Long-term enhancement of REM sleep by the pituitary adenylyl cyclase-activating polypeptide (PACAP) in the pontine reticular formation of the rat
Ahnaou, A. ; Basille, M. ; Gonzalez, B. ; Vaudry, H. ; Hamon, M. ; Adrien, J. ; Bourgin, P.
Oxford, UK : Blackwell Science Ltd
Published 1999
Oxford, UK : Blackwell Science Ltd
Published 1999
ISSN: |
1460-9568
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Source: |
Blackwell Publishing Journal Backfiles 1879-2005
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Topics: |
Medicine
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Notes: |
In rats, rapid eye movement (REM) sleep can be elicited by microinjection of vasoactive intestinal polypeptide (VIP) into the oral pontine reticular nucleus (PnO). In the present study, we investigated whether this area could also be a REM-promoting target for a peptide closely related to VIP: the pituitary adenylyl cyclase-activating polypeptide (PACAP). When administered into the posterior part of the PnO, but not in nearby areas, of freely moving chronically implanted rats, PACAP-27 and PACAP-38 (0.3 and 3 pmol) induced a marked enhancement (60–85% over baseline) of REM sleep for 8 h that could be prevented by prior infusion of the antagonist PACAP-(6–27) (3 pmol) into the same site. Moreover, injections of PACAP into the centre of the posterior PnO resulted in REM sleep enhancement which could last for up to 11 consecutive days. Quantitative autoradiography using [125I]PACAP-27 revealed the presence in the PnO of specific binding sites with high affinity for PACAP-27 and PACAP-38 (IC50 = 2.4 and 3.2 nm, respectively), but very low affinity for VIP (IC50 〉 1 μm). These data suggest that PACAP within the PnO may play a key role in REM sleep regulation, and provide evidence for long-term (several days) mechanisms involved in such a control. PAC1 receptors which have a much higher affinity for PACAP than for VIP might mediate this long-term action of PACAP on REM sleep.
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Type of Medium: |
Electronic Resource
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URL: |
_version_ | 1798290159905538049 |
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autor | Ahnaou, A. Basille, M. Gonzalez, B. Vaudry, H. Hamon, M. Adrien, J. Bourgin, P. |
autorsonst | Vaudry, H. Hamon, M. Adrien, J. Bourgin, P. |
book_url | http://dx.doi.org/10.1046/j.1460-9568.1999.00811.x |
datenlieferant | nat_lic_papers |
hauptsatz | hsatz_simple |
identnr | NLZ242446876 |
insertion_date | 2012-04-27 |
issn | 1460-9568 |
journal_name | European journal of neuroscience |
materialart | 1 |
notes | In rats, rapid eye movement (REM) sleep can be elicited by microinjection of vasoactive intestinal polypeptide (VIP) into the oral pontine reticular nucleus (PnO). In the present study, we investigated whether this area could also be a REM-promoting target for a peptide closely related to VIP: the pituitary adenylyl cyclase-activating polypeptide (PACAP). When administered into the posterior part of the PnO, but not in nearby areas, of freely moving chronically implanted rats, PACAP-27 and PACAP-38 (0.3 and 3 pmol) induced a marked enhancement (60–85% over baseline) of REM sleep for 8 h that could be prevented by prior infusion of the antagonist PACAP-(6–27) (3 pmol) into the same site. Moreover, injections of PACAP into the centre of the posterior PnO resulted in REM sleep enhancement which could last for up to 11 consecutive days. Quantitative autoradiography using [125I]PACAP-27 revealed the presence in the PnO of specific binding sites with high affinity for PACAP-27 and PACAP-38 (IC50 = 2.4 and 3.2 nm, respectively), but very low affinity for VIP (IC50 〉 1 μm). These data suggest that PACAP within the PnO may play a key role in REM sleep regulation, and provide evidence for long-term (several days) mechanisms involved in such a control. PAC1 receptors which have a much higher affinity for PACAP than for VIP might mediate this long-term action of PACAP on REM sleep. |
package_name | Blackwell Publishing |
publikationsjahr_anzeige | 1999 |
publikationsjahr_facette | 1999 |
publikationsjahr_intervall | 8004:1995-1999 |
publikationsjahr_sort | 1999 |
publikationsort | Oxford, UK |
publisher | Blackwell Science Ltd |
reference | 11 (1999), S. 0 |
search_space | articles |
shingle_author_1 | Ahnaou, A. Basille, M. Gonzalez, B. Vaudry, H. Hamon, M. Adrien, J. Bourgin, P. |
shingle_author_2 | Ahnaou, A. Basille, M. Gonzalez, B. Vaudry, H. Hamon, M. Adrien, J. Bourgin, P. |
shingle_author_3 | Ahnaou, A. Basille, M. Gonzalez, B. Vaudry, H. Hamon, M. Adrien, J. Bourgin, P. |
shingle_author_4 | Ahnaou, A. Basille, M. Gonzalez, B. Vaudry, H. Hamon, M. Adrien, J. Bourgin, P. |
shingle_catch_all_1 | Ahnaou, A. Basille, M. Gonzalez, B. Vaudry, H. Hamon, M. Adrien, J. Bourgin, P. Long-term enhancement of REM sleep by the pituitary adenylyl cyclase-activating polypeptide (PACAP) in the pontine reticular formation of the rat Blackwell Science Ltd In rats, rapid eye movement (REM) sleep can be elicited by microinjection of vasoactive intestinal polypeptide (VIP) into the oral pontine reticular nucleus (PnO). In the present study, we investigated whether this area could also be a REM-promoting target for a peptide closely related to VIP: the pituitary adenylyl cyclase-activating polypeptide (PACAP). When administered into the posterior part of the PnO, but not in nearby areas, of freely moving chronically implanted rats, PACAP-27 and PACAP-38 (0.3 and 3 pmol) induced a marked enhancement (60–85% over baseline) of REM sleep for 8 h that could be prevented by prior infusion of the antagonist PACAP-(6–27) (3 pmol) into the same site. Moreover, injections of PACAP into the centre of the posterior PnO resulted in REM sleep enhancement which could last for up to 11 consecutive days. Quantitative autoradiography using [125I]PACAP-27 revealed the presence in the PnO of specific binding sites with high affinity for PACAP-27 and PACAP-38 (IC50 = 2.4 and 3.2 nm, respectively), but very low affinity for VIP (IC50 〉 1 μm). These data suggest that PACAP within the PnO may play a key role in REM sleep regulation, and provide evidence for long-term (several days) mechanisms involved in such a control. PAC1 receptors which have a much higher affinity for PACAP than for VIP might mediate this long-term action of PACAP on REM sleep. 1460-9568 14609568 |
shingle_catch_all_2 | Ahnaou, A. Basille, M. Gonzalez, B. Vaudry, H. Hamon, M. Adrien, J. Bourgin, P. Long-term enhancement of REM sleep by the pituitary adenylyl cyclase-activating polypeptide (PACAP) in the pontine reticular formation of the rat Blackwell Science Ltd In rats, rapid eye movement (REM) sleep can be elicited by microinjection of vasoactive intestinal polypeptide (VIP) into the oral pontine reticular nucleus (PnO). In the present study, we investigated whether this area could also be a REM-promoting target for a peptide closely related to VIP: the pituitary adenylyl cyclase-activating polypeptide (PACAP). When administered into the posterior part of the PnO, but not in nearby areas, of freely moving chronically implanted rats, PACAP-27 and PACAP-38 (0.3 and 3 pmol) induced a marked enhancement (60–85% over baseline) of REM sleep for 8 h that could be prevented by prior infusion of the antagonist PACAP-(6–27) (3 pmol) into the same site. Moreover, injections of PACAP into the centre of the posterior PnO resulted in REM sleep enhancement which could last for up to 11 consecutive days. Quantitative autoradiography using [125I]PACAP-27 revealed the presence in the PnO of specific binding sites with high affinity for PACAP-27 and PACAP-38 (IC50 = 2.4 and 3.2 nm, respectively), but very low affinity for VIP (IC50 〉 1 μm). These data suggest that PACAP within the PnO may play a key role in REM sleep regulation, and provide evidence for long-term (several days) mechanisms involved in such a control. PAC1 receptors which have a much higher affinity for PACAP than for VIP might mediate this long-term action of PACAP on REM sleep. 1460-9568 14609568 |
shingle_catch_all_3 | Ahnaou, A. Basille, M. Gonzalez, B. Vaudry, H. Hamon, M. Adrien, J. Bourgin, P. Long-term enhancement of REM sleep by the pituitary adenylyl cyclase-activating polypeptide (PACAP) in the pontine reticular formation of the rat Blackwell Science Ltd In rats, rapid eye movement (REM) sleep can be elicited by microinjection of vasoactive intestinal polypeptide (VIP) into the oral pontine reticular nucleus (PnO). In the present study, we investigated whether this area could also be a REM-promoting target for a peptide closely related to VIP: the pituitary adenylyl cyclase-activating polypeptide (PACAP). When administered into the posterior part of the PnO, but not in nearby areas, of freely moving chronically implanted rats, PACAP-27 and PACAP-38 (0.3 and 3 pmol) induced a marked enhancement (60–85% over baseline) of REM sleep for 8 h that could be prevented by prior infusion of the antagonist PACAP-(6–27) (3 pmol) into the same site. Moreover, injections of PACAP into the centre of the posterior PnO resulted in REM sleep enhancement which could last for up to 11 consecutive days. Quantitative autoradiography using [125I]PACAP-27 revealed the presence in the PnO of specific binding sites with high affinity for PACAP-27 and PACAP-38 (IC50 = 2.4 and 3.2 nm, respectively), but very low affinity for VIP (IC50 〉 1 μm). These data suggest that PACAP within the PnO may play a key role in REM sleep regulation, and provide evidence for long-term (several days) mechanisms involved in such a control. PAC1 receptors which have a much higher affinity for PACAP than for VIP might mediate this long-term action of PACAP on REM sleep. 1460-9568 14609568 |
shingle_catch_all_4 | Ahnaou, A. Basille, M. Gonzalez, B. Vaudry, H. Hamon, M. Adrien, J. Bourgin, P. Long-term enhancement of REM sleep by the pituitary adenylyl cyclase-activating polypeptide (PACAP) in the pontine reticular formation of the rat Blackwell Science Ltd In rats, rapid eye movement (REM) sleep can be elicited by microinjection of vasoactive intestinal polypeptide (VIP) into the oral pontine reticular nucleus (PnO). In the present study, we investigated whether this area could also be a REM-promoting target for a peptide closely related to VIP: the pituitary adenylyl cyclase-activating polypeptide (PACAP). When administered into the posterior part of the PnO, but not in nearby areas, of freely moving chronically implanted rats, PACAP-27 and PACAP-38 (0.3 and 3 pmol) induced a marked enhancement (60–85% over baseline) of REM sleep for 8 h that could be prevented by prior infusion of the antagonist PACAP-(6–27) (3 pmol) into the same site. Moreover, injections of PACAP into the centre of the posterior PnO resulted in REM sleep enhancement which could last for up to 11 consecutive days. Quantitative autoradiography using [125I]PACAP-27 revealed the presence in the PnO of specific binding sites with high affinity for PACAP-27 and PACAP-38 (IC50 = 2.4 and 3.2 nm, respectively), but very low affinity for VIP (IC50 〉 1 μm). These data suggest that PACAP within the PnO may play a key role in REM sleep regulation, and provide evidence for long-term (several days) mechanisms involved in such a control. PAC1 receptors which have a much higher affinity for PACAP than for VIP might mediate this long-term action of PACAP on REM sleep. 1460-9568 14609568 |
shingle_title_1 | Long-term enhancement of REM sleep by the pituitary adenylyl cyclase-activating polypeptide (PACAP) in the pontine reticular formation of the rat |
shingle_title_2 | Long-term enhancement of REM sleep by the pituitary adenylyl cyclase-activating polypeptide (PACAP) in the pontine reticular formation of the rat |
shingle_title_3 | Long-term enhancement of REM sleep by the pituitary adenylyl cyclase-activating polypeptide (PACAP) in the pontine reticular formation of the rat |
shingle_title_4 | Long-term enhancement of REM sleep by the pituitary adenylyl cyclase-activating polypeptide (PACAP) in the pontine reticular formation of the rat |
sigel_instance_filter | dkfz geomar wilbert ipn albert |
source_archive | Blackwell Publishing Journal Backfiles 1879-2005 |
timestamp | 2024-05-06T08:12:17.930Z |
titel | Long-term enhancement of REM sleep by the pituitary adenylyl cyclase-activating polypeptide (PACAP) in the pontine reticular formation of the rat |
titel_suche | Long-term enhancement of REM sleep by the pituitary adenylyl cyclase-activating polypeptide (PACAP) in the pontine reticular formation of the rat |
topic | WW-YZ |
uid | nat_lic_papers_NLZ242446876 |