humulene and Brain-Edema

Excitotoxicity is a paradigm used to explain the biochemical events in both acute neuronal damage and in slowly progressive, neurodegenerative diseases. Here, we show in a longitudinal magnetic resonance imaging study that Delta(9)-tetrahydrocannabinol (Delta(9)-THC), the main active compound in marijuana, reduces neuronal injury in neonatal rats injected intracerebrally with the Na(+)/K(+)-ATPase inhibitor ouabain to elicit excitotoxicity. In the acute phase Delta(9)-THC reduced the volume of cytotoxic edema by 22%. After 7 d, 36% less neuronal damage was observed in treated rats compared with control animals. Coadministration of the CB(1) cannabinoid receptor antagonist SR141716 prevented the neuroprotective actions of Delta(9)-THC, indicating that Delta(9)-THC afforded protection to neurons via the CB(1) receptor. In Delta(9)-THC-treated rats the volume of astrogliotic tissue was 36% smaller. The CB(1) receptor antagonist did not block this effect. These results provide evidence that the cannabinoid system can serve to protect the brain against neurodegeneration.

Topics: Acute Disease; Animals; Animals, Newborn; Brain; Brain Edema; Cannabis; Chronic Disease; Corpus Striatum; Dose-Response Relationship, Drug; Dronabinol; Enzyme Inhibitors; Longitudinal Studies; Magnetic Resonance Imaging; Microinjections; Neuroprotective Agents; Ouabain; Rats; Rats, Wistar; Receptors, Cannabinoid; Receptors, Drug; Sodium-Potassium-Exchanging ATPase; Water