard physiological gas exchange.
D. CO2 + 6 H2O -> C6H12O6 + 6 O2: This formula represents the endergonic process of photosynthesis occurring in photoautotrophic organisms. It describes the fixation of inorganic carbon into organic compounds using light energy. Eukaryotic animal cells lack the chloroplasts necessary to drive this specific anabolic reaction.
E. 6 O2 + 6 H2O -> C6H12O6 + 6 CO2: The combination of oxygen and water does not spontaneously synthesize glucose molecules in biological systems. This equation fails to account for the carbon source required for carbohydrate formation. It violates the fundamental thermodynamic principles governing respiratory substrate breakdown and energy release.
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