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Gluconeogenesis: Reactions and Regulation

Gluconeogenesis: Reactions and Regulation

Gluconeogenesis: Reactions and Regulation

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Gluconeogenesis Overview - Sweet Rebirth

  • Definition: Metabolic pathway generating new glucose from diverse non-carbohydrate precursors like lactate, pyruvate, glycerol, and specific amino acids.
  • Primary Function: Maintains blood glucose during fasting, starvation, or prolonged exercise.
  • Major Sites:
    • Liver (primary, ~90%)
    • Kidney cortex (secondary, ~10%)
  • Cellular Location:
    • Mitochondria
    • Cytosol
    • Endoplasmic Reticulum (ER - final step) Glucose-Alanine Cycle: Hepatocyte and Muscle Cell

⭐ Gluconeogenesis is NOT a simple reversal of glycolysis; it bypasses three irreversible glycolytic reactions using distinct enzymes.

Gluconeogenesis Substrates - Fueling Glucose Up

  • Lactate: From anaerobic glycolysis (muscle, RBCs); via Cori cycle. $Lactate \rightarrow Pyruvate$.
  • Pyruvate: Central entry point.
  • Glycerol: From triglyceride breakdown (adipose); forms Dihydroxyacetone Phosphate (DHAP).
  • Glucogenic Amino Acids: All except Leucine & Lysine (📌 "L"ovely "L"adies are ketogenic). Enter as pyruvate or TCA intermediates.

    ⭐ Alanine (muscle; Glucose-Alanine cycle) is a key gluconeogenic amino acid.

  • Propionyl CoA: From odd-chain fatty acids, some AAs; forms succinyl CoA.

Gluconeogenesis substrates and pathways

Gluconeogenesis Reactions - The Uphill Sugar Path

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Gluconeogenesis Regulation - Glucose Traffic Cops

Gluconeogenesis (GNG) is precisely regulated by hormones and allosteric molecules, with $F-2,6-BP$ as a key reciprocal switch.

Regulator TypeKey ActivatorsKey Inhibitors
HormonalGlucagon, Epinephrine: ↑cAMP → PKA. PKA → ↑FBPase-2/↓PFK-2 activity → ↓$F-2,6-BP$; Induce PEPCK, $G_6Pase$.Insulin: ↓cAMP; Represses PEPCK, $G_6Pase$, $FBPase-1$.
Cortisol: ↑AAs (protein catabolism); Induces GNG enzymes.
AllostericAcetyl-CoA: + Pyruvate Carboxylase.AMP: - $FBPase-1$.
Citrate: + $FBPase-1$.$F-2,6-BP$: - $FBPase-1$.

Gluconeogenesis and Glycolysis Regulation in Liver

Gluconeogenesis Clinicals - Sweetness Gone Sour

  • Impaired GNG causes Hypoglycemia:
    • Alcohol intoxication: ↑NADH/NAD+ ratio diverts pyruvate $\rightarrow$ lactate & oxaloacetate (OAA) $\rightarrow$ malate.
    • Enzyme deficiencies: Glucose-6-phosphatase (Von Gierke's), PEPCK, Fructose-1,6-bisphosphatase.
  • Type 2 Diabetes: Excessive gluconeogenesis contributes to hyperglycemia.

⭐ Alcohol-induced hypoglycemia is primarily due to the increased NADH/NAD+ ratio, which inhibits the conversion of lactate to pyruvate and malate to oxaloacetate, thus limiting gluconeogenic precursors.

High‑Yield Points - ⚡ Biggest Takeaways

  • Gluconeogenesis is the synthesis of new glucose from non-carbohydrate precursors like lactate, glycerol, and amino acids.
  • Primarily occurs in the liver; minor extent in the kidney cortex.
  • Bypasses irreversible steps of glycolysis using pyruvate carboxylase, PEPCK, fructose-1,6-bisphosphatase, and glucose-6-phosphatase.
  • Fructose-1,6-bisphosphatase is a key regulatory enzyme; inhibited by AMP and fructose-2,6-bisphosphate.
  • Acetyl-CoA allosterically activates pyruvate carboxylase.
  • Stimulated by glucagon and cortisol; inhibited by insulin.
  • Glucose-6-phosphatase, present only in liver and kidney, releases free glucose into blood.

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