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Article: Administration of melatonin after onset of ischemia reduces the volume of cerebral infarction in a rat middle cerebral artery occlusion stroke model
Title | Administration of melatonin after onset of ischemia reduces the volume of cerebral infarction in a rat middle cerebral artery occlusion stroke model |
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Authors | |
Keywords | Melatonin Middle cerebral artery occlusion Neuroprotection Rats Stroke, experimental |
Issue Date | 2003 |
Publisher | Lippincott Williams & Wilkins. The Journal's web site is located at http://stroke.ahajournals.org |
Citation | Stroke, 2003, v. 34 n. 3, p. 770-775 How to Cite? |
Abstract | Background and Purpose - In both permanent and transient 3-hour middle cerebral artery occlusion rat stroke models, a single intraperitoneal injection of melatonin at 5 or 15 mg/kg given before ischemia was shown to reduce infarct volume at 72 hours. The present study was conducted to examine the treatment time window when melatonin was commenced after onset of ischemia. Methods - Adult male Sprague-Dawley rats were anesthetized to undergo right-sided middle cerebral artery occlusion for 3 hours. A single intraperitoneal injection of vehicle or melatonin at 5 mg/kg was given at 0, 1, or 3 hours after onset of ischemia. Other groups received multiple injections of vehicle or melatonin at 5 mg/kg with the first injection given at 1, 2, or 3 hours after onset of ischemia and the second and third injections at 24 and 48 hours, respectively. Multiple injections of melatonin at 15 mg/kg with the first injection given at 3 hours were also made. The infarct volume was determined at 72 hours. Results - A single dose of melatonin at 5 mg/kg given at 0 or 1 but not 3 hours after onset of ischemia reduced the infarct volume. Multiple doses of melatonin at 5 mg/kg also reduced the infarct volume when the first dose was given at 1 or 2 but not 3 hours after onset. Significant hemodynamic effects were not observed. Conclusions - Our results indicate that melatonin at 5 mg/kg given as a single injection or multiple injections protects against focal cerebral ischemia when commenced within 2 hours of onset. |
Persistent Identifier | http://hdl.handle.net/10722/77538 |
ISSN | 2023 Impact Factor: 7.8 2023 SCImago Journal Rankings: 2.450 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Pei, Z | en_HK |
dc.contributor.author | Pang, SF | en_HK |
dc.contributor.author | Cheung, RTF | en_HK |
dc.date.accessioned | 2010-09-06T07:32:59Z | - |
dc.date.available | 2010-09-06T07:32:59Z | - |
dc.date.issued | 2003 | en_HK |
dc.identifier.citation | Stroke, 2003, v. 34 n. 3, p. 770-775 | en_HK |
dc.identifier.issn | 0039-2499 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/77538 | - |
dc.description.abstract | Background and Purpose - In both permanent and transient 3-hour middle cerebral artery occlusion rat stroke models, a single intraperitoneal injection of melatonin at 5 or 15 mg/kg given before ischemia was shown to reduce infarct volume at 72 hours. The present study was conducted to examine the treatment time window when melatonin was commenced after onset of ischemia. Methods - Adult male Sprague-Dawley rats were anesthetized to undergo right-sided middle cerebral artery occlusion for 3 hours. A single intraperitoneal injection of vehicle or melatonin at 5 mg/kg was given at 0, 1, or 3 hours after onset of ischemia. Other groups received multiple injections of vehicle or melatonin at 5 mg/kg with the first injection given at 1, 2, or 3 hours after onset of ischemia and the second and third injections at 24 and 48 hours, respectively. Multiple injections of melatonin at 15 mg/kg with the first injection given at 3 hours were also made. The infarct volume was determined at 72 hours. Results - A single dose of melatonin at 5 mg/kg given at 0 or 1 but not 3 hours after onset of ischemia reduced the infarct volume. Multiple doses of melatonin at 5 mg/kg also reduced the infarct volume when the first dose was given at 1 or 2 but not 3 hours after onset. Significant hemodynamic effects were not observed. Conclusions - Our results indicate that melatonin at 5 mg/kg given as a single injection or multiple injections protects against focal cerebral ischemia when commenced within 2 hours of onset. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Lippincott Williams & Wilkins. The Journal's web site is located at http://stroke.ahajournals.org | en_HK |
dc.relation.ispartof | Stroke | en_HK |
dc.rights | Stroke. Copyright © Lippincott Williams & Wilkins. | en_HK |
dc.subject | Melatonin | - |
dc.subject | Middle cerebral artery occlusion | - |
dc.subject | Neuroprotection | - |
dc.subject | Rats | - |
dc.subject | Stroke, experimental | - |
dc.subject.mesh | Animals | en_HK |
dc.subject.mesh | Brain Edema - pathology | en_HK |
dc.subject.mesh | Cerebral Infarction - etiology - pathology - prevention & control | en_HK |
dc.subject.mesh | Disease Models, Animal | en_HK |
dc.subject.mesh | Dose-Response Relationship, Drug | en_HK |
dc.subject.mesh | Infarction, Middle Cerebral Artery - complications - drug therapy - pathology | en_HK |
dc.subject.mesh | Injections, Intraperitoneal | en_HK |
dc.subject.mesh | Ischemic Attack, Transient - complications - drug therapy - pathology | en_HK |
dc.subject.mesh | Male | en_HK |
dc.subject.mesh | Melatonin - pharmacology | en_HK |
dc.subject.mesh | Neuroprotective Agents - pharmacology | en_HK |
dc.subject.mesh | Rats | en_HK |
dc.subject.mesh | Rats, Sprague-Dawley | en_HK |
dc.subject.mesh | Reperfusion | en_HK |
dc.subject.mesh | Time Factors | en_HK |
dc.title | Administration of melatonin after onset of ischemia reduces the volume of cerebral infarction in a rat middle cerebral artery occlusion stroke model | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0039-2499&volume=34&spage=770&epage=775&date=2003&atitle=Administration+of+melatonin+after+onset+of+ischemia+reduces+the+volume+of+cerebral+infarction+in+a+rat+middle+cerebral+artery+occlusion+stroke+model | en_HK |
dc.identifier.email | Cheung, RTF:rtcheung@hku.hk | en_HK |
dc.identifier.authority | Cheung, RTF=rp00434 | en_HK |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1161/01.STR.0000057460.14810.3E | en_HK |
dc.identifier.pmid | 12624306 | - |
dc.identifier.scopus | eid_2-s2.0-0037335690 | en_HK |
dc.identifier.hkuros | 87549 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0037335690&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 34 | en_HK |
dc.identifier.issue | 3 | en_HK |
dc.identifier.spage | 770 | en_HK |
dc.identifier.epage | 775 | en_HK |
dc.identifier.isi | WOS:000181466700041 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Pei, Z=23051646800 | en_HK |
dc.identifier.scopusauthorid | Pang, SF=7402528719 | en_HK |
dc.identifier.scopusauthorid | Cheung, RTF=7202397498 | en_HK |
dc.identifier.issnl | 0039-2499 | - |