VIP (Vasoactive Intestinal Peptide)
VIP (Vasoactive Intestinal Peptide) — neuropeptide with potent anti-inflammatory, bronchodilatory, and gut motility effects used in chronic inflammatory and autonomic conditions.
- Potent anti-inflammatory — suppresses NF-kB and reduces Th1/Th17 inflammatory cytokines
- Bronchodilatory — relaxes airway smooth muscle and reduces neurogenic inflammation
- Gut motility support — relaxes smooth muscle for peristalsis regulation
- Neuroprotective — reduces neuroinflammation in CNS tissue
- Immune tolerance induction — promotes regulatory T-cells and reduces autoimmune activity
Dosage Calculator
Reference dosing by experience level. For research use only — always consult a licensed healthcare provider.
⚠ For research reference only. VIP (Vasoactive Intestinal Peptide) is not approved for human use. Always consult a qualified healthcare professional.
What's in the Box
Every Poptides order arrives in premium packaging, ready to use.
VIP (Vasoactive Intestinal Peptide) Vial
Your selected amount of lyophilized VIP (Vasoactive Intestinal Peptide) in a sealed, sterile glass vial with silver crimp cap. COA included on request.
BAC Water 3mL
Bacteriostatic water for reconstitution, included with every injectable peptide order. Maintains sterility for multi-dose use.
Syringe Kit
5 × insulin syringes with orange caps, individually sealed, in a dedicated Poptides-branded box.
Research Guide Card + Thank You Note
A QR code card linking to your product's research guide, plus a personal thank you note from the Poptides team.
Discreet Outer Packaging
All orders ship in plain, unmarked outer packaging with no reference to Poptides on the exterior.
How VIP (Vasoactive Intestinal Peptide) Works
The mechanism of action, step by step.
NF-kB Suppression
VIP binds VPAC1 and VPAC2 receptors on immune cells, activating adenylyl cyclase and elevating cAMP. Elevated cAMP activates PKA, which phosphorylates and inhibits NF-kB — the master transcription factor for pro-inflammatory cytokine production. This downstream cascade produces broad anti-inflammatory effects across multiple cell types.
Regulatory T-Cell Induction
VIP promotes the differentiation of naive T-cells toward the regulatory T-cell (Treg) phenotype while simultaneously suppressing the differentiation of Th1 and Th17 effector T-cells. This immune-skewing toward tolerance is relevant in autoimmune conditions where Th1/Th17 activity drives tissue destruction.
Airway Smooth Muscle Relaxation
VIP acts as a non-adrenergic non-cholinergic (NANC) bronchodilator via VPAC2 receptor activation on airway smooth muscle cells. Elevated cAMP relaxes smooth muscle via protein kinase A-dependent mechanisms, widening airways independent of beta-adrenergic pathways — making it relevant in beta-agonist-refractory airway conditions.
Neuroprotective Anti-Neuroinflammation
VIP is naturally produced by neurons and reduces glial-derived neuroinflammation. VPAC2 receptor activation on microglia suppresses IL-6, TNF-alpha, and nitric oxide production in the CNS, protecting neurons from inflammatory injury. This mechanism is studied in Parkinson's disease, ALS, and multiple sclerosis research.
Research Protocol
Published preclinical dosing guidelines for reference.
The Science Behind It
Peer-reviewed research supporting the mechanism of VIP (Vasoactive Intestinal Peptide).
VIP suppresses NF-kB and produces immunological tolerance in autoimmune models
VIP treatment significantly reduced collagen-induced arthritis severity in murine models, associated with decreased Th1/Th17 cytokines (IFN-gamma, IL-17), increased Treg populations, and inhibition of synovial NF-kB activation — establishing its immunomodulatory mechanism in autoimmune inflammation.
Journal of Immunology, 2004Inhaled VIP for pulmonary arterial hypertension — phase 2 trial
Inhaled VIP in patients with pulmonary arterial hypertension significantly improved pulmonary vascular resistance, 6-minute walk distance, and dyspnoea scores compared to placebo, with a mechanism involving pulmonary vasodilation and anti-remodelling inflammatory suppression.
Annals of Internal Medicine, 2004VIP as neuroprotective agent in neuroinflammation models
VIP administration significantly reduced microglial activation, suppressed pro-inflammatory cytokine production, and protected dopaminergic neurons from LPS-induced death in an in vivo neuroinflammation model — establishing its CNS anti-inflammatory mechanism relevant to neurodegenerative disease.
Journal of Neuroinflammation, 2009Customer Reviews
Verified purchases from Canadian customers.
Changed my autoimmune inflammatory baseline
Running VIP alongside BPC-157 for 3 months. CRP dropped from 4.1 to 0.8. My rheumatologist commented on the improvement in my inflammatory markers without changing my disease-modifying drugs. Remarkable compound.
CIRS protocol — meaningful improvement
Using VIP intranasal as part of a Shoemaker CIRS protocol. Cognitive symptoms and fatigue that had been present for 2 years began improving at week 6. The inflammatory suppression mechanism is the right target for this condition.
Gut motility improvement was the first thing I noticed
Started VIP primarily for its anti-inflammatory properties. Within 2 weeks gut motility and IBS symptoms improved significantly. The smooth muscle relaxation effect on the GI tract is very real.
Frequently Asked Questions
VIP (Vasoactive Intestinal Peptide)