VIP

Also known as: Vasoactive Intestinal Peptide

A neuropeptide with anti-inflammatory and tissue-protective properties.

Overview

Vasoactive Intestinal Peptide is a 28-amino acid neuropeptide with widespread tissue distribution. It acts as a neurotransmitter and neuromodulator with potent anti-inflammatory and cytoprotective effects.

Mechanism of Action

VIP binds VPAC1 and VPAC2 receptors, activating cAMP pathways. Inhibits pro-inflammatory cytokine production, promotes regulatory T cells, and has direct neuroprotective effects.

Pharmacokinetics

Very short half-life (1-2 minutes in plasma). Often administered intranasally or via sustained-release formulations.

Dosing Protocols

Note: These are research protocols from literature. This is not medical advice.

1

Intranasal

Dose

50 mcg

Frequency

4x daily

Duration

4-8 weeks

CIRS protocol

2

Subcutaneous

Dose

50-100 mcg

Frequency

Once daily

Duration

4 weeks

Systemic anti-inflammatory

Stacking Recommendations

Peptides that may be combined based on complementary mechanisms in research settings.

Rationale: Multi-system healing

Synergy: Neurological and GI support

Research Areas

Autoimmune DiseasesNeuroprotectionCIRS/Mold IllnessPulmonary Hypertension

Key Research Findings

  • 1Reduced inflammation in rheumatoid arthritis models
  • 2Neuroprotective in Parkinson's and Alzheimer's models
  • 3Benefits in chronic inflammatory response syndrome (CIRS)
  • 4Pulmonary vasodilator effects

Side Effects & Contraindications

Reported Side Effects

  • Nasal irritation
  • Flushing
  • Hypotension

Contraindications

  • Hypotension
  • Cardiac conduction abnormalities

Safety Considerations

Generally well-tolerated. Hypotension possible with higher doses due to vasodilatory effects.

Storage Requirements

Store at 2-8C. Protect from light.

Scientific References

Quick Reference

Sequence
HSDAVFTDNYTRLRKQMAVKKYLNSILN
Molecular Weight
3326 g/mol
Half-Life
1-2 minutes
Bioavailability
Low oral; intranasal or injection preferred
Research Stage
clinical phase 2
Administration
Intranasal, subcutaneous, or intravenous