Abstract | OBJECTIVE: METHODS: Ninety adult male Wistar rats weighing 320-350 g were randomly divided into the following groups (n=5): (a) sham control group; (b) vehicle group, subjected to middle cerebral artery occlusion and received vehicle intraperitoneally; (c-e) baicalin groups, which were subjected to the middle cerebral artery occlusion and treated with baicalin 25, 50 and 100 mg/kg, respectively. The neurological scores were determined at postoperative 1, 3 and 7 d after the treatment. The expression of protease-activated receptor-1 (PAR-1), PAR-1 mRNA and Caspase-3 were determined using Western blot, reverse transcription polymerase chain reaction (RTPCR) analysis and immunohistochemistry, respectively. RESULTS: Significant decrease was noted in the neurological score in the baicalin group compared with that of the vehicle group (P<0.01). Additionally, down-regulation of PAR-1 mRNA, PAR-1 and Caspase-3 was observed in the baicalin groups compared with those obtained from the vehicle group (P<0.01). Compared with the low-dose baicalin group (25 mg/kg), remarkable decrease was noted in neurological score, and the expression of PAR-1 mRNA, PAR-1 as well as Caspase-3 in the high-dose group (P<0.05). CONCLUSION:
Baicalin showed neuro-protective effects in focal cerebral ischemic reperfusion injury through inhibiting the expression of PAR-1 and apoptosis.
|
Authors | Qing-bo Zhou, Cheng-zhu Duan, Qing Jia, Ping Liu, Lu-yang Li |
Journal | Chinese journal of integrative medicine
(Chin J Integr Med)
Vol. 20
Issue 2
Pg. 116-22
(Feb 2014)
ISSN: 1672-0415 [Print] China |
PMID | 23504578
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
- Flavonoids
- RNA, Messenger
- Receptor, PAR-1
- baicalin
- Caspase 3
|
Topics |
- Animals
- Apoptosis
(drug effects)
- Brain Ischemia
(complications, drug therapy, genetics, pathology)
- Caspase 3
(metabolism)
- Flavonoids
(administration & dosage, pharmacology, therapeutic use)
- Gene Expression Regulation
(drug effects)
- Male
- RNA, Messenger
(genetics, metabolism)
- Rats
- Rats, Wistar
- Receptor, PAR-1
(antagonists & inhibitors, genetics, metabolism)
- Reperfusion Injury
(complications, drug therapy, genetics, pathology)
|