Carnosine is neuroprotective against permanent focal cerebral ischemia in mice.

Abstract

BACKGROUND AND PURPOSE:

Carnosine is a naturally occurring dipeptide with multiple neuroprotective properties. In addition, it is well tolerated in high doses with minimal side effects. The purposes of this study were to determine whether carnosine is neuroprotective in permanent focal cerebral ischemia and to determine potential mechanisms of neuroprotection.

METHODS:

We investigated the efficacy of carnosine in a mouse model of permanent focal cerebral ischemia. The effects of carnosine were investigated with respect to neuronal damage and infarct formation, endogenous antioxidant status, and matrix metalloproteinase activity.

RESULTS:

Carnosine significantly decreased infarct size and neuronal damage when administered at time points both before and after the induction of ischemia. Carnosine also decreased reactive oxygen species levels in the ischemic brain, preserved normal glutathione levels, and decreased matrix metalloproteinase protein levels and activity.

CONCLUSIONS:

Carnosine is neuroprotective in focal cerebral ischemia and appears to influence deleterious pathological processes that are activated after the onset of ischemia.

• Authors: G K Rajanikant, Daniel Zemke, Marie-Claude Senut, Mark B Frenkel, Alex F Chen, Rishi Gupta, Arshad Majid
• Journal: Stroke (Stroke) Vol. 38 Issue 11 Pg. 3023-31 (Nov 2007) ISSN: 1524-4628 [Electronic] United States
• PMID: 17916766 (Publication Type: Journal Article)

Chemical References

• Antioxidants
• Free Radical Scavengers
• Matrix Metalloproteinase Inhibitors
• Neuroprotective Agents
• Reactive Oxygen Species
• Carnosine
• Matrix Metalloproteinases
• Glutathione

Topics

• Animals
• Antioxidants (pharmacology, therapeutic use)
• Brain (drug effects, pathology, physiopathology)
• Brain Ischemia (drug therapy, metabolism, physiopathology)
• Carnosine (metabolism, pharmacology, therapeutic use)
• Cell Death (drug effects, physiology)
• Cerebral Infarction (drug therapy, physiopathology, prevention & control)
• Cerebrovascular Circulation (drug effects, physiology)
• Disease Models, Animal
• Dose-Response Relationship, Drug
• Enzyme Activation (drug effects, physiology)
• Free Radical Scavengers (pharmacology, therapeutic use)
• Glutathione (agonists, metabolism)
• Infarction, Middle Cerebral Artery (drug therapy, metabolism, physiopathology)
• Male
• Matrix Metalloproteinase Inhibitors
• Matrix Metalloproteinases (metabolism)
• Mice
• Mice, Inbred C57BL
• Nerve Degeneration (drug therapy, physiopathology, prevention & control)
• Neuroprotective Agents (pharmacology, therapeutic use)
• Oxidative Stress (drug effects, physiology)
• Reactive Oxygen Species (antagonists & inhibitors, metabolism)
• Treatment Outcome