gpi-5693 and Disease-Models--Animal

Excitotoxic glutamate release occurs in several neurological disorders. One source is derived from the hydrolysis of the neuropeptide N-acetyl aspartyl glutamate (NAAG) by glutamate carboxypeptidase II (GCPII, also known as NAALADase). Drugs that attenuate glutamate transmission have been shown to relieve neuropathic pain, however side effects have limited their clinical use. It appears that GCPII is exclusively recruited to provide a glutamate source in hyperglutamatergic, excitotoxic conditions and therefore would be devoid of such side effects. Here we report on the therapeutic effects of an orally bio-available GCP II inhibitor on established painful and sensory neuropathy in the spontaneously diabetic BB/Wor rat. It significantly improved hyperalgesia, nerve conduction velocity and underlying myelinated fiber atrophy. The data suggest that GCP II inhibition may provide a meaningful and effective approach to the treatment of painful diabetic neuropathy.

Topics: Analysis of Variance; Animals; Diabetic Neuropathies; Disease Models, Animal; Female; Glutamate Carboxypeptidase II; Glutarates; Male; Nerve Fibers, Myelinated; Neural Conduction; Pain; Pain Measurement; Rats; Rats, Inbred BB; Reaction Time; Sodium-Potassium-Exchanging ATPase; Sulfhydryl Compounds