V1 (Vasopressin) Receptors
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General Pharm
- Gs / Gi Pathway
- Gq Signaling Pathway
- Alpha-1 (Adrenergic) Receptors
- Alpha-2 (Adrenergic) Receptors
- Beta-1 (Adrenergic) Receptors
- Beta-2 (Adrenergic) Receptors
- Beta-3 (Adrenergic) Receptors
- M1 (Muscarinic) Receptors
- M2 (Muscarinic) Receptors
- M3 (Muscarinic) Receptors
- D1 (Dopamine) Receptors
- D2 (Dopamine) Receptors
- H1 (Histamine) Receptors
- H2 (Histamine) Receptors
- V1 (Vasopressin) Receptors
- V2 (Vasopressin) Receptors
Summary
V1 receptors are a type of G-protein coupled receptor activated by vasopressin, a hormone also known as antidiuretic hormone (ADH). V1 receptors are primarily located on vascular smooth muscle, and binding by vasopressin activates a Gq protein subunit, activating a signaling cascade that eventually leads to smooth muscle contraction and vasoconstriction. The resulting increase in systemic vascular resistance increases blood pressure.
Key Points
- V1 (Vasopressin) Receptors
- GPCR that responds to Vasopressin / ADH
- Activates a Gq subunit
- Locations
- Vascular smooth muscle
- Actions
- Vasoconstriction
- Think: vaso- = vessel, -pressin = constriction
- Increase in systemic vascular resistance increases blood pressure.
- Vasoconstriction
- GPCR that responds to Vasopressin / ADH