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GAP-43 expression and pathological changes of temporal infarction in rats and effects of batroxobin.

AbstractUNLABELLED:
To study the changes of the expression of growth-associated protein-43 (GAP-43) and pathology in temporal infarction of rats photochemically induced and the effects of batroxobin.
METHODS:
Immunohistochemical technique and hematoxylin-eosin stain was used to show the changes of the expression of GAP-43 and pathology.
RESULTS:
In infarction group, GAP-43 expression was markedly increased on the infarction and surrounding tissues at 24 h cerebral infarction. The expression reached peak level at 72 h after cerebral infarction and was decreased at 7 d after cerebral infarction. However, in batroxobin-treated group, GAP-43 expression was increased and the pathological changes were much slight as compared with infarction group.
CONCLUSION:
The expression of GAP-43 increases in infarction of temporal neocortex and batroxobin promotes the expression of GAP-43 and ameliorates the pathological changes in infarction of temporal neocortex.
AuthorsWeiping Wu, Xingzhi Guan, Xiaoshu Zhang, Peigen Kuang
JournalJournal of traditional Chinese medicine = Chung i tsa chih ying wen pan (J Tradit Chin Med) Vol. 22 Issue 1 Pg. 42-6 (Mar 2002) ISSN: 0255-2922 [Print] China
PMID11977521 (Publication Type: Journal Article)
Chemical References
  • Fibrinolytic Agents
  • GAP-43 Protein
  • Batroxobin
Topics
  • Animals
  • Batroxobin (pharmacology)
  • Brain Infarction (metabolism, pathology)
  • Fibrinolytic Agents (pharmacology)
  • GAP-43 Protein (biosynthesis, genetics)
  • Male
  • Neocortex (pathology)
  • Random Allocation
  • Rats
  • Rats, Wistar
  • Temporal Lobe (pathology)

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