Mesial temporal lobe epilepsy (MTLE), the most common form of partial epilepsy, affects the majority of patients with uncontrolled seizures. Seizures do not strike randomly but occur in daily patterns. Studies have shown that seizures can cluster at sleep-wake transitions or occur in diurnal or nocturnal patterns. Possible influences on the timing of seizures include the sleep-wake state, exogenous cycles such as the light- dark cycle, or endogenous rhythms of the biological clock. Because of the difficulty in testing these influences in humans, possible mechanisms have not been compared under rigorous conditions. The distinctions among these cycles is important because of their different physiology and potential effects on the timing of seizures. Understanding the temporal influences on seizure occurrences is a critical step in determining the factors that permit expression of seizures. This proposal examines the temporal distribution of spontaneous, limbic seizures in an animal model of partial epilepsy that shares clinical, electrographic, and histological similarities with human MTLE. Preliminary results show that limbic seizures occur non-randomly in a daily rhythm similar to that found in MTLE. In this study we will examine the role of endogenous circadian rhythms, measured by markers of motor activity and body temperature, on seizure timing. We will test these hypothesis. 1) Limbic seizures and the epileptic state alter circadian rhythms. 2) The distribution of limbic seizures is tied to phases of the sleep-wake state. 3) Limbic seizure occurrence is influenced occurrence is influenced by endogenous, circadian rhythms. In summary, the results will determine the chronobiological factors that facilitate partial seizure expression and may provide new perspectives into treatments for poorly controlled epilepsy.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08NS002021-03
Application #
2891460
Study Section
NST-2 Subcommittee (NST)
Program Officer
Jacobs, Margaret
Project Start
1997-09-30
Project End
2000-08-31
Budget Start
1999-09-01
Budget End
2000-08-31
Support Year
3
Fiscal Year
1999
Total Cost
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