REGULATORYRFK Jr.: 14 peptides returning to Category 1 — FDA advisory committee July 2026TRENDINGHexarelin: ↑↑ Surging ��� Trends score 100 as of May 2026UPDATESemaglutide and tirzepatide compounding ended — shortage resolved Feb/May 2025REGULATORYBPC-157, TB-500, thymosin alpha-1, CJC-1295, ipamorelin: expected Category 1 reclassification pendingEVENTpep-talk con ��� First US Peptide Convention · August 2026 · Anaheim CAFDAFDA advisory committee meetings scheduled: late July 2026REGULATORYRFK Jr.: 14 peptides returning to Category 1 — FDA advisory committee July 2026TRENDINGHexarelin: ↑↑ Surging ��� Trends score 100 as of May 2026UPDATESemaglutide and tirzepatide compounding ended — shortage resolved Feb/May 2025REGULATORYBPC-157, TB-500, thymosin alpha-1, CJC-1295, ipamorelin: expected Category 1 reclassification pendingEVENTpep-talk con ��� First US Peptide Convention · August 2026 · Anaheim CAFDAFDA advisory committee meetings scheduled: late July 2026

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Peptide Library

VIP

Vasoactive Intestinal Peptide / Aviptadil

Cognitive & Neuro

Vasoactive Intestinal Peptide (VIP) is a 28-amino acid neuropeptide originally isolated from porcine intestinal tissue that functions as a potent vasodilator, immunomodulator, and neurotransmitter throughout the body. It has gained significant research attention for its potential role in treating Chronic Inflammatory Response Syndrome (CIRS) associated with mold illness, as well as pulmonary arterial hypertension. VIP is typically administered via nasal inhalation in clinical research settings, though injectable forms also exist.

Mechanism of Action

Endogenous 28-amino-acid neuropeptide with broad physiological roles. Potent vasodilator, bronchodilator, and immunomodulator. Promotes neuronal survival, regulates circadian rhythm via SCN, inhibits NF-kB-mediated inflammation, and modulates gut-brain axis signaling.

Research Protocols

For research purposes only. Not medical advice.

Research protocols use 50-200mcg intranasally 1-3 times daily. IV research doses used in ARDS studies were 100-300pmol/kg/min. Subcutaneous protocols not well-established due to rapid degradation.

Research Notes

Clinical Research Status

VIP has been studied extensively in the context of CIRS by Dr. Ritchie Shoemaker and others, with intranasal administration showing improvements in inflammatory markers and pulmonary artery pressures. Research in pulmonary hypertension has demonstrated VIP's ability to reduce pulmonary vascular resistance and improve exercise capacity in small clinical trials. It is not FDA-approved for any indication, and its use remains investigational with ongoing debate about optimal dosing protocols.

Key Published Findings

Studies demonstrate VIP's ability to downregulate inflammatory cytokines including TGF-beta, MMP-9, and complement split products C3a and C4a in CIRS patients. In pulmonary hypertension models, VIP reduces right ventricular systolic pressure and pulmonary vascular remodeling through cAMP-mediated smooth muscle relaxation. Neuroprotective properties have been documented in models of Parkinson's disease and Alzheimer's disease through anti-inflammatory and anti-apoptotic mechanisms.

Safety Profile

VIP is generally well-tolerated at therapeutic doses, with the most common side effects being nasal congestion, flushing, and transient hypotension due to its vasodilatory properties. Diarrhea and abdominal cramping may occur at higher doses, reflecting its original physiological role in gut motility regulation. Caution is warranted in patients with existing hypotension or those on antihypertensive medications due to additive blood pressure lowering effects.

Comparison to Related Compounds

VIP belongs to the secretin/glucagon superfamily and shares structural homology with PACAP (Pituitary Adenylate Cyclase-Activating Polypeptide), though VIP has greater selectivity for VPAC1 and VPAC2 receptors. Unlike synthetic vasodilators, VIP provides combined anti-inflammatory and vasodilatory effects through a single molecular pathway. Compared to other CIRS treatments in the Shoemaker protocol, VIP is typically used as a final-step intervention after other markers have been normalized.

Community Observations

Patients using VIP for CIRS report improvements in fatigue, cognitive function, and respiratory symptoms, often describing it as the final piece in their recovery protocol. Sourcing pharmaceutical-grade VIP remains challenging, and proper cold-chain storage is critical for maintaining peptide stability. Some users report rebound symptoms upon discontinuation, suggesting the need for gradual tapering or ongoing maintenance dosing.

Half-Life

~1-2 minutes (IV); ~30 min (intranasal)

Reconstitution

Sterile saline for IV; saline for nasal spray

Storage

Lyophilized

Store at -20C. Extremely sensitive to degradation.

Reconstituted

Prepare fresh. Use within hours of reconstitution.

US Legal Status

Research chemical (in clinical trials for ARDS)

Also Known As

Vasoactive Intestinal PeptideAviptadil

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