This project will assess the basic neurochemical changes which accompany normal pregnancy. It has been known for many years that there is a marked reduction in the levels of vitamin B6 in the blood of pregnant women, and that in the pathologic pregnancies preeclampsia and eclampsia, this deficit is even greater. The significance of this observation is that vitamin B6 deficiency is known to be a predisposing factor for the development of seizures, and eclampsia is characterized by generalized seizures which are life-threatening to mother and fetus alike. Vitamin B6 is required for synthesis and degradation of several neurotransmitters including norepinephrine, dopamine, serotonin and Gamma-aminobutyric acid. During vitamin B6 deficiency there is, presumably, an alteration in the functioning of these neurotransmitter pathways, and it is this which results in predisposition to seizures. An enzyme which is induced in the livers of pregnant mice, Pi-aldehyde dehydrogenase (Pi-A1DH), is capable of metabolizing a form of vitamin B6, pyridoxal. It is likely that the development of seizures in pregnancy (eclampsia) is due partly to increased metabolism of vitamin B6 by Pi-A1DH. The experiments in this proposal are designed to test this hypothesis. Levels and turnover rates of the neurotransmitters (above) will be studied in regions of mouse brain during pregnancy. Blood levels of vitamin B6 will be followed and efforts will be made to relieve the deficiency of vitamin B6 by dietary supplementation with at least two forms of the vitamin. Lastly, attempts will be made to inhibit Pi-A1DH in vivo in an effort to halt the excessive metabolism of vitamin B6, and restore neuronal function and seizure susceptibility to normal. The incidence of preeclampsia and eclampsia have remained constant in pregnancy, and approximately 4% are affected to some degree. Eclampsia remains a major cause of maternal and neonatal morbidity and mortality. Since the cause of the disease is unknown, treatment is symptomatic, and methods of prevention are unknown. These studies should reveal the nature of the neurochemical changes which precede eclampsia and allow for a rational approach to the prevention of eclampsia.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS020748-03
Application #
3401311
Study Section
Neurology A Study Section (NEUA)
Project Start
1984-04-01
Project End
1988-03-31
Budget Start
1986-04-01
Budget End
1988-03-31
Support Year
3
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Colorado at Boulder
Department
Type
Graduate Schools
DUNS #
City
Boulder
State
CO
Country
United States
Zip Code
80309
Smolen, A; Smolen, T N (1989) Reproducibility of ethanol elimination rates in long-sleep and short-sleep mice. J Stud Alcohol 50:519-24
Smolen, T N; Smolen, A (1989) Blood and brain ethanol concentrations during absorption and distribution in long-sleep and short-sleep mice. Alcohol 6:33-8
Furth-Walker, D; Leibman, D; Smolen, A (1989) Changes in pyridoxal phosphate and pyridoxamine phosphate in blood, liver and brain in the pregnant mouse. J Nutr 119:750-6
Smolen, A; Smolen, T N; van de Kamp, J L (1987) Sensitivity of inbred and selectively bred mice to ethanol. Alcohol 4:57-62
Smolen, A; Smolen, T N; van de Kamp, J L (1987) Alterations in brain catecholamines during pregnancy. Pharmacol Biochem Behav 26:613-8
Wehner, J M; Murphy-Erdosh, C; Smolen, A et al. (1987) Genetic variation in paraoxonase activity and sensitivity to diisopropylphosphofluoridate in inbred mice. Pharmacol Biochem Behav 28:317-20
Smolen, A; Smolen, T N (1987) Demonstration of a threshold concentration for ethanol at the time of regaining the righting response in long-sleep and short-sleep mice. Alcohol Drug Res 7:279-83
Smolen, A; Smolen, T N; van de Kamp, J L (1986) The effect of naloxone administration on pregnancy-associated seizures. Life Sci 38:1899-905
Smolen, A; Smolen, T N (1986) Genetic influence on increased seizure susceptibility in pregnancy. Life Sci 39:1525-30