Drug intelligence / Profile preview

PACAP 6-38

Development stage
Preclinical
Modality
Peptides
Administration
Intrathecal, Intracerebroventricular, Intravenous, Topical
01

Overview

PACAP 6-38 is a truncated peptide fragment of the endogenous neuropeptide pituitary adenylate cyclase-activating polypeptide (PACAP-38), consisting of amino acid residues 6 through 38. It is widely utilized in pharmacological research as a potent and selective competitive antagonist of the **PAC1 receptor**, although it also exhibits antagonistic activity at the **VPAC2 receptor**. In preclinical studies, PACAP 6-38 is used to investigate the role of PACAP signaling in diverse physiological and pathological conditions, including chronic pain (such as neuropathic pain and Parkinson's disease-related hyperalgesia), stress-induced drug seeking, neuroinflammation, and learning and memory consolidation. Interestingly, it has also been identified as a functional antagonist for the **cocaine- and amphetamine-regulated transcript (CART) receptor**. While it is a critical tool in neuroscience and pharmacology research, it is currently employed as a research reagent rather than a clinical therapeutic asset.

Other names
pituitary adenylate cyclase-activating polypeptide 6-38PACAP(6-38)
02

Targets

VIPR2 (Vasoactive intestinal polypeptide receptor 2)ADCYAP1R1 (Pituitary adenylate cyclase-activating polypeptide receptor PAC1)VIPR1 (Vasoactive intestinal peptide receptor 1)

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