VIP
peptideevidence: observational · v1.0.0Vasoactive intestinal peptide discussed in CIRS/neuroinflammation contexts.
Neuro-immune and inflammatory signaling.
In plain terms, VIP tells blood vessels and smooth muscle to relax and tells parts of the immune system to calm down. That is why it widens airways and blood vessels and lowers some inflammatory signals.
Technically, VIP binds two receptors called VPAC1 and VPAC2. These are G-protein-coupled receptors that raise cyclic AMP inside cells, which drives the muscle-relaxing and anti-inflammatory effects. VIP also acts in the brain's master clock (the suprachiasmatic nucleus), which links it to circadian timing.
Targets: VPAC1 and VPAC2 receptors (cAMP signaling). Reported actions: vasodilation, smooth-muscle relaxation, immune modulation. Main limitation: human outcome evidence is thin for most marketed uses. [Source: Peptide Dosing Protocols]
VIP helps relax blood vessels and smooth muscles, reducing inflammation and calming the immune system.
- People with pancreatitis history or elevated lipase
- People with low blood pressure
- People with active cancer should discuss first
- Pregnant or breastfeeding people (safety not established)
- Dizziness or lightheadedness
- Loose stools
- Mild headache
- Flushing
- Lipase before starting and during use
- Lipase rechecked after the first dose, about two weeks in, and after any increase
- The effect that matters most for safety monitoring is the pancreas.
- VIP has a very short biological half-life, which is why divided daily dosing is common.
Provider-only reference. This page does not constitute medical advice, a recommendation, or dosing guidance.