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- Publisher Website: 10.1002/cne.903600108
- Scopus: eid_2-s2.0-0028840333
- PMID: 7499557
- WOS: WOS:A1995RT21200007
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Article: Time-course of neuropeptide changes in peri-ischemic zone and amygdala following focal ischemia in rats
Title | Time-course of neuropeptide changes in peri-ischemic zone and amygdala following focal ischemia in rats |
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Authors | |
Keywords | dynorphin insular cortex leucine‐enkephalin neuropeptide Y neurotensin |
Issue Date | 1995 |
Publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/31248 |
Citation | Journal Of Comparative Neurology, 1995, v. 360 n. 1, p. 101-120 How to Cite? |
Abstract | Previously, using a middle cerebral artery occlusion model in Wistar rat, we showed autonomic disturbances similar to those seen clinically and observed striking neurochemical changes in cortical and subcortical sites at 5 days following stroke. The neurochemical changes may account for functional recovery and/or autonomic disturbances after focal ischemia. To understand the possible mechanisms and to facilitate future studies, it is necessary to define the time-courses of these changes. Using immunohistochemical staining with the peroxidase-antiperoxidase reaction, the changes in several neuropeptides over the peri-ischemic region and the ipsilateral central and basolateral nucleus of the amygdala were investigated at different times after middle cerebral artery occlusion. In the experimental group, neuropeptide Y immunoreactivity appeared to increase by 6 hours in the peri- ischemic region. Using image analysis to quantify the staining intensity, the change became statistically significant at 1 day, peaked around 3 days, and subsided at 10 days. There was a delayed increase in neuropeptide Y in the ipsilateral basolateral nucleus of the amygdala with a peak around 3 days. Immunoreactive staining for leucine-enkephalin, dynorphin, and neurotensin demonstrated an increase that was localized to the ipsilateral central nucleus of the amygdala with a peak around 3 days and a return to baseline levels by 10 days. The results support a specific time-course for each of the neuropeptides studied and indicate that a survival time of 3 days after focal ischemia is the critical period for examining the relationship between neuropeptide responses and neuronal or functional recovery. |
Persistent Identifier | http://hdl.handle.net/10722/162066 |
ISSN | 2023 Impact Factor: 2.3 2023 SCImago Journal Rankings: 1.218 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Cheung, RTF | en_US |
dc.contributor.author | Diab, T | en_US |
dc.contributor.author | Cechetto, DF | en_US |
dc.date.accessioned | 2012-09-05T05:17:01Z | - |
dc.date.available | 2012-09-05T05:17:01Z | - |
dc.date.issued | 1995 | en_US |
dc.identifier.citation | Journal Of Comparative Neurology, 1995, v. 360 n. 1, p. 101-120 | en_US |
dc.identifier.issn | 0021-9967 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/162066 | - |
dc.description.abstract | Previously, using a middle cerebral artery occlusion model in Wistar rat, we showed autonomic disturbances similar to those seen clinically and observed striking neurochemical changes in cortical and subcortical sites at 5 days following stroke. The neurochemical changes may account for functional recovery and/or autonomic disturbances after focal ischemia. To understand the possible mechanisms and to facilitate future studies, it is necessary to define the time-courses of these changes. Using immunohistochemical staining with the peroxidase-antiperoxidase reaction, the changes in several neuropeptides over the peri-ischemic region and the ipsilateral central and basolateral nucleus of the amygdala were investigated at different times after middle cerebral artery occlusion. In the experimental group, neuropeptide Y immunoreactivity appeared to increase by 6 hours in the peri- ischemic region. Using image analysis to quantify the staining intensity, the change became statistically significant at 1 day, peaked around 3 days, and subsided at 10 days. There was a delayed increase in neuropeptide Y in the ipsilateral basolateral nucleus of the amygdala with a peak around 3 days. Immunoreactive staining for leucine-enkephalin, dynorphin, and neurotensin demonstrated an increase that was localized to the ipsilateral central nucleus of the amygdala with a peak around 3 days and a return to baseline levels by 10 days. The results support a specific time-course for each of the neuropeptides studied and indicate that a survival time of 3 days after focal ischemia is the critical period for examining the relationship between neuropeptide responses and neuronal or functional recovery. | en_US |
dc.language | eng | en_US |
dc.publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/31248 | en_US |
dc.relation.ispartof | Journal of Comparative Neurology | en_US |
dc.subject | dynorphin | - |
dc.subject | insular cortex | - |
dc.subject | leucine‐enkephalin | - |
dc.subject | neuropeptide Y | - |
dc.subject | neurotensin | - |
dc.subject.mesh | Amygdala - Blood Supply - Metabolism | en_US |
dc.subject.mesh | Animals | en_US |
dc.subject.mesh | Cerebral Cortex - Metabolism | en_US |
dc.subject.mesh | Dynorphins - Metabolism | en_US |
dc.subject.mesh | Enkephalin, Leucine - Metabolism | en_US |
dc.subject.mesh | Ischemic Attack, Transient - Metabolism | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Neuropeptide Y - Metabolism | en_US |
dc.subject.mesh | Neuropeptides - Metabolism | en_US |
dc.subject.mesh | Neurotensin - Metabolism | en_US |
dc.subject.mesh | Rats | en_US |
dc.subject.mesh | Rats, Wistar | en_US |
dc.subject.mesh | Time Factors | en_US |
dc.subject.mesh | Tyrosine 3-Monooxygenase - Metabolism | en_US |
dc.title | Time-course of neuropeptide changes in peri-ischemic zone and amygdala following focal ischemia in rats | en_US |
dc.type | Article | en_US |
dc.identifier.email | Cheung, RTF:rtcheung@hku.hk | en_US |
dc.identifier.authority | Cheung, RTF=rp00434 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1002/cne.903600108 | en_US |
dc.identifier.pmid | 7499557 | en_US |
dc.identifier.scopus | eid_2-s2.0-0028840333 | en_US |
dc.identifier.volume | 360 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.spage | 101 | en_US |
dc.identifier.epage | 120 | en_US |
dc.identifier.isi | WOS:A1995RT21200007 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Cheung, RTF=7202397498 | en_US |
dc.identifier.scopusauthorid | Diab, T=6603290337 | en_US |
dc.identifier.scopusauthorid | Cechetto, DF=7006226109 | en_US |
dc.identifier.issnl | 0021-9967 | - |