Deakin University

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The effects of neuropeptide Y and its fragments upon basal and electrically stimulated ion secretion in rat jejunum mucosa

journal contribution
posted on 1990-01-01, 00:00 authored by Helen CoxHelen Cox, A W Cuthbert
1. The effects of neuropeptide Y (NPY) and a range of C terminal fragments were investigated both on basal short circuit current (s.c.c.) and electrical field stimulated responses in voltage clamped preparations in rat jejunal mucosa. 2. Most of the NPY fragments tested had direct effects upon the mucosa, reducing baseline s.c.c. with EC50 values of 1 μM or more. NPY was 30 times more effective than any of the fragments tested and the order of potency was: NPY >> NPY (11-36) ≥ (12-36) ≥ (13-36) ≥ (14-36). NPY (15-36), (16-36), (20-36) and (22-36), were still less effective and complete concentration response curves could not be constructed. NPY (26-36), des amido NYP and the C-terminal flanking peptide or NPY (CPON) were all inactive and did not significantly alter responses to NPY. 3. Electrical field stimulation (EFS) of mucosal preparations elicited rapid transient secretory responses in the presence of hexamethonium and atropine. NPY and fragments attenuated these secretory responses and where concentration-response relationships could be compared at a given time point the following order of potency was obtained: NPY >> NPY (11-36) > NPY (13-36). Again NPY (26-36), des amido NPY and CPON were ineffective, while at single concentrations (300 nM) a graded attenuation of EFS responses was obtained with NPY (14-36) ≥ NPY (15-36) > NPY (16-36) ≥ NPY (20-36) > NPY (22-36). 4. The attenuation of EFS responses by the these peptides was not dependent upon the basal secretory state. Pretreatment of tissues with piroxicam reduced s.c. and attenuated further reductions in s.c.c. by NPY, but had no effect upon NPY-mediated inhibition of electrically-stimulated secretory responses. 5. NPY fragments attenuated both basal and EFS generated secretion. Since fragments are effective these receptors must, by definition be Y2-like NPY (11-36) and NPY (13-36) at 300 nM and 1 μM did not significantly attenuate secretory responses to either carbachol (CCh) or substance P (SP). A 1 μM concentration of either fragment was equivalent in effect to 30 nM NPY upon basal current, but NPY at this concentration significantly reduced both CCh- and SP-induced secretion. The reduced spectrum of fragment activity together with the different order and potency ratios obtained with these three peptides indicates a presynaptic action for NPY and the fragments.



British Journal of Pharmacology






247 - 252



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