Protective effects of phenolic alkaloids from Menispermum dauricum on inflammatory injury following focal cerebral ischemia-reperfusion in rats.
- Author:
Xiao-juan ZHANG
1
;
Lian-jun GUO
;
Ling QU
;
Qing LÜ
Author Information
- Publication Type:Journal Article
- MeSH: Alkaloids; isolation & purification; pharmacology; Animals; Anti-Inflammatory Agents, Non-Steroidal; pharmacology; Benzylisoquinolines; isolation & purification; pharmacology; Brain Ischemia; complications; metabolism; Cell Adhesion; drug effects; Cerebral Cortex; metabolism; Female; Hippocampus; metabolism; Intercellular Adhesion Molecule-1; metabolism; Leukocytes; pathology; Male; Menispermum; chemistry; Neuroprotective Agents; pharmacology; Neutrophil Infiltration; drug effects; Nitric Oxide; metabolism; Peroxidase; metabolism; Plants, Medicinal; chemistry; Rats; Rats, Wistar; Reperfusion Injury; etiology; metabolism; pathology; Tetrahydroisoquinolines; isolation & purification; pharmacology
- From: Acta Pharmaceutica Sinica 2004;39(8):661-665
- CountryChina
- Language:Chinese
-
Abstract:
AIMTo study the protective effects of phenolic alkaloids from Menispermum dauricum (PAMd) on inflammatory injury following focal cerebral ischemia-reperfusion in rats.
METHODSThe right middle cerebral artery of the rat was occluded by inserting a nylon suture through the internal carotid artery for 2 h, followed by reperfusion by withdrawing the suture. The expression of intercellular adhesion molecule-1 (ICAM-1) was observed by immunohistochemistry staining. The adhesiveness and infiltration of leucocytes were observed by HE staining. The activity of myeloperoxidase (MPO) and the content of nitric oxide (NO) in the cortex and hippocampus were measured.
RESULTSPAMd was shown to markedly inhibit ICAM-1 expression, alleviate the adhesiveness and infiltration of leucocytes, and decrease the MPO activity and the NO content in ischemic cortex and hippocampus.
CONCLUSIONPAMd has protective effects on inflammatory injury following focal cerebral ischemia-reperfusion by inhibiting ICAM-1 expression, alleviating the adhesiveness and infiltration of leucocytes and decreasing the generation of NO.
