Mesial temporal lobe epilepsy (MTLE), the most common partial epilepsy, accounts for the majority of patients with uncontrolled seizures. Seizures in MTLE do not strike randomly but occur in daily patterns. Possible influences on the timing of seizures include those factors that underlie circadian oscillation and that facilitate or inhibit seizures. Influences provided by the hypothalamicpituitaryadrenal axis (HPAA) are logical candidates to modulate seizures and will be the focus of the proposed experiments. This proposal examines the temporal distribution of spontaneous, limbic seizures in a unique animal model of partial epileps~ that shares clinical, electrographic, histological, and timing similarities with MTLE.
The specific aim of this proposal is to evaluate the role of endogenous rhythmicity of the HPAA in the circadian modulation of experimental limbic epilepsy. Hypothesis 1. Rhythmicity of the HPAA is intact in experimental epilepsy. Hypothesis 2. Corticosterone releasing hormone (CRH) is differentially affected within the hypothalamus and limbic system by lesions at different levels of the clockHPAA system. Our data suggests that circadian mechanisms continue to function in the epileptic rat and that neuronal density in regions important in HPAA regulation is normal. We will evaluate whether CRH expression remains rhythmic in intact animals as well as in animals that have lesions of the clock or of the HPAA. Hypothesis 3. The normal variations of CRH and corticosterone are necessary for circadian recurrence of limbic seizures. We predict that alterations of inputs into the HPAA will cause changes in the circadian distribution of seizures. Previous results show that seizures occur in an endogenously mediated circadian rhythm.. In summary, these studies will provide insight into the chronoblological factors that facilitate partial seizure expression and may provide new perspectives into treatments for poorly controlled partial epilepsy.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Clinical Investigator Award (CIA) (K08)
Project #
2K08NS002021-04
Application #
6341405
Study Section
NST-2 Subcommittee (NST)
Program Officer
Jacobs, Margaret
Project Start
1997-09-30
Project End
2003-05-31
Budget Start
2001-06-15
Budget End
2002-05-31
Support Year
4
Fiscal Year
2001
Total Cost
$127,845
Indirect Cost
Name
University of Virginia
Department
Neurology
Type
Schools of Medicine
DUNS #
001910777
City
Charlottesville
State
VA
Country
United States
Zip Code
22904
Quigg, Mark; Kiely, James M; Johnson, Michael L et al. (2006) Interictal and postictal circadian and ultradian luteinizing hormone secretion in men with temporal lobe epilepsy. Epilepsia 47:1452-9
Quigg, Mark; Taft, William (2004) Stroboscopic artifact in digital video-EEG. J Clin Neurophysiol 21:96-8
Quigg, Mark; Broshek, Donna K; Heidal-Schiltz, Susan et al. (2003) Depression in intractable partial epilepsy varies by laterality of focus and surgery. Epilepsia 44:419-24
Quigg, Mark; Kiely, James M; Shneker, Bassel et al. (2002) Interictal and postictal alterations of pulsatile secretions of luteinizing hormone in temporal lobe epilepsy in men. Ann Neurol 51:559-66
Quigg, M; Straume, M; Smith, T et al. (2001) Seizures induce phase shifts of rat circadian rhythms. Brain Res 913:165-9
Quigg, M (2000) Circadian rhythms: interactions with seizures and epilepsy. Epilepsy Res 42:43-55
Quigg, M; Clayburn, H; Straume, M et al. (2000) Effects of circadian regulation and rest-activity state on spontaneous seizures in a rat model of limbic epilepsy. Epilepsia 41:502-9
Frucht, M M; Quigg, M; Schwaner, C et al. (2000) Distribution of seizure precipitants among epilepsy syndromes. Epilepsia 41:1534-9
Quigg, M; Straume, M (2000) Dual epileptic foci in a single patient express distinct temporal patterns dependent on limbic versus nonlimbic brain location. Ann Neurol 48:117-20
Quigg, M; Clayburn, H; Straume, M et al. (1999) Hypothalamic neuronal loss and altered circadian rhythm of temperature in a rat model of mesial temporal lobe epilepsy. Epilepsia 40:1688-96