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Development of a New Enzyme-Linked Immunosorbent Assay (ELISA) for Measuring the Content of PACAP in Mammalian Tissue and Plasma
被引:1
|作者:
Obara, Elisabeth Anne Adanma
[1
]
Georg, Birgitte
[1
]
Hannibal, Jens
[1
]
机构:
[1] Univ Copenhagen, Bispebjerg & Frederiksberg Hosp, Fac Hlth Sci, Dept Clin Biochem, Nielsine Nielsens Vej 4, DK-2400 Copenhagen NV, Denmark
关键词:
PACAP;
ELISA;
assay validation;
migraine;
CYCLASE-ACTIVATING POLYPEPTIDE;
DIPEPTIDYL-PEPTIDASE-IV;
CENTRAL-NERVOUS-SYSTEM;
ADENYLATE-CYCLASE;
FUNCTIONAL EXPRESSION;
RAT;
MIGRAINE;
RECEPTOR;
BRAIN;
IMMUNOREACTIVITY;
D O I:
10.3390/ijms242015102
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Pituitary adenylate cyclase-activating polypeptide (PACAP) is a naturally occurring neuropeptide found in both the central and peripheral nervous systems of vertebrates. Recent studies have revealed the presence of PACAP and its corresponding receptors, namely, the pituitary adenylate cyclase-activating polypeptide type I receptor (PAC1R), vasoactive intestinal peptide receptor 1 (VIPR1), and vasoactive intestinal peptide receptor 2 (VIPR2), in various structures implicated in migraine pathophysiology, including sensory trigeminal neurons. Human studies have demonstrated that when infused, PACAP can cause dilation of cranial vessels and result in delayed migraine-like attacks. In light of this, we present a novel ELISA assay that has been validated for quantifying PACAP in tissue extracts and human plasma. Using two well characterized antibodies specifically targeting PACAP, we successfully developed a sandwich ELISA assay, capable of detecting and accurately quantifying PACAP without any cross-reactivity to closely related peptides. The quantification range was between 5.2 pmol/L and 400 pmol/L. The recovery in plasma ranged from 98.2% to 100%. The increasing evidence pointing to the crucial role of PACAP in migraine pathophysiology necessitates the availability of tools capable of detecting changes in the circulatory levels of PACAP and its potential application as a reliable biomarker.
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