VIP (Vasoactive Intestinal Peptide)
Overview
VIP, or vasoactive intestinal peptide, is a neuropeptide with broad signaling roles across the nervous, immune, and vascular systems. Its widespread receptor distribution and involvement in multiple physiological axes make it a well-studied tool compound in neuro-immune and neuroendocrine research.
In preclinical research, VIP has been studied for its interactions with the VPAC1 and VPAC2 receptors and downstream cAMP signaling, and for its modeled roles in immune-modulation, vasodilation, and circadian and neuroendocrine pathways. Investigators examining how a single neuropeptide coordinates across systems have used it as a research material to probe these mechanisms.
What makes VIP a useful catalog entry is the breadth of pathways in which it participates, from immune regulation to circadian signaling. Whether these mechanisms translate to female physiology remains an open research question; our evidence review tracks how many of the underlying studies included women.
Summary
VIP is an endogenous neuropeptide with broad roles in vasodilation, secretion, and immune regulation, studied extensively as a signaling molecule. Its synthetic therapeutic form (aviptadil) has been investigated in conditions such as ARDS and sarcoidosis with mixed results; human data are not analyzed for female-specific outcomes.
Evidence in women
Mechanism
Activates VPAC1/VPAC2 receptors to relax smooth muscle, stimulate secretion, and modulate immune and inflammatory signaling.
Free research guide
How to tell real female data from male-extrapolated claims, with the questions to ask about any compound.
Citations (PMID)
Related peptides
Educational information for laboratory and research use only. Not medical advice, a recommendation, or a claim of safety or efficacy; no personal dosing. “Unstudied” means no qualifying study was found, not that a compound is safe or unsafe.