VIP

Vasoactive Intestinal Peptide (VIP) is a multifunctional peptide with regenerative properties.

Not FDA Approved Emerging Research
Reviewed by Peptide Treatments Medical Advisory Board (Medical Advisory Board) 1 min read

VIP: At a Glance

VIP works by binding to specific receptors, promoting vasodilation and modulating immune responses.

  • Improves respiratory function
  • Enhances neuroprotection
  • Hypotension
Not FDA Approved Emerging Research

Research Summary

VIP is a 28-amino acid neuropeptide with broad physiological effects including immunomodulation, neuroprotection, and anti-inflammatory activities. Research demonstrates promising results in neurodegenerative diseases, inflammatory bowel disease, and respiratory conditions through VPAC1/VPAC2 receptor signaling.

What is VIP?

Vasoactive Intestinal Peptide (VIP) is a neuropeptide that was initially discovered in the gut but is now known to have widespread actions throughout the body. It is composed of 28 amino acids and is involved in numerous physiological processes, including vasodilation, immune regulation, and neurotransmission. VIP is considered a potential therapeutic agent in regenerative medicine due to its ability to modulate inflammatory responses and promote tissue repair.

Mechanism of Action

VIP exerts its effects by binding to specific receptors on cell surfaces, namely VPAC1 and VPAC2. When VIP binds to these receptors, it triggers a cascade of intracellular events that lead to the relaxation of smooth muscle, dilation of blood vessels, and modulation of the immune response. This neuropeptide has a significant role in the central nervous system and peripheral tissues, making it a promising candidate in various therapeutic applications.

Clinical Applications

VIP has shown potential in treating a variety of conditions due to its diverse biological activities. In regenerative medicine, VIP is being explored for its benefits in respiratory diseases such as chronic obstructive pulmonary disease (COPD) and asthma, where it helps improve lung function and reduce inflammation. Additionally, VIP’s neuroprotective properties are being studied for potential applications in neurodegenerative diseases like Alzheimer’s and Parkinson’s diseases. Its ability to modulate immune responses also makes it a candidate for treating chronic inflammatory conditions.

Safety & Side Effects

VIP is generally considered safe when used in controlled clinical settings. However, like any biologically active compound, it may have side effects. The most commonly reported side effect of VIP administration is hypotension, or low blood pressure, due to its vasodilatory effects. Therefore, monitoring and appropriate dosing are crucial when using VIP in therapeutic settings to minimize adverse effects and optimize its regenerative potential.

Related Conditions

References

  1. 1

    Overexpression of colonic VIP ameliorates cognitive function and barrier system damage caused by sevoflurane anesthesia and surgery in aged rats with fragile brain functions.

    Liao H, Wang X, Yang C, Wang Z, Liu X, et al.

    Experimental neurology 2025 study
  2. 2

    Increased Expression of the Neuropeptides PACAP/VIP in the Brain of Mice with CNS Targeted Production of IL-6 Is Mediated in Part by Trans-Signalling.

    Castorina A, Scheller J, Keay KA, Marzagalli R, Rose-John S, et al.

    International journal of molecular sciences 2024 study
  3. 3

    Differential Expression of PACAP/VIP Receptors in the Post-Mortem CNS White Matter of Multiple Sclerosis Donors.

    Jansen MI, Musumeci G, Castorina A

    International journal of molecular sciences 2024 study
  4. 4

    Targeting the PAC1 receptor mitigates degradation of myelin and synaptic markers and diminishes locomotor deficits in the cuprizone demyelination model.

    Jansen MI, Mahmood Y, Lee J, Broome ST, Waschek JA, et al.

    Journal of neurochemistry 2024 study
  5. 5

    Extracellular vesicles from primary human macrophages stimulated with VIP or PACAP mediate anti-SARS-CoV-2 activities in monocytes through NF-κB signaling pathway.

    Arteaga-Blanco LA, Temerozo JR, Tiné LPS, Dantas-Pereira L, Sacramento CQ, et al.

    Microbes and infection 2024 study
  6. 6

    The impact of exogenous vasoactive intestinal polypeptide on inflammatory responses and mRNA expression of tight junction genes in lambs fed a high-grain diet.

    Mia GK, Hawley E, Yusuf M, Amat S, Ward AK, et al.

    Journal of animal science 2024 study

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