VIP 6 MG - kit by
Peptide Hubs

VIP 6 MG

CLASSIFICATION: NEUROPEPTIDE / GASTROINTESTINAL MODULATOR
ACTIVE SUBSTANCE: VASOACTIVE INTESTINAL PEPTIDE (VIP)
FORM: LYOPHILIZED POWDER (2 ML VIAL x 6 MG)
ACTIVE HALF-LIFE: APPROX. 2–5 MINUTES (IN VIVO)
DOSAGE: 2–6 MG PER WEEK (RESEARCH USE ONLY)
ACNE: NO
WATER RETENTION: NO
HIGH BLOOD PRESSURE (HBP): NO
HEPATOTOXICITY: NONE
AROMATIZATION: NO
MANUFACTURER: PEPTIDE HUBS

Out of stock

VIP 6 MG Detailed

VIP 6 mg – Vasoactive Intestinal Peptide for Inflammation & Neuroimmune Research

VIP (Vasoactive Intestinal Peptide) is a 28-amino acid neuropeptide naturally produced in the gut, brain, and immune tissues. It is involved in a wide range of physiological processes, including smooth muscle relaxation, immune modulation, gastrointestinal function, and circadian rhythm regulation. This 6 mg (2 mL) vial by Peptide Hubs is a high-purity peptide formulation intended for research use only.

What Is Vasoactive Intestinal Peptide (VIP)?

VIP is a pleiotropic signaling molecule with potent anti-inflammatory and immunomodulatory properties. It plays a critical role in regulating the enteric nervous system, pulmonary function, cardiovascular tone, and neuroprotection. According to published data on PubMed, VIP has been shown to suppress pro-inflammatory cytokines while enhancing regulatory T-cell activity, making it an attractive compound for inflammatory and autoimmune research.

Key Research Applications

  • Gut-brain axis signaling and motility regulation
  • Anti-inflammatory and immunomodulatory models
  • Research into pulmonary hypertension and asthma
  • Neuroprotective peptide in CNS and neurodegenerative models
  • Autoimmune disease and systemic inflammation studies

Suggested Dosage in Research

Typical preclinical studies use VIP at 2–6 mg per week, divided into subcutaneous or intravenous injections. Due to its short half-life in vivo, some research protocols utilize stabilized formulations or frequent dosing. VIP is not bioavailable orally and should be handled with sterile technique under lab-controlled conditions.

Synergistic Peptides for Research Stacking

Researchers commonly combine VIP with other anti-inflammatory or neuroactive peptides for synergistic benefit:

  • BPC-157 – for GI tract healing and gut-brain axis studies
  • Selank – supports neuroimmune balance and stress regulation
  • GHK-Cu – for regenerative and anti-inflammatory synergy
  • SS-31 – mitochondrial protection and oxidative stress modulation
  • Thymalin – systemic immune normalization in aging and chronic disease models

Safety Profile

VIP has demonstrated a favorable safety profile in early human trials and preclinical models. It does not affect sex hormones or metabolic functions and shows no evidence of toxicity to liver, kidney, or cardiovascular systems. Because of its short half-life, dosing protocols may require precision timing or peptide stabilization methods.

USA Domestic Shipping & Quality Control

Peptide Hubs provides fast and discreet USA domestic shipping for VIP 6 mg and all peptide research products. Every vial is manufactured in GMP-compliant labs and batch-tested for purity and sterility. VIP is a high-value research tool for gastrointestinal, neurological, and immune applications.

Frequently Asked Questions

What is VIP used for in research?

VIP is used in research focused on neuroimmune signaling, inflammation control, pulmonary health, and gastrointestinal motility.

Is VIP a hormone or a neurotransmitter?

VIP acts as both a neurotransmitter and hormone-like peptide, involved in smooth muscle relaxation, immune signaling, and circadian rhythm regulation.

Can VIP be stacked with other research peptides?

Yes, VIP is often stacked with BPC-157, Selank, or SS-31 for advanced gut-brain axis, anti-inflammatory, and neuroprotective research.

Is VIP safe in preclinical models?

VIP has shown good tolerability in early-phase research with no known toxicity in preclinical models. It is research-use only and not approved for therapeutic use.

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