VIP
Vasoactive Intestinal Peptide (VIP) is a multifunctional peptide with regenerative properties.
VIP works by binding to specific receptors, promoting vasodilation and modulating immune responses.
- Improves respiratory function
- Enhances neuroprotection
VIP is not FDA approved and is available primarily for research purposes.
Emerging Research
Growing body of clinical evidence with promising results.
Important: Always consult with a qualified healthcare provider before starting any treatment. This information is for educational purposes only and should not be considered medical advice.
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.
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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.
VIP Research References
- 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.
PubMedStudy2025PMID: 40456433Liao H, Wang X, Yang C, Wang Z, Liu X, et al.
Experimental neurology
- 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.
PubMedStudy2024PMID: 39273398Castorina A, Scheller J, Keay KA, Marzagalli R, Rose-John S,...
International journal of molecular sciences
- 3
Differential Expression of PACAP/VIP Receptors in the Post-Mortem CNS White Matter of Multiple Sclerosis Donors.
PubMedStudy2024PMID: 39201536Jansen MI, Musumeci G, Castorina A
International journal of molecular sciences
- 4
Targeting the PAC1 receptor mitigates degradation of myelin and synaptic markers and diminishes locomotor deficits in the cuprizone demyelination model.
PubMedStudy2024PMID: 39115025Jansen MI, Mahmood Y, Lee J, Broome ST, Waschek JA, et al.
Journal of neurochemistry
- 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.
PubMedStudy2024PMID: 39069117Arteaga-Blanco LA, Temerozo JR, Tiné LPS, Dantas-Pereira L, ...
Microbes and infection
- 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.
PubMedStudy2024PMID: 39396104Mia GK, Hawley E, Yusuf M, Amat S, Ward AK, et al.
Journal of animal science
Click on any reference to view the full publication. References are listed in order of relevance.
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Medical Disclaimer
This content is for informational purposes only and does not constitute medical advice. Always consult with a qualified healthcare provider before starting any treatment, making changes to existing treatment, or making decisions about your health. Individual results may vary, and the information presented here should not replace professional medical judgment.