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Protective effect of pharmacological preconditioning of total flavones of abelmoschl manihot on cerebral ischemic reperfusion injury in rats.

Abstract
The present study was to investigate the effect of pharmacological preconditioning of total flavones of abelmoschl manihot (TFA) on cerebral ischemic reperfusion injury in rats. Rat cerebral ischemia/reperfusion injury was induced by occluding the right middle cerebral artery (MCA). The infarct size was determined by staining with 2,3,5-triphenyl tetrazalium chloride (TTC). The serum malonaldehyde (MDA), nitric oxide (NO) and lactate dehydrogenase (LDH) levels were measured by using spectrophotometry; Inducible NO synthase (iNOS) mRNA expression was detected by RT-PCR method. The percentage of cerebral infarction volume was 28.1 +/- 0.8 in the model group, while TFA or nimodipine (Nim) pretreatment 36 hours prior to the ischemic insult significantly decreased the infarction volume. Increases of serum LDH activity and MDA level were observed after ischemia/reperfusion, but these changes were inhibited in rats pretreated with either TFA (20, 40, 80, 160 mg/kg) or Nim, indicating a delayed protective effect of TFA preconditioning on cerebral ischemic reperfusion injury. In addition, the serum NO level and the cerebral iNOS mRNA were up-regulated, suggesting a possible mechanism for the protective effect of TFA pretreatment on cerebral ischemic reperfusion injury.
AuthorsJi-Yue Wen, Zhi-Wu Chen
JournalThe American journal of Chinese medicine (Am J Chin Med) Vol. 35 Issue 4 Pg. 653-61 ( 2007) ISSN: 0192-415X [Print] Singapore
PMID17708631 (Publication Type: Journal Article)
Chemical References
  • Drugs, Chinese Herbal
  • Flavones
  • RNA, Messenger
  • Nitric Oxide
  • Malondialdehyde
  • L-Lactate Dehydrogenase
  • Nitric Oxide Synthase Type II
Topics
  • Abelmoschus
  • Animals
  • Brain Ischemia (prevention & control)
  • Cerebral Infarction (metabolism, pathology)
  • Disease Models, Animal
  • Drugs, Chinese Herbal (therapeutic use)
  • Female
  • Flavones (therapeutic use)
  • Ischemic Preconditioning (methods)
  • L-Lactate Dehydrogenase (blood)
  • Lipid Peroxidation (drug effects)
  • Male
  • Malondialdehyde (blood)
  • Nitric Oxide (blood)
  • Nitric Oxide Synthase Type II (metabolism)
  • RNA, Messenger (metabolism)
  • Rats
  • Reperfusion Injury (prevention & control)

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