Metabolic Hormones: Overview - Metabolic Maestros

- Major Types & Origin:
- Peptides: Insulin, Glucagon (Pancreas).
- Amines: Epinephrine (Adrenal Medulla), Thyroid hormones (Thyroid).
- Steroids: Cortisol (Adrenal Cortex).
- Core Function: Regulate flux through metabolic pathways; maintain energy balance & glucose homeostasis.
- Signaling: Act via cell surface or intracellular receptors to alter enzyme activity or gene expression.
⭐ Insulin is the major anabolic hormone; Glucagon is its primary counter-regulatory catabolic hormone, crucial for glucose balance.
Insulin: The Anabolic Chief - Anabolic Architect
- Source: Pancreatic β-cells.
- Nature: Peptide; key anabolic hormone.
- Secretion Stimuli: ↑ Blood glucose (primary, >70 mg/dL), amino acids, GLP-1, GIP.
- Receptor: Tyrosine Kinase (RTK).
- Mechanism: Activates PI3K/Akt & MAPK pathways.
- Overall: Promotes fuel storage.
- Key Actions:
- ↑ Glucose uptake (GLUT4: muscle, adipose).
- ↑ Glycogenesis; ↓ Glycogenolysis.
- ↑ Glycolysis (liver); ↓ Gluconeogenesis.
- ↑ Lipogenesis; ↓ Lipolysis.
- ↑ Protein synthesis.
- ↑ K+ cellular uptake. 📌 (Mnemonic: InsulIN K+ goes IN)
⭐ Insulin's promotion of K+ entry into cells is used to treat hyperkalemia.

Glucagon & Co: Catabolic Crew - Catabolic Champions
- Glucagon (Pancreatic α-cells):
- Stimuli: ↓ Glucose, ↑ Amino acids (e.g., arginine).
- Actions: ↑ Liver glycogenolysis, gluconeogenesis, ketogenesis; ↑ Lipolysis.
- Mechanism: GPCR (Gs → ↑$cAMP$).
⭐ Glucagon primarily targets the liver; muscle lacks glucagon receptors.
- Epinephrine (Adrenal Medulla):
- Stimuli: Stress, hypoglycemia.
- Actions: ↑ Glycogenolysis (liver, muscle); ↑ Lipolysis; ↑ Glucagon secretion, ↓ Insulin secretion.
- Cortisol (Adrenal Cortex):
- Stimulus: Stress (via ACTH).
- Actions (slow, permissive): ↑ Muscle proteolysis; ↑ Lipolysis; ↑ Liver gluconeogenesis (induces PEPCK); ↓ Peripheral glucose utilization.
- Growth Hormone (GH; Anterior Pituitary):
- Actions (anti-insulin): ↓ Tissue glucose uptake; ↑ Lipolysis.
Metabolic States: Hormonal Control - Fuel State Symphony
Hormones orchestrate fuel flux, adapting to nutritional and physiological demands. Key players: Insulin, Glucagon, Epinephrine, Cortisol.
- Fed State (↑ Insulin:Glucagon ratio):
- Insulin dominant: ↑ Glucose uptake (GLUT4), ↑ Glycogenesis, ↑ Lipogenesis, ↑ Protein synthesis.
- Anabolic processes favored.
- Fasting State (↓ Insulin:Glucagon ratio):
- Glucagon dominant: ↑ Glycogenolysis, ↑ Gluconeogenesis.
- Epinephrine, Cortisol: ↑ Lipolysis, ↑ Proteolysis (prolonged).
- Prolonged fasting: ↑ Ketogenesis.
- Stress/Exercise:
- Sympathetic drive: ↑ Epinephrine.
- ↑ Cortisol, ↑ Glucagon: Mobilize fuels (glucose, Free Fatty Acids) for immediate energy.

⭐ Insulin is the primary anabolic hormone, promoting storage of carbohydrates, fats, and proteins after a meal, and its deficiency or resistance leads to diabetes mellitus.
High‑Yield Points - ⚡ Biggest Takeaways
- Insulin: key anabolic hormone; ↑ glucose uptake (GLUT4), glycogenesis, lipogenesis.
- Glucagon: primary catabolic hormone; ↑ glycogenolysis, gluconeogenesis.
- Epinephrine: rapid stress response via cAMP; ↑ glycogenolysis (liver/muscle), lipolysis.
- Cortisol: permissive action; ↑ gluconeogenesis, protein breakdown in chronic stress.
- Insulin/Glucagon ratio dictates metabolic flux: high (fed), low (fasting).
- Growth Hormone opposes insulin's glucose action; can be diabetogenic.
- Thyroid hormones (T3/T4): ↑ BMR, sensitize tissues to catecholamines.
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