Behavioral methods used in the study of long-chain polyunsaturated fatty acid nutrition in primate infants

Authors
Citation
Se. Carlson, Behavioral methods used in the study of long-chain polyunsaturated fatty acid nutrition in primate infants, AM J CLIN N, 71(1), 2000, pp. 268S-274S
Citations number
45
Categorie Soggetti
Endocrynology, Metabolism & Nutrition","Endocrinology, Nutrition & Metabolism
Journal title
AMERICAN JOURNAL OF CLINICAL NUTRITION
ISSN journal
00029165 → ACNP
Volume
71
Issue
1
Year of publication
2000
Supplement
S
Pages
268S - 274S
Database
ISI
SICI code
0002-9165(200001)71:1<268S:BMUITS>2.0.ZU;2-3
Abstract
Domains of behavior may be broadly categorized as sensory, motor, motivatio nal and arousal, cognitive, and social. Differences in these domains occur because of changes in brain structure and function. Docosahexaenoic acid (D HA; 22:6-23) and arachidonic acid (AA; 20:4-26) are major structural compon ents of the brain that decrease when diets deficient in the essential fatty acids (EFA) alpha-linolenic acid and linoleic acid are consumed. Early ele ctrophysiologic and behavioral studies in EFA-deficient rodents showed beha vioral effects attributable to lower-than-normal accumulation of DKA and AA in the brain. More recently, electrophysiologic and behavioral studies in EFA-deficient primate infants and analogous studies in human infants have b een conducted. The human infants were fed formulas that could result in low er-than-optimal accumulation of long-chain polyunsaturated fatty acids (LCP UFAs) in the brain during critical periods of development. This article des cribes the behavioral methods that have been used to study primate infants. These methods may be unfamiliar to many physicians and nutritionists who w ish to read and interpret the human studies. The behavioral outcomes that h ave been evaluated in LCPUFA studies represent only a fraction of those ava ilable in the behavioral sciences. Specific developmental domains have been studied less often than global development, even though studies of nonhuma n primates deficient in EFAs suggest that the former provide more informati on that could help target the underlying mechanisms of action of LCPUFAs in the brain.