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Second messenger systems (cAMP, cGMP, Ca2+)

Second messenger systems (cAMP, cGMP, Ca2+)

Second messenger systems (cAMP, cGMP, Ca2+)

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Second Messengers - Cellular Gossip Girls

  • cAMP System (Gs/Gi): Ligand → Gs/Gi protein → Adenylyl Cyclase (AC) → ↑/↓cAMP → Protein Kinase A (PKA).
  • IP3/DAG System (Gq): Ligand → Gq protein → Phospholipase C (PLC) → PIP2 cleaved to IP3 + DAG.
    • IP3 → ↑Ca²⁺ release from ER.
    • DAG + Ca²⁺ → Protein Kinase C (PKC).
  • cGMP System: Nitric Oxide (NO) or ANP → Guanylyl Cyclase (GC) → ↑cGMP → Protein Kinase G (PKG).

Cholera Toxin permanently activates Gs by ADP-ribosylation, causing massive ↑cAMP, leading to severe secretory diarrhea.

cAMP and IP3/Ca2+ Second Messenger Pathways

cAMP Pathway - The 'On' Switch

  • Mechanism: Ligand binding to a Gs-protein coupled receptor (GPCR) triggers the exchange of GDP for GTP on the Gαs subunit.
  • Activation: The activated Gαs subunit dissociates and activates adenylyl cyclase.
  • Second Messenger: Adenylyl cyclase converts ATP to cyclic AMP (cAMP).
  • Effector: cAMP activates Protein Kinase A (PKA), which phosphorylates target proteins, causing a cellular response.

GPCR signaling pathways and second messengers

Cholera toxin permanently activates Gαs by ADP-ribosylation, leading to a massive ↑ in cAMP in intestinal cells. This causes continuous phosphorylation of the CFTR channel, resulting in severe secretory diarrhea.

📌 Mnemonic (Gs-coupled receptors): "FLAT ChAMP" - FSH, LH, ACTH, TSH, CRH, hCG, Adrenaline/Noradrenaline (β-receptors), MSH, PTH.

cGMP Pathway - The 'Relax' Signal

  • Activator: Nitric Oxide (NO) & natriuretic peptides (ANP, BNP).
  • Enzyme: Guanylate Cyclase (converts GTP → cGMP).
  • Effector: Protein Kinase G (PKG).

Mechanism of Action:

  • NO, often from endothelial cells or drugs like nitroglycerin, activates soluble guanylate cyclase.
  • ↑ cGMP activates Protein Kinase G.
  • PKG activation leads to ↓ intracellular Ca²⁺ and activation of Myosin Light Chain Phosphatase.
  • Result: Smooth muscle relaxation → vasodilation.

Second messenger systems in smooth muscle contraction

Clinical Pearl: Phosphodiesterase-5 (PDE-5) inhibitors like sildenafil prevent the breakdown of cGMP, prolonging vasodilation. Co-administration with nitrates can cause life-threatening hypotension.

📌 Mnemonic: cGMP = Causes Generous Muscle Paralysis (relaxation).

IP₃/DAG/Ca²⁺ Pathway - The 'Release' Crew

  • Trigger: Ligand binds to a Gq-protein coupled receptor (GPCR).
  • Mechanism:
    • Gq activates Phospholipase C (PLC).
    • PLC cleaves membrane lipid PIP₂ into IP₃ (Inositol trisphosphate) and DAG (Diacylglycerol).
    • IP₃ travels to the endoplasmic reticulum → triggers release of stored Ca²⁺.
    • DAG and ↑Ca²⁺ co-activate Protein Kinase C (PKC) → cellular response via phosphorylation.

📌 Mnemonic (Gq receptors): "HAVe 1 M&M" → H₁, α₁, V₁, M₁, M₃.

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Exam Favorite: Lithium, used for bipolar disorder, inhibits inositol monophosphatase, dampening this pathway by depleting recyclable inositol precursors.

High‑Yield Points - ⚡ Biggest Takeaways

  • G-protein coupled receptors (GPCRs) are central to second messenger signaling.
  • Gs (stimulatory) and Gi (inhibitory) modulate adenylyl cyclase to control cAMP levels, which in turn activates Protein Kinase A (PKA).
  • Gq activates phospholipase C, yielding IP₃ (releases intracellular Ca²⁺) and DAG (activates Protein Kinase C).
  • Nitric oxide (NO) stimulates guanylyl cyclase, increasing cGMP to cause smooth muscle relaxation.
  • Phosphodiesterases degrade cAMP/cGMP; inhibitors prolong their signals.

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