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VIP

Product information

$62.99

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VIP (5mg)

$ 62.99

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Product description

Vasoactive Intestinal Peptide (VIP) is a neuropeptide hormone composed of 28 amino acid residues. It is widely distributed in the central and peripheral nervous systems, as well as in the digestive, respiratory, reproductive, and cardiovascular systems. VIP exhibits a range of biological functions, including vasodilation, smooth muscle relaxation, secretion regulation, and immunomodulation. As a neurotransmitter and neuromodulator, VIP plays a crucial role in maintaining homeostasis and has shown potential therapeutic applications in various disorders, such as inflammatory diseases, neurodegenerative conditions, and cancer.

Product Usage: This product is intended solely for use as a research chemical in vitro and laboratory experimentation by licensed, qualified professionals. It is not approved for human or animal consumption. Misuse, misbranding, or mislabeling as a drug, food, or cosmetic is strictly prohibited. All information provided is for educational purposes only.

Table of Contents

  1. Characteristics
  2. How does VIP work?
  3. Benefits
  4. Side Effects
  5. Summary
  6. Certificate of Analysis (COA)
  7. References

Characteristics

Molecular Formula

C147H238N44O42S

CAS

137525-51-0

Molar Mass

773.895 g/mol

Amino Acid Sequence

His-Ser-Asp-Ala-Val-Phe-Thr-Asp-Asn-Tyr-Thr-Arg-Leu-Arg-Lys-Gln-Met-Ala-Val-Lys-Lys-Tyr-Leu-Asn-Ser-Ile-Leu-Asn

Synonyms

VIP, Vasoactive Intestinal Polypeptide, PHM27

Solubility

Soluble in Water

Organoleptic Profile

White powder

Composition

Lyophilized powder

How does VIP work?

VIP exerts its effects by binding to specific G protein-coupled receptors, namely VPAC1 and VPAC2. These receptors are expressed in various tissues, including the brain, lungs, intestines, and immune cells. Upon binding, VIP activates adenylate cyclase, leading to an increase in intracellular cyclic AMP (cAMP) levels. This, in turn, triggers a cascade of signaling events that regulate diverse physiological processes.

VIP's vasodilatory effects are mediated through the relaxation of smooth muscle cells in blood vessels, resulting in increased blood flow and reduced blood pressure. In the digestive system, VIP stimulates the secretion of water and electrolytes, promoting digestion and nutrient absorption. Additionally, VIP acts as a potent anti-inflammatory agent by inhibiting the production of pro-inflammatory cytokines and modulating the activity of immune cells, such as T lymphocytes and macrophages.

Benefits

  • Anti-inflammatory properties: VIP has demonstrated significant anti-inflammatory effects in various experimental models. It inhibits the production of pro-inflammatory cytokines, such as TNF-α, IL-6, and IL-12, while promoting the release of anti-inflammatory cytokines like IL-10. This makes VIP a promising candidate for the treatment of inflammatory disorders, including rheumatoid arthritis, inflammatory bowel disease, and sepsis.

  • Neuroprotection: VIP has shown neuroprotective properties in several studies. It protects neurons from oxidative stress, excitotoxicity, and apoptosis, which are common pathological processes in neurodegenerative diseases like Alzheimer's and Parkinson's. VIP also promotes neurogenesis, enhances synaptic plasticity, and improves cognitive function, suggesting its potential as a therapeutic agent for neurodegenerative disorders.

  • Immunomodulation: VIP plays a crucial role in regulating the immune system. It modulates the balance between T helper 1 (Th1) and T helper 2 (Th2) responses, favoring a shift towards the anti-inflammatory Th2 response. This immunomodulatory effect makes VIP a potential treatment for autoimmune diseases, such as multiple sclerosis and type 1 diabetes.

  • Cardiovascular protection: VIP's vasodilatory and anti-inflammatory properties contribute to its cardiovascular protective effects. It reduces blood pressure, improves endothelial function, and attenuates the development of atherosclerosis. VIP also exhibits cardioprotective effects in ischemia-reperfusion injury, reducing infarct size and preserving cardiac function.

  • Respiratory benefits: VIP has been shown to have bronchodilatory effects, making it a potential therapeutic target for respiratory disorders like asthma and chronic obstructive pulmonary disease (COPD). It relaxes airway smooth muscle, reduces airway inflammation, and promotes mucus secretion, improving overall respiratory function.

  • Gastrointestinal regulation: VIP is a key regulator of gastrointestinal function. It stimulates the secretion of water, electrolytes, and bicarbonate, promoting digestion and nutrient absorption. VIP also exhibits protective effects in gastrointestinal disorders, such as inflammatory bowel disease and colitis, by reducing inflammation and promoting mucosal healing.

Side Effects

While VIP has shown promising therapeutic potential, it is essential to consider potential side effects. Some reported side effects of VIP administration include:

  1. Hypotension: Due to its potent vasodilatory effects, VIP may cause a significant decrease in blood pressure, leading to dizziness, lightheadedness, or fainting.

  2. Gastrointestinal disturbances: VIP's effects on gastrointestinal secretion and motility may result in side effects such as diarrhea, abdominal cramps, and nausea.

  3. Flushing: Administration of VIP may cause flushing, a sudden redness of the skin, particularly on the face and neck.

  4. Headache: Some individuals may experience headaches following VIP administration, possibly due to its vasodilatory effects.

Summary

Vasoactive Intestinal Peptide (VIP) is a multifunctional neuropeptide with a wide range of biological effects, including vasodilation, smooth muscle relaxation, secretion regulation, and immunomodulation. Its anti-inflammatory, neuroprotective, immunomodulatory, cardiovascular protective, respiratory, and gastrointestinal regulatory properties make it a promising therapeutic target for various disorders. However, potential side effects, such as hypotension, gastrointestinal disturbances, flushing, and headache, should be considered when exploring VIP as a treatment option.

References

  1. Moody TW, Hill JM, Jensen RT. VIP as a trophic factor in the CNS and cancer cells. Peptides. 2003 Jan;24(1):163-77. doi: 10.1016/s0196-9781(02)00290-5. PMID: 12576099.

  2. Gozes I, Brenneman DE. VIP: molecular biology and neurobiological function. Mol Neurobiol. 1989 Winter;3(4):201-36. doi: 10.1007/BF02740606. PMID: 2698176.

  3. Bellinger DL, Lorton D, Brouxhon S, Felten S, Felten DL. The significance of vasoactive intestinal polypeptide (VIP) in immunomodulation. Adv Neuroimmunol. 1996;6(1):5-27. doi: 10.1016/s0960-5428(96)00008-3. PMID: 8790778.

  4. Robert J Henning, Darrell R Sawmiller, Vasoactive intestinal peptide: cardiovascular effects, Cardiovascular Research, Volume 49, Issue 1, January 2001, Pages 27–37

  5. Delgado, M., Pozo, D. and Ganea, D., 2004. The significance of vasoactive intestinal peptide in immunomodulation. Pharmacological reviews, 56(2), pp.249-290.

  6. Fahrenkrug, J., 1993. Transmitter role of vasoactive intestinal peptide.

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