Mammalian Fuel Metabolism: Integration and Regulation
Mammalian Fuel Metabolism: Integration and Regulation
Matching
Glucokinase Activity: Increases with high blood glucose. (Answer: G - Liver)
Kidney Function: Excretes urea and other waste products from the blood. (Answer: K - Urea)
Cori Cycle: Provides a pathway for the metabolic use of lactate for glucose production. (Answer: C - Cori cycle)
Endocrine Glands: Secrete hormones that result in numerous cellular responses. (Answer: H - Hormones)
Epinephrine Binding: Binding to the α-adrenergic receptor causes an increase in intracellular [Ca^{2+}]. (Answer: A - α-adrenergic receptor)
Prolonged Starvation: Ketone bodies are used as fuel by the brain. (Answer: J - Ketone bodies)
Acetyl CoA: The degradation product of glucose, fatty acids, and ketogenic amino acids. (Answer: I - Acetyl CoA)
Starvation & Glucose: During starvation, the kidney generates as much as 50% of the body's glucose supply. (Answer: L - Kidney)
Brain's Energy Needs: The brain stores very little glycogen and therefore requires a steady supply of glucose from the blood. (Answer: M - Brain)
Leptin Deficiency: Mice lacking the protein leptin are genetically obese. (Answer: E - Leptin)
Multiple Choice
Preferred Muscle Fuel: Glucose is the preferred fuel of muscles because it can be metabolized under anaerobic conditions. (Answer: A)
Muscle Glucose Transporter: The glucose transporter in muscle cells is GLUT4. (Answer: D)
Adenylate Cyclase Reaction: Adenylate cyclase catalyzes the reaction ATP → cAMP + PPi. (Answer: A)
Phospholipase C Cleavage: Phospholipase C cleaves PIP2, generating IP3 and DAG (inositol-1,4,5-trisphosphate and 1,2-diacylglycerol). (Answer: A)
Balanced Meal Digestion:
Fatty acids are absorbed by the intestinal mucosa and circulated through the lymph.
Proteins are digested into monomer amino acids and absorbed by the intestinal mucosa, after which the majority is delivered to the liver. (Answer: C)
Glucose Production Limitation: Animals lack the ability to produce glucose from fatty acids. (Answer: B)
Common Products of Fuel Metabolism: The common products of fuel metabolism in mammals are pyruvate and acetyl-CoA. (Answer: B)
ATP Regeneration Mechanisms: ATP regeneration mechanisms are utilized in the following order: phosphocreatine, glycolysis, oxidative phosphorylation. (Answer: B)
Glucokinase Regulation: Glucokinase is regulated by glucokinase regulatory protein and fructose-6-phosphate. (Answer: A)
Metabolic Fate of Glucose-6-Phosphate: The metabolic fates of glucose-6-phosphate include glycogen, glucose, ribose-5-phosphate, and acetyl-CoA. (Answer: E)
Hepatocyte Response to Insulin (FALSE): Glucose uptake is increased in the liver (it's not directly stimulated by insulin). (Answer: D)
Pancreatic β Cells: Insulin is secreted by the β cells in response to high glucose levels. (Answer: C)
Effects of Insulin Secretion:
Muscle and adipose tissue are stimulated to take up glucose.
Glycogen synthesis increases in the liver.
Gluconeogenesis is inhibited in the liver and kidney. (Answer: C)
Appetite Stimulating Protein: Ghrelin stimulates the appetite. (Answer: B)
Leptin (FALSE): Obesity in humans leads to a decrease in leptin production (actually, obesity leads to increased leptin production and then resistance). (Answer: C)
Blood Glucose in Non-Insulin Dependent Diabetics: Blood glucose levels of diabetics tend to be variable and higher than normal individuals. (Answer: B)
Insulin-Dependent (Type 1) Diabetes: Is associated with a deficiency of pancreatic β-cells. (Answer: A)
Aerobic Activity Under Stress: Glycolysis occurs in the muscle; glycogenolysis occurs in the muscle and liver. (Answer: A)
Interorgan Nitrogen Transport: The interorgan pathway that allows transport of nitrogen from muscle to the liver utilizes pyruvate as an amino group acceptor in the transamination reaction generating alanine. (Answer: E)
AMPK Function: AMP-dependent protein kinase (AMPK) activates ATP-generating metabolic pathways and inhibits biosynthetic pathways. (Answer: A)
Liver Glucose Production at Low Concentrations: At low glucose concentrations (≤5mM), the majority of glucose produced by liver cells is due to the action of glucose-6-phosphatase. (Answer: C)
Liver Glycogen Depletion: In an average individual, liver glycogen is depleted during starvation in approximately 18-24 hours. (Answer: C)
Excess Glucosylation in Diabetics: Excess glucosylation of lens proteins in diabetics leads to cataracts. (Answer: A)
Glucokinase Activity Curve: The curve labeled C corresponds to activity of glucokinase under conditions with no inhibition. The binding of F6P to the regulating protein would result in kinetic behavior represented by curve B.
Brain Glucose Usage: The majority of glucose in the brain is used to produce ATP for membrane Na^+-K^+ ATPase required for nerve impulse transmission. (Answer: B)
Triacylglycerol Synthesis Dependence: Synthesis of triacylglycerols is dependent on the availability of glycerol-3-phosphate, the uptake of glucose from the bloodstream, the enzyme responsible for reduction of dihydroxyacetone phosphate, and the circulation of lipoprotein. (Answer: E)
Adipose Tissue:Secretes hormones that regulate metabolism. (Answer: A)
Generates Glucose: Kidney and liver generates glucose. (Answer: C)
Occurs During Starvation: During starvation the brain utilizes ketone bodies as a fuel source; the adipose tissue releases fatty acids and gluconeogenesis occurs in the liver. (Answer: B)
Metabolizes Ketone Bodies: Brain and muscle metabolizes ketone bodies. (Answer: C)
Muscle Metabolism Hormonal Control: Muscle metabolism is controlled hormonally by insulin and epinephrine. (Answer: D)
Regulation of Metabolism: Metabolism is regulated by receptor tyrosine kinase, adenylate cyclase and phosphoinositide pathway. (Answer: D)
Muscle and Liver interaction: None of the options are correct. (Answer: E)
Glucose Update: Glucose update in the muscle is increased in response to insulin due to increased expression of GLUT4. (Answer: B)
Activation of AMPK activity: Accomplished by AMP induced conformational changes facilitating phosphorylation. (Answer: A)
Lifespan Extension in Rodents: Evidence suggests that the lifespan of a rodent may be extended 50% by a 30-40% reduction in calorie intake. (Answer: B)
Type 2 Diabetes: Can develop due to a mutation in the insulin receptor and can develop in individuals with insulin resistance. (Answer: B)
Stored Caloric Energy During Prolonged Starvation: During prolonged starvation the majority of the stored caloric energy comes from fat stores. Muscle protein provides the second largest caloric energy total. (Answer: D)
Metabolic Syndrome Characteristics: Insulin resistance and infammation are characteristics of metabolic syndrome. (Answer: A)
Metformin and Thiazolidinediones (TZDs): Are used to treat type 2 diabetes and produce a(an) increase in AMPK activity. (Answer: B)