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d-galactose administration induces memory loss and energy metabolism disturbance in mice: protective effects of catalpol.

Abstract
The neuroprotective effects of catalpol, an iridoid glycoside isolated from the fresh rehmannia roots, on the behavior and brain energy metabolism in senescent mice induced by d-galactose were assessed. Except control group, mice were subcutaneously injected with d-galactose (150 mg/kg body weight) for 6 weeks. From the fifth week, drug group mice were treated with catalpol (2.5, 5, 10 mg/kg body weight) and piracetam (300 mg/kg body weight) for the last 2 weeks. Behavioral changes including open field test and passive avoidance were examined after drug administration. To determine the brain damage, pathological alterations were measured by hematoxylin and eosin (HE) staining. The activities of lactate dehydrogenase (LDH), glutathione S-transferase (GSH-ST), glutamine synthetase (GS), creatine kinase (CK) in brain cortex and hippocampus were determined using different biochemical methods. Consistent with the cognition deficits, the activities of GSH-ST, GS and CK decreased while the activity of LDH increased in aging mice brain. Administration of catalpol for 2-weeks not only ameliorated cognition deficit, but also reversed the biochemical markers mentioned above and reduced the histological lesions in mouse brain. These results suggest that catalpol has protective effects on memory damage and energy metabolism failure in aging model mice and is worth testing for further preclinical study aimed for senescence or neurodegenerative diseases such as Alzheimer's disease (AD) and Parkinson's disease (PD).
AuthorsXiu-Li Zhang, Li-Jia An, Yong-Ming Bao, Jing-Yun Wang, Bo Jiang
JournalFood and chemical toxicology : an international journal published for the British Industrial Biological Research Association (Food Chem Toxicol) Vol. 46 Issue 8 Pg. 2888-94 (Aug 2008) ISSN: 0278-6915 [Print] England
PMID18573305 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Glucosides
  • Indicators and Reagents
  • Iridoid Glucosides
  • Iridoids
  • catalpol
  • L-Lactate Dehydrogenase
  • Glutathione Transferase
  • Creatine Kinase
  • Glutathione
  • Galactose
Topics
  • Aging (physiology, psychology)
  • Animals
  • Avoidance Learning (drug effects)
  • Brain (pathology)
  • Brain Chemistry (drug effects)
  • Cerebral Cortex (drug effects, metabolism)
  • Cognition (drug effects)
  • Creatine Kinase (metabolism)
  • Energy Metabolism (drug effects)
  • Female
  • Galactose (antagonists & inhibitors, toxicity)
  • Glucosides (pharmacology)
  • Glutathione (metabolism)
  • Glutathione Transferase (metabolism)
  • Hippocampus (drug effects, metabolism)
  • Indicators and Reagents
  • Iridoid Glucosides
  • Iridoids (pharmacology)
  • L-Lactate Dehydrogenase (metabolism)
  • Male
  • Memory Disorders (chemically induced, psychology)
  • Mice
  • Motor Activity (drug effects)
  • Plant Roots (chemistry)
  • Rehmannia (chemistry)

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