Inhibition of stimulated cyclic AMP production by multiple neuropeptide Y receptors in the rat brainstem
(1997) In Neuroscience Letters 221(2-3). p.113-116- Abstract
Neuropeptide Y (NPY) has been shown to modulate blood pressure, heart rate and to inhibit the baroreceptor reflex at the level of nucleus tractus solitarius (NTS). The aim of this study was to examine effects of NPY and its related peptides on forskolin (1 microM)-stimulated cyclic AMP production in slices of the rat NTS. Each peptide was present at 0.3 microM. Pretreatment with NPY inhibited the stimulated increase in cyclic AMP levels in slices of rat NTS. Also [Pro34]NPY, an analog, which activates Y1, Y3 (and Y5) receptors inhibited the stimulated increase in cyclic AMP levels. However, pretreatment with the Y1 receptor-selective antagonist BIBP3226 (3 microM) did not affect the [Pro34]NPY-evoked inhibition of cyclic AMP levels. In... (More)
Neuropeptide Y (NPY) has been shown to modulate blood pressure, heart rate and to inhibit the baroreceptor reflex at the level of nucleus tractus solitarius (NTS). The aim of this study was to examine effects of NPY and its related peptides on forskolin (1 microM)-stimulated cyclic AMP production in slices of the rat NTS. Each peptide was present at 0.3 microM. Pretreatment with NPY inhibited the stimulated increase in cyclic AMP levels in slices of rat NTS. Also [Pro34]NPY, an analog, which activates Y1, Y3 (and Y5) receptors inhibited the stimulated increase in cyclic AMP levels. However, pretreatment with the Y1 receptor-selective antagonist BIBP3226 (3 microM) did not affect the [Pro34]NPY-evoked inhibition of cyclic AMP levels. In addition, [Leu31,Pro34]NPY, an Y1 (and PP1/Y4 and Y5) receptor agonist did not inhibit the stimulated increase in cyclic AMP production. Also the Y2 receptor-selective agonist C2-NPY inhibited the stimulated elevation of cyclic AMP levels, while peptide YY, which does not recognize Y3 receptors did not significantly affect the stimulated cyclic AMP production. In conclusion, it seems that Y2 and Y3 receptors are coupled to inhibition of adenylate cyclase activity in the rat NTS.
(Less)
- author
- Ny, L and Grundemar, L LU
- publishing date
- 1997-01-17
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Animals, Arginine/analogs & derivatives, Colforsin/pharmacology, Cyclic AMP/biosynthesis, Male, Neuropeptide Y/analogs & derivatives, Rats, Rats, Sprague-Dawley, Receptors, Neuropeptide Y/agonists, Solitary Nucleus/drug effects
- in
- Neuroscience Letters
- volume
- 221
- issue
- 2-3
- pages
- 113 - 116
- publisher
- Elsevier
- external identifiers
-
- pmid:9121677
- scopus:0343907285
- ISSN
- 0304-3940
- DOI
- 10.1016/s0304-3940(96)13302-4
- language
- English
- LU publication?
- no
- id
- 2e8adc94-02c9-48cd-9ab7-d28f5a288b04
- date added to LUP
- 2019-09-03 13:57:38
- date last changed
- 2024-01-01 18:33:59
@article{2e8adc94-02c9-48cd-9ab7-d28f5a288b04,
abstract = {{<p>Neuropeptide Y (NPY) has been shown to modulate blood pressure, heart rate and to inhibit the baroreceptor reflex at the level of nucleus tractus solitarius (NTS). The aim of this study was to examine effects of NPY and its related peptides on forskolin (1 microM)-stimulated cyclic AMP production in slices of the rat NTS. Each peptide was present at 0.3 microM. Pretreatment with NPY inhibited the stimulated increase in cyclic AMP levels in slices of rat NTS. Also [Pro34]NPY, an analog, which activates Y1, Y3 (and Y5) receptors inhibited the stimulated increase in cyclic AMP levels. However, pretreatment with the Y1 receptor-selective antagonist BIBP3226 (3 microM) did not affect the [Pro34]NPY-evoked inhibition of cyclic AMP levels. In addition, [Leu31,Pro34]NPY, an Y1 (and PP1/Y4 and Y5) receptor agonist did not inhibit the stimulated increase in cyclic AMP production. Also the Y2 receptor-selective agonist C2-NPY inhibited the stimulated elevation of cyclic AMP levels, while peptide YY, which does not recognize Y3 receptors did not significantly affect the stimulated cyclic AMP production. In conclusion, it seems that Y2 and Y3 receptors are coupled to inhibition of adenylate cyclase activity in the rat NTS.</p>}},
author = {{Ny, L and Grundemar, L}},
issn = {{0304-3940}},
keywords = {{Animals; Arginine/analogs & derivatives; Colforsin/pharmacology; Cyclic AMP/biosynthesis; Male; Neuropeptide Y/analogs & derivatives; Rats; Rats, Sprague-Dawley; Receptors, Neuropeptide Y/agonists; Solitary Nucleus/drug effects}},
language = {{eng}},
month = {{01}},
number = {{2-3}},
pages = {{113--116}},
publisher = {{Elsevier}},
series = {{Neuroscience Letters}},
title = {{Inhibition of stimulated cyclic AMP production by multiple neuropeptide Y receptors in the rat brainstem}},
url = {{http://dx.doi.org/10.1016/s0304-3940(96)13302-4}},
doi = {{10.1016/s0304-3940(96)13302-4}},
volume = {{221}},
year = {{1997}},
}