Effect of Theophylline and Trimethobenzamide When Given During Kainate-Induced Status Epilepticus: An Improved Histopathologic Rat Model of Human Hippocampal Sclerosis
Article first published online: 2 AUG 2005
Volume 41, Issue 11, pages 1390–1399, November 2000
How to Cite
Katzir, H., Mendoza, D. and Mathern, G. W. (2000), Effect of Theophylline and Trimethobenzamide When Given During Kainate-Induced Status Epilepticus: An Improved Histopathologic Rat Model of Human Hippocampal Sclerosis. Epilepsia, 41: 1390–1399. doi: 10.1111/j.1528-1157.2000.tb00114.x
- Issue published online: 2 AUG 2005
- Article first published online: 2 AUG 2005
- Accepted June 23, 2000
- Blood flow;
Summary: Purpose: The most common pathology in temporal lobe epilepsy (TLE) is hippocampal sclerosis. It is controversial whether status epilepticus (SE) or prolonged seizures plus secondary cerebral injuries are pathogenic mechanisms of hippocampal sclerosis. This study addressed this question in rat models of TLE.
Methods: Hippocampal neuron densities and supragranular mossy fiber sprouting were determined in adult rats subjected to systemic kainate-induced SE (KA-only) and KA-induced SE followed 75 minutes later by theophylline (KA/Theo) or trimethobenzamide (KA/Tri). These drugs probably decrease seizure-induced cerebral hyperemia or hypertension.
Results: Compared with controls and KA-only rats, KA/Tri and KA/Theo rats showed decreased CA3b and CA1 neuron densities (i.e., greater Sommer's sector injury). In addition, KA/Tri rats showed that increased trimethobenzamide dosages were associated with decreased hilar, CA3c, CA3b, CA1, and subiculum neuron densities. There were no significant differences in supragranular mossy fiber sprouting between KA-only, KA/Tri, and KA/Theo rats.
Conclusions: Pharmacologic manipulations during KA-induced SE are associated with differences in hippocampal pathology, especially in Sommer's sector, and the final pattern of damage and axon sprouting shows histopathologic similarities to that in patients with hippocampal sclerosis. Our findings support the hypothesis that secondary physiologic insults during SE that are likely to decrease seizure-induced cerebral hyperemia and hypertension may generate greater hippocampal neuronal injury compared with SE alone, and this may be a pathogenic mechanism of human hippocampal sclerosis in patients with TLE.