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PACAP Receptor Knockout and Transgenics: What Have We Learnt?

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Pituitary Adenylate Cyclase-Activating Polypeptide

Part of the book series: Endocrine Updates ((ENDO,volume 20))

Abstract

Since the discovery of PACAP, originally isolated from hypothalamus in 1989 (Miyata et al, 1989), numerous studies devoted to the expression of this peptide have clearly demonstrated that it is not restricted to hypothalamic level but it is also expressed in various other brain areas and peripheral tissues. Functional studies have also established that the role of PACAP is not restricted to activation of the hypothalamic-pituitary complex, but that PACAP serves additional functions in the brain and peripheral organs. Most of these studies, herein reported in the precedent chapters, have been conducted both in vitro by incubation of PACAP, VIP and related peptides on either tumoral cell lines, primary cell cultures, or isolated perfused organs; and in vivo by injection of PACAP, or by administration of antagonists or PACAP antibodies to block the peptide activity. These approaches had the advantage of being technically simple, reproducible and/or relatively fast but were limited to a cellular or tissular context and to application of exogenous drugs. Recently, an alternative more appropriate approach to studying the physiology of PACAP has been the generation of mouse strains deficient in PACAP type 1 receptor and overexpressing the VIP (vasoactive intestinal peptide)/PACAP type 2 receptor (VPAC2).

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Brabet, P., Jamen, F., Rodriguez-Henche, N., Bertrand, G., Bockaert, J. (2003). PACAP Receptor Knockout and Transgenics: What Have We Learnt?. In: Vaudry, H., Arimura, A. (eds) Pituitary Adenylate Cyclase-Activating Polypeptide. Endocrine Updates, vol 20. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-0243-2_15

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