Unidirectional Cross‐tolerance from Levetiracetam to Carbamazepine in Amygdala‐kindled Seizures

• Published in: Epilepsia (Copenhagen) 2003-12, Vol.44 (12), p.1487-1493
• Main Authors: Zhang, Zhang‐Jin, Xing, Guo‐Qiang, Russell, Shani, Obeng, Kris, Post, Robert M.
• Format: Article
• Language: English
• Subjects: Amygdala - drug effects; Animals; Anticonvulsants - pharmacology; Biological and medical sciences; Carbamazepine; Carbamazepine - pharmacology; Cross‐tolerance; Drug Tolerance; Electroencephalography - drug effects; Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy; Injections, Intraperitoneal; Kindling; Kindling, Neurologic - drug effects; Levetiracetam; Long-Term Care; Male; Medical sciences; Nervous system (semeiology, syndromes); Neurology; Piracetam - analogs & derivatives; Piracetam - pharmacology; Rat; Rats; Rats, Sprague-Dawley
• ISSN: 0013-9580; 1528-1167
• DOI: 10.1111/j.0013-9580.2003.34803.x

Purpose: Tolerance is a potential problem in long‐term anticonvulsant therapy of epilepsy, bipolar disorder, and neuropathic pain. The present study was designed to determine whether cross‐tolerance occurs between levetiracetam (LEV) and carbamazepine (CBZ) in amygdala‐kindled rats. Methods: Male Sprague–Dawley rats were implanted with an electrode into the left amygdala. While kindling stimulation was started, animals received repeated treatment (i.p.) with saline (n = 7) or LEV (150 mg/kg, n = 8). Saline‐injected rats were subsequently challenged with a single dose of 150 mg/kg LEV when full kindling developed (stage ≥4). Both groups of rats were then administered long‐term CBZ (5 mg/kg) until rats developed complete tolerance. All CBZ‐tolerant rats were subsequently reexposed to LEV (150 mg/kg) for an additional 10 consecutive days. Results: Repeated LEV treatment significantly suppressed the increase in seizure stage, seizure duration, and afterdischarge duration induced by amygdala stimulation, markedly increasing the number of stimulations to achieve a kindling major motor seizure. The LEV challenge produced a more robust suppression of seizure stage in saline‐injected rats compared with LEV‐treated animals. CBZ treatment markedly suppressed fully kindled seizures in rats initially injected with saline, and then anticonvulsant tolerance rapidly developed after 3–4 days of repeated treatment. In contrast, rats that had initially received repeated LEV treatment did not show a response to treatment with CBZ (5 mg/kg). When CBZ‐tolerant rats were subsequently exposed to LEV (150 mg/kg), noticeable anticonvulsant effects were observed; but these were gradually lost with increasing numbers of LEV exposures. Conclusions: Whereas LEV shows potent antiepileptogenic and anticonvulsant effects in amygdala‐kindled rats, its repeated treatment induces anticonvulsant tolerance and unidirectional cross‐tolerance to CBZ. In contrast, anticonvulsant tolerance to CBZ does not transfer to LEV. The mechanistic implications of the present results for clinical therapeutics remain to be evaluated.